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1 ontal cortex, hippocampus, amygdala, and bed nucleus of the stria terminalis).
2 othalamus, the central amygdala, and the bed nucleus of the stria terminalis.
3 rontal cortex, basolateral amygdala, and bed nucleus of the stria terminalis.
4 anced startle (LES), is dependent on the bed nucleus of the stria terminalis.
5 nded amygdala, and the posterior lateral bed nucleus of the stria terminalis.
6 ved in the zona incerta and the interstitial nucleus of the stria terminalis.
7 striatum, the central amygdala, and the bed nucleus of the stria terminalis.
8 ajor downstream projection structure-the bed nucleus of the stria terminalis.
9 amygdala and at 17 and 24 months in the bed nucleus of the stria terminalis.
10 that project out of the CeA and into the bed nucleus of the stria terminalis.
11 le, central nucleus of the amygdala, and bed nucleus of the stria terminalis.
12 medial amygdala, cortical amygdala, and bed nucleus of the stria terminalis.
13 nocellular preoptic nucleus (SI/MA), and bed nucleus of the stria terminalis.
14 odorsal medial amygdala, and 103% in the bed nucleus of the stria terminalis.
15 terminalis and scattered throughout the bed nucleus of the stria terminalis.
16 of the anterior commissure nucleus, and bed nucleus of the stria terminalis.
17 leasing factor-containing neurons of the bed nucleus of the stria terminalis.
18 e that CeA CRF1 neurons project into the bed nucleus of the stria terminalis.
19 en receptors (AR) in the medial anterior bed nucleus of the stria terminalis, a key brain area that c
20 ociated with increased metabolism in the bed nucleus of the stria terminalis, a key component of the
22 N(SF1) fibers projecting to the anterior bed nucleus of the stria terminalis (aBNST), but not to othe
23 ng while activation of AgRP --> anterior bed nucleus of the stria terminalis (aBNST)vl projections, d
24 tified a discrete region of the anterior bed nucleus of the stria terminalis (aBST) as a candidate fo
25 a circumscribed portion of the anterior bed nucleus of the stria terminalis (aBST), which we previou
27 er of FLI neurons in the lateral septum, bed nucleus of the stria terminalis, amygdala, paraventricul
28 with anxiety and stress behaviors (i.e., bed nucleus of the stria terminalis, amygdala, periaqueducta
29 dial pallium, lateral and medial septum, bed nucleus of the stria terminalis, amygdala, preoptic area
30 that P metabolites have an effect on the bed nucleus of the stria terminalis and anxiety rather than
32 d in several other regions including the bed nucleus of the stria terminalis and central amygdala.
33 ventricular nucleus, supraoptic nucleus, bed nucleus of the stria terminalis and central nucleus of t
35 sed heroin intake when injected into the bed nucleus of the stria terminalis and shell of the nucleus
36 the coordinated activation of D2R in the bed nucleus of the stria terminalis and the central amygdala
37 ptum, the ventromedial hypothalamus, the bed nucleus of the stria terminalis and the medial amygdala.
38 acid lesions of the medial amygdala, the bed nucleus of the stria terminalis and the medial preoptic
39 the medial nucleus of the amygdala, the bed nucleus of the stria terminalis and the medial preoptic
41 nduced c-fos expression in the principle bed nucleus of the stria terminalis and the ventrolateral di
42 ontinuous with the medial aspects of the bed nucleus of the stria terminalis and the ventromedial str
43 ing the central nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area i
44 ing the central nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area i
46 abundant in the medial preoptic nucleus, bed nucleus of the stria terminalis, and anterior hypothalam
47 nsely expressed in the stress-responsive bed nucleus of the stria terminalis, and bilateral injection
48 induced Fos-IR changes (caudate putamen, bed nucleus of the stria terminalis, and CA1 region of the h
49 tral nuclei of the amygdala and anterior bed nucleus of the stria terminalis, and densely to the late
51 e allocortex, claustrum, lateral septum, bed nucleus of the stria terminalis, and in many hypothalami
52 bers throughout the hypothalamus, in the bed nucleus of the stria terminalis, and in the amygdala.
53 f the nucleus accumbens (AccSh), lateral bed nucleus of the stria terminalis, and intermediate zone o
54 lateral septum, dorsolateral area of the bed nucleus of the stria terminalis, and lateral habenular n
55 ucleus, central nucleus of the amygdala, bed nucleus of the stria terminalis, and lateral septum.
56 uclei, amygdalostriatal transition area, bed nucleus of the stria terminalis, and medial habenular nu
57 campus, central nucleus of the amygdala, bed nucleus of the stria terminalis, and medial parvocellula
58 Fos protein expression in the amygdala, bed nucleus of the stria terminalis, and medial preoptic are
59 gray, thalamus, hypothalamus, amygdala, bed nucleus of the stria terminalis, and other central sites
60 layer, dentate gyrus polymorphic layer, bed nucleus of the stria terminalis, and paraventricular nuc
61 s, amygdala (central and corticomedial), bed nucleus of the stria terminalis, and prefrontal cortical
62 the shell of the nucleus accumbens, the bed nucleus of the stria terminalis, and the central nucleus
63 tic area, periventricular preoptic area, bed nucleus of the stria terminalis, and the medial amygdala
64 es within the hippocampus, amygdala, the bed nucleus of the stria terminalis, and the prefrontal cort
65 r neurons in the amygdala, hypothalamus, bed nucleus of the stria terminalis, and to a remarkable ext
66 terogenous regions such as the amygdala, bed nucleus of the stria terminalis, and ventral forebrain.
67 lar hypothalamus, premammillary nucleus, bed nucleus of the stria terminalis, and ventral posterior a
68 wer neurons in the central amygdala, the bed nucleus of the stria terminalis, and visceral cortices w
69 dial and lateral hypothalamus, amygdala, bed nucleus of the stria terminalis, and visceral cortices.
70 nificant effect on Fos expression in the bed nucleus of the stria terminalis, another forebrain area
71 , including notable contributions of the bed nucleus of the stria terminalis, anterior insula, and th
72 strates that the medial amygdala and the bed nucleus of the stria terminalis are not involved in the
73 central nucleus of the amygdala and the bed nucleus of the stria terminalis as glucocorticoid-sensit
74 reoptic area of the hypothalamus and the bed nucleus of the stria terminalis as well as novel dimorph
75 ses of neurons in the lateral septum and bed nucleus of the stria terminalis, as well as in several o
76 o, infusion of antisauvagine-30 into the bed nucleus of the stria terminalis (BNST) 15 min, but not i
78 o identified in hippocampus, the lateral bed nucleus of the stria terminalis (BNST) and globus pallid
79 increased CRF mRNA within the amygdala, bed nucleus of the stria terminalis (BNST) and paraventricul
80 to the posteromedial subdivision of the bed nucleus of the stria terminalis (BNST) and to the medial
81 ales in the cingulate cortex and rostral bed nucleus of the stria terminalis (BNST) at 2 h, and in th
82 araventricular nucleus (PVN) or into the bed nucleus of the stria terminalis (BNST) but not into the
84 sts norepinephrine (NE) signaling in the bed nucleus of the stria terminalis (BNST) could have a role
85 medial amygdala (MeA) and reduced in the bed nucleus of the stria terminalis (BNST) during novelty ex
90 factor (CRF)-mediated mechanisms in the bed nucleus of the stria terminalis (BNST) have a pivotal ro
91 of an alpha2-receptor agonist, into the bed nucleus of the stria terminalis (BNST) in rats markedly
92 e identify a surprising new role for the bed nucleus of the stria terminalis (BNST) in the coordinate
94 vement of the central amygdala (CeA) and bed nucleus of the stria terminalis (BNST) in the genesis of
95 nal data support a critical role for the bed nucleus of the stria terminalis (BNST) in the interactio
96 Fos results, we determined the effect of bed nucleus of the stria terminalis (BNST) injections of nor
98 entral nucleus of the amygdala (CeA) and bed nucleus of the stria terminalis (BNST) is a critical com
106 buse, and noradrenergic signaling in the bed nucleus of the stria terminalis (BNST) is thought to be
110 ctivating peptide (PACAP) systems in the bed nucleus of the stria terminalis (BNST) mediates many con
111 vestigated the effects of lesions of the bed nucleus of the stria terminalis (BNST) on conditioned fe
113 ha2-adrenergic receptors (AR) within the bed nucleus of the stria terminalis (BNST) reduce stress-rew
114 Although specific neuronal groups in the bed nucleus of the stria terminalis (BNST) related to anxiet
115 cific had lower levels of peptide in the bed nucleus of the stria terminalis (BNST) than isolated ani
116 eract in a serial manner to activate the bed nucleus of the stria terminalis (BNST) to drive stress-
117 The responsiveness of neurons of the bed nucleus of the stria terminalis (BNST) to infralimbic co
118 d pretraining excitotoxic lesions of the bed nucleus of the stria terminalis (BNST) to that of sham r
119 tential role of CRF projections from the bed nucleus of the stria terminalis (BNST) to the VTA, CRF n
120 al nucleus of the amygdala (BlA), or the bed nucleus of the stria terminalis (BNST) were evaluated on
121 dy examined the role of the amygdala and bed nucleus of the stria terminalis (BNST), 2 systems that h
122 h dynorphin and KOR are expressed in the bed nucleus of the stria terminalis (BNST), a brain region a
123 ssessed the role of CRF receptors in the bed nucleus of the stria terminalis (BNST), a brain region i
124 hese catecholamines are found within the bed nucleus of the stria terminalis (BNST), a brain relay nu
125 in extracellular dopamine levels is the bed nucleus of the stria terminalis (BNST), a CRF-rich compo
126 entify a precise neural mechanism in the bed nucleus of the stria terminalis (BNST), a limbic brain r
127 Here, we study 5-HT inputs into the bed nucleus of the stria terminalis (BNST), a major subdivis
128 depresses excitatory transmission in the bed nucleus of the stria terminalis (BNST), a region critica
129 ctions innervate distinct regions of the bed nucleus of the stria terminalis (BNST), a structure that
130 tral amygdaloid nucleus (CeA) and in the bed nucleus of the stria terminalis (BNST), although robust
131 e of affecting 5-HT systems, such as the bed nucleus of the stria terminalis (BNST), amygdala, and ha
133 , central nucleus of the amygdala (CeA), bed nucleus of the stria terminalis (BNST), and insular cort
134 l nucleus of the amygdala (CeA), lateral bed nucleus of the stria terminalis (BNST), and nucleus accu
135 TD) of glutamatergic transmission in the bed nucleus of the stria terminalis (BNST), and that ex vivo
136 r nucleus (PVN) of the hypothalamus, the bed nucleus of the stria terminalis (BNST), and the central
137 the amygdala, periqueductal gray (PAG), bed nucleus of the stria terminalis (BNST), anterior cingula
138 uding the insular gustatory cortex (IC), bed nucleus of the stria terminalis (BNST), central nucleus
139 ructures like the gustatory cortex (GC), bed nucleus of the stria terminalis (BNST), central nucleus
141 al nucleus of the amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), each of which ha
142 imulation of the CeA, or the neighboring bed nucleus of the stria terminalis (BNST), initiates bouts
143 in both 2-DG and c-fos activity), e.g., bed nucleus of the stria terminalis (BNST), lateral habenula
144 reatly reduced in the dorsal and ventral bed nucleus of the stria terminalis (BNST), lateral septum,
145 ) in several brain regions including the bed nucleus of the stria terminalis (BNST), medial preoptic
146 The extended amygdala, including the bed nucleus of the stria terminalis (BNST), modulates fear a
147 e accessory olfactory bulb (gr-AOB), the bed nucleus of the stria terminalis (BNST), MPOA, the medial
148 atum, various subfields of the amygdala, bed nucleus of the stria terminalis (BNST), optic tectum, va
149 induced in several nuclei including the bed nucleus of the stria terminalis (BNST), paraventricular
150 us accumbens (Acb), preoptic area (POA), bed nucleus of the stria terminalis (BNST), posterior dorsal
151 at in the dorsolateral and ventrolateral bed nucleus of the stria terminalis (BNST), recruitment of G
152 central nucleus of the amygdala and the bed nucleus of the stria terminalis (BNST), respectively.
153 m, several preoptic nuclei, the anterior bed nucleus of the stria terminalis (BNST), the anterior par
154 r these effects require NA inputs to the bed nucleus of the stria terminalis (BNST), vehicle or sapor
156 A are from the medial amygdala (MeA) and bed nucleus of the stria terminalis (BNST), which mediate th
157 dence implicates a tiny brain region-the bed nucleus of the stria terminalis (BNST)-in the body's str
158 may specifically increase long-duration bed nucleus of the stria terminalis (BNST)-mediated aversive
163 tal cortex, nucleus accumbens (NAc), and bed nucleus of the stria terminalis (BNST)], whereas protrac
164 atic [SCN]) and extended amygdala (i.e., bed nucleus of the stria terminalis [BNST] and medial amygda
167 the amygdala (CeAL) and the dorsolateral bed nucleus of the stria terminalis (BNSTDL) coordinate the
168 nucleus of the amygdala, dorsal lateral bed nucleus of the stria terminalis (BNSTdl), anterior parav
169 al nucleus of the amygdala (CN), ventral bed nucleus of the stria terminalis (BNSTv), and nucleus acc
170 ine-induced c-fos mRNA expression in the bed nucleus of the stria terminalis (BST) and amygdala of ma
171 othalamic nucleus, medial preoptic area, bed nucleus of the stria terminalis (BST) and hippocampus (C
172 ole-rats had very few VP-ir cells in the bed nucleus of the stria terminalis (BST) and none in the su
174 ed with prosocial behavior including the bed nucleus of the stria terminalis (BST) and the medial amy
175 eus of the amygdala (Ce) and the lateral bed nucleus of the stria terminalis (BST) are highly similar
176 e medial preoptic area and posteromedial bed nucleus of the stria terminalis (BST) in aged rats relat
177 ermetabolism in a cluster comprising the bed nucleus of the stria terminalis (BST) in rats expressing
178 erous lines of evidence suggest that the bed nucleus of the stria terminalis (BST) is well positioned
179 ant peptide vasopressin (AVP) within the bed nucleus of the stria terminalis (BST) of adult brain is
180 central nucleus of the amygdala (Ce) and bed nucleus of the stria terminalis (BST) than in hamsters h
182 food intake by acting on neurons of the bed nucleus of the stria terminalis (BST), a component of ex
183 n the forebrain of amniotes has been the bed nucleus of the stria terminalis (BST), but numerous rece
184 ral nucleus of the amygdala (Ce) and the bed nucleus of the stria terminalis (BST), the two major sub
187 hat project to the principal part of the bed nucleus of the stria terminalis (BST; 43%), and the perc
188 ia terminalis (BSTv), whereas the dorsal bed nucleus of the stria terminalis (BSTd) and the medial an
190 ation of the HPA response in the lateral bed nucleus of the stria terminalis (BSTL), compared to outb
193 ells in the dorsolateral division of the bed nucleus of the stria terminalis (BSTld), part of the cri
194 central amygdala (ceA) and laterodorsal bed nucleus of the stria terminalis (BSTLD), the blunting of
196 oid receptor labeling in the POM, medial bed nucleus of the stria terminalis (BSTm), and periaqueduct
197 gdala (CEAl) and the oval nucleus of the bed nucleus of the stria terminalis (BSTov) have been linked
198 ygdala (CEAl/c) and oval division of the bed nucleus of the stria terminalis (BSTov), which form part
200 express T-induced Fos: the posteromedial bed nucleus of the stria terminalis (BSTPM), posteromedial a
202 ng norepinephrine release in the ventral bed nucleus of the stria terminalis (BSTv) with the alpha2-a
203 dial preoptic area (MPO) and the ventral bed nucleus of the stria terminalis (BSTv), whereas the dors
205 rons project mainly to the ventrolateral bed nucleus of the stria terminalis (BSTvl), the pre-locus c
206 gustatory region of the thalamus and the bed nucleus of the stria terminalis but not in the insular c
207 icular reduced amygdala AT1 receptor and bed nucleus of the stria terminalis c-Fos messenger RNA leve
208 r neurons were visualized in the cortex, bed nucleus of the stria terminalis, central amygdala, hypot
209 in the infralimbic and insular cortices, bed nucleus of the stria terminalis, central nucleus of the
210 er and electrolyte balance including the bed nucleus of the stria terminalis, central nucleus of the
211 the anterior olfactory nucleus, LS, and bed nucleus of the stria terminalis, compared with naive LD
212 exceptions were the posterointermediate bed nucleus of the stria terminalis, containing more neurons
213 lity in the amygdalohippocampal area and bed nucleus of the stria terminalis correlated positively wi
214 in-releasing factor (CRF) neurons in the bed nucleus of the stria terminalis (CRF(BNST)) in mice.
217 dose) administered into the dorsolateral bed nucleus of the stria terminalis (dlBNST) immediately pri
219 ene mapping highlighted the dorsolateral bed nucleus of the stria terminalis (dlBST) as a structure p
220 ly; however, both triggered increases in bed nucleus of the stria terminalis dorsal (BNSTd) and later
221 deep brain structures such as amygdala, bed nucleus of the stria terminalis, dorsal raphe, and later
223 ple labeled neurons were observed in the bed nucleus of the stria terminalis following WGA-Au-HRP inj
224 havioral responses: the amygdala and the bed nucleus of the stria terminalis for sustaining adaptive
226 ons of either the medial amygdala or the bed nucleus of the stria terminalis have no effect on the di
227 were apparent in the nucleus accumbens, bed nucleus of the stria terminalis, hippocampus, and cortex
228 area (LPOA) and ventral division of the bed nucleus of the stria terminalis; however, lesions of the
229 esent in the suprachiasmatic nucleus and bed nucleus of the stria terminalis; however, there are exte
230 mmunoreactive cells were observed in the bed nucleus of the stria terminalis, hypothalamic paraventri
231 ed cells in several areas, including the bed nucleus of the stria terminalis, hypothalamic regions, t
232 teroventral periventricular nucleus, and bed nucleus of the stria terminalis in a distribution consis
233 ) binding was higher in the encapsulated bed nucleus of the stria terminalis in males than females fo
234 k implicating PACAP signaling within the bed nucleus of the stria terminalis in mediating the consequ
235 Abundant GnIH-ir fibers were observed in the nucleus of the stria terminalis in the telencephalon; ha
236 rentiation: the principal nucleus of the bed nucleus of the stria terminalis, in which males have mor
237 uch as the septum, the amygdala, and the bed nucleus of the stria terminalis; in areas involved in en
239 e central nucleus of the amygdala (CeA), bed nucleus of the stria terminalis (lateral-dorsal division
240 s (AON), and more OT binding in the AON, bed nucleus of the stria terminalis, LS, and lateral amygdal
242 nd posteroventral medial amygdala (MeA), bed nucleus of the stria terminalis, medial preoptic nucleus
243 ncreased significantly in the claustrum, bed nucleus of the stria terminalis, medial preoptic nucleus
244 tive cells were seen unilaterally in the bed nucleus of the stria terminalis, medial ventral pallidum
245 moderate projections from the posterior bed nucleus of the stria terminalis, mesocortical structures
246 in the preoptic area, amygdala, septum, bed nucleus of the stria terminalis, midline thalamus, and t
247 ea (POA) and medial preoptic area/medial bed nucleus of the stria terminalis (mPOA/BSTm), and the hig
250 n and OT/c-fos cells in the medioventral bed nucleus of the stria terminalis of female mice but not m
251 ding in the medial preoptic area and the bed nucleus of the stria terminalis of non-responsive mice t
252 ynaptic transmission was enhanced in the bed nucleus of the stria terminalis of rats that performed a
254 did not increase FLI in caudate-putamen, bed nucleus of the stria terminalis, or ventral pallidum.
255 e staining in the septum, diagonal band, bed nucleus of the stria terminalis, organum vasculosum, nuc
256 eling from the nPGi was prominent in the bed nucleus of the stria terminalis, paraventricular nucleus
257 hypothalamus and a larger volume of the bed nucleus of the stria terminalis, paraventricular nucleus
258 within nucleus accumbens shell, lateral bed nucleus of the stria terminalis, paraventricular nucleus
259 halamus, arcuate nucleus, preoptic area, bed nucleus of the stria terminalis, paraventricular thalamu
260 ough its interactions with the amygdala, bed nucleus of the stria terminalis, periaqueductal gray, hi
261 ed autonomic effector regions, including bed nucleus of the stria terminalis, perifornical and anteri
262 entral pallium; nucleus basalis Meynert; bed nucleus of the stria terminalis; preoptic area; paravent
263 injections of RXFP3 antagonist into the bed nucleus of the stria terminalis significantly decreased
264 elds of the cholinergic basal forebrain, bed nucleus of the stria terminalis, striohypothalamic regio
265 erminals were encountered in the septum, bed nucleus of the stria terminalis, substantia innominata,
266 ing also failed a-Helical CRF9-41 in the bed nucleus of the stria terminalis suggested that this area
267 amic nuclei, the nucleus prepositus, and the nucleus of the stria terminalis suggests that each recep
268 inuum with the substantia innominata and bed nucleus of the stria terminalis, supporting the concept
269 al cortex, medial septum, preoptic area, bed nucleus of the stria terminalis, supraoptic nucleus, par
270 frontal cortex (dmPFC), anterior insula, bed nucleus of the stria terminalis, thalamus, and midbrain
271 of GABAA-IPSCs (D1-LTPGABA) in the oval bed nucleus of the stria terminalis that was positively corr
272 ontrol descending output (via the CNA or bed nucleus of the stria terminalis) that in turn regulates
273 , the central tegmental field (CTF), the bed nucleus of the stria terminalis, the anterior hypothalam
274 eus, anteromedial and oval nuclei of the bed nucleus of the stria terminalis, the central nucleus of
275 the central EA structures of the lateral bed nucleus of the stria terminalis, the central sublenticul
276 rkinje cell layer of the cerebellum, the bed nucleus of the stria terminalis, the claustrum (alpha1G)
277 ortices, the lateral septal nucleus, the bed nucleus of the stria terminalis, the fundus striati, the
278 cleus of the amygdala and to the lateral bed nucleus of the stria terminalis, the latter region recei
279 uding the lateral and medial septum, the bed nucleus of the stria terminalis, the medial and central
280 ppocampus and septum, the basal ganglia, bed nucleus of the stria terminalis, the thalamus including
281 d in other aggression areas, such as the bed nucleus of the stria terminalis, the ventrolateral hypot
282 sal premammillary nucleus, and principal bed nucleus of the stria terminalis, this is the first indic
283 e mainly observed in the medial amygdala/bed nucleus of the stria terminalis to lateral septum circui
285 enic cytokine, can act on neurons of the bed nucleus of the stria terminalis to reduce food intake vi
287 rolateral (subcommissural) aspect of the bed nucleus of the stria terminalis (vBNST) in motivational
291 d after castration in the interstitial (bed) nucleus of the stria terminalis, ventral aspect (INSTv),
292 I in caudate-putamen, nucleus accumbens, bed nucleus of the stria terminalis, ventral pallidum, centr
293 olfactory bulb, lateral septal nucleus, bed nucleus of the stria terminalis, ventromedial hypothalam
297 rexin cell field from lateral septum and bed nucleus of the stria terminalis were Fos-activated durin
298 ns participate in specific nuclei of the bed nucleus of the stria terminalis, which plays essential r
299 f the amygdala and then to the principal bed nucleus of the stria terminalis, which suppresses territ
300 report a sex difference in ERbeta in the bed nucleus of the stria terminalis, with males showing grea
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