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 ubparaventricular zone, and the hypothalamic paraventricular and dorsomedial nuclei.

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

5 the SCN to neurons producing oxytocin in the paraventricular and periventricular nuclei (PVN and PeVN

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

7 amygdala, septum, preoptic region, lateral, paraventricular and posterior hypothalamus, zona incerta

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

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

10 ion was most pronounced in the ventromedial, paraventricular, and arcuate nuclei, neuron populations

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

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

13 including the hippocampus, amygdala and the paraventricular, arcuate and dorsomedial nuclei of the h

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

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

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

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

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

19 Our findings suggest that paraventricular hypothalamic neurons directly control bo

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

21 OS in stress-responsive central amygdala and paraventricular hypothalamic neurons, nor did SD elevate

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

23 mutant ARH targets including dorsomedial and paraventricular hypothalamic nuclei.

24 ucleus (SON), 1.6-times in the magnocellular paraventricular hypothalamic nucleus (mPVN), 4.1-times i

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

26 The paraventricular hypothalamic nucleus (PVH) contains many

27 ns do not target HPA effector neurons in the paraventricular hypothalamic nucleus (PVH) directly, dis

28 The paraventricular hypothalamic nucleus (PVH) receives dire

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

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

31 oendocrine effector mechanisms housed in the paraventricular hypothalamic nucleus (PVH).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 neurons of the MBH, oxytocin neurons of the paraventricular hypothalamus, and neurons within the bra

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

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

53 and elicited direct depolarizing actions on paraventricular neurons in hypothalamic slices.

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

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

56 ed GPCR101 mRNA expression in supraoptic and paraventricular nuclei from late pregnancy to late lacta

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

58 ic sites, including the central amygdala and paraventricular nuclei of the hypothalamus and thalamus.

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

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

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

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

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

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

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

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

67 TH release, in the parvocellular division of paraventricular nucleus (pcPVN), and (2) mFSS-induced ac

68 g hormone (CRH) neurons in the parvocellular paraventricular nucleus (pPVN) play a key role in coordi

69 e Arc and its projection to the hypothalamic paraventricular nucleus (PVH) are both components of the

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

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

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

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

74 ey rats with both a push-pull cannula in the paraventricular nucleus (PVN) and a catheter in the jugu

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 CRF and oxytocin mRNA expression in the paraventricular nucleus (PVN) and supraoptic nucleus (SO

82 The paraventricular nucleus (PVN) and supraoptic nucleus (SO

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

84 These prominently included the hypothalamic paraventricular nucleus (PVN) and the nucleus of the sol

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

86 m laminae terminalis (OVLT) and hypothalamic paraventricular nucleus (PVN) each contribute significan

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

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

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

90 The development of the hypothalamic paraventricular nucleus (PVN) involves several factors t

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

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

93 1 receptor (NMDA-NR1) expression within the paraventricular nucleus (PVN) is critically linked to th

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

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

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

97 The hypothalamic paraventricular nucleus (PVN) is responsive to hypoxic s

98 te mechanisms regulating the excitability of paraventricular nucleus (PVN) neurones that project dire

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

100 increased by angiotensin II (Ang II) within paraventricular nucleus (PVN) neurons of normotensive ra

101 The paraventricular nucleus (PVN) of the hypothalamus contro

102 The paraventricular nucleus (PVN) of the hypothalamus is a k

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

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

105 Glutamatergic inputs in the paraventricular nucleus (PVN) of the hypothalamus mainta

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

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

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

109 ttributable to global hypocellularity of the paraventricular nucleus (PVN) of the hypothalamus.

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

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

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

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

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

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

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

117 The hypothalamic paraventricular nucleus (PVN) regulates numerous homeost

118 The paraventricular nucleus (PVN) regulates sympathetic outf

119 Hypothalamic projections from the paraventricular nucleus (PVN) release oxytocin (OT) to m

120 rolateral medulla (RVLM) from neurons in the paraventricular nucleus (PVN) that release arginine vaso

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

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

123 or (CRF) mRNA expression in the hypothalamic paraventricular nucleus (PVN), and plasma cortisol and A

124 Neuronal activity in the hypothalamic paraventricular nucleus (PVN), as well as sympathetic ou

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

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

127 in neurons of the supraoptic nucleus (SON), paraventricular nucleus (PVN), locus coeruleus (LC), ros

128 in the bed nucleus of the stria terminalis, paraventricular nucleus (PVN), posterior hypothalamus, p

129 Fos-like immunoreactive (IR) neurons in the paraventricular nucleus (PVN), supraoptic nucleus (SON)

130 The rostral region, containing the paraventricular nucleus (PVN), was defined by discrete l

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

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

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

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

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

136 te several hypothalamic areas, including the paraventricular nucleus (PVN).

137 ERbeta immunoreactive cell numbers in ARH or paraventricular nucleus (PVN).

138 elicited by the stimulation of hypothalamic paraventricular nucleus (PVN).

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

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

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

142 RVLM-projecting neurons of the hypothalamic paraventricular nucleus (PVN-RVLM) contributes to an imb

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

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

145 4Rs only in SIM1 neurons in the hypothalamic paraventricular nucleus and neurons in the amygdala was

146 , galanin, enkephalin, and dynorphin, in the paraventricular nucleus and orexin and melanin-concentra

147 s in Arc NPY projections areas (hypothalamic paraventricular nucleus and perifornical area) after Arc

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

149 er intake, was increased in the hypothalamic paraventricular nucleus and the subfornical organ.

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

151 oinjection of muscimol into the hypothalamic paraventricular nucleus failed to reduce changes evoked

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

153 The rat paraventricular nucleus has three major divisions: desce

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

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

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

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

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

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

160 ied by reduced GLP-1 immunoreactivity in the paraventricular nucleus of hypothalamus, suggesting rele

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

162 stinct from that of Utx, specifically in the paraventricular nucleus of the hypothalamus (high Uty) a

163 ion between the circumventricular organs and paraventricular nucleus of the hypothalamus (PVH) and th

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

165 its were identified in subpopulations of the paraventricular nucleus of the hypothalamus (PVH) by dou

166 The paraventricular nucleus of the hypothalamus (PVH) consis

167 The paraventricular nucleus of the hypothalamus (PVH) contai

168 The paraventricular nucleus of the hypothalamus (PVH) coordi

169 The paraventricular nucleus of the hypothalamus (PVH) plays

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

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

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

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

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

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

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

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

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

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

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

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

182 is critical for energy homeostasis, and the paraventricular nucleus of the hypothalamus (PVN) is a k

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

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

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

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

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

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

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

190 mone (ACTH) secretagogue biosynthesis in the paraventricular nucleus of the hypothalamus (PVN).

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

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

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

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

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

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

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

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

199 tivate c-fos expression in the hind brain or paraventricular nucleus of the hypothalamus indicating t

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

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

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

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

204 tive axonal projections and terminals in the paraventricular nucleus of the hypothalamus, arcuate nuc

205 ular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalamus, IPe, arcuat

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

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

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

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

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

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

212 TS and reduction of GLP-1 innervation to the paraventricular nucleus of the hypothalamus.

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

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

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

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

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

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

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

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

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

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

223 The posterior paraventricular nucleus of the thalamus (THPVP) has been

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

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

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

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

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

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

230 lis in the telencephalon; habenular nucleus, paraventricular nucleus of the thalamus, preoptic area,

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

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

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

234 Intra-paraventricular nucleus oxytocin injections reduced beha

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

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

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

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

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

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

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

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

243 preoptic area (POA; homolog of the mammalian paraventricular nucleus), Purkinje cell layer of the cer

244 In the paraventricular nucleus, although temporal changes in ox

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

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

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

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

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

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

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

252 nucleus, ventromedial hypothalamic nucleus, paraventricular nucleus, dorsomedial hypothalamic nucleu

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

254 hanisms of chronic stress integration in the paraventricular nucleus, focusing on the role of glucoco

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

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

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

258 autonomic brain regions (i.e., hypothalamic paraventricular nucleus, rostral ventrolateral medulla a

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

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

261 ns, including the arcuate nucleus (ARC), the paraventricular nucleus, the medial preoptic area, the l

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

263 llular and magnocellular subdivisions of the paraventricular nucleus, with greater increases ipsilate

264 -1Rs) in the vagus nerve, area postrema, and paraventricular nucleus.

265 releasing factor immunoreactive cells in the paraventricular nucleus.

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

267 ed c-fos mRNA expression in the hypothalamic paraventricular nucleus.

268 entromedial parvocellular subdivision of the paraventricular nucleus.

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

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

271 ation of GLP-1 into the arcuate, but not the paraventricular, nucleus of the hypothalamus reduced hep

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

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

274 The paraventricular (PV) and paratenial (PT) nuclei are prom

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

276 d include the hypothalamic arcuate (Arc) and paraventricular (PVN) nuclei, and the nucleus of the sol

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

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

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

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

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

282 nt study examines subcortical connections of paraventricular thalamic nucleus (Pa) following small an

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

284 Paraventricular thalamic nucleus (PVT) neurons receive h

285 odorsal, reuniens, and, most prominently the paraventricular thalamic nucleus), hypothalamus (medial

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

287 ly concentrated in the medial preoptic area, paraventricular thalamic nucleus, the subparaventricular

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

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

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

291 The paraventricular thalamus balances the competing behavior

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

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

294 c area, bed nucleus of the stria terminalis, paraventricular thalamus, periaqueductal gray, and preco

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

296 -334867 increased Fos expression in mPFC and 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-