ライフサイエンスコーパス: paraventricular

1 medial, and lateral hypothalamus), thalamus (paraventricular and centromedian thalamus), and limbic s

2 , in particular the forebrain, including the paraventricular and dorsomedial nuclei of the hypothalam

3 the stria terminalis, the thalamus including paraventricular and parafascicular nuclei, the hypothala

4 lar and rhomboid nuclei of the thalamus, and paraventricular and periventricular nuclei of the hypoth

5 and magnocellular peptidergic neurons in the paraventricular and supraoptic hypothalamus.

6 to the melanocortin 4 receptor (MC4R) in the paraventricular and ventromedial neurons of the hypothal

7 H-expressing neurons in the periventricular, paraventricular, and arcuate hypothalamic nuclei and loc

8 stria; anterior hypothalamic area; arcuate, paraventricular, and dorsomedial hypothalamic nuclei; la

9 d obese animals include the medial preoptic, paraventricular, and dorsomedial nuclei.

10 ei of terminal stria; anterior hypothalamus; paraventricular, arcuate, and dorsomedial hypothalamic n

11 estingly, p21 expression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the

12 ion) in multiple nuclei in the hypothalamus (paraventricular, dorsomedial, and lateral hypothalamus),

13 hat deletion of BMAL1, a core clock gene, in paraventricular hypothalamic (PVH) neurons reduces diurn

14 for glucagon-like peptide 1 (GLP-1)-mediated paraventricular hypothalamic circuit coordinating the gl

15 ectively engages a MAP kinase pathway in rat paraventricular hypothalamic CRH (corticotropin-releasin

16 Our findings suggest that paraventricular hypothalamic neurons directly control bo

17 Scn9a deletion in AGRP, POMC, or paraventricular hypothalamic neurons reduced EPSP durati

18 s found in the preoptic, ventromedial (VMH), paraventricular hypothalamic nuclei, and in the bed nucl

19 egions such as the arcuate, dorsomedial, and paraventricular hypothalamic nuclei, lateral hypothalami

20 mutant ARH targets including dorsomedial and paraventricular hypothalamic nuclei.

21 first localized cell groups afferent to the paraventricular hypothalamic nucleus (PVH) (the initiato

22 The paraventricular hypothalamic nucleus (PVH) receives dire

23 selectively recorded from OT neurons in the paraventricular hypothalamic nucleus (PVH) to show that

24 GABAergic neurons project extensively to the paraventricular hypothalamic nucleus (PVH), and optogene

25 The paraventricular hypothalamic nucleus (PVH), lateral hypo

26 y inhibiting hypophysiotropic neurons in the paraventricular hypothalamic nucleus (PVH).

27 e severely diminished GABAergic input to the paraventricular hypothalamic nucleus (PVH).

28 rosis factor alpha receptor 1 (TNFR1) in the paraventricular hypothalamic nucleus (PVN), a critical n

29 ndocrine (medial parvicellular region of the paraventricular hypothalamic nucleus [PaMP]) and autonom

30 ctions from non-POMC non-AgRP neurons to the paraventricular hypothalamic nucleus in promoting postwe

31 nd from these to HPA effector neurons in the paraventricular hypothalamic nucleus, and to aspects of

32 posterior division of the thalamic nucleus, paraventricular hypothalamic nucleus, arcuate hypothalam

33 One involves SFO-dependent activation of the paraventricular hypothalamic nucleus, elevations in plas

34 ocus ceruleus, ventrolateral septal nucleus, paraventricular hypothalamic nucleus, lateral hypothalam

35 he horizontal limb of the diagonal band, the paraventricular hypothalamic nucleus, several visual tha

36 he area postrema, the subfornical organ, the paraventricular hypothalamic nucleus, the arcuate nucleu

37 bens and amygdala while increasing it in the paraventricular hypothalamic nucleus.

38 of CREB phosphorylation in a reduced ex vivo paraventricular hypothalamic preparation, making this si

39 Indeed, we show that the paraventricular hypothalamicnucleus sends direct oxytoci

40 (PFH; 30%), ventromedial hypothalamus (34%), paraventricular hypothalamus (34%), paraventricular thal

41 rectly innervated by oxytocin neurons in the paraventricular hypothalamus (Oxt(PVH) neurons), which m

42 tor (MC4R)-expressing satiety neurons in the paraventricular hypothalamus (PVH(MC4R) neurons).

43 s, MC4Rs on SIM1(+) neurons, possibly in the paraventricular hypothalamus (PVH) and/or amygdala, regu

44 nstrate that selective Ntrk2 deletion within paraventricular hypothalamus (PVH) leads to severe hyper

45 SIM1-expressing paraventricular hypothalamus (PVH) neurons are key regul

46 An inhibitory circuit with paraventricular hypothalamus (PVH) neurons substantially

47 The paraventricular hypothalamus (PVH) plays a pivotal role

48 ere, we identify a novel projection from the paraventricular hypothalamus (PVH) to the ventral latera

49 t one of the major subsets of neurons in the paraventricular hypothalamus (PVH), a critical brain reg

50 of the appetitive network by focusing on the paraventricular hypothalamus (PVH), a key region respons

51 uitary-adrenal (HPA) effector neurons in the paraventricular hypothalamus (PVH).

52 red activity in hundreds of neurons in mouse paraventricular hypothalamus (PVH).

53 f GABAergic input to target cells across the paraventricular hypothalamus and ventral thalamus, supre

54 bitory influences to HPA-effector neurons in paraventricular hypothalamus during acute stress, notabl

55 vealed that inhibition of avBST input to the paraventricular hypothalamus enhanced stress hormonal ou

56 ala, brainstem, globus pallidus, lateral and paraventricular hypothalamus, and olfactory tubercle.

57 ic distension) in part via signalling to the paraventricular hypothalamus.

58 These findings demonstrate that paraventricular neurons are major contributors to the ef

59 In the paraventricular nuclei (PVN) of the hypothalamus, DOC pr

60 amin D regulates glucose homeostasis via the paraventricular nuclei and energy homeostasis via the ar

61 found a vasopressinergic projection from the paraventricular nuclei of the hypothalamus (PVN) to the

62 magnocellular neurons in the supraoptic and paraventricular nuclei of the hypothalamus.

63 containing neurons within the supraoptic and paraventricular nuclei of the hypothalamus.

64 os expression in the oxytocin neurons of the paraventricular nuclei of WT but not HDC-KO mice.

65 pothalamic nuclei (dorsomedial, lateral, and paraventricular nuclei).

66 ons including the arcuate, ventromedial, and paraventricular nuclei.

67 ons in the hypothalamic supraoptic (SON) and paraventricular nuclei.

68 hypothalamic feeding nuclei/cell types, the paraventricular nucleus (GLP-1RKD(DeltaSim1cre)) and pro

69 uropeptide Y (NPY) levels in the DMH and the paraventricular nucleus (P < 0.05).

70 TH+) and somatostatin (SST+) neurons in the paraventricular nucleus (PaVN) of the hypothalamus of ad

71 for glutamatergic input to the hypothalamic paraventricular nucleus (PVH) in stress-induced activati

72 ablished orexigenic peptide and hypothalamic paraventricular nucleus (PVH) is one major brain site th

73 ral brain regions including the hypothalamic paraventricular nucleus (PVH), the anteroventral periven

74 and to the medial parvocellular part of the paraventricular nucleus (PVHmp).

75 ors are highly expressed in the hypothalamic paraventricular nucleus (PVN) and arcuate nucleus (ARC).

76 ssure, and heart rate via projections to the paraventricular nucleus (PVN) and dorsomedial hypothalam

77 by parvocellular neurons of the hypothalamic paraventricular nucleus (PVN) and released into the port

78 ns in other hypothalamic regions such as the paraventricular nucleus (PVN) and rostral preoptic area

79 f E2 exposure, rats were sacrificed, and the paraventricular nucleus (PVN) and rostral ventrolateral

80 opressin (AVP) neurons from the hypothalamic paraventricular nucleus (PVN) and supraoptic nucleus (SO

81 fspring stress regulating brain regions, the paraventricular nucleus (PVN) and the bed nucleus of str

82 t the effects of NPS within the hypothalamic paraventricular nucleus (PVN) are mediated via actions o

83 utyric acid (GABA)-projecting neurons in the paraventricular nucleus (PVN) have been shown to inhibit

84 in stimulates VP neurons in the hypothalamic paraventricular nucleus (PVN) in a nutritional state-dep

85 The paraventricular nucleus (PVN) in mammals is the main hyp

86 lenges such as dehydration, the hypothalamic paraventricular nucleus (PVN) is activated and drives SN

87 The hypothalamic paraventricular nucleus (PVN) is critically involved in

88 1 receptor (NMDA-NR1) expression within the paraventricular nucleus (PVN) is critically linked to th

89 (NMDA) receptor activity in the hypothalamic paraventricular nucleus (PVN) is crucial for the sympath

90 Increased glutamatergic input in the paraventricular nucleus (PVN) is important for high symp

91 NMDAR activity in the hypothalamic paraventricular nucleus (PVN) is increased and criticall

92 elaxin-3/RXFP3 signaling in the hypothalamic paraventricular nucleus (PVN) is necessary for the expre

93 tocin- and arginine-vasopressin-synthesizing paraventricular nucleus (PVN) magnocellular neurosecreto

94 oxidase (NOX) in AVP-expressing hypothalamic paraventricular nucleus (PVN) neurons in "menopausal" fe

95 The paraventricular nucleus (PVN) of the hypothalamus contro

96 -aspartate receptor (NMDAR) activity, in the paraventricular nucleus (PVN) of the hypothalamus is clo

97 asing factor (CRF) that is released from the paraventricular nucleus (PVN) of the hypothalamus is ess

98 d-aspartate receptor (NMDAR) activity in the paraventricular nucleus (PVN) of the hypothalamus is inv

99 Preautonomic neurons in the paraventricular nucleus (PVN) of the hypothalamus play a

100 The hyperphagia derived from the paraventricular nucleus (PVN) of the hypothalamus, where

101 rticotropin-releasing hormone (CRH) from the paraventricular nucleus (PVN) of the hypothalamus.

102 sed c-Fos immunoreactivity of neurons in the paraventricular nucleus (PVN) of the hypothalamus.

103 scription factor abundantly expressed in the paraventricular nucleus (PVN) of the hypothalamus.

104 by microdialysis, either in the hypothalamic paraventricular nucleus (PVN) or in the ventromedial nuc

105 SB334867 microinjected into the hypothalamic paraventricular nucleus (PVN) or into the bed nucleus of

106 During social interactions, activity in paraventricular nucleus (PVN) OXT neurons increased.

107 amatergic synaptic input in the hypothalamic paraventricular nucleus (PVN) plays a critical role in r

108 eceptor (NMDAR) activity in the hypothalamic paraventricular nucleus (PVN) plays a major role in elev

109 thetic drive emanating from the hypothalamic paraventricular nucleus (PVN) plays a major role in the

110 The hypothalamic paraventricular nucleus (PVN) regulates numerous homeost

111 The paraventricular nucleus (PVN) regulates sympathetic outf

112 Whether leptin acts in the paraventricular nucleus (PVN) to increase sympathetic ne

113 Tmem18 expression in the murine hypothalamic paraventricular nucleus (PVN) was altered by changes in

114 At the end, the paraventricular nucleus (PVN) was analyzed by Real-time

115 s of the amygdala (CeA) and the hypothalamic paraventricular nucleus (PVN) were evaluated in male rhe

116 ened glutamate signaling in the hypothalamic paraventricular nucleus (PVN), a key central coordinator

117 a terminalis, central amygdala, hypothalamic paraventricular nucleus (PVN), Barrington's nucleus and

118 tic nucleus (SCN), supraoptic nucleus (SON), paraventricular nucleus (PVN), dorsomedial nucleus (DM),

119 development of HPA axis regions, such as the paraventricular nucleus (PVN), in addition to blood pres

120 ack CREB1 in SIM1-expressing neurons, of the paraventricular nucleus (PVN), which are known to be MC4

121 um intake evoked an endogenous, hypothalamic paraventricular nucleus (PVN)-specific, decrease (sodium

122 -dependent dysregulation of the hypothalamic paraventricular nucleus (PVN).

123 rticotropin releasing hormone neurons in the paraventricular nucleus (PVN).

124 eptors (MC4R) in neurons of the hypothalamic paraventricular nucleus (PVN).

125 on mediated in part through the hypothalamic paraventricular nucleus (PVN).

126 tor blockade in the ipsilateral hypothalamic paraventricular nucleus (PVN).

127 bition of SNA by neuropeptide Y (NPY) in the paraventricular nucleus (PVN).

128 ate nucleus-median eminence (ARC-ME) and the paraventricular nucleus (PVN).

129 LHA (22%), zona incerta (ZI, 15%), CeA (5%), paraventricular nucleus (PVN, 13%), SLEA (66%), and MPA

130 neurons that express ENK in the hypothalamic paraventricular nucleus and central nucleus of the amygd

131 ated neuronal activation in the hypothalamic paraventricular nucleus and medial nucleus of the amygda

132 4Rs only in SIM1 neurons in the hypothalamic paraventricular nucleus and neurons in the amygdala was

133 ut had normal activation in the hypothalamic paraventricular nucleus and the amygdalar central nucleu

134 easing hormone (TRH)-positive neurons in the paraventricular nucleus area of the hypothalamus and thu

135 ry tract and arcuate hypothalamic nucleus -> paraventricular nucleus axonal fiber outgrowth.

136 ngle-minded 1 neurons, we show dependence of paraventricular nucleus GLP-1 signaling in the coordinat

137 ut of the X-linked Fgf13 in the hypothalamic paraventricular nucleus impairs sympathetic output to br

138 somatodendritic release of vasopressin from paraventricular nucleus neurones.

139 enetic stimulation of ARC TH axons inhibited paraventricular nucleus neurons by dopamine and GABA co-

140 of their postsynaptic targets (Arc POMC and paraventricular nucleus neurons), where ATP dramatically

141 at increased OT/c-fos colocalizations in the paraventricular nucleus of both sexes.

142 and increased mitochondrial function in the paraventricular nucleus of hypertensive rats by promotin

143 atory function in the supraoptic nucleus and paraventricular nucleus of hypertensive rats that contri

144 se system, and decreased inflammation in the paraventricular nucleus of hypertensive rats.

145 vation, and proinflammatory cytokines in the paraventricular nucleus of hypothalamus.

146 The paraventricular nucleus of thalamus (PVT), which project

147 neurotropic factor-expressing neurons in the paraventricular nucleus of the hypothalamus (BDNF(PVH)).

148 Neurons within the paraventricular nucleus of the hypothalamus (PVH) are a

149 ve absent Crh mRNA and peptide mainly in the paraventricular nucleus of the hypothalamus (PVH) but pr

150 The paraventricular nucleus of the hypothalamus (PVH) consis

151 The paraventricular nucleus of the hypothalamus (PVH) contai

152 ogenetic activation of OT neurons within the paraventricular nucleus of the hypothalamus (PVH) of mal

153 The paraventricular nucleus of the hypothalamus (PVH) plays

154 ed mainly to the hypothalamus, including the paraventricular nucleus of the hypothalamus (PVH), later

155 altered POMC projections to the preautonomic paraventricular nucleus of the hypothalamus (PVH), pancr

156 utonomic nervous system, particularly in the paraventricular nucleus of the hypothalamus (PVH), play

157 ons provide a distinctive innervation of the paraventricular nucleus of the hypothalamus (PVH), with

158 tream melanocortin-4 receptors (MC4R) in the paraventricular nucleus of the hypothalamus (PVH).

159 the mouse and send direct projections to the paraventricular nucleus of the hypothalamus (PVH).

160 tion factor necessary for development of the paraventricular nucleus of the hypothalamus (PVH).

161 nd behavioral responses are regulated by the paraventricular nucleus of the hypothalamus (PVH).

162 es in the anterior parvicellular part of the paraventricular nucleus of the hypothalamus (PVHap) and

163 xpression of IRS2 and TRPV1 receptors in the paraventricular nucleus of the hypothalamus (PVN) and do

164 reduced binding of both radioligands in the paraventricular nucleus of the hypothalamus (PVN) and me

165 We tested the hypotheses that (1) the paraventricular nucleus of the hypothalamus (PVN) and th

166 ation of firing activity of neurons from the paraventricular nucleus of the hypothalamus (PVN) by alp

167 d female rats, nanoinjection of NPY into the paraventricular nucleus of the hypothalamus (PVN) dose-d

168 ysiological properties of CRF neurons in the paraventricular nucleus of the hypothalamus (PVN) found

169 ocellular cells and fiber projections of the paraventricular nucleus of the hypothalamus (PVN) of mal

170 d the Cre/lox system to delete AT1a from the paraventricular nucleus of the hypothalamus (PVN) of mic

171 We found that neurons of the paraventricular nucleus of the hypothalamus (PVN) send d

172 ly glutamatergic and send projections to the paraventricular nucleus of the hypothalamus (PVN) that a

173 gly, we found bilateral projections from the paraventricular nucleus of the hypothalamus (PVN) to RAI

174 e hypocretin neurons project directly to the paraventricular nucleus of the hypothalamus (PVN), and S

175 tal cortex, striatum, nucleus accumbens, and paraventricular nucleus of the hypothalamus (PVN), in bo

176 Within the paraventricular nucleus of the hypothalamus (PVN), OXT-i

177 Bilateral nanoinjection of SHU9119 into the paraventricular nucleus of the hypothalamus (PVN), to bl

178 the hindbrain send robust projections to the paraventricular nucleus of the hypothalamus (PVN), which

179 in G(s)alpha in brain regions outside of the paraventricular nucleus of the hypothalamus (PVN).

180 ith hypothalamic brain nuclei, including the paraventricular nucleus of the hypothalamus (PVN).

181 and oxytocin- (OC) containing neurons of the paraventricular nucleus of the hypothalamus (PVN).

182 ropin-releasing hormone (CRH) neurons in the paraventricular nucleus of the hypothalamus (PVN).

183 These neurons densely populate the paraventricular nucleus of the hypothalamus (PVN).

184 noreactive cells and OT messenger RNA in the paraventricular nucleus of the hypothalamus and an incre

185 withdrawal induces OT neuroplasticity in the paraventricular nucleus of the hypothalamus and dorsal r

186 uroplasticity in OT-producing neurons in the paraventricular nucleus of the hypothalamus and its effe

187 mmunication in hypertension originating from paraventricular nucleus of the hypothalamus and presenti

188 n releasing factor-containing neurons of the paraventricular nucleus of the hypothalamus and primaril

189 sympathoexcitatory brain centres such as the paraventricular nucleus of the hypothalamus and the rost

190 found that PACAP increased CRF levels in the paraventricular nucleus of the hypothalamus and, importa

191 c and anorexigenic neural projections to the paraventricular nucleus of the hypothalamus at PN 28.

192 hat knockdown of VP and OT production in the paraventricular nucleus of the hypothalamus exerts diver

193 in-releasing hormone (CRH) released from the paraventricular nucleus of the hypothalamus is a major r

194 -releasing factor type 1 receptor within the paraventricular nucleus of the hypothalamus is an import

195 ective activation of oxytocin neurons in the paraventricular nucleus of the hypothalamus stimulates i

196 g there make appositions onto neurons in the paraventricular nucleus of the hypothalamus that are als

197 Oxytocinergic neurons in the paraventricular nucleus of the hypothalamus that project

198 ina terminals and vasopressin neurons in the paraventricular nucleus of the hypothalamus, and further

199 n type-1a receptor-containing neurons of the paraventricular nucleus of the hypothalamus, the goal be

200 ss responsiveness and transcriptomics of the paraventricular nucleus of the hypothalamus.

201 -releasing factor (CRF) immunodensity in the paraventricular nucleus of the hypothalamus.

202 with high levels of oxidative stress in the paraventricular nucleus of the hypothalamus.

203 effect that is dependent upon VDR within the paraventricular nucleus of the hypothalamus.

204 ssion in the brain that was localized to the paraventricular nucleus of the hypothalamus.

205 er, bed nucleus of the stria terminalis, and paraventricular nucleus of the hypothalamus.

206 mpanied by increased oxytocin release in the paraventricular nucleus of the hypothalamus.

207 olved in the development and function of the paraventricular nucleus of the hypothalamus.

208 ely the locus coeruleus, raphe pallidus, and paraventricular nucleus of the hypothalamus.

209 d nucleus of the stria terminalis (BNST) and paraventricular nucleus of the hypothalamus.

210 parvocellular neurosecretory neurons of the paraventricular nucleus of the hypothalamus.

211 precursor peptide, prepro-TRH (ppTRH) in the paraventricular nucleus of the rat hypothalamus and the

212 sted that OrxA transmission in the posterior paraventricular nucleus of the thalamus (pPVT) participa

213 ting neurons of the posterior portion of the paraventricular nucleus of the thalamus (pPVT).

214 Recently, we reported that activation of the paraventricular nucleus of the thalamus (PVT) abolished

215 thway from the prelimbic cortex (PrL) to the paraventricular nucleus of the thalamus (PVT) decreases

216 We focus on the temporal recruitment of the paraventricular nucleus of the thalamus (PVT) for the re

217 Here, we show that the paraventricular nucleus of the thalamus (PVT) orchestrat

218 estigated the functional organization of the paraventricular nucleus of the thalamus (PVT), a midline

219 Here we show a key role for the rat paraventricular nucleus of the thalamus (PVT), a nucleus

220 ian brain, one putative stress sensor is the paraventricular nucleus of the thalamus (PVT), an area t

221 entiates excitatory transmission between the paraventricular nucleus of the thalamus and D2-receptor-

222 Here we identify the paraventricular nucleus of the thalamus as a prominent i

223 Activity in the paraventricular nucleus of the thalamus to nucleus accum

224 ay- and cell-type-specific plasticity in the paraventricular nucleus of the thalamus to nucleus accum

225 The Gpr151-expressing neurons in the paraventricular nucleus of the thalamus was primarily co

226 ives dense DA innervation via the fr and the paraventricular nucleus of the thalamus, a stress sensit

227 grade and anterograde tracing identified the paraventricular nucleus of the thalamus, bed nucleus of

228 e midbrain periaqueductal gray (PAG) and the paraventricular nucleus of the thalamus, two brain areas

229 and some of which innervate both the PAG and paraventricular nucleus of the thalamus.

230 bed nuclei of the stria terminalis, and the paraventricular nucleus of the thalamus.

231 Intra-paraventricular nucleus oxytocin injections reduced beha

232 Together, our data demonstrate that paraventricular nucleus oxytocin mediates the social buf

233 Transcriptomic analysis of the paraventricular nucleus revealed widespread changes in e

234 damage to the ventromedial hypothalamus and paraventricular nucleus showed severe obesity and insuli

235 m hypothalamic neuroendocrine neurons in the paraventricular nucleus stimulates neighboring (~100 mum

236 ng hormone (CRH) neurons in the hypothalamic paraventricular nucleus that govern neuroendocrine stres

237 ns from oxytocin neurons in the hypothalamic paraventricular nucleus to midbrain DA regions.

238 nate extract reduces oxidative stress in the paraventricular nucleus to relieve hypertension.

239 le, the locus coeruleus, medial amygdala and paraventricular nucleus), implicating a prominent role o

240 action, reduces melanocortin content in the paraventricular nucleus, and markedly increases suscepti

241 ary tract, periaqueductal gray, hypothalamic paraventricular nucleus, and medial preoptic area, sites

242 dalar nucleus (CAmy), anterior hypothalamus, paraventricular nucleus, and posterior lateral hypothala

243 and improving mitochondrial function in the paraventricular nucleus, and reveal multiple novel targe

244 ndant in the area postrema, arcuate nucleus, paraventricular nucleus, and ventromedial hypothalamus.

245 lateral hypothalamus, somatosensory cortex, paraventricular nucleus, and zona incerta; no regions we

246 n carotid bodies, striatum, and hypothalamic paraventricular nucleus, but not in the nucleus tractus

247 somatosensory/insular cortex, preoptic area, paraventricular nucleus, dorsomedial nucleus and lateral

248 with RFRP-3 immunoreactivity enhanced in the paraventricular nucleus, dorsomedial nucleus, and Arc of

249 n a modest increase in CRH expression in the paraventricular nucleus, hypoplastic adrenal glands and

250 terminals, originating from the hypothalamic paraventricular nucleus, in the CA2 of mice.

251 tion of BM-derived cells to the hypothalamic paraventricular nucleus, presumably via a mechanism of d

252 ed their projections from the arcuate to the paraventricular nucleus, reduced energy expenditure, and

253 unexpectedly, emanates from the hypothalamic paraventricular nucleus, specifically from subsets of ne

254 entricular nucleus, medial preoptic nucleus, paraventricular nucleus, suprachiasmatic nucleus, and ve

255 rticotrophin releasing factor neurons in the paraventricular nucleus, which when activated result in

256 mpaired c-fos activation in the hypothalamic paraventricular nucleus.

257 -1Rs) in the vagus nerve, area postrema, and paraventricular nucleus.

258 releasing factor immunoreactive cells in the paraventricular nucleus.

259 e number of synapses has been doubled in the paraventricular nucleus.

260 ventromedial hypothalamus, and hypothalamic paraventricular nucleus.

261 ARC TH cells project to the hypothalamic paraventricular nucleus; optogenetic stimulation of ARC

262 ntacting (CSF-c) neurons of the hypothalamic paraventricular organ and the central canal of the spina

263 retromamillary areas and, in particular, the paraventricular organ showed immunoreactivity to dopamin

264 novel intrahypothalamic mechanism involving paraventricular oxytocin neurons that express the neurop

265 ea and the hypothalamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammil

266 ala, and hypothalamic structures such as the paraventricular (PVH) and dorsomedial (DMH), the arcuate

267 Cells in the paraventricular (PVN) and parabrachial (PBN) nuclei and

268 neuropeptide elaborated by the hypothalamic paraventricular (PVN) and supraoptic (SON) nuclei.

269 from laser micro-dissected arcuate (ARC) and paraventricular (PVN) hypothalamic nuclei.

270 osynaptic input include the lateral (LH) and paraventricular (PVN) nuclei of the hypothalamus, parasu

271 lamus including supraoptic, periventricular, paraventricular (PVN), arcuate nuclei and ventromedial a

272 , and that RFRP-3 neurons are present in the paraventricular (PVN), dorsomedial (DMH), and ventromedi

273 n multiple nuclei in the hypothalamus (i.e., paraventricular [PVN], supraoptic [SON], and suprachiasm

274 e, mainly from the central medial (CMT), and paraventricular (PVT) nuclei.

275 re observed in pallial and subpallial areas, paraventricular region, tuberal and retromammillary hypo

276 ucleus of the stria terminalis, hypothalamic paraventricular, supraoptic, dorsomedial, infundibular (

277 s (34%), paraventricular hypothalamus (34%), paraventricular thalamic nucleus (64%), and cerebral cor

278 The paraventricular thalamic nucleus (PVT) is a component of

279 Paraventricular thalamic nucleus (PVT) neurons receive h

280 -stress paradigms, with the exception of the paraventricular thalamic nucleus, in which responsivenes

281 l cortex neurons projecting to the posterior paraventricular thalamus (mPFC->pPVT) during social expo

282 GABA) neurons or their axonal projections to paraventricular thalamus (PVT) excitatory neurons immedi

283 Here we show a role for the paraventricular thalamus (PVT) in behavioral control dur

284 The paraventricular thalamus (PVT) is an interface for brain

285 (2020) examine the contributions of distinct paraventricular thalamus (PVT) outputs to contextual opi

286 trate a critical role for the input from the paraventricular thalamus (PVT), a hub for cortical, sens

287 VMH SF1 neurons project dense fibers to the paraventricular thalamus (PVT), selective chemo/optogene

288 from AgRP neurons to insular cortex via the paraventricular thalamus and basolateral amygdala.

289 ity marker c-fos in the ventral hippocampus, paraventricular thalamus and lateral septum correlated w

290 The paraventricular thalamus balances the competing behavior

291 Here we show a role for the paraventricular thalamus, a nucleus of the dorsal midlin

292 We show that the paraventricular thalamus, a nucleus of the dorsal midlin

293 G neurons include the hippocampal formation, paraventricular thalamus, and prefrontal cortex.

294 tral subiculum (vSub), basolateral amygdala, paraventricular thalamus, and ventral medial prefrontal

295 -334867 increased Fos expression in mPFC and paraventricular thalamus.

296 eral aspects of the lateral habenula and the paraventricular thalamus.

297 in boundaries and subdivisions in the optic, paraventricular, tuberal, and mammillary hypothalamic re

298 Labeled cells were found in the paraventricular, ventromedial, and dorsomedial nuclei as

299 Most newly formed cells in chicks leave the paraventricular zone after hatching, but a pool of neuro

300 In the forebrain ventricular and paraventricular zones, the density of bromodeoxyuridine-