Details about the neuroanatomical projections from ILA to Br

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Report IDSending structure Receiving structureProjection strengthTechniqueGeneral description projectionCollatorAssociated reference
2796 Infralimbic areaLateral hypothalamic area lightHRP/WGA
Case pg267, fig12. Soma notes not specified.. Terminal notes WGA-HRP inj.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
2797 Infralimbic areaSupramammillary nucleus lightPHAL
Case pg261. Soma notes 9 Injs centred in ILC?In expt R652 (fig2B) in which dorsal peduncular cortex & tenia tecta were excluded from inj site
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
2798 Infralimbic areaEndopiriform nucleus very lightHRP/WGA
Case pg264. Soma notes previous injections were fibres of passage. Terminal notes WGA-HRP inj.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70515 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70516 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70517 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70518 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70519 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70520 Infralimbic areaPrelimbic area moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70521 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70522 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70523 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70524 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70525 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70526 Infralimbic areaAnterior cingulate area dorsal part moderatePHAL
The dorsal efferent pathway from the ILC innervated mainly layers I, V, and VI of the prelimbic and anterior cingulate cortices (Fig. 3A). Finely arborized axons and boutons were found throughout these regions. Collator note: Fig 3A corresponds to Atlas Level 14, Swanson 2004 Atlas. Collator note: we consider here a combinatorial approach, since there is no additional information about the layer specificity of connections.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70527 Infralimbic areaPiriform area moderate/strongPHAL
The piriform cortex received innervation via both the lateral and ventral pathways (see Fig. 3A-D). Labelled fibers were observed throughout the rostral piriform cortex. primarily in the molecular and polymorph layers. Fibers in the molecular layer demonstrated varicosities along their lengths, whereas labelled fibers in the polymorph layers only occasionally exhibited swellings. At rostral levels, the dorsolateral portion of the piriform cortex demonstrated a slightly heavier innervation as compared to other parts of the piriform cortex. These fibers apparently arose from the lateral efferent pathway. By the level of the septum and proceeding further caudally, the density of innervation in the piriform cortex began to shift ventrally and arose primarily from the ventral efferent pathway. The majority of labelled fibers formed a dense plexus within the molecular layer. Some labelled fibers pierced the pyramidal layer perpendicular to the pial surface and entered the polymorph cell layer. Collator note: molecular layer, considered as a separate record.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70528 Infralimbic areaPiriform area moderate/strongPHAL
The piriform cortex received innervation via both the lateral and ventral pathways (see Fig. 3A-D). Labelled fibers were observed throughout the rostral piriform cortex. primarily in the molecular and polymorph layers. Fibers in the molecular layer demonstrated varicosities along their lengths, whereas labelled fibers in the polymorph layers only occasionally exhibited swellings. At rostral levels, the dorsolateral portion of the piriform cortex demonstrated a slightly heavier innervation as compared to other parts of the piriform cortex. These fibers apparently arose from the lateral efferent pathway. By the level of the septum and proceeding further caudally, the density of innervation in the piriform cortex began to shift ventrally and arose primarily from the ventral efferent pathway. The majority of labelled fibers formed a dense plexus within the molecular layer. Some labelled fibers pierced the pyramidal layer perpendicular to the pial surface and entered the polymorph cell layer. Collator note: polymorph layer, considered as a separate record.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70529 Infralimbic areaPiriform area strongPHAL
The piriform cortex received innervation via both the lateral and ventral pathways (see Fig. 3A-D). Labelled fibers were observed throughout the rostral piriform cortex. primarily in the molecular and polymorph layers. Fibers in the molecular layer demonstrated varicosities along their lengths, whereas labelled fibers in the polymorph layers only occasionally exhibited swellings. At rostral levels, the dorsolateral portion of the piriform cortex demonstrated a slightly heavier innervation as compared to other parts of the piriform cortex. These fibers apparently arose from the lateral efferent pathway. By the level of the septum and proceeding further caudally, the density of innervation in the piriform cortex began to shift ventrally and arose primarily from the ventral efferent pathway. The majority of labelled fibers formed a dense plexus within the molecular layer. Some labelled fibers pierced the pyramidal layer perpendicular to the pial surface and entered the polymorph cell layer. Collator note: molecular layer, considered as a separate record.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70530 Infralimbic areaPiriform area strongPHAL
The piriform cortex received innervation via both the lateral and ventral pathways (see Fig. 3A-D). Labelled fibers were observed throughout the rostral piriform cortex. primarily in the molecular and polymorph layers. Fibers in the molecular layer demonstrated varicosities along their lengths, whereas labelled fibers in the polymorph layers only occasionally exhibited swellings. At rostral levels, the dorsolateral portion of the piriform cortex demonstrated a slightly heavier innervation as compared to other parts of the piriform cortex. These fibers apparently arose from the lateral efferent pathway. By the level of the septum and proceeding further caudally, the density of innervation in the piriform cortex began to shift ventrally and arose primarily from the ventral efferent pathway. The majority of labelled fibers formed a dense plexus within the molecular layer. Some labelled fibers pierced the pyramidal layer perpendicular to the pial surface and entered the polymorph cell layer. Collator note: polymorph layer, considered as a separate record.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70531 Infralimbic areaEndopiriform nucleus dorsal part moderatePHAL
Deep to the piriform cortex, the endopiriform nucleus contained a number of short, fine labelled fibers that had few varicosities along their lengths and ran perpendicular to the external capsule (Fig. 3A). Collator note: we were unable to unequivocally assign a qualitative density for this connection. See Fig. 3A from the associated paper.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70532 Infralimbic areaAgranular insular area dorsal part moderatePHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70533 Infralimbic areaAgranular insular area dorsal part moderate/strongPHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70534 Infralimbic areaAgranular insular area ventral part moderatePHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70535 Infralimbic areaAgranular insular area ventral part moderate/strongPHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70536 Infralimbic areaAgranular insular area posterior part light/moderatePHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70537 Infralimbic areaAgranular insular area posterior part moderatePHAL
The density of labelled fibers in the agranular insular cortex was most pronounced in layer I (Fig. 3A,B). Most PHA-L containing fibers within this region were largely short, demonstrated boutons along their lengths and were radially oriented. Labelled fibers in layer I tended to be of a thicker caliber than the smaller numbers of scattered fibers present in the deeper layers of the insular cortex. Collator note: the terminal fields extend in all divisions of the AI (Figs 3 A, B, which correspond to Atlas Leves 13-14 and 17-18, respectively). We consider here 2 separate entries for each AI region: one for the general region, and one for layer I.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70538 Infralimbic areaCentral nucleus of amygdala medial part very strongPHAL
The medial subdivision of the central nucleus was particularly heavily innervated by thin and medium caliber fibers demonstrating numerous varicosities (Fig. 4A). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70539 Infralimbic areaCentral nucleus of amygdala lateral part very strongPHAL
Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70540 Infralimbic areaCentral nucleus of amygdala capsular part very strongPHAL
Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70541 Infralimbic areaMedial nucleus of the amygdala anterodorsal part very strongPHAL
Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70542 Infralimbic areaMedial nucleus of the amygdala anteroventral part very strongPHAL
Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70543 Infralimbic areaBasolateral nucleus of the amygdala anterior part moderatePHAL
Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 26-29, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70544 Infralimbic areaCortical nucleus of the amygdala anterior part strongPHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70545 Infralimbic areaCortical nucleus of the amygdala posterior part moderate/strongPHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70546 Infralimbic areaBed nucleus of the accessory olfactory part strongPHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70547 Infralimbic areaNucleus of the lateral olfactory tract moderatePHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70548 Infralimbic areaNucleus of the lateral olfactory tract moderatePHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Collator note: the termination field in the rostral amygdala is particularly heavy from the external capsule-amygdalar capsule down to the optic tract. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70549 Infralimbic areaLateral nucleus of the amygdala light/moderatePHAL
The basolateral and lateral nuclei of the amygdala contained fewer labelled fibers than the adjacent cortical and medial nuclei (Fig. 3E,F). Afferents to the rostral lateral nucleus were oriented in a dorsoventral fashion and primarily distributed in the dorsolateral subdivision of the nucleus, though in more caudal sections the labelled fibers were observed in the ventral parts as well. Collator note: Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70550 Infralimbic areaEndopiriform nucleus ventral part moderatePHAL
Collator note: Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70551 Infralimbic areaIntercalated nuclei of the amygdala moderatePHAL
Collator note: Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70552 Infralimbic areaNucleus of the lateral olfactory tract light/moderatePHAL
Collator note: NLOT3 (dorsal cap) appears to be labeleed light-to-moderate. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70553 Infralimbic areaBasolateral nucleus of the amygdala posterior part moderatePHAL
Labelling was comparatively more sparse [collator note: than in the rostral amygdalar nuclei] in the caudal amygdala (Fig. 3G,H). Both smooth and varicose labelled fibers were found in the posterior basolateral and the basomedial nuclei. Collator note: Figures 3H-G that include the amygdalar nuclei may correspond to Swanson Atlas Levels 31-36, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70554 Infralimbic areaBasomedial nucleus of the amygdala posterior part moderatePHAL
Labelling was comparatively more sparse [collator note: than in the rostral amygdalar nuclei] in the caudal amygdala (Fig. 3G,H). Both smooth and varicose labelled fibers were found in the posterior basolateral and the basomedial nuclei. Collator note: Figures 3H-G that include the amygdalar nuclei may correspond to Swanson Atlas Levels 31-36, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70555 Infralimbic areaPosterior nucleus of the amygdala light/moderatePHAL
Labelling was comparatively more sparse [collator note: than in the rostral amygdalar nuclei] in the caudal amygdala (Fig. 3G,H). Both smooth and varicose labelled fibers were found in the posterior basolateral and the basomedial nuclei. Collator note: Figures 3H-G that include the amygdalar nuclei may correspond to Swanson Atlas Levels 31-36, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70556 Infralimbic areaOrbital area ventrolateral part strongPHAL
Collator note: all MEApd zones appear labeled heavily in Figures 3C-F, even though there is no supporting textual information. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70557 Infralimbic areaPerirhinal area strongPHAL
Collator note: all MEApd zones appear labeled heavily in Figures 3C-F, even though there is no supporting textual information. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70558 Infralimbic areaPosterior parietal association areas strongPHAL
Collator note: all MEApd zones appear labeled heavily in Figures 3C-F, even though there is no supporting textual information. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70559 Infralimbic areaMedial nucleus of the amygdala posteroventral part strongPHAL
Collator note: MEApv zones appears labeled heavily in Figures 3D-E, even though there is no supporting textual information. Exception maybe is in Figure 3F, which shows an empty field, just below the optic tract labeled as "MEA" by authors. This would correspond to MEApv in Swanson Atlas, level 29. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70560 Infralimbic areaMedial nucleus of the amygdala posteroventral part not presentPHAL
Collator note: MEApv zones appears labeled heavily in Figures 3D-E, even though there is no supporting textual information. Exception maybe is in Figure 3F, which shows an empty field, just below the optic tract labeled as "MEA" by authors. This would correspond to MEApv in Swanson Atlas, level 29. We therefore consider this as an "absent" projection. Figures 3C-F that include the amygdalar nuclei may correspond to Swanson Atlas Levels 24-30, but this mapping may be valid only to ventral half.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70561 Infralimbic areaCortical nucleus of the amygdala posterior part lateral zone light/moderatePHAL
The posterior cortical nucleus of the amygdala also contained a few labelled medium and fine caliber fibers with boutons along their lengths. Finally, the amygdalo-hippocampal transition area was innervated by medium caliber fibers with frequent boutons. Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70562 Infralimbic areaCortical nucleus of the amygdala posterior part medial zone light/moderatePHAL
The posterior cortical nucleus of the amygdala also contained a few labelled medium and fine caliber fibers with boutons along their lengths. Finally, the amygdalo-hippocampal transition area was innervated by medium caliber fibers with frequent boutons. Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70563 Infralimbic areaPiriform-amygdaloid area light/moderatePHAL
The posterior cortical nucleus of the amygdala also contained a few labelled medium and fine caliber fibers with boutons along their lengths. Finally, the amygdalo-hippocampal transition area was innervated by medium caliber fibers with frequent boutons. Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70564 Infralimbic areaSubiculum ventral part lightPHAL
[...] the dorsal and ventral presubiculum were innervated by fibers with comparatively fewer varicosities and the hippocampus proper contained only a few PHA-L labelled fibers, mainly in the molecular layer of the CA1 cell field (Fig. 3H). Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34. Most fibers are shown in the temporal (ventral) part of the hippocampal regions, and only rostrally (there are no Figures showing the intermediate or caudal parts.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70565 Infralimbic areaField CA1 lightPHAL
[...] the dorsal and ventral presubiculum were innervated by fibers with comparatively fewer varicosities and the hippocampus proper contained only a few PHA-L labelled fibers, mainly in the molecular layer of the CA1 cell field (Fig. 3H). Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34. Most fibers are shown in the temporal (ventral) part of the hippocampal regions, and only rostrally (there are no Figures showing the intermediate or caudal parts.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70566 Infralimbic areaField CA3 lightPHAL
[...] the dorsal and ventral presubiculum were innervated by fibers with comparatively fewer varicosities and the hippocampus proper contained only a few PHA-L labelled fibers, mainly in the molecular layer of the CA1 cell field (Fig. 3H). Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34. Most fibers are shown in the temporal (ventral) part of the hippocampal regions, and only rostrally (there are no Figures showing the intermediate or caudal parts.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70567 Infralimbic areaDentate gyrus lightPHAL
[...] the dorsal and ventral presubiculum were innervated by fibers with comparatively fewer varicosities and the hippocampus proper contained only a few PHA-L labelled fibers, mainly in the molecular layer of the CA1 cell field (Fig. 3H). Collator note: Figures 3G-H that include the amygdalar nuclei roughly correspond to Swanson Atlas Levels 31-34. Most fibers are shown in the temporal (ventral) part of the hippocampal regions, and only rostrally (there are no Figures showing the intermediate or caudal parts.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70568 Infralimbic areaEntorhinal area, lateral part moderatePHAL
The lateral entorhinal cortex received a projection of medium caliber fibers with boutons which were primarily distributed to the deeper cortical layers. A few labelled fibers were observed in layers I and III.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70569 Infralimbic areaEntorhinal area, lateral part lightPHAL
The lateral entorhinal cortex received a projection of medium caliber fibers with boutons which were primarily distributed to the deeper cortical layers. A few labelled fibers were observed in layers I and III.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70570 Infralimbic areaEntorhinal area, lateral part lightPHAL
The lateral entorhinal cortex received a projection of medium caliber fibers with boutons which were primarily distributed to the deeper cortical layers. A few labelled fibers were observed in layers I and III.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70571 Infralimbic areaBed nuclei of the stria terminalis anterolateral area strongPHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-18. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70572 Infralimbic areaBed nuclei of the stria terminalis anterior division anteroventral area strongPHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-19. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70573 Infralimbic areaBed nuclei of the stria terminalis anterior division anterodorsal area light/moderatePHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-19. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70574 Infralimbic areaBed nuclei of the stria terminalis, anterior division, subcommisural zone not presentPHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-19. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA. BSTsc, however, appears to be devoid of fibers. This can be a criterion for demarcation of BSTsc, or at least of a specific neuron population...
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70575 Infralimbic areaBed nuclei of the stria terminalis anterior division dorsomedial nucleus light/moderatePHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-18. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA. BSTsc, however, appears to be devoid of fibers. Very few fibers in the BSTdm, if any....
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70576 Infralimbic areaNucleus accumbens very strongPHAL
The nucleus accumbens (Fig. 3A) exhibited numerous fascicles of labelled fibers that followed a diagonal trajectory across the nucleus from dorsomedial to ventrolateral. Fine and medium caliber individual labelled fibers branched profusely, exhibiting numerous boutons along their lengths. Collator note: Fig. 3A corresponds to Swanson Atlas Levels 14-15 (lot as a fiducial point). The labeled fibers and terminal fields appear to extend into the fundus of striatum, but seem to avoid the SI (notice the specific shape of the unlabeled tissue, ventral to ACb and dorsal to OT), at least at this level.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70577 Infralimbic areaCaudoputamen strongPHAL
In the ventral putamen (Fig. 3A), smooth labelled fibers clustered together to form several fascicles. In addition to these bundles of labelled axons, a dense plexus of labelled fibers was also present throughout the ventral putamen. These fibers were of medium or fine caliber, were oriented in a medial to lateral direction, and exhibited numerous branch points and boutons along their lengths. Collator note: Fig. 3A corresponds to Swanson Atlas Levels 14-15 (lot as a fiducial point).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70578 Infralimbic areaFundus of the striatum moderatePHAL
In the ventral putamen (Fig. 3A), smooth labelled fibers clustered together to form several fascicles. In addition to these bundles of labelled axons, a dense plexus of labelled fibers was also present throughout the ventral putamen. These fibers were of medium or fine caliber, were oriented in a medial to lateral direction, and exhibited numerous branch points and boutons along their lengths. Collator note: Fig. 3A corresponds to Swanson Atlas Levels 14-15 (lot as a fiducial point).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70579 Infralimbic areaParataenial nucleus strongPHAL
The midline thalamic nuclei contained labelled fibers that appeared to arise from the dorsal component of the ventral efferent pathway that ran along the wall of the third ventricle caudal to the anterior commissure. In the most rostral portion of the thalamus, medium and fine labelled fibers with densely clustered varicosities were found predominantly in the dorsomedial part of the ipsilateral paratenial nucleus where they were oriented in a dorsoventral direction (Fig. 3C). Collator note: Fig 3C roughly corresponds to Swanson Atlas Level 24. PT appears to be labeled entirely.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70580 Infralimbic areaParaventricular nucleus of the thalamus moderatePHAL
A smaller number [collator note:than those labeled in PT] of finer fibers with boutons along their lengths, also oriented in a dorsoventral direction, were present in the paraventricular nucleus of the thalamus (Fig. 3D-F). Collator note: Fig. 3D-F correspond Swanson Atlas Levels 24-30.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70581 Infralimbic areaInteranterodorsal nucleus of the thalamus moderatePHAL
The midline thalamic nuclei contained labelled fibers that appeared to arise from the dorsal component of the ventral efferent pathway that ran along the wall of the third ventricle caudal to the anterior commissure. Collator note:see Fig. 3D-F. Fig. 3D-F correspond Swanson Atlas Levels 24-30.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70582 Infralimbic areaMediodorsal nucleus of the thalamus medial part very strongPHAL
Labeled fibers tended to cluster along the medial edge of the mediodorsal nucleus where they were oriented in a dorsoventral direction (Fig. 5A).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70583 Infralimbic areaMediodorsal nucleus of the thalamus lateral part very strongPHAL
Labeled fibers tended to cluster along the medial edge of the mediodorsal nucleus where they were oriented in a dorsoventral direction (Fig. 5A).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70584 Infralimbic areaInteranteromedial nucleus of the thalamus moderatePHAL
Labeled fibers tended to cluster along the medial edge of the mediodorsal nucleus where they were oriented in a dorsoventral direction (Fig. 5A). IAM appears to be labeled, at least in its ventral part.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70585 Infralimbic areaCentral medial nucleus of the thalamus moderatePHAL
Labeled fibers tended to cluster along the medial edge of the mediodorsal nucleus where they were oriented in a dorsoventral direction (Fig. 5A). CM appears to be labeled, at least in its dorsal part.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70586 Infralimbic areaNucleus reuniens rostral division dorsal part moderate/strongPHAL
In the reuniens nucleus, (Fig. 3D) labelled fibers of medium and fine caliber exhibited numerous swellings and boutons along their lengths. These axons were oriented in a mediolateral direction, though along the midline of the nucleus there were several fibers that coursed in a dorsoventral direction, apparently ascending as part of the dorsal component of the ventral pathway toward the paraventricular and paratenial thalamic nuclei.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70587 Infralimbic areaNucleus reuniens rostral division lateral part moderate/strongPHAL
In the reuniens nucleus, (Fig. 3D) labelled fibers of medium and fine caliber exhibited numerous swellings and boutons along their lengths. These axons were oriented in a mediolateral direction, though along the midline of the nucleus there were several fibers that coursed in a dorsoventral direction, apparently ascending as part of the dorsal component of the ventral pathway toward the paraventricular and paratenial thalamic nuclei.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70588 Infralimbic areaNucleus reuniens rostral division median part moderate/strongPHAL
In the reuniens nucleus, (Fig. 3D) labelled fibers of medium and fine caliber exhibited numerous swellings and boutons along their lengths. These axons were oriented in a mediolateral direction, though along the midline of the nucleus there were several fibers that coursed in a dorsoventral direction, apparently ascending as part of the dorsal component of the ventral pathway toward the paraventricular and paratenial thalamic nuclei.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70589 Infralimbic areaNucleus reuniens caudal division dorsal part strongPHAL
In more caudal sections the innervation of the reuniens nucleus became so dense that the orientation of individual fibers was obscured, though the terminal-like processes seemed largely to be located in the ventral half of the nucleus (see Fig. 3C-F).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70590 Infralimbic areaNucleus reuniens caudal division median part strongPHAL
In more caudal sections the innervation of the reuniens nucleus became so dense that the orientation of individual fibers was obscured, though the terminal-like processes seemed largely to be located in the ventral half of the nucleus (see Fig. 3C-F).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70591 Infralimbic areaNucleus reuniens caudal division posterior part strongPHAL
In more caudal sections the innervation of the reuniens nucleus became so dense that the orientation of individual fibers was obscured, though the terminal-like processes seemed largely to be located in the ventral half of the nucleus (see Fig. 3C-F).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70592 Infralimbic areaParafascicular nucleus moderatePHAL
In more caudal sections through the thalamus, labelled efferents were seen within the parafasicular and subparafasicular nuclei (Fig. 3G). These fibers were of a relatively thin caliber with few swellings or varicosities.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70593 Infralimbic areaLateral hypothalamic area moderatePHAL
[...] principal target was the lateral hypothalamic area, in particular its ventrolateral and perifornical regions (Figs. 3D-G, 5C,D). Although innervation of the anterior part of the lateral hypothalamic area was scant, varicose fibers running in a mediolateral direction were prominent in the retrochiasmatic area.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70596 Infralimbic areaLateral hypothalamic area strongPHAL
[...] principal target was the lateral hypothalamic area, in particular its ventrolateral and perifornical regions (Figs. 3D-G, 5C,D). Although innervation of the anterior part of the lateral hypothalamic area was scant, varicose fibers running in a mediolateral direction were prominent in the retrochiasmatic area.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70597 Infralimbic areaTuberal nucleus strongPHAL
[....]a dense terminal field in the tuberomamillary nucleus.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70598 Infralimbic areaBed nuclei of the stria terminalis oval nucleus moderatePHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-19. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA. BSTov and BStju may be targets of ILA, but Fig 3B does not show the characteristic internal capsule, lateral to these 2 nuclei.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70599 Infralimbic areaBed nuclei of the stria terminalis oval nucleus moderatePHAL
The bed nucleus of the stria terminalis contained a number of fine to medium caliber fibers that exhibited numerous varicosities along their lengths. These fibers were clustered primarily in the lateral and ventrolateral subdivisions of this cell group (Figs. 3B, 4B). Collator note: Figure 3B corresponds to Swanson Atlas Levels 17-19. Only the rostral part of the BST was mapped in this case. It is possible that nuclei caudal to this level (approx. 0 mm from bregma) are also targets of the ILA. BSTov and BStju may be targets of ILA, but Fig 3B does not show the characteristic internal capsule, lateral to these 2 nuclei.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70600 Infralimbic areaAnterior hypothalamic nucleus anterior part lightPHAL
Collator note: few fibers in what appears to be AHNc and AHNa, Swanson Atlas Levels 23-25.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70601 Infralimbic areaAnterior hypothalamic central part lightPHAL
Collator note: few fibers in what appears to be AHNc and AHNa, Swanson Atlas Levels 23-25.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70602 Infralimbic areaAnteroventral periventricular nucleus moderatePHAL
At the rostral tip of the third ventricle labelled fibers oriented in a dorsoventral direction were seen within the anteroventral periventricular nucleus (Fig. 3B). The fibers were of either medium or fine caliber with varicosities and stalks distributed along their lengths. Some terminals also appeared as punctate labelling covering neuronal cell bodies.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70603 Infralimbic areaMedial preoptic area moderatePHAL
Within the medial preoptic area labelled fibers, organized in a mediolateral orientation, were generally of a medium diameter with boutons and stalk-like appendages distributed along their lengths (Fig. 3B). These fibers gave off branches that were thinner than the parent fiber and tended to be smooth. In addition, many well-filled fibers of a larger caliber crossed the preoptic region on a diagonal, arcing in a ventromedial to dorsolateral direction.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70604 Infralimbic areaAnteroventral preoptic nucleus moderatePHAL
Within the medial preoptic area labelled fibers, organized in a mediolateral orientation, were generally of a medium diameter with boutons and stalk-like appendages distributed along their lengths (Fig. 3B). These fibers gave off branches that were thinner than the parent fiber and tended to be smooth. In addition, many well-filled fibers of a larger caliber crossed the preoptic region on a diagonal, arcing in a ventromedial to dorsolateral direction. Collator note: Fig 3B, which roughly corresponds to Swanson Atlas Level 19. Fibers appear to turn into AVP, towards LPO and NDB.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70605 Infralimbic areaSuprachiasmatic nucleus moderatePHAL
Labelled fibers were more numerous in the dorsal half of the suprachiasmatic nucleus than in the ventral half (Figs. 3C, 6; also Swanson et al., '87). Fibers in the dorsal half of the nucleus were either of fine caliber and smooth with an occasional varicosity, or were of a medium caliber, exhibiting numerous varicosities along their lengths. Collator note: Fig 3C roughly corresponds to Swanson Atlas Levels 23-24. It is unclear what is the pattern of labeling in the rostral part of the SCH.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70606 Infralimbic areaSuprachiasmatic nucleus light/moderatePHAL
Labelled fibers in the ventral half of the suprachiasmatic nucleus were generally smooth, exhibiting only a few bouton-like structures. Collator note: Fig 3C roughly corresponds to Swanson Atlas Levels 23-24. It is unclear what is the pattern of labeling in the rostral part of the SCH.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70607 Infralimbic areaSupraoptic nucleus moderatePHAL
Labelled fibers coursed along the dorsolateral border of the supraoptic nucleus (Fig. 3C,D). A few medium caliber fibers with occasional varicosities entered the nucleus and distributed themselves amongst the most peripherally located magnocellular neurons. These regions of termination were concentrated in the more lateral aspects of the nucleus. In addition, a few smooth labelled fibers were seen within the ipsilateral optic tract. These labelled fibers then ran directly into the supraoptic nucleus where they branched and demonstrated varicosities along their lengths. These fibers did not proceed very far into the nucleus, but appeared to maintain a close association with the optic tract. Coillator note: Swanson Atlas Levels 24-27. The pattern of terminals of SO is complex enough to support a possible remapping of SO.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70608 Infralimbic areaParaventricular nucleus of the hypothalamus, descending division, medial parvicellular part, ventral zone light/moderatePHAL
Like the supraoptic nucleus, the paraventricular nucleus of the hypothalamus was also surrounded by a plexus of medium caliber fibers with terminal processes that closely followed the contours of its borders (Fig. 3D). A few thin, labelled fibers that exhibited occasional boutons and varicosities along their lengths were also observed coursing through the parvocellular portion of the paraventricular nucleus. Collator note: Swanson Atlas Levels 26-27.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70609 Infralimbic areaParaventricular nucleus of the hypothalamus, magnocellular division, posterior magnocellular part, lateral zone light/moderatePHAL
Like the supraoptic nucleus, the paraventricular nucleus of the hypothalamus was also surrounded by a plexus of medium caliber fibers with terminal processes that closely followed the contours of its borders (Fig. 3D). A few thin, labelled fibers that exhibited occasional boutons and varicosities along their lengths were also observed coursing through the parvocellular portion of the paraventricular nucleus. Collator note: Swanson Atlas Levels 26-27.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70610 Infralimbic areaParaventricular nucleus of the hypothalamus, parvicellular division, medial parvicellular part, dorsal zone light/moderatePHAL
Like the supraoptic nucleus, the paraventricular nucleus of the hypothalamus was also surrounded by a plexus of medium caliber fibers with terminal processes that closely followed the contours of its borders (Fig. 3D). A few thin, labelled fibers that exhibited occasional boutons and varicosities along their lengths were also observed coursing through the parvocellular portion of the paraventricular nucleus. Collator note: Swanson Atlas Levels 26-27.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70611 Infralimbic areaIntermediate periventricular nucleus of the hypothalamus light/moderatePHAL
Like the supraoptic nucleus, the paraventricular nucleus of the hypothalamus was also surrounded by a plexus of medium caliber fibers with terminal processes that closely followed the contours of its borders (Fig. 3D). A few thin, labelled fibers that exhibited occasional boutons and varicosities along their lengths were also observed coursing through the parvocellular portion of the paraventricular nucleus. Collator note: Swanson Atlas Levels 26-27. PVI is labeled with termination fields rostrocaudally, the direction of fibers being dorso-ventral.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70612 Infralimbic areaDorsomedial nucleus of the hypothalamus anterior part moderate/strongPHAL
Within the dorsal hypothalamic area (just dorsal to the dorsomedial nucleus in Fig. 3F), there were fibers of both fine and medium caliber that exhibited multiple branches with numerous boutons, varicosities, and stalk-like appendages as they followed the dorsal contour of the paraventricular nucleus. In addition a number of labelled fibers appeared to cross the midline just above the third ventricle.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70613 Infralimbic areaDorsomedial nucleus of the hypothalamus posterior part moderate/strongPHAL
Within the dorsal hypothalamic area (just dorsal to the dorsomedial nucleus in Fig. 3F), there were fibers of both fine and medium caliber that exhibited multiple branches with numerous boutons, varicosities, and stalk-like appendages as they followed the dorsal contour of the paraventricular nucleus. In addition a number of labelled fibers appeared to cross the midline just above the third ventricle.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70614 Infralimbic areaDorsomedial nucleus of the hypothalamus ventral part moderate/strongPHAL
Within the dorsal hypothalamic area (just dorsal to the dorsomedial nucleus in Fig. 3F), there were fibers of both fine and medium caliber that exhibited multiple branches with numerous boutons, varicosities, and stalk-like appendages as they followed the dorsal contour of the paraventricular nucleus. In addition a number of labelled fibers appeared to cross the midline just above the third ventricle.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70615 Infralimbic areaPosterior hypothalamic nucleus moderate/strongPHAL
Within the dorsal hypothalamic area (just dorsal to the dorsomedial nucleus in Fig. 3F), there were fibers of both fine and medium caliber that exhibited multiple branches with numerous boutons, varicosities, and stalk-like appendages as they followed the dorsal contour of the paraventricular nucleus. In addition a number of labelled fibers appeared to cross the midline just above the third ventricle. Collator note: the direction of the terminal fields in PH at this level (27-30) is dorso-ventral.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70616 Infralimbic areaPosterior hypothalamic nucleus strongPHAL
As the caudal third ventricle ascended to join the cerebral aqueduct, medium and thin caliber labelled fibers in the posterior hypothalamic area formed a crisscrossing network of axons bearing terminal processes (Fig. 3G). Collator note: Swanson Atlas Levels 31-32.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70617 Infralimbic areaSupramammillary nucleus moderate/strongPHAL
The infralimbic cortex projects to the supramamillary nucleus while the more ventrally located dorsal peduncular cortex projects to the region of the mamillary body immediately ventral to the ILC terminal field.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70618 Infralimbic areaSupramammillary nucleus lateral part light/moderatePHAL
The infralimbic cortex projects to the supramamillary nucleus while the more ventrally located dorsal peduncular cortex projects to the region of the mamillary body immediately ventral to the ILC terminal field. Collator note: very difficult to assess the qualitative strength of this connection.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70619 Infralimbic areaMedial mammillary nucleus moderate/strongPHAL
The infralimbic cortex projects to the supramamillary nucleus while the more ventrally located dorsal peduncular cortex projects to the region of the mamillary body immediately ventral to the ILC terminal field. Collator note: we include this connection, because DP is included in the ILA as defined by Swanson. Only the dorsal part of the MM is labeled with terminal fields.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70620 Infralimbic areaLateral mammillary nucleus moderate/strongPHAL
The infralimbic cortex projects to the supramamillary nucleus while the more ventrally located dorsal peduncular cortex projects to the region of the mamillary body immediately ventral to the ILC terminal field. Collator note: we include this connection, because DP is included in the ILA as defined by Swanson. Only the dorsal part of the MM is labeled with terminal fields.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70621 Infralimbic areaPeriaqueductal gray medial division moderatePHAL
Labelled fibers in the medial forebrain bundle swept dorsomedially through the posterior hypothalamic area into the ventrolateral quadrant of the periaqueductal gray matter (Fig. 3I).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70622 Infralimbic areaPeriaqueductal gray ventrolateral division moderatePHAL
Labelled fibers in the medial forebrain bundle swept dorsomedially through the posterior hypothalamic area into the ventrolateral quadrant of the periaqueductal gray matter (Fig. 3I).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70623 Infralimbic areaVentral tegmental area moderatePHAL
Collator note: see Figure 3I, which roughly corresponds to Swanson Atlas Levels 39-40.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70624 Infralimbic areaEdinger-Westphal nucleus lightPHAL
Some of these fibers ran through the Edinger-Westphal nucleus into the periaqueductal gray matter and dorsal raphe nucleus. Collator note: few terminal fields, if any in EW.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70625 Infralimbic areaMesencephalic reticular nucleus moderatePHAL
Collator note: in MRN, fibers travel in a diagonal fashion, towards the AQ. The label density is variable, see Figs 3I and 3J (Swanson Atlas Levels 39-40 and 45, respectively).
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70626 Infralimbic areaInterpeduncular nucleus apical subnucleus light/moderatePHAL
Labelled fibers which traveled in the ventromedial tegmental pathway innervated the interpeduncular nucleus. These fibers were primarily located in the dorsal part of the nucleus and while generally smooth did exhibit occasional terminal boutons (Fig. 3J). Collator note: Fgiure 3J roughly corresponds to Swanson Atlas Level 45.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70627 Infralimbic areaInterpeduncular nucleus dorsomedial subnucleus light/moderatePHAL
Labelled fibers which traveled in the ventromedial tegmental pathway innervated the interpeduncular nucleus. These fibers were primarily located in the dorsal part of the nucleus and while generally smooth did exhibit occasional terminal boutons (Fig. 3J). Collator note: Fgiure 3J roughly corresponds to Swanson Atlas Level 45.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70628 Infralimbic areaInterpeduncular nucleus central subnucleus light/moderatePHAL
Labelled fibers which traveled in the ventromedial tegmental pathway innervated the interpeduncular nucleus. These fibers were primarily located in the dorsal part of the nucleus and while generally smooth did exhibit occasional terminal boutons (Fig. 3J). Collator note: Fgiure 3J roughly corresponds to Swanson Atlas Level 45.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70629 Infralimbic areaParabrachial nucleus lateral division central lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70630 Infralimbic areaParabrachial nucleus lateral division dorsal lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70631 Infralimbic areaParabrachial nucleus lateral division external lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70632 Infralimbic areaParabrachial nucleus lateral division internal lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70633 Infralimbic areaParabrachial nucleus lateral division superior lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70634 Infralimbic areaParabrachial nucleus lateral division ventral lateral part moderatePHAL
Terminal labelling within the parabrachial nucleus arose as a caudal and lateral extension of the fibers coursing through the periaqueductal gray matter and central tegmental fields (see Fig. 7B; see also Fig. 3L,M). In the rostral parabrachial nucleus, a few labelled fibers of fine caliber found in the superior lateral subnucleus exhibited infrequent swellings along their lengths. Within the central lateral subnucleus there was a denser collection of spinelike processes and boutons along the lengths of fine caliber fibers as they coursed laterally from the periaqueductal gray matter. Both medium and fine caliber fibers, observed within the dorsal and external lateral subnuclei, exhibited boutons and varicosities along their lengths. In the ventrolateral parabrachial subnucleus fine caliber fibers were observed, which also demonstrated varicosities along their lengths. In caudal sections through the parabrachial nucleus, labeling within these subnuclei grew denser. Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70635 Infralimbic areaParabrachial nucleus medial division external medial part moderatePHAL
Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70636 Infralimbic areaParabrachial nucleus medial division ventral medial part moderatePHAL
Labeled fibers within the medial subnucleus were oriented in a mediolateral direction. These tended to be smooth with occasional swellings along their lengths in the more lateral part of the subnucleus. In the more medial part of the nucleus, these labelled fibers branched and gave rise to finer axons with complex bouton-bearing processes. Collator note: Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51. The terminals fields in PB are organized around the superior cerebellar peduncle. KF is not labeled in this experiment.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70637 Infralimbic areaLaterodorsal tegmental nucleus light/moderatePHAL
Collator note. The terminal field in PB extends medially into LDT, see Fig 3L, M. Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70638 Infralimbic areaPedunculopontine nucleus light/moderatePHAL
Collator note. The terminal field in PB may extend ventrally into PPN, see Fig 3L, M. Fig 3L-M roughly corresponds to Swanson Atlas Levels 47-51.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70639 Infralimbic areaMesencephalic nucleus of the trigeminal lightPHAL
Other structures in the pontine tegmentum that demonstrated PHA-L containing fibers included the mesencephalic trigeminal nucleus and the locus coeruleus (see Fig. 3M). Only a few medium-size fibers were seen coursing among the large neurons of the mesencephalic trigeminal nucleus, but an occasional varicosity was seen in close proximity to a cell body. Smooth labelled fibers with occasional boutons were present in the dorsal, rostral portion of the locus coeruleus.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70640 Infralimbic areaLocus coeruleus light/moderatePHAL
Other structures in the pontine tegmentum that demonstrated PHA-L containing fibers included the mesencephalic trigeminal nucleus and the locus coeruleus (see Fig. 3M). Only a few medium-size fibers were seen coursing among the large neurons of the mesencephalic trigeminal nucleus, but an occasional varicosity was seen in close proximity to a cell body. Smooth labelled fibers with occasional boutons were present in the dorsal, rostral portion of the locus coeruleus.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70641 Infralimbic areaSuperior central nucleus raphe medial part lightPHAL
Collator note: see Fig 3L (Swanson Atlas Levels 47-48). Several fibers cross CSM and they appear to leave few terminal fields.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70642 Infralimbic areaParvicellular reticular nucleus light/moderatePHAL
Collator note: see Figure 3N, which roughly corresponds to Swanson Atlas Level 53.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70643 Infralimbic areaMedullary reticular nucleus ventral part light/moderatePHAL
Collator note: MDRNv appears to be crossed by several fibers ventro-dorsally towards the NTS.See Figure 3O-R, which roughly correspond to Swanson Atlas Level 56-70.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70644 Infralimbic areaNucleus of the solitary tract central part moderatePHAL
Labelled fibers ran dorsally in a position medial to the spinal trigeminal nucleus and innervated the ventrolateral, medial and commissural subdivisions of the nucleus of the solitary tract as well as the dorsal motor vagal nucleus (see Figs. 30-R, 7C,D). In sections through the rostral nucleus of the solitary tract there were numerous medium and fine wavy fibers with many varicosities along their lengths. Labeled fibers were not seen in the rostral nucleus of the solitary tract in experiment R678 in which the injection site was confined to the ILC, indicating that this projection may originate from the prelimbic cortex (see below). In experiment R651, the pattern of fibers seen in the medial subdivision of the nucleus of the solitary tract was similar to the rostral subdivision, with the addition that finel abelled fibers with boutons and swellings swept into the layer of ependymal cells lining the fourth ventricle (Fig. 7D). The ventrolateral portion of the nucleus of the solitary tract was innervated by fibers that appeared to be a continuation of the thick, straight axons of the lateral tegmental pathway. These axons branched profusely giving rise to numerous medium and fine caliber fibers bearing boutons and varicosities along their lengths. The commissural portion of the nucleus of the solitary tract was innervated by a few fine-labelled fibers that had stalk-like processes and boutons along their lengths.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70645 Infralimbic areaNucleus of the solitary tract commissural part moderatePHAL
Labelled fibers ran dorsally in a position medial to the spinal trigeminal nucleus and innervated the ventrolateral, medial and commissural subdivisions of the nucleus of the solitary tract as well as the dorsal motor vagal nucleus (see Figs. 30-R, 7C,D). In sections through the rostral nucleus of the solitary tract there were numerous medium and fine wavy fibers with many varicosities along their lengths. Labeled fibers were not seen in the rostral nucleus of the solitary tract in experiment R678 in which the injection site was confined to the ILC, indicating that this projection may originate from the prelimbic cortex (see below). In experiment R651, the pattern of fibers seen in the medial subdivision of the nucleus of the solitary tract was similar to the rostral subdivision, with the addition that finel abelled fibers with boutons and swellings swept into the layer of ependymal cells lining the fourth ventricle (Fig. 7D). The ventrolateral portion of the nucleus of the solitary tract was innervated by fibers that appeared to be a continuation of the thick, straight axons of the lateral tegmental pathway. These axons branched profusely giving rise to numerous medium and fine caliber fibers bearing boutons and varicosities along their lengths. The commissural portion of the nucleus of the solitary tract was innervated by a few fine-labelled fibers that had stalk-like processes and boutons along their lengths.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70646 Infralimbic areaNucleus of the solitary tract gelatinous part moderatePHAL
Labelled fibers ran dorsally in a position medial to the spinal trigeminal nucleus and innervated the ventrolateral, medial and commissural subdivisions of the nucleus of the solitary tract as well as the dorsal motor vagal nucleus (see Figs. 30-R, 7C,D). In sections through the rostral nucleus of the solitary tract there were numerous medium and fine wavy fibers with many varicosities along their lengths. Labeled fibers were not seen in the rostral nucleus of the solitary tract in experiment R678 in which the injection site was confined to the ILC, indicating that this projection may originate from the prelimbic cortex (see below). In experiment R651, the pattern of fibers seen in the medial subdivision of the nucleus of the solitary tract was similar to the rostral subdivision, with the addition that finel abelled fibers with boutons and swellings swept into the layer of ependymal cells lining the fourth ventricle (Fig. 7D). The ventrolateral portion of the nucleus of the solitary tract was innervated by fibers that appeared to be a continuation of the thick, straight axons of the lateral tegmental pathway. These axons branched profusely giving rise to numerous medium and fine caliber fibers bearing boutons and varicosities along their lengths. The commissural portion of the nucleus of the solitary tract was innervated by a few fine-labelled fibers that had stalk-like processes and boutons along their lengths.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70647 Infralimbic areaNucleus of the solitary tract lateral part moderatePHAL
Labelled fibers ran dorsally in a position medial to the spinal trigeminal nucleus and innervated the ventrolateral, medial and commissural subdivisions of the nucleus of the solitary tract as well as the dorsal motor vagal nucleus (see Figs. 30-R, 7C,D). In sections through the rostral nucleus of the solitary tract there were numerous medium and fine wavy fibers with many varicosities along their lengths. Labeled fibers were not seen in the rostral nucleus of the solitary tract in experiment R678 in which the injection site was confined to the ILC, indicating that this projection may originate from the prelimbic cortex (see below). In experiment R651, the pattern of fibers seen in the medial subdivision of the nucleus of the solitary tract was similar to the rostral subdivision, with the addition that finel abelled fibers with boutons and swellings swept into the layer of ependymal cells lining the fourth ventricle (Fig. 7D). The ventrolateral portion of the nucleus of the solitary tract was innervated by fibers that appeared to be a continuation of the thick, straight axons of the lateral tegmental pathway. These axons branched profusely giving rise to numerous medium and fine caliber fibers bearing boutons and varicosities along their lengths. The commissural portion of the nucleus of the solitary tract was innervated by a few fine-labelled fibers that had stalk-like processes and boutons along their lengths.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70648 Infralimbic areaNucleus of the solitary tract medial part moderatePHAL
Labelled fibers ran dorsally in a position medial to the spinal trigeminal nucleus and innervated the ventrolateral, medial and commissural subdivisions of the nucleus of the solitary tract as well as the dorsal motor vagal nucleus (see Figs. 30-R, 7C,D). In sections through the rostral nucleus of the solitary tract there were numerous medium and fine wavy fibers with many varicosities along their lengths. Labeled fibers were not seen in the rostral nucleus of the solitary tract in experiment R678 in which the injection site was confined to the ILC, indicating that this projection may originate from the prelimbic cortex (see below). In experiment R651, the pattern of fibers seen in the medial subdivision of the nucleus of the solitary tract was similar to the rostral subdivision, with the addition that finel abelled fibers with boutons and swellings swept into the layer of ependymal cells lining the fourth ventricle (Fig. 7D). The ventrolateral portion of the nucleus of the solitary tract was innervated by fibers that appeared to be a continuation of the thick, straight axons of the lateral tegmental pathway. These axons branched profusely giving rise to numerous medium and fine caliber fibers bearing boutons and varicosities along their lengths. The commissural portion of the nucleus of the solitary tract was innervated by a few fine-labelled fibers that had stalk-like processes and boutons along their lengths.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70649 Infralimbic areaDorsal motor nucleus of the vagus nerve moderatePHAL
[...] the dorsal motor vagal nucleus was also innervated by fine caliber fibers that ran along its dorsal surface and gave rise to numerous fine branches which entered the nucleus and exhibited varicosities.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70650 Infralimbic areaNucleus ambiguus dorsal division moderatePHAL
The compact zone of the nucleus ambiguus received a small number of short, fine labelled axons that exhibited swellings and boutons. This innervation appeared to become denser more caudally and extended into the external formation of the nucleus.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70651 Infralimbic areaNucleus ambiguus, ventral division moderatePHAL
The compact zone of the nucleus ambiguus received a small number of short, fine labelled axons that exhibited swellings and boutons. This innervation appeared to become denser more caudally and extended into the external formation of the nucleus.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70652 Infralimbic areaNucleus of the diagonal band strongPHAL
Collator note: see Fig 3A, which roughly corresponds to Swanson Atlas Level 14. The terminal field is oriented dorso-ventral.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70653 Infralimbic areaMedial septal nucleus strongPHAL
Collator note: see Fig 3A, which roughly corresponds to Swanson Atlas Level 14. The terminal field is oriented dorso-ventral.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70654 Infralimbic areaSeptohippocampal nucleus moderatePHAL
Collator note: see Fig 3A, which roughly corresponds to Swanson Atlas Level 14. The terminal field is oriented dorso-ventral. Terminal fields are at least in the rostral part of the SH.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70655 Infralimbic areaMain olfactory bulb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70656 Infralimbic areaMain olfactory bulb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70657 Infralimbic areaMain olfactory bulb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70658 Infralimbic areaMain olfactory bulb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70659 Infralimbic areaMain olfactory bulb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70660 Infralimbic areaAccessory olfactory bulb, glomerular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70661 Infralimbic areaAccessory olfactory bulb, mitral layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70662 Infralimbic areaAccessory olfactory bulb, granular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70663 Infralimbic areaEntorhinal area medial part, dorsal zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70664 Infralimbic areaEntorhinal area medial part, ventral zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70665 Infralimbic areaPresubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70666 Infralimbic areaPostsubiculum layers 1-6 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70667 Infralimbic areaAnteroventral nucleus of thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70668 Infralimbic areaAnteromedial nucleus of thalamus dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70669 Infralimbic areaAnteromedial nucleus of thalamus ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70670 Infralimbic areaAnterodorsal nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70671 Infralimbic areaLateral dorsal nucleus of thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70672 Infralimbic areaMediodorsal nucleus of the thalamus central part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70673 Infralimbic areaIntermediodorsal nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70674 Infralimbic areaSubmedial nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70675 Infralimbic areaPerireunensis nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70676 Infralimbic areaNucleus reuniens rostral division rostral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70677 Infralimbic areaNucleus reuniens rostral division ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70678 Infralimbic areaNucleus reuniens caudal division caudal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70679 Infralimbic areaRhomboid nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70680 Infralimbic areaParacentral nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70681 Infralimbic areaCentral lateral nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70682 Infralimbic areaLateral posterior nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70683 Infralimbic areaPosterior complex of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70684 Infralimbic areaSuprageniculate nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70685 Infralimbic areaPosterior limiting nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70686 Infralimbic areaVentral anterior-lateral complex of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70687 Infralimbic areaVentral medial nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70688 Infralimbic areaBed nuclei of the stria terminalis juxtacapsular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70689 Infralimbic areaBed nuclei of the stria terminalis rhomboid nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70690 Infralimbic areaBed nuclei of the stria terminalis anterior division dorsolateral nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70691 Infralimbic areaBed nuclei of the stria terminalis anterior division fusiform nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70692 Infralimbic areaBed nuclei of the stria terminalis anterior division ventral nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70693 Infralimbic areaBed nuclei of the stria terminalis anterior division magnocellular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70694 Infralimbic areaBed nuclei of the stria terminalis posterior division principal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70695 Infralimbic areaBed nuclei of the stria terminalis posterior division interfascicular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70696 Infralimbic areaBed nuclei of the stria terminalis posterior division transverse nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70697 Infralimbic areaBed nuclei of the stria terminalis posterior division premedullary nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70698 Infralimbic areaBed nuclei of the stria terminalis posterior division dorsal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70699 Infralimbic areaBed nuclei of the stria terminalis posterior division strial extension not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70700 Infralimbic areaBed nuclei of the stria terminalis posterior division cell-sparse zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70701 Infralimbic areaBed nucleus of the anterior commissure not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70702 Infralimbic areaBed nucleus of the stria medularis not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70703 Infralimbic areaVascular organ of the lamina terminalis not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70704 Infralimbic areaSuprachiasmatic preoptic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70705 Infralimbic areaMedian preoptic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70706 Infralimbic areaPreoptic periventricular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70707 Infralimbic areaSupraoptic nucleus, retrochiasmatic part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70708 Infralimbic areaSupraoptic nucleus, accessory supraoptic group, nucleus circularis not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70709 Infralimbic areaParaventricular nucleus of the hypothalamus, descending division, dorsal parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70710 Infralimbic areaParaventricular nucleus of the hypothalamus, descending division, lateral parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70711 Infralimbic areaParaventricular nucleus of the hypothalamus, descending division, forniceal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70712 Infralimbic areaParaventricular nucleus of the hypothalamus, magnocellular division, anterior magnocellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70713 Infralimbic areaParaventricular nucleus of the hypothalamus, magnocellular division, medial magnocellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70714 Infralimbic areaParaventricular nucleus of the hypothalamus, magnocellular division, posterior magnocellular part, medial zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70715 Infralimbic areaParaventricular nucleus of the hypothalamus, parvicellular division, anterior parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70716 Infralimbic areaParaventricular nucleus of the hypothalamus, parvicellular division, periventricular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70717 Infralimbic areaAnterior amygdaloid area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70718 Infralimbic areaMedial nucleus of the amygdala posterodorsal part,sublayer a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70719 Infralimbic areaMedial nucleus of the amygdala posterodorsal part,sublayer b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70720 Infralimbic areaMedial nucleus of the amygdala posterodorsal part,sublayer c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70721 Infralimbic areaAnterior periventricular nucleus of the hypothalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70722 Infralimbic areaArcuate nucleus of the hypothalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70723 Infralimbic areaPosterior periventricular nucleus of the hypothalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70724 Infralimbic areaMedial preoptic nucleus lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70725 Infralimbic areaMedial preoptic nucleus medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70726 Infralimbic areaMedial preoptic nucleus central part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70727 Infralimbic areaAnterodorsal preoptic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70728 Infralimbic areaPosterodorsal preoptic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70729 Infralimbic areaParastrial nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70730 Infralimbic areaAnterior hypothalamic posterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70731 Infralimbic areaAnterior hypothalamic dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70732 Infralimbic areaSuprachiasmatic nucleus dorsomedial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70733 Infralimbic areaSuprachiasmatic nucleus ventrolateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70734 Infralimbic areaSubparaventricular zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70735 Infralimbic areaRetrochiasmatic area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70736 Infralimbic areaVentromedial nucleus of the hypothalamus anterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70737 Infralimbic areaVentromedial nucleus of the hypothalamus dorsomedial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70738 Infralimbic areaVentromedial nucleus of the hypothalamus central part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70739 Infralimbic areaVentromedial nucleus of the hypothalamus ventrolateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70740 Infralimbic areaVentral premammillary nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70741 Infralimbic areaTuberomammillary nucleus dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70742 Infralimbic areaTuberomammillary nucleus ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70743 Infralimbic areaSupramammillary nucleus medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70744 Infralimbic areaDorsal premammillary nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70745 Infralimbic areaMedial mammillary nucleus median part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70746 Infralimbic areaLateral preoptic area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70747 Infralimbic areaSubthalamic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70748 Infralimbic areaVentral posterolateral nucleus of the thalamus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70749 Infralimbic areaVentral posteromedial nucleus of the thalamus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70750 Infralimbic areaMedial geniculate complex dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70751 Infralimbic areaMedial geniculate complex ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70752 Infralimbic areaMedial geniculate complex medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70753 Infralimbic areaDorsal part of the lateral geniculate complex not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70754 Infralimbic areaSubfornical organ not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70755 Infralimbic areaMedial habenula dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70756 Infralimbic areaMedial habenula ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70757 Infralimbic areaLateral habenula not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70758 Infralimbic areaReticular nucleus of the thalamus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70759 Infralimbic areaIntergeniculate leaflet of the lateral geniculate complex not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70760 Infralimbic areaVentral part of the lateral geniculate complex lateral zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70761 Infralimbic areaVentral part of the lateral geniculate complex medial zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70762 Infralimbic areaZona incerta dopaminergic group not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70763 Infralimbic areaFields of Forel not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70764 Infralimbic areaZona incerta proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70765 Infralimbic areaPeripeduncular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70766 Infralimbic areaSubparafascicular nucleus magnocellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70767 Infralimbic areaSubparafascicular nucleus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70768 Infralimbic areaOlfactory tubercle molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70769 Infralimbic areaOlfactory tubercle pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70770 Infralimbic areaOlfactory tubercle polymorph layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70771 Infralimbic areaIslands of Calleja not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70772 Infralimbic areaMajor island of Calleja not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70773 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part dorsal zone rostral region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70774 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part dorsal zone dorsal region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70775 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part dorsal zone lateral region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70776 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part dorsal zone ventral region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70777 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part ventral zone medial region dorsal domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70778 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part ventral zone medial region ventral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70779 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part ventral zone intermediate region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70780 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part ventral zone lateral region dorsal domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70781 Infralimbic areaLateral septal nucleus caudal (caudodorsal) part ventral zone lateral region ventral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70782 Infralimbic areaLateral septal nucleus rostral (rostroventral) part medial zone dorsal region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70783 Infralimbic areaLateral septal nucleus rostral (rostroventral) part medial zone ventral region rostral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70784 Infralimbic areaLateral septal nucleus rostral (rostroventral) part medial zone ventral region caudal domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70785 Infralimbic areaLateral septal nucleus rostral (rostroventral) part ventrolateral zone dorsal region medial domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70786 Infralimbic areaLateral septal nucleus rostral (rostroventral) part ventrolateral zone dorsal region lateral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70787 Infralimbic areaLateral septal nucleus rostral (rostroventral) part ventrolateral zone ventral region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70788 Infralimbic areaLateral septal nucleus rostral (rostroventral) part dorsolateral zone medial region dorsal domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70789 Infralimbic areaLateral septal nucleus rostral (rostroventral) part dorsolateral zone medial region ventral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70790 Infralimbic areaLateral septal nucleus rostral (rostroventral) part dorsolateral zone lateral region dorsal domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70791 Infralimbic areaLateral septal nucleus rostral (rostroventral) part dorsolateral zone lateral region ventral domain not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70792 Infralimbic areaLateral septal nucleus ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70793 Infralimbic areaSeptofimbrial nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70794 Infralimbic areaGlobus pallidus lateral segment not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70795 Infralimbic areaGlobus pallidus medial segment not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70796 Infralimbic areaSubstantia innominata not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70797 Infralimbic areaMagnocellular preoptic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70798 Infralimbic areaTriangular nucleus of the septum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70799 Infralimbic areaSuperior colliculus zonal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70800 Infralimbic areaSuperior colliculus superficial gray layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70801 Infralimbic areaSuperior colliculus optic layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70802 Infralimbic areaSuperior colliculus intermediate gray layer sublayer a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70803 Infralimbic areaSuperior colliculus intermediate gray layer sublayer b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70804 Infralimbic areaSuperior colliculus intermediate gray layer sublayer c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70805 Infralimbic areaSuperior colliculus intermediate white layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70806 Infralimbic areaSuperior colliculus intermediate deep gray layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70807 Infralimbic areaSuperior colliculus intermediate deep white layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70808 Infralimbic areaParageminal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70809 Infralimbic areaOlivary pretectal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70810 Infralimbic areaNucleus of the optic tract not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70811 Infralimbic areaPosterior pretectal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70812 Infralimbic areaNucleus of the posterior commissure not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70813 Infralimbic areaAnterior pretectal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70814 Infralimbic areaMedial pretectal area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70815 Infralimbic areaMedial terminal nucleus of the accessory optic tract not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70816 Infralimbic areaLateral terminal nucleus of the accessory optic tract not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70817 Infralimbic areaDorsal terminal nucleus of the accessory optic tract not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70818 Infralimbic areaTrigeminal ganglion not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70819 Infralimbic areaPrincipal sensory nucleus of the trigeminal not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70820 Infralimbic areaSpinal nucleus of the trigeminal oral part ventrolateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70821 Infralimbic areaSpinal nucleus of the trigeminal oral part rostral dorsomedial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70822 Infralimbic areaSpinal nucleus of the trigeminal oral part middle dorsomedial part, dorsal zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70823 Infralimbic areaSpinal nucleus of the trigeminal oral part middle dorsomedial part, ventral zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70824 Infralimbic areaSpinal nucleus of the trigeminal oral part caudal dorsomedial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70825 Infralimbic areaSpinal nucleus of the trigeminal interpolar part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70826 Infralimbic areaSpinal nucleus of the trigeminal caudal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70827 Infralimbic areaParatrigeminal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70828 Infralimbic areaGracile nucleus median part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70829 Infralimbic areaGracile nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70830 Infralimbic areaCuneate nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70831 Infralimbic areaNucleus z not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70832 Infralimbic areaExternal cuneate nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70833 Infralimbic areaDorsal coclear nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70834 Infralimbic areaVentral coclear nucleus anterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70835 Infralimbic areaVentral coclear nucleus posterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70836 Infralimbic areaSubpeduncular granular region of the cochlear nuclei not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70837 Infralimbic areaGranular lamina of the cochlear nuclei not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70838 Infralimbic areaInterstitial nucleus of the auditory nerve not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70839 Infralimbic areaNucleus of the trapezoid body not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70840 Infralimbic areaSuperior olivary complex medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70841 Infralimbic areaSuperior olivary complex lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70842 Infralimbic areaSuperior olivary complex periolivary region not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70843 Infralimbic areaNucleus of the lateral lemniscus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70844 Infralimbic areaInferior colliculus external nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70845 Infralimbic areaInferior colliculus dorsal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70846 Infralimbic areaInferior colliculus central nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70847 Infralimbic areaNucleus of the brachium of the inferior colliculus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70848 Infralimbic areaNucleus sagulum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70849 Infralimbic areaMedial vestibular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70850 Infralimbic areaLateral vestibular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70851 Infralimbic areaSuperior vestibular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70852 Infralimbic areaSpinal vestibular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70853 Infralimbic areaNucleus intercalatus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70854 Infralimbic areaNucleus prepositus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70855 Infralimbic areaNucleus of Roller not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70856 Infralimbic areaInterstitial nucleus of the vestibular nerve not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70857 Infralimbic areaNucleus x not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70858 Infralimbic areaNucleus y not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70859 Infralimbic areaInfracerebellar nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70860 Infralimbic areaNucleus of the solitary tract medial part rostral zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70861 Infralimbic areaNucleus of the solitary tract medial part caudal zone not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70862 Infralimbic areaArea postrema not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70863 Infralimbic areaParabrachial nucleus lateral division extreme lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70864 Infralimbic areaKolliker-Fuse subnucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70865 Infralimbic areaParabrachial nucleus medial division medial medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70866 Infralimbic areaMedial accessory nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70867 Infralimbic areaOculomotor nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70868 Infralimbic areaTrochlear nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70869 Infralimbic areaAccesory abducens nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70870 Infralimbic areaAbducens nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70871 Infralimbic areaMotor nucleus of the trigeminal parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70872 Infralimbic areaMotor nucleus of the trigeminal proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70873 Infralimbic areaSubstantia nigra compact part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70874 Infralimbic areaSubstantia nigra reticular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70875 Infralimbic areaPrecommissural nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70876 Infralimbic areaCommissural nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70877 Infralimbic areaPeriaqueductal gray rostromedial division not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70878 Infralimbic areaPeriaqueductal gray rostrolateral division not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70879 Infralimbic areaPeriaqueductal gray dorsal division not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70880 Infralimbic areaPeriaqueductal gray dorsolateral division not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70881 Infralimbic areaInterstitial nucleus of Cajal not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70882 Infralimbic areaNucleus of Darkschewitsch not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70883 Infralimbic areaDorsal tegmental nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70884 Infralimbic areaVentral tegmental nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70885 Infralimbic areaAnterior tegmental nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70886 Infralimbic areaLateral tegmental nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70887 Infralimbic areaSublaterodorsal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70888 Infralimbic areaSubcoeruleus nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70889 Infralimbic areaBarrington nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70890 Infralimbic areaSupargenual nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70891 Infralimbic areaPontine central gray not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70892 Infralimbic areaInterfascicular nucleus raphe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70893 Infralimbic areaRostral linear nucleus raphe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70894 Infralimbic areaCentral linear nucleus raphe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70895 Infralimbic areaSuperior central nucleus raphe lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70896 Infralimbic areaDorsal nucleus raphe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70897 Infralimbic areaNucleus incertus compact part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70898 Infralimbic areaNucleus incertus diffuse part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70899 Infralimbic areaNucleus raphe pontis not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70900 Infralimbic areaNucleus raphe magnus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70901 Infralimbic areaNucleus raphe pallidus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70902 Infralimbic areaNucleus raphe obscurus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70903 Infralimbic areaInterpeduncular nucleus rostral subnucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70904 Infralimbic areaInterpeduncular nucleus lateral subnucleus dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70905 Infralimbic areaInterpeduncular nucleus lateral subnucleus intermediate part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70906 Infralimbic areaInterpeduncular nucleus lateral subnucleus ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70907 Infralimbic areaInterpeduncular nucleus lateral subnucleus rostral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70908 Infralimbic areaInterpeduncular nucleus intermediate subnucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70909 Infralimbic areaRetrorubral area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70910 Infralimbic areaCuneiform nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70911 Infralimbic areaPontine reticular nucleus caudal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70912 Infralimbic areaPontine reticular nucleus rostral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70913 Infralimbic areaGigantocellular reticular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70914 Infralimbic areaParagigantocellular reticular nucleus dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70915 Infralimbic areaParagigantocellular reticular nucleus lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70916 Infralimbic areaParapyramidal nucleus deep part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70917 Infralimbic areaParapyramidal nucleus superficial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70918 Infralimbic areaMagnocellular reticular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70919 Infralimbic areaSupratrigeminal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70920 Infralimbic areaMedullary reticular nucleus dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70921 Infralimbic areaMarginal zone of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70922 Infralimbic areaSubstantia gelatinosa of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70923 Infralimbic areaNucleus proprius of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70924 Infralimbic areaReticular nucleus of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70925 Infralimbic areaLateral cervical nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70926 Infralimbic areaLateral spinal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70927 Infralimbic areaCentral cervical nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70928 Infralimbic areaDorsal nucleus of the spinal cord caudal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70929 Infralimbic areaIntermediomedial column of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70930 Infralimbic areaDorsal commissural nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70931 Infralimbic areaIntercalated nucleus of the spinal cord not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70932 Infralimbic areaIntermediolateral column of the spinal cord sympathetic column not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70933 Infralimbic areaIntermediolateral column of the spinal cord parasympathetic column not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70934 Infralimbic areaNucleus of the bulbocavernosus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70935 Infralimbic areaOnuf nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70936 Infralimbic areaPhrenic nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70937 Infralimbic areaPrimary motor area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70938 Infralimbic areaSecondary motor area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70939 Infralimbic areaPrimary auditory area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70940 Infralimbic areaDorsal auditory areas not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70941 Infralimbic areaVentral auditory areas not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70942 Infralimbic areaGustatory areas not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70943 Infralimbic areaAnterior olfactory nucleus dorsal part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70944 Infralimbic areaAnterior olfactory nucleus dorsal part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70945 Infralimbic areaAnterior olfactory nucleus external part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70946 Infralimbic areaAnterior olfactory nucleus external part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70947 Infralimbic areaAnterior olfactory nucleus lateral part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70948 Infralimbic areaAnterior olfactory nucleus lateral part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70949 Infralimbic areaAnterior olfactory nucleus medial part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70950 Infralimbic areaAnterior olfactory nucleus medial part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70951 Infralimbic areaAnterior olfactory nucleus posteroventral part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70952 Infralimbic areaAnterior olfactory nucleus posteroventral part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70953 Infralimbic areaTaenia tecta dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70954 Infralimbic areaTaenia tecta dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70955 Infralimbic areaTaenia tecta dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70956 Infralimbic areaTaenia tecta dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70957 Infralimbic areaTaenia tecta ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70958 Infralimbic areaTaenia tecta ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70959 Infralimbic areaTaenia tecta ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70960 Infralimbic areaPiriform area molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70961 Infralimbic areaPiriform area pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70962 Infralimbic areaPiriform area polymorph layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70963 Infralimbic areaPostpiriform transition area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70964 Infralimbic areaPrimary somatosensory area barrel field not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70965 Infralimbic areaPrimary somatosensory area lower limb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70966 Infralimbic areaPrimary somatosensory area mouth not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70967 Infralimbic areaPrimary somatosensory area nose not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70968 Infralimbic areaPrimary somatosensory area trunk not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70969 Infralimbic areaPrimary somatosensory area upper limb not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70970 Infralimbic areaSupplemental somatosensory area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70971 Infralimbic areaVisceral area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70972 Infralimbic areaAnterior laterolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70973 Infralimbic areaAnterolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70974 Infralimbic areaAnteromedial visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70975 Infralimbic areaIntermediolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70976 Infralimbic areaLaterolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70977 Infralimbic areaMediolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70978 Infralimbic areaPosterolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70979 Infralimbic areaPrimary visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70980 Infralimbic areaRostrolateral visual area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70981 Infralimbic areaAnterior cingulate area ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70982 Infralimbic areaEctorhinal area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70983 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70984 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70985 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70986 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70987 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70988 Infralimbic areaParasubiculum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70989 Infralimbic areaSubiculum dorsal part molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70990 Infralimbic areaSubiculum dorsal part stratum radiatum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70991 Infralimbic areaSubiculum dorsal part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70992 Infralimbic areaSubiculum ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70993 Infralimbic areaSubiculum ventral part stratum radiatum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70994 Infralimbic areaSubiculum ventral part pyramidal layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70995 Infralimbic areaField CA1 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70996 Infralimbic areaField CA1 pyramidal layer, deep not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70997 Infralimbic areaField CA1 pyramidal layer, superficial not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70998 Infralimbic areaField CA1 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
70999 Infralimbic areaField CA2 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71000 Infralimbic areaField CA2 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71001 Infralimbic areaField CA2 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71002 Infralimbic areaField CA2 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71003 Infralimbic areaField CA3 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71004 Infralimbic areaField CA3 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71005 Infralimbic areaField CA3 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71006 Infralimbic areaField CA3 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71007 Infralimbic areaDentate gyrus crest molecular layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71008 Infralimbic areaDentate gyrus crest granule cell layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71009 Infralimbic areaDentate gyrus crest polymorph layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71010 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71011 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71012 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71013 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71014 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71015 Infralimbic areaDentate gyrus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71016 Infralimbic areaInduseum griseum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71017 Infralimbic areaFasciola cinerea not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71018 Infralimbic areaInfralimbic area not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71019 Infralimbic areaOrbital area lateral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71020 Infralimbic areaOrbital area medial part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71021 Infralimbic areaOrbital area ventral part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71022 Infralimbic areaRetrosplenial area dorsal part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71023 Infralimbic areaRetrosplenial area lateral agranular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71024 Infralimbic areaRetrosplenial area ventral part zone a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71025 Infralimbic areaRetrosplenial area ventral part zone b/c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71026 Infralimbic areaVentral temporal association areas not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71027 Infralimbic areaLayer 6b, isocortex not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71028 Infralimbic areaClaustrum not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71029 Infralimbic areaBasomedial nucleus of the amygdala anterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71030 Infralimbic areaLingula (l) not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71031 Infralimbic areaCentral lobule, lobule II sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71032 Infralimbic areaCentral lobule, lobule II sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71033 Infralimbic areaCentral lobule, lobule III sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71034 Infralimbic areaCentral lobule, lobule III sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71035 Infralimbic areaCulmen lobule IV not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71036 Infralimbic areaCulmen lobule V not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71037 Infralimbic areaDeclive, sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71038 Infralimbic areaDeclive, sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71039 Infralimbic areaDeclive, sublobule c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71040 Infralimbic areaDeclive, sublobule d not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71041 Infralimbic areaFolium-tuber vermis (VII) not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71042 Infralimbic areaPyramus sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71043 Infralimbic areaPyramus sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71044 Infralimbic areaUvula (IX) sublobule ab not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71045 Infralimbic areaUvula (IX) sublobule c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71046 Infralimbic areaNodulus sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71047 Infralimbic areaNodulus sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71048 Infralimbic areaSimple lobule sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71049 Infralimbic areaSimple lobule sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71050 Infralimbic areaAnsiform lobule crus 1 sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71051 Infralimbic areaAnsiform lobule crus 1 sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71052 Infralimbic areaAnsiform lobule crus 1 sublobule c not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71053 Infralimbic areaAnsiform lobule crus 1 sublobule d not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71054 Infralimbic areaAnsiform lobule crus 2 sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71055 Infralimbic areaAnsiform lobule crus 2 sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71056 Infralimbic areaParamedian lobule not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71057 Infralimbic areaCopula pyramidis sublobule a not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71058 Infralimbic areaCopula pyramidis sublobule b not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71059 Infralimbic areaParaflocculus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71060 Infralimbic areaFlocculus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71061 Infralimbic areaFastigial nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71062 Infralimbic areaInterposed nucleus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71063 Infralimbic areaInterposed nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71064 Infralimbic areaDentate nucleus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71065 Infralimbic areaDentate nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71066 Infralimbic areaRetina, outer nuclear layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71067 Infralimbic areaRetina, outer plexiform layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71068 Infralimbic areaRetina, inner nuclear layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71069 Infralimbic areaRetina, inner plexiform layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71070 Infralimbic areaRetina, ganglion cell layer not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71071 Infralimbic areaTegmental reticular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71072 Infralimbic areaPontine gray proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71073 Infralimbic areaDorsal accessory olive not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71074 Infralimbic areaMedial accessory olive not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71075 Infralimbic areaPrincipal olive not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71076 Infralimbic areaLateral reticular nucleus magnocellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71077 Infralimbic areaLateral reticular nucleus parvicellular part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71078 Infralimbic areaLinear nucleus of the medulla not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71079 Infralimbic areaParamedian reticular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71080 Infralimbic areaParasolitary nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71081 Infralimbic areaRed nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71082 Infralimbic areaAccessory facial nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71083 Infralimbic areaFacial nucleus_proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71084 Infralimbic areaEfferent cochlear group not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71085 Infralimbic areaEfferent vesstibular nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71086 Infralimbic areaNucleus ambiguus dorsal division, stylopharyngeal motoneurons not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71087 Infralimbic areaNucleus ambiguus dorsal division proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71088 Infralimbic areaNucleus of the spinal accessory nerve not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71089 Infralimbic areaHypoglossal nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71090 Infralimbic areaSuperior salivatory nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71091 Infralimbic areaInferior salivatory nucleus not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71092 Infralimbic areaLateral hypothalamic area proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71093 Infralimbic areaMedial preoptic area proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71094 Infralimbic areaAnterior hypothalamic area proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71095 Infralimbic areaSupraoptic nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71096 Infralimbic areaMesencephalic reticular nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71097 Infralimbic areaLocus coeruleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71098 Infralimbic areaBed nuclei of the stria terminalis anterior division anterodorsal area proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71099 Infralimbic areaBed nuclei of the stria terminalis anterior division anterodorsal area central core not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71100 Infralimbic areaLaterodorsal tegmental nucleus proper not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71101 Infralimbic areaField CA3 not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71102 Infralimbic areaPituitary gland, neural lobe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71103 Infralimbic areaMedian eminence external lamina not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71104 Infralimbic areaMedian eminence internal lamina not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71105 Infralimbic areaInfundibulum external lamina not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71106 Infralimbic areaInfundibulum internal lamina not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71107 Infralimbic areaPituitary gland, anterior lobe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71108 Infralimbic areaPituitary gland, intermediate lobe not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
71109 Infralimbic areaNucleus reuniens rostral division anterior part not presentPHAL
Collator note: this connection is considered to be absent, because all of the atlas levels were inspected by authors.
Hurley KM, Herbert H, Moga MM, Saper CB., 1991
General description technique/protocol: not provided

Further details associated to record number 70638:
Position of injection: everywhere
Topological position of injection: identical
Extension of injection outside: small
The injection was performed in: left hemisphere
Position of terminal field: dorsal
Topological position of terminal field: is contained
Extension of terminal field outside: none
The terminal field was found: ipsilateral