ライフサイエンスコーパス: hypothalamus

1 hylome (whole-genome bisulfite sequencing of hypothalamus).

2 the medial and lateral preoptic area of the hypothalamus.

3 jor neuronal populations of the ventromedial hypothalamus.

4 ocus on accumbens projections to the lateral hypothalamus.

5 wo distinct functional DA modules within the hypothalamus.

6 ajor regional subdivisions of the developing hypothalamus.

7 ed in dorsal (cortical) patterning(5) in the hypothalamus.

8 ng hormone and orexin neurons in the lateral hypothalamus.

9 iatum, has substantial connectivity with the hypothalamus.

10 altered NR3C1 and CRH gene expression in the hypothalamus.

11 as well as more reactive mitochondria in the hypothalamus.

12 ogical and behavioral functions requires the hypothalamus.

13 urons and through projections to the lateral hypothalamus.

14 known as hypocretin) neurons of the lateral hypothalamus.

15 n part via signalling to the paraventricular hypothalamus.

16 role in leptin's anorexigenic effects in the hypothalamus.

17 inhibit hunger-promoting AgRP neurons in the hypothalamus.

18 or feed-forward multi-order command from the hypothalamus.

19 y a loss of hypocretin (hcrt) neurons in the hypothalamus.

20 ocess that relies on opioid signaling in the hypothalamus.

21 d pattern of neurogenesis within the tuberal hypothalamus.

22 bonafide subpopulation of Klb+ cells in the hypothalamus.

23 n of developmental regulatory genes in adult hypothalamus.

24 n the motor cortex, thalamus, subiculum, and hypothalamus.

25 ations that were randomly distributed in the hypothalamus.

26 d wake-promoting neuropeptide-in the lateral hypothalamus.

27 nd MCH neurons from the mouse late embryonic hypothalamus.

28 mperature when exogenously injected into the hypothalamus.

29 ral insula and negatively connected with the hypothalamus.

30 envector centrality nodes from cortex to the hypothalamus.

31 e dynamic encoding of spatial context in the hypothalamus.

32 ed throughout the rostrocaudal extent of the hypothalamus.

33 nucleus, and the dorsomedial nucleus of the hypothalamus.

34 for expression in the arcuate nucleus of the hypothalamus.

35 striatum, has minimal connectivity with the hypothalamus.

36 eural genes act independently in the tuberal hypothalamus.

37 ced activation of neurons within the arcuate hypothalamus.

38 medial and lateral mammillary nuclei in the hypothalamus.

39 pallidus, and paraventricular nucleus of the hypothalamus.

40 homeostasis both depend on the preoptic (PO) hypothalamus [15, 16].

41 ensitivity in the preoptic area (POA) of the hypothalamus, a critical thermoregulatory region.

42 in the suprachiasmatic nucleus (SCN) of the hypothalamus, a region critical for coordinating periphe

43 of single cell RNA sequencing data from the hypothalamus, a region with particularly significant mWA

44 In the hypothalamus, ACBP is enriched in arcuate nucleus (ARC)

45 f early-born neurons within the ventromedial hypothalamus, acting independently of Ascl1 In addition,

46 in male mice, orexin neurons in the lateral hypothalamus activated a small population of glutamic ac

47 rmone-producing neurons (MCH neurons) in the hypothalamus actively contribute to forgetting in rapid

48 se data demonstrate that leptin stimulates a hypothalamus-adrenal medulla-BAT axis, which is necessar

49 lt-onset ablation of Sh2b1 in the mediobasal hypothalamus also impairs the SNS/BAT/thermogenesis axis

50 eft anterior insula, periaqueductal grey and hypothalamus among other areas.

51 and circuits, including the lateral septum, hypothalamus, amygdala, bed nucleus of the stria termina

52 evidence that the melanocortin system of the hypothalamus, an important neural circuit controlling fe

53 yed anophthalmia, a reduction of the ventral hypothalamus and a disorganization of diencephalic nucle

54 er RNA in the paraventricular nucleus of the hypothalamus and an increase in OT receptor density in t

55 wnstream synaptic partners, the ventromedial hypothalamus and bed nucleus of the stria terminalis tha

56 ns differentially innervate the ventromedial hypothalamus and bed nucleus of the stria terminalis, an

57 dentified neuronal populations in the medial hypothalamus and brainstem that encode defensive respons

58 ently activated G(q) proteins and PLC in the hypothalamus and cerebellum but not in cortex.

59 sense transcripts by postnatal day 2 (P2) in hypothalamus and day 9 (P9) in cortex, compared to wild-

60 ticity in the paraventricular nucleus of the hypothalamus and dorsal raphe nucleus to increase anxiet

61 ork of brain regions including the amygdala, hypothalamus and dorsolateral prefrontal cortex.

62 ulation of energy expenditure, including the hypothalamus and extended amygdala.

63 we studied development of the diencephalon, hypothalamus and eyes in mutant mice in which the Ftm/Rp

64 of cilia in development of the diencephalon, hypothalamus and eyes via the region-specific control of

65 and PSST3 are only expressed in cells of the hypothalamus and in some hindbrain lateral reticular neu

66 which lack distal projections outside of the hypothalamus and influence locomotion through unknown me

67 eurons in the paraventricular nucleus of the hypothalamus and its efferent targets was measured.

68 as a main source of excitatory inputs to the hypothalamus and key mediators for mating and fighting i

69 ) signaling from the caudal brainstem to the hypothalamus and limbic forebrain.

70 st with exposure to LLbright, except IL-6 in hypothalamus and liver.

71 Otx2bhu3625/hu3625 fish have a small hypothalamus and low expression of pituitary growth horm

72 r 5-HT-ir cell groups were identified in the hypothalamus and one group in the pretectum.

73 on experiments suggest that the ventromedial hypothalamus and periaqueductal gray play distinct roles

74 se anatomical proximity to the optic chiasm, hypothalamus and pituitary gland.

75 li was associated with greater activation of hypothalamus and right amygdala and reduced connectivity

76 ht amygdala and reduced connectivity between hypothalamus and right orbitofrontal cortex, amygdala, a

77 shape the developmental architecture of the hypothalamus and show how neuronal heterogeneity is tran

78 on requires mPFC communications with lateral hypothalamus and showed that disconnection of that syste

79 The responsivity of the hypothalamus and the crosstalk of the hypothalamus with

80 to show functional connectivity between the hypothalamus and the reward-related brain regions during

81 show similar temporal regulation except the hypothalamus and two hypothalamic nuclei display sexuall

82 t to target cells across the paraventricular hypothalamus and ventral thalamus, supressing their acti

83 transcriptome (RNA sequencing of cortex and hypothalamus) and methylome (whole-genome bisulfite sequ

84 day in brain (nidopallium, hippocampus, and hypothalamus) and peripheral tissues (liver, spleen, and

85 ession in the piriform-entorhinal cortex and hypothalamus, and a modest loss of Purkinje cells.

86 rs, including lateral hypothalamus, anterior hypothalamus, and anteromedial BNST (BNSTam).

87 UCMS in the prefrontal cortex, hippocampus, hypothalamus, and blood were associated with inflammator

88 Among 33 regions, cerebral cortex areas, hypothalamus, and cerebellar gray and white matter evolv

89 eurons in the paraventricular nucleus of the hypothalamus, and further indicate that activation of th

90 tochrome oxidase activities in the cerebrum, hypothalamus, and hippocampus.

91 brain regions such as the cortex, striatum, hypothalamus, and hippocampus.

92 ygdala, ventral lateral septum, ventromedial hypothalamus, and hypothalamic paraventricular nucleus.

93 he otx2b gene is expressed in the developing hypothalamus, and otx2bhu3625/hu3625 fish exhibit multip

94 ducted scRNA-Seq analysis of embryonic mouse hypothalamus, and PanoView was able to reveal known cell

95 nd those expressed in the retina, hindbrain, hypothalamus, and pituitary.

96 ations in the cerebellum, brainstem, cortex, hypothalamus, and striatum with hippocampus of rats chro

97 activity differences, including the pallium, hypothalamus, and tectum.

98 ing the suprachiasmatic nucleus, dorsomedial hypothalamus, and tuberomammillary nucleus region), the

99 lling defensive behaviors, including lateral hypothalamus, anterior hypothalamus, and anteromedial BN

100 (POMC) neurons in the arcuate nucleus of the hypothalamus (ARC) also regulate overall glucose homeost

101 essing neurons in the arcuate nucleus of the hypothalamus (ARC).

102 show that neurons in the mouse ventromedial hypothalamus are activated both by the presence of a soc

103 (POMC) neurons in the arcuate nucleus of the hypothalamus are activated by energy surfeits and inhibi

104 AT1 receptors in the hypothalamus are endogenously activated to sustain NMDA

105 NMDA receptor phosphorylation levels in the hypothalamus are increased in a rat genetic model of hyp

106 REM sleep-active MCH neurons in the hypothalamus are thus involved in active forgetting in t

107 Y/AgRP neurons in the arcuate nucleus of the hypothalamus (ARH) are derived from the same progenitors

108 ronal nuclei from the arcuate nucleus of the hypothalamus (ARH) reveal differentially methylated geno

109 d centrally (less activated microglia in the hypothalamus) as well as more reactive mitochondria in t

110 in the early morphogenesis of the developing hypothalamus, as a key player in establishing the early

111 ments showed that the arcuate nucleus of the hypothalamus, as a major site for regulation of food int

112 hat is co-expressed with GAL in amygdala and hypothalamus, as being important in the protein kinase C

113 mass in a part of the right and left medial hypothalamus associated functionally with physiological

114 in the pharmacometabolome in the plasma and hypothalamus associated with OLZ-induced hyperphagia and

115 ng to the GnRH1 promoter increased in monkey hypothalamus at the onset of puberty as determined by ch

116 of fever) in the anteroventral region of the hypothalamus (AVPO; an important site for Tb control), o

117 eurons in the paraventricular nucleus of the hypothalamus (BDNF(PVH)).

118 Low densities were found in the pallidum, hypothalamus, brainstem and cerebellum.

119 d Pdyn subpopulations project heavily to the hypothalamus, but not to the cortex, basal forebrain, or

120 regions of the preoptic area, thalamus, and hypothalamus, but was also observed in sensory and senso

121 ddPCR in the rodent hypothalamus confirmed that, although expression levels

122 The hypothalamus contains catecholaminergic neurons marked b

123 ases, whereas impairment of HIF2alpha in the hypothalamus contributes to weight gain and glucose diso

124 rine command systems intercalated within the hypothalamus control the most fundamental physiological

125 The ventromedial hypothalamus controls both social aggression and avoidan

126 versity along temporal and spatial scales of hypothalamus development(3).

127 regions, including the pallium, subpallium, hypothalamus, diencephalon, optic tectum, midbrain tegme

128 mice we show that neurons in the dorsomedial hypothalamus (DMH) are responsible for the majority of s

129 ory and inhibitory inputs to the dorsomedial hypothalamus (DMH) determines the level of activation of

130 ined sleep-promoting neurons in the preoptic hypothalamus does not facilitate anesthesia.

131 he subpallium, preoptic area (POA), anterior hypothalamus, dorsal thalamus, posterior tuberculum, mid

132 ltiple neuronal populations in the zebrafish hypothalamus during defensive responses to a variety of

133 These findings reveal how the hypothalamus dynamically encodes spatial and sensory cue

134 bition of avBST input to the paraventricular hypothalamus enhanced stress hormonal output and subsequ

135 lating neurons in the arcuate nucleus of the hypothalamus, exerting an orexigenic effect via an as ye

136 xpressing (th2+) DA neurons in the zebrafish hypothalamus fire phasic bursts of activity to acutely p

137 regulated by multiple interactions with the hypothalamus from regions overlapping with centers for f

138 ubunit alpha2 (GABRA2) expression in lateral hypothalamus GABAergic (LH(GABA)) neurons.

139 signals of current physiological state with hypothalamus-gated amygdala inputs that signal upcoming

140 ed within the suprachiasmatic nucleus in the hypothalamus governs peripheral clocks present in all sy

141 (cerebral cortex, cerebral nuclei, thalamus, hypothalamus) has distinct intrinsic network topological

142 us, thereby highlighting a novel hippocampus-hypothalamus-hindbrain pathway regulating meal size cont

143 Like neurons in the amygdala and lateral hypothalamus, hippocampal neurons discriminated between

144 These findings identify a hypothalamus-hippocampus projection that may link endocr

145 ron-producing beta-endorphin peptides in the hypothalamus in a postnatal rat model of fetal alcohol s

146 the blood-brain barrier and localizes to the hypothalamus in primates.

147 e zona incerta (ZI)-a region assigned to the hypothalamus in the ARA-where every TH-ir neuron express

148 here were abnormally few GABA neurons in the hypothalamus in the mutant larvae, and expression of glu

149 ng of GABAergic neurons in the mouse lateral hypothalamus in vivo.

150 the rEPN, and possibly immediately adjacent hypothalamus, in driving basal activities and valence pr

151 stributed manner, in multiple regions of the hypothalamus (including the suprachiasmatic nucleus, dor

152 ections of TRH into the RVLM and dorsomedial hypothalamus increase SNA, highlighting these nuclei as

153 Synthesis of triiodothyronine (T(3)) in the hypothalamus induces marked seasonal neuromorphology cha

154 The ventromedial hypothalamus is a central node of the mammalian predator

155 The hypothalamus is a central regulator of many innate behav

156 The hypothalamus is composed of many neuropeptidergic cell p

157 The tuberal hypothalamus is comprised of the dorsomedial, ventromedi

158 rom the paraventricular nucleus (PVN) of the hypothalamus is essential for mediating stress response

159 The hypothalamus is implicated in memory disorders, but how

160 he major efferent target of the ventromedial hypothalamus is the dorsal periaqueductal gray (dPAG), a

161 The suprachiasmatic nucleus (SCN) of the hypothalamus is the principal circadian timekeeper of ma

162 IGF-1 signaling in the brain, especially the hypothalamus, is important for regulation of systemic me

163 in the suprachiasmatic nucleus (SCN) of the hypothalamus, it is unclear how firing of individual SCN

164 kisspeptin-expressing neurons in the arcuate hypothalamus (Kiss1(ARH)) of female mice control the dai

165 al connectivity with a network including the hypothalamus (known to regulate physiological stress) pr

166 found that inhibitory neurons in the lateral hypothalamus (LH(vgat)) show unique activity patterns du

167 tivation of LS(Nts) terminals in the lateral hypothalamus (LH) also decreases food intake.

168 cell types and their projections to lateral hypothalamus (LH) and ventral tegmental area (VTA).

169 we show that CeA projections to the lateral hypothalamus (LH) are preferentially activated in male r

170 A pivotal role of the lateral hypothalamus (LH) in regulating appetitive and reward-re

171 that activating the downstream NAc->lateral hypothalamus (LH) pathway also prevents relapse.

172 ng connection between the IC and the lateral hypothalamus (LH) with a monosynaptic relay in the CeA a

173 of connection between the IC and the lateral hypothalamus (LH), which engages numerous LH-projecting

174 trating hormone (MCH) neurons in the lateral hypothalamus (LH), which regulate REM sleep initiation a

175 bens medial shell (NAcmSh), and with lateral hypothalamus (LH)-projecting D1-MSN hyperexcitability me

176 ully withheld licking responses, but lateral hypothalamus (LH)-projecting neurons were more active in

177 ally on VTA(Vgat) projections to the lateral hypothalamus (LH).

178 om the central amygdala (CeA) to the lateral hypothalamus (LH)] mediates avoidance of stress-associat

179 nvergent projections into the caudal lateral hypothalamus (LHA) encompassing the parasubthalamic nucl

180 Celastrol increased LCN2 protein levels in hypothalamus, liver, fat, muscle, and bone marrow, as we

181 t growth factor 1 (FGF1), and the mediobasal hypothalamus (MBH) was recently implicated as the brain

182 energy regulatory centers of the mediobasal hypothalamus (MBH).

183 ia, amygdaloid complex, preoptic area, basal hypothalamus, mesencephalic tectum and tegmentum, latero

184 d into the lower hindbrain together with the hypothalamus midbrain and pons, yet R222 showed normal s

185 ry bulb, telencephalon, preoptic area (POA), hypothalamus, midbrain, hindbrain, and spinal cord.

186 to the medioposterior arcuate nucleus of the hypothalamus (mpARH) and GE-ERalpha(vlVMH) neurons prefe

187 in both neuronal cell body and axons in the hypothalamus of 4.1N(+/+) mice, it was only expressed in

188 significantly more microglia present in the hypothalamus of adult AF animals, and their hypothalamic

189 in the paraventricular nucleus (PaVN) of the hypothalamus of adult rats and results in discrete behav

190 >79,000 single-cell transcriptomes from the hypothalamus of diabetic Lep(ob/ob) mice obtained on Day

191 aviorally triggered NE release in the LC and hypothalamus of freely moving mice.

192 rebellum, cortex, hippocampus, striatum, and hypothalamus of lipopolysaccharide-treated mice (vs.

193 ease in MKRN3 expression in the medial basal hypothalamus of mice before the initiation of reproducti

194 ave a profound impact on ciliogenesis in the hypothalamus of neonatal mice; through these effects the

195 tress-related genes were up-regulated in the hypothalamus of neonates born to obese mothers.

196 by designer drugs (DREADD) viruses into the hypothalamus of normoglycaemic and diabetic AgRP-ires-cr

197 as in mice, MKRN3 expression is high in the hypothalamus of rats and nonhuman primates early in life

198 in teleosts compare to the POA and anterior hypothalamus of tetrapods.SIGNIFICANCE STATEMENT Studies

199 In general, the diencephalon and hypothalamus of the tree pangolin follow the organizatio

200 tions and neurogenesis (e.g., dentate gyrus, hypothalamus, olfactory areas, cerebellum) in the whole-

201 timulus-specific slow neural dynamics in the hypothalamus, on a time scale orders of magnitude longer

202 iated Dusp8 overexpression in the mediobasal hypothalamus, or metyrapone-induced chemical adrenalecto

203 Then we showed that lateral hypothalamus orexin-producing neurons project to the mPF

204 lar nucleus, dorsomedial nucleus and lateral hypothalamus, PAG, and LPB.

205 (LH) and paraventricular (PVN) nuclei of the hypothalamus, parasubthalamic nucleus, lateral division

206 ion of panic responses, such as perifornical hypothalamus (PeF), periaqueductal gray, amygdala and fr

207 in young men owing to organic disease of the hypothalamus, pituitary gland or testes has been treated

208 dies suggesting regulation occurs within the hypothalamus, pituitary, or gonads.

209 uncover a novel role for 4.1N in the axis of hypothalamus-pituitary gland-reproductive system.

210 ss hormone that is the primary output of the hypothalamus-pituitary-adrenal (HPA) axis, has been hypo

211 ress responses through the activation of the hypothalamus-pituitary-adrenal axis and the sympathetic

212 melatonin, and endocannabinoid systems; the hypothalamus-pituitary-adrenal axis; and adenosine and n

213 ivate the sympathetic nervous system and the hypothalamus-pituitary-adrenal endocrine axis.

214 The hypothalamus-pituitary-thyroid (HPT) axis plays a crucia

215 in/hypocretin neurons located in the lateral hypothalamus play a critical role in the maintenance of

216 s increasing evidence that DA neurons in the hypothalamus play a locomotor role, their precise contri

217 ojecting neurons in the preoptic area of the hypothalamus (POA(PAG) neurons) elicited USV production

218 is mediated by the preoptic area of anterior hypothalamus (POA), with ~30% of its neurons sensitive t

219 is upregulated in the preoptic area-anterior hypothalamus (POA-AH) of nest-holding, courting type I m

220 cortin neurons in the arcuate nucleus of the hypothalamus (POMC(ARH) neurons) associated with decreas

221 , inferior and superior colliculus homologs, hypothalamus, preoptic area, septum, nucleus of the diag

222 early inactivation of Nkx2.1 in the ventral hypothalamus prevented the onset of Pomc expression.

223 vasopressin and oxytocin neurones in the rat hypothalamus project to the posterior pituitary, where t

224 These neurons inhibit the lateral hypothalamus-projecting neurons in the ventrolateral par

225 mediated through projections to the lateral hypothalamus, promotes selective avoidance of food and f

226 ns within the paraventricular nucleus of the hypothalamus (PVH) are a key component of the satiety re

227 ective Ntrk2 deletion within paraventricular hypothalamus (PVH) leads to severe hyperphagic obesity.

228 SIM1-expressing paraventricular hypothalamus (PVH) neurons are key regulators of energy

229 ns within the paraventricular nucleus of the hypothalamus (PVH) of male mice (OT-Ires-Cre) enhanced s

230 The paraventricular hypothalamus (PVH) plays a pivotal role in regulating en

231 a novel projection from the paraventricular hypothalamus (PVH) to the ventral lateral septum (LSv) t

232 hundreds of neurons in mouse paraventricular hypothalamus (PVH).

233 ulated by the paraventricular nucleus of the hypothalamus (PVH).

234 ctions to the paraventricular nucleus of the hypothalamus (PVH).

235 eurons in the paraventricular nucleus of the hypothalamus (PVN) found no significant changes in synap

236 ctions to the paraventricular nucleus of the hypothalamus (PVN) that appear to synapse onto vasopress

237 ions from the paraventricular nucleus of the hypothalamus (PVN) to RAIC.

238 Within the paraventricular nucleus of the hypothalamus (PVN), OXT-induced anxiolysis is mediated,

239 including the paraventricular nucleus of the hypothalamus (PVN).

240 eurons in the paraventricular nucleus of the hypothalamus (PVN).

241 as it was determined by the calculus of the hypothalamus quotient, suggesting that the development o

242 hibition of AT1 receptor-PKC activity in the hypothalamus reduces arterial blood pressure and sympath

243 f the diagonal band of Broca, preoptic area, hypothalamus, rostral pallium, nucleus accumbens, ventra

244 ricted areas of the brain, especially in the hypothalamus, septum, thalamic reticular nucleus, certai

245 either LepR neuron-specific or adult-onset, hypothalamus-specific ablation of Sh2b1 develop obesity,

246 ide, and selectively interrogate, an updated hypothalamus structure-function network model to encoura

247 6, exclusively neuronal, cell types from the hypothalamus, subthalamus, midbrain, hippocampus, thalam

248 eptors in the suprachiasmatic nucleus of the hypothalamus, synchronizing the physiology and behaviour

249 eurons in the paraventricular nucleus of the hypothalamus that project to extrahypothalamic brain are

250 medium spiny neuron terminals in the lateral hypothalamus that promotes overeating.

251 a specific neuronal population in the mouse hypothalamus that serves as a core regulator of torpor.

252 om structures, such as prefrontal cortex and hypothalamus, that are broadcast to downstream limbic ta

253 a small, circumscribed region of the lateral hypothalamus, the anterior dorsal region (LHAad), stains

254 ion studies suggest that, in addition to the hypothalamus, the brainstem is essential for non-rapid e

255 rk has focused on projections to the lateral hypothalamus, the role of NAc projections to the VTA in

256 nduces responses to stress through acting on hypothalamus to activate the sympathetic nervous system

257 and NPY/AgRP neurons in the developing mouse hypothalamus to decipher the transcriptional codes behin

258 hat 17alpha-E2 may act through the liver and hypothalamus to improve metabolic parameters in male mic

259 Here we identify a hypothalamus to telencephalon neural pathway for regulat

260 eracts with the brain's appetite center, the hypothalamus, to stimulate feeding behavior is unknown.

261 of the organization of the diencephalon and hypothalamus using a range of standard and immunohistoch

262 , which also includes nodes in the amygdala, hypothalamus, ventral striatum, thalamus, and specific b

263 s, and the interbrain is subdivided into the hypothalamus ventrally and thalamus dorsally.

264 Although the ventromedial hypothalamus ventrolateral area (VMHvl) is now well esta

265 ial preoptic area (MPOA) or the ventromedial hypothalamus, ventrolateral subdivision (VMHvl) revealed

266 nd integrate this status with input from the hypothalamus via GnRH receptor signaling to regulate rep

267 relin (Ghr) stimulates hunger signals in the hypothalamus via growth hormone secretagogue receptor (G

268 a synaptic connections with the ventromedial hypothalamus (VmH) and bed nucleus of the stria terminal

269 ltiple brain regions, including ventromedial hypothalamus (VMH) and lateral parabrachial nucleus (LPB

270 (PR)-expressing neurons in the ventromedial hypothalamus (VMH) are active and required during this b

271 of efferent projections to the ventromedial hypothalamus (VMH) or lateral periaqueductal gray (lPAG)

272 The ventromedial hypothalamus (VMH) plays chief roles regulating energy a

273 It is well recognized that ventromedial hypothalamus (VMH) serves as a satiety center in the bra

274 In the rat ventromedial hypothalamus (VMH), leptin-induced action potential firi

275 the dorsomedial division of the ventromedial hypothalamus (VMHdm) and the dPAG.

276 and central subdivisions of the ventromedial hypothalamus (VMHdm/c) that express the nuclear receptor

277 entrolateral subdivision of the ventromedial hypothalamus (VMHvl(Esr1)) play a causal role in the con

278 ) and ventrolateral part of the ventromedial hypothalamus (VMHvl) are essential regions for male sexu

279 entrolateral subdivision of the ventromedial hypothalamus (VMHvl) contains ~4,000 neurons that projec

280 entrolateral subdivision of the ventromedial hypothalamus (VMHvl).

281 The ventromedial nucleus of the hypothalamus (VMN) has an important role in diverse beha

282 The ventromedial nucleus of the hypothalamus (VMN) is involved in the counterregulatory

283 The ventral posterior hypothalamus (VPH) is an anatomically complex brain regi

284 ul trigeminal stimulation, activation of the hypothalamus was present within the last 48 hours before

285 f Tlr4 or knockdown of the Ikbke gene in the hypothalamus was sufficient to reverse the metabolic out

286 onnection (macroconnection) data for the rat hypothalamus were extracted from the primary literature.

287 ess than 50% of TH-expressing neurons in the hypothalamus were found to express DAT.

288 ons of the ventral thalamus, epithalamus, or hypothalamus were noted.

289 CK neurons project rostrally to the preoptic hypothalamus, whereas CALCA neurons also project caudall

290 iet exhibit macrophage infiltration into the hypothalamus, whereas females were protected irrespectiv

291 opressin (AVP) in the pituitary gland or the hypothalamus, whereas nephrogenic DI results from resist

292 in the suprachiasmatic nucleus (SCN) of the hypothalamus, which governs daily rhythms in physiology

293 eurons present in the arcuate nucleus of the hypothalamus, which release Pomc-encoded melanocortins,

294 lly significant expansion of a region of the hypothalamus, while females showed significant expansion

295 y reduced GAL expression in the amygdala and hypothalamus whilst producing a corresponding reduction

296 ect cellular and functional diversity in the hypothalamus whose neurodevelopment remains poorly studi

297 of the hypothalamus and the crosstalk of the hypothalamus with reward-related brain regions were inve

298 ven the interactions of the diencephalon and hypothalamus with virtually all portions of the central

299 eurons are generated in the postnatal rodent hypothalamus, with a subset of tanycytes in the third ve

300 ventrolateral preoptic nucleus (VLPO) of the hypothalamus would modulate sleep/wake states and alter