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1 ippocampus, amygdala, and bed nucleus of the stria terminalis).
2 neurons project into the bed nucleus of the stria terminalis.
3 esponse to high-frequency stimulation of the stria terminalis.
4 central amygdala, and the bed nucleus of the stria terminalis.
5 nnections that project primarily through the stria terminalis.
6 and the posterior lateral bed nucleus of the stria terminalis.
7 basolateral amygdala, and bed nucleus of the stria terminalis.
8 LES), is dependent on the bed nucleus of the stria terminalis.
9 projection structure-the bed nucleus of the stria terminalis.
10 t of the CeA and into the bed nucleus of the stria terminalis.
11 scattered throughout the bed nucleus of the stria terminalis.
12 r commissure nucleus, and bed nucleus of the stria terminalis.
13 s no changes were observed within the BLA or stria terminalis.
14 containing neurons of the bed nucleus of the stria terminalis.
15 R) in the medial anterior bed nucleus of the stria terminalis, a key brain area that controls social
16 creased metabolism in the bed nucleus of the stria terminalis, a key component of the central extende
17 rojecting to the anterior bed nucleus of the stria terminalis (aBNST), but not to other brain areas i
18 tion of AgRP --> anterior bed nucleus of the stria terminalis (aBNST)vl projections, distinct from Ag
19 te region of the anterior bed nucleus of the stria terminalis (aBST) as a candidate for fulfilling th
20 ibed, anterior part of the bed nuclei of the stria terminalis (aBST) that houses stress-sensitive, PV
21 ic neurons within anterior bed nuclei of the stria terminalis (aBST) that integrates and relays inhib
22 d portion of the anterior bed nucleus of the stria terminalis (aBST), which we previously identified
24 d stress behaviors (i.e., bed nucleus of the stria terminalis, amygdala, periaqueductal gray, raphe a
25 ateral and medial septum, bed nucleus of the stria terminalis, amygdala, preoptic area, ventral hypot
27 tes have an effect on the bed nucleus of the stria terminalis and anxiety rather than on the amygdala
29 noradrenaline transmission in bed nucleus of stria terminalis and central amygdala, and dopamine, CRF
32 ed in the anterior cingulate, bed nucleus of stria terminalis and perirhinal area of oxytocin pretrea
33 asolateral amygdala (BLA) inputs through the stria terminalis and projects back to the anterior BLA a
34 amygdalostriatal transition area (AStr) and stria terminalis and scattered throughout the bed nucleu
36 the medial amygdala, the bed nucleus of the stria terminalis and the medial preoptic area on the dis
38 pression in the principle bed nucleus of the stria terminalis and the ventrolateral division of the v
39 the medial aspects of the bed nucleus of the stria terminalis and the ventromedial striatum, forming
40 nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area in the shell of
41 nucleus of the amygdala, bed nucleus of the stria terminalis, and a transition area in the shell of
43 medial preoptic nucleus, bed nucleus of the stria terminalis, and anterior hypothalamic area, wherea
44 in the stress-responsive bed nucleus of the stria terminalis, and bilateral injections of RXFP3 anta
45 changes (caudate putamen, bed nucleus of the stria terminalis, and CA1 region of the hippocampus).
46 the amygdala and anterior bed nucleus of the stria terminalis, and densely to the lateral hypothalamu
47 The dorsal and hippocampal cingulum bundle, stria terminalis, and fornix were investigated as region
50 laustrum, lateral septum, bed nucleus of the stria terminalis, and in many hypothalamic regions inclu
51 ccumbens (AccSh), lateral bed nucleus of the stria terminalis, and intermediate zone of the lateral s
54 striatal transition area, bed nucleus of the stria terminalis, and medial habenular nucleus display a
55 nucleus of the amygdala, bed nucleus of the stria terminalis, and medial parvocellular paraventricul
58 gyrus polymorphic layer, bed nucleus of the stria terminalis, and paraventricular nucleus of the hyp
59 tral nucleus of the amygdala, bed nucleus of stria terminalis, and posterior ventral tegmental area.
61 eptum, posterior division of the bed nucleus stria terminalis, and the medial nucleus of the amygdala
62 a, the oval nucleus of the bed nuclei of the stria terminalis, and the paraventricular nucleus of the
64 e amygdala, hypothalamus, bed nucleus of the stria terminalis, and to a remarkable extent, the globus
66 the central amygdala, the bed nucleus of the stria terminalis, and visceral cortices were infected co
67 on Fos expression in the bed nucleus of the stria terminalis, another forebrain area implicated in s
68 able contributions of the bed nucleus of the stria terminalis, anterior insula, and thalamus during t
69 ojection pattern of a tiny bed nuclei of the stria terminalis anteromedial group differentiation, the
70 e medial amygdala and the bed nucleus of the stria terminalis are not involved in the behavioral resp
71 the hypothalamus and the bed nucleus of the stria terminalis as well as novel dimorphic islands in t
72 in the lateral septum and bed nucleus of the stria terminalis, as well as in several other limbic sit
73 n, EphA5 protein was found in the claustrum, stria terminalis, barrel cortex, and striatal patches, a
74 dial extended amygdala and bed nuclei of the stria terminalis; basal telencephalic cholinergic and no
76 anted DBS electrodes from the bed nucleus of stria terminalis (BNST area) in 12 patients (5 OCD, 7 MD
77 antisauvagine-30 into the bed nucleus of the stria terminalis (BNST) 15 min, but not immediately, pri
78 hippocampus, the lateral bed nucleus of the stria terminalis (BNST) and globus pallidus at 60 and 12
79 mRNA within the amygdala, bed nucleus of the stria terminalis (BNST) and paraventricular nucleus of t
80 gulate cortex and rostral bed nucleus of the stria terminalis (BNST) at 2 h, and in the caudal BNST a
81 nucleus (PVN) or into the bed nucleus of the stria terminalis (BNST) but not into the ventral tegment
83 ine (NE) signaling in the bed nucleus of the stria terminalis (BNST) could have a role in mediating t
84 (MeA) and reduced in the bed nucleus of the stria terminalis (BNST) during novelty exposure, regardl
86 ong these structures, the bed nucleus of the stria terminalis (BNST) has been implicated in emotional
89 ediated mechanisms in the bed nucleus of the stria terminalis (BNST) have a pivotal role in stress-in
90 rprising new role for the bed nucleus of the stria terminalis (BNST) in the coordinated modulation of
92 entral amygdala (CeA) and bed nucleus of the stria terminalis (BNST) in the genesis of fear versus an
93 t a critical role for the bed nucleus of the stria terminalis (BNST) in the interaction between stres
94 determined the effect of bed nucleus of the stria terminalis (BNST) injections of nor-BNI (4 mug/sid
96 of the amygdala (CeA) and bed nucleus of the stria terminalis (BNST) is a critical component of the n
99 iously, we found that the bed nucleus of the stria terminalis (BNST) is also necessary for the enhanc
104 renergic signaling in the bed nucleus of the stria terminalis (BNST) is thought to be a source of thi
107 ere we tested whether the bed nucleus of the stria terminalis (BNST) mediates anxiogenic effects of O
108 de (PACAP) systems in the bed nucleus of the stria terminalis (BNST) mediates many consequences of ch
109 effects of lesions of the bed nucleus of the stria terminalis (BNST) on conditioned fear and anxiety.
111 receptors (AR) within the bed nucleus of the stria terminalis (BNST) reduce stress-reward interaction
112 lter BI and metabolism in the bed nucleus of stria terminalis (BNST) region and that individual diffe
113 ic neuronal groups in the bed nucleus of the stria terminalis (BNST) related to anxiety and reward ci
115 al manner to activate the bed nucleus of the stria terminalis (BNST) to drive stress- or cue-induced
116 iveness of neurons of the bed nucleus of the stria terminalis (BNST) to infralimbic cortex (ILCx) exc
118 CRF projections from the bed nucleus of the stria terminalis (BNST) to the VTA, CRF neurons in this
119 he amygdala (BlA), or the bed nucleus of the stria terminalis (BNST) were evaluated on excessive inta
120 KOR are expressed in the bed nucleus of the stria terminalis (BNST), a brain region associated with
121 e of CRF receptors in the bed nucleus of the stria terminalis (BNST), a brain region implicated in st
122 ines are found within the bed nucleus of the stria terminalis (BNST), a brain relay nucleus in the ex
123 ar dopamine levels is the bed nucleus of the stria terminalis (BNST), a CRF-rich component of the ext
124 e neural mechanism in the bed nucleus of the stria terminalis (BNST), a limbic brain region involved
125 tudy 5-HT inputs into the bed nucleus of the stria terminalis (BNST), a major subdivision of the exte
126 atory transmission in the bed nucleus of the stria terminalis (BNST), a region critical to the integr
127 e distinct regions of the bed nucleus of the stria terminalis (BNST), a structure that mediates behav
128 5-HT systems, such as the bed nucleus of the stria terminalis (BNST), amygdala, and habenula, could c
129 hors examined whether the bed nucleus of the stria terminalis (BNST), an area involved in stress and
131 e amygdala (CeA), lateral bed nucleus of the stria terminalis (BNST), and nucleus accumbens shell (NA
132 ergic transmission in the bed nucleus of the stria terminalis (BNST), and that ex vivo induction of t
133 periqueductal gray (PAG), bed nucleus of the stria terminalis (BNST), anterior cingulate cortex (ACC)
134 ar gustatory cortex (IC), bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala
135 he gustatory cortex (GC), bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala
137 he amygdala (CeA) and the bed nucleus of the stria terminalis (BNST), each of which has been implicat
138 e CeA, or the neighboring bed nucleus of the stria terminalis (BNST), initiates bouts of fictive call
139 in the dorsal and ventral bed nucleus of the stria terminalis (BNST), lateral septum, and nucleus acc
140 ain regions including the bed nucleus of the stria terminalis (BNST), medial preoptic area (MPOA), pa
141 d amygdala, including the bed nucleus of the stria terminalis (BNST), modulates fear and anxiety, but
142 ubfields of the amygdala, bed nucleus of the stria terminalis (BNST), optic tectum, various tegmental
143 cb), preoptic area (POA), bed nucleus of the stria terminalis (BNST), posterior dorsal and posterior
144 lateral and ventrolateral bed nucleus of the stria terminalis (BNST), recruitment of G(q)-linked rece
146 ptic nuclei, the anterior bed nucleus of the stria terminalis (BNST), the anterior paraventricular nu
147 require NA inputs to the bed nucleus of the stria terminalis (BNST), vehicle or saporin toxin conjug
148 e lateral division of the bed nucleus of the stria terminalis (BNST), which forms part of the circuit
149 elated regions, including the bed nucleus of stria terminalis (BNST), which is implicated in sustaine
150 medial amygdala (MeA) and bed nucleus of the stria terminalis (BNST), which mediate the female-stimul
151 s a tiny brain region-the bed nucleus of the stria terminalis (BNST)-in the body's stress response an
152 ly increase long-duration bed nucleus of the stria terminalis (BNST)-mediated aversive responses (ie,
157 leus accumbens (NAc), and bed nucleus of the stria terminalis (BNST)], whereas protracted alcohol abs
158 extended amygdala (i.e., bed nucleus of the stria terminalis [BNST] and medial amygdala [MeA]), and
159 nterolateral group of the bed nucleus of the stria terminalis (BNSTALG ) is a critical modulator of a
161 eAL) and the dorsolateral bed nucleus of the stria terminalis (BNSTDL) coordinate the expression of s
162 he amygdala (CN), ventral bed nucleus of the stria terminalis (BNSTv), and nucleus accumbens shell (N
163 ry few VP-ir cells in the bed nucleus of the stria terminalis (BST) and none in the suprachiasmatic n
165 al behavior including the bed nucleus of the stria terminalis (BST) and the medial amygdala (MeA).
167 dala (Ce) and the lateral bed nucleus of the stria terminalis (BST) are highly similar regions that s
168 Nuclei in the amygdala and bed nuclei of the stria terminalis (BST) form functionally organized units
169 a cluster comprising the bed nucleus of the stria terminalis (BST) in rats expressing contextual anx
171 evidence suggest that the bed nucleus of the stria terminalis (BST) is well positioned to relay limbi
172 opressin (AVP) within the bed nucleus of the stria terminalis (BST) of adult brain is dependent upon
173 ed the hypothesis that the bed nuclei of the stria terminalis (BST) provides this compensatory plasti
174 of the amygdala (Ce) and bed nucleus of the stria terminalis (BST) than in hamsters housed in long p
175 sion of GAD67 mRNA in the bed nucleus of the stria terminalis (BST) was minimally affected by acute r
176 acting on neurons of the bed nucleus of the stria terminalis (BST), a component of extended amygdala
177 synaptic terminals in the bed nuclei of the stria terminalis (BST), a projection area for mPFC corti
178 of amniotes has been the bed nucleus of the stria terminalis (BST), but numerous recent investigatio
179 ld was iontophoresed into the bed nucleus of stria terminalis (BST), central nucleus of the amygdala
180 d shell), olfactory tubercle, bed nucleus of stria terminalis (BST), medial, central, cortical, and b
181 the amygdala (Ce) and the bed nucleus of the stria terminalis (BST), the two major subdivisions of th
184 the principal part of the bed nucleus of the stria terminalis (BST; 43%), and the percentage likely t
185 ended amygdala (primarily the bed nucleus of stria terminalis; BST), on the whole, the BST contained
186 anterolateral group of the bed nuclei of the stria terminalis (BSTalg) contains four distinct cell gr
187 e anteromedial area of the bed nuclei of the stria terminalis (BSTam) is the relatively undifferentia
188 anteromedial) group of the bed nuclei of the stria terminalis (BSTamg), which also includes the more
190 A response in the lateral bed nucleus of the stria terminalis (BSTL), compared to outbred Sprague-Daw
192 solateral division of the bed nucleus of the stria terminalis (BSTld), part of the critical brain are
194 beling in the POM, medial bed nucleus of the stria terminalis (BSTm), and periaqueductal gray (PAG).
195 and oval division of the bed nucleus of the stria terminalis (BSTov), which form part of the central
196 Neurons in the principal bed nucleus of the stria terminalis (BSTp) integrate hormonal and sensory i
197 e principal nucleus of the bed nuclei of the stria terminalis (BSTp) is sexually dimorphic and partic
199 ed Fos: the posteromedial bed nucleus of the stria terminalis (BSTPM), posteromedial amygdala (MeP),
200 The principal part of the bed nucleus of the stria terminalis (BSTpr) and the anteroventral periventr
201 ne release in the ventral bed nucleus of the stria terminalis (BSTv) with the alpha2-autoreceptor ant
203 inly to the ventrolateral bed nucleus of the stria terminalis (BSTvl), the pre-locus coeruleus (pre-L
205 that extended through the medial part of the stria terminalis, but they remained confined to the mole
207 visualized in the cortex, bed nucleus of the stria terminalis, central amygdala, hypothalamic paraven
208 yte balance including the bed nucleus of the stria terminalis, central nucleus of the amygdala, diago
209 bic and insular cortices, bed nucleus of the stria terminalis, central nucleus of the amygdala, peria
211 e the posterointermediate bed nucleus of the stria terminalis, containing more neurons heavily labele
212 gdalohippocampal area and bed nucleus of the stria terminalis correlated positively with individual d
217 hlighted the dorsolateral bed nucleus of the stria terminalis (dlBST) as a structure putatively invol
218 th triggered increases in bed nucleus of the stria terminalis dorsal (BNSTd) and lateral septum (LS).
219 uctures such as amygdala, bed nucleus of the stria terminalis, dorsal raphe, and lateral hypothalamus
220 ewise, in vivo intra-oval bed nucleus of the stria terminalis DRD1 pharmacological blockade reduced l
221 ses: the amygdala and the bed nucleus of the stria terminalis for sustaining adaptive fear-related be
222 itudinal fasciculus, bilateral fornix (cres)/stria terminalis, genu and splenium of the corpus callos
223 eriment 1, lesions of the bed nucleus of the stria terminalis had no influence on CTA or COA acquisit
224 posterior division of the bed nuclei of the stria terminalis has three major nuclei: principal, inte
225 he medial amygdala or the bed nucleus of the stria terminalis have no effect on the display of paced
227 actory bulb, cerebral cortex, bed nucleus of stria terminalis, hippocampus, habenular nucleus, amygda
228 prachiasmatic nucleus and bed nucleus of the stria terminalis; however, there are extensive VP-ir fib
229 ells were observed in the bed nucleus of the stria terminalis, hypothalamic paraventricular, supraopt
230 iventricular nucleus, and bed nucleus of the stria terminalis in a distribution consistent with previ
231 oles for the anteroventral bed nuclei of the stria terminalis in inhibiting both stress hormone outpu
232 igher in the encapsulated bed nucleus of the stria terminalis in males than females for all four vole
233 ACAP signaling within the bed nucleus of the stria terminalis in mediating the consequences of stress
234 2 expression in the amygdala and bed nucleus stria terminalis in response to stress, whereas males ex
235 r fibers were observed in the nucleus of the stria terminalis in the telencephalon; habenular nucleus
236 principal nucleus of the bed nucleus of the stria terminalis, in which males have more neurons than
237 um, the amygdala, and the bed nucleus of the stria terminalis; in areas involved in endocrine regulat
239 ended amygdala, including the bed nucleus of stria terminalis, interstitial nucleus of the posterior
242 oreactive staining in the bed nucleus of the stria terminalis may predict paternal behavior because i
243 al medial amygdala (MeA), bed nucleus of the stria terminalis, medial preoptic nucleus, ventrolateral
244 seen unilaterally in the bed nucleus of the stria terminalis, medial ventral pallidum, arcuate nucle
245 examined areas, including the bed nucleus of stria terminalis,medial amygdala, and medial parabrachia
246 ctions from the posterior bed nucleus of the stria terminalis, mesocortical structures and the hippoc
247 dial preoptic area/medial bed nucleus of the stria terminalis (mPOA/BSTm), and the highest AR express
250 ssion was enhanced in the bed nucleus of the stria terminalis of rats that performed an operant task
252 nPGi was prominent in the bed nucleus of the stria terminalis, paraventricular nucleus (PVN), posteri
253 accumbens shell, lateral bed nucleus of the stria terminalis, paraventricular nucleus of the hypotha
254 nd a larger volume of the bed nucleus of the stria terminalis, paraventricular nucleus, and medial am
255 e nucleus, preoptic area, bed nucleus of the stria terminalis, paraventricular thalamus, periaqueduct
256 cussations or the inferior thalamic peduncle-stria terminalis pathway from the posterior thalamus, an
258 ctions with the amygdala, bed nucleus of the stria terminalis, periaqueductal gray, hippocampus, and
259 und in the hippocampal cingulum, fornix, and stria terminalis, posterior corona radiata, and superior
260 effects on the hippocampal cingulum, fornix, stria terminalis, posterior corona radiata, and superior
261 ntral part of the anterior bed nuclei of the stria terminalis (presently discussed as being involved
262 ricular nucleus (PVN) and the bed nucleus of stria terminalis, revealed global pattern changes in tra
263 varying density were noted in bed nucleus of stria terminalis, septal nuclei, nucleus accumbens, caud
264 RXFP3 antagonist into the bed nucleus of the stria terminalis significantly decreased self-administra
267 ncountered in the septum, bed nucleus of the stria terminalis, substantia innominata, various thalami
268 a-Helical CRF9-41 in the bed nucleus of the stria terminalis suggested that this area is a site at w
269 (dmPFC), anterior insula, bed nucleus of the stria terminalis, thalamus, and midbrain consistently ac
270 ated cellular processes in the region of the stria terminalis that extended into the presumptive BSTp
271 (D1-LTPGABA) in the oval bed nucleus of the stria terminalis that was positively correlated with mot
272 ng output (via the CNA or bed nucleus of the stria terminalis) that in turn regulates pontine REM gen
273 al and oval nuclei of the bed nucleus of the stria terminalis, the central nucleus of the amygdala, t
274 structures of the lateral bed nucleus of the stria terminalis, the central sublenticular EA, and the
275 teral septal nucleus, the bed nucleus of the stria terminalis, the fundus striati, the amygdala, the
276 sal forebrain structures, the bed nucleus of stria terminalis, the lateral preoptic area, the entoped
277 ygdala and to the lateral bed nucleus of the stria terminalis, the latter region receiving comparativ
278 al and medial septum, the bed nucleus of the stria terminalis, the medial and central amygdala, the p
279 including the preoptic area, the bed nuclei stria terminalis, the paraventricular nucleus thalamus,
280 distinct cell group of the bed nuclei of the stria terminalis, the rhomboid nucleus (BSTrh), was anal
281 eptum, the basal ganglia, bed nucleus of the stria terminalis, the thalamus including paraventricular
282 ession areas, such as the bed nucleus of the stria terminalis, the ventrolateral hypothalamus, and th
283 nd principal nuclei of the bed nuclei of the stria terminalis; the caudate-putamen; the globus pallid
285 nhibitory projection from bed nucleus of the stria terminalis to patch/exo-patch neurons was revealed
286 can act on neurons of the bed nucleus of the stria terminalis to reduce food intake via the IL-18 rec
287 that projections from the MEApd through the stria terminalis to the BSTpr may be specified initially
291 onal pathways specific to the amygdala (i.e. stria terminalis, ventral amygdalofugal pathway and unci
292 teral part of the ventral bed nucleus of the stria terminalis (vlBNST) is a critical site for the ant
294 binding in the posterior bed nucleus of the stria terminalis was greater in males irrespective of ag
295 and ventral nuclei (of the bed nuclei of the stria terminalis) was analyzed with the Phaseolus vulgar
297 d from lateral septum and bed nucleus of the stria terminalis were Fos-activated during cocaine CPP i
298 in specific nuclei of the bed nucleus of the stria terminalis, which plays essential roles in anxiety
299 and then to the principal bed nucleus of the stria terminalis, which suppresses territorial aggressio
300 fference in ERbeta in the bed nucleus of the stria terminalis, with males showing greater expression
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