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1 nduced NGF receptor expression in the medial septal nucleus.
2 audate putamen, corpus callosum, and lateral septal nucleus.
3 d by microinfusions restricted to the medial septal nucleus.
4 led neurons were also present in the lateral septal nucleus, a system that receives hippocampal input
5 anges in forebrain regions, particularly the septal nucleus and amygdala.
6 icantly correlated with gating in the medial septal nucleus and brainstem reticular nucleus, but not
7 mbers of Fos-positive neurons in the lateral septal nucleus and in both the parvocellular and magnoce
8 ucleus, central nucleus of amygdala, lateral septal nucleus and lateral habenular nucleus.
9 tions to forebrain structures, including the septal nucleus and nucleus accumbens (NAC), and within t
10                       Neurons in the lateral septal nucleus and the medial amygdaloid nucleus, which
11 8 and originate in pacemaker circuits in the septal nucleus and the piriform cortex.
12 aves are initiated at pacemaker sites in the septal nucleus and ventral cortex.
13 us, and limbic regions including the lateral septal nucleus and ventral subiculum.
14 nd trkA-immunoreactive neurons in the medial septal nucleus and vertical limb of the diagonal band as
15 upraoptic nucleus, as well as in the cortex, septal nucleus, and preoptical area.
16 s, habenula, hippocampus, subiculum, lateral septal nucleus, anterior cingulate cortex, infralimbic c
17 ty for p75 and trkA antibodies in the medial septal nucleus as compared to controls.
18 nificant 50% increase in GAD activity in the septal nucleus at 12 months of age.
19 luded aspects of the olfactory bulb, lateral septal nucleus, bed nucleus of the stria terminalis, ven
20 areas: CA3 region of the hippocampus, medial septal nucleus, brainstem reticular nucleus, and the aud
21 imilar and included cerebral cortex, lateral septal nucleus, cingulum, hippocampus, thalamus, amygdal
22 ization and burst firing in rat dorsolateral septal nucleus (DLSN) neurons and results in long-term p
23 tivation extending anteriorly to the lateral septal nucleus, dorsally to the thalamic paraventricular
24 cortin induced Fos expression in the lateral septal nucleus, Edinger-Westphal nucleus, dorsal raphe n
25 y and loss of axons entering the ipsilateral septal nucleus followed by ipsilateral septal atrophy.
26                               In the lateral septal nucleus, GABAergic neuronal activity was signific
27                      However, in the lateral septal nucleus, helpless animals showed significantly re
28 ial nucleus, suprachiasmatic nucleus, medial septal nucleus, hippocampus (CA1 region), or cingulate c
29 area, ventral tegmental area, and the medial septal nucleus in P17 pups.
30 d projection mapping showed that the lateral septal nucleus (LS) contained the densest accumulation o
31 tic-anterior hypothalamus (MPOA-AH), lateral septal nucleus (LS), bed nucleus of stria terminalis (BN
32 tic-anterior hypothalamus (MPOA-AH), lateral septal nucleus (LS), bed nucleus of the stria terminalis
33 cy of each distinct cell type in the lateral septal nucleus (LSN) region of mouse forebrain.
34        Expression in insular cortex, lateral septal nucleus, medial preoptic area, rostral linear nuc
35 rrogate transcriptomic changes within medial septal nucleus (MSN) BFCNs.
36 d of several structures including the medial septal nucleus (MSN), nucleus of the diagonal band (DB),
37 ng the rat entorhinal cortex (EC) and medial septal nucleus (MSN), two promising areas for DBS treatm
38 gh levels also in thalamus, caudate putamen, septal nucleus, nucleus accumbens, amygdala, and anterio
39 and olfactory bulb, with lower levels in the septal nucleus, nucleus accumbens, amygdala, and hypotha
40 tants, including the caudate-putamen, medial septal nucleus, nucleus of the diagonal band, and magnoc
41  the amygdala, locus ceruleus, ventrolateral septal nucleus, paraventricular hypothalamic nucleus, la
42 tions end in the olfactory tubercle, lateral septal nucleus, posterior basolateral amygdalar nucleus,
43 rtex, the diagonal band of Broca, the medial septal nucleus, reticular thalamic nucleus, the striatum
44 areas, including the olfactory bulb, lateral septal nucleus, septohypothalamic nucleus, anteromedial
45 ta also demonstrate the presence of a medial septal nucleus that is histochemically comparable to the
46 nsular, and ectorhinal cortices, the lateral septal nucleus, the bed nucleus of the stria terminalis,
47 inals are unevenly distributed in the medial septal nucleus, the diagonal band, and the nucleus basal
48 ojections to the ventral part of the lateral septal nucleus, the parastrial nucleus, and the region a
49 beled in the infralimbic cortex, the lateral septal nucleus, the paraventricular thalamic nucleus, th
50 cholinergic efferent network from the medial septal nucleus to the hippocampus plays an important rol
51  decipher neural circuits emanating from the septal nucleus to the lateral hypothalamus (LH) that con
52 l amygdalar nucleus, to the adjacent lateral septal nucleus, to the nucleus accumbens and substantia
53 egions, including the preoptic area, lateral septal nucleus, ventral subiculum, and supramammillary n
54 e-labeled fibers were present in the lateral septal nucleus, ventromedial preoptic nucleus, lateral h
55  in the olfactory tubercle, striatum, medial septal nucleus, vertical and horizontal limbs of the dia
56 l volumes of cholinergic cells in the medial septal nucleus were assessed after an additional 10 mont
57  were identified that project to the lateral septal nucleus, which houses a prominent UCN-ir terminal
58 e brainstem reticular nucleus and the medial septal nucleus, while relatively few neurons responded i