ライフサイエンスコーパス: preoptic area

1 soma and near fiber-fiber appositions in the preoptic area.

2 paraventricular nucleus and the ventromedial preoptic area.

3 and in a dense fiber network throughout the preoptic area.

4 ivation of neurons in the medial part of the preoptic area.

5 to the thermoregulatory command center, the preoptic area.

6 ing the medial ganglionic eminence (MGE) and preoptic area.

7 commissures, and more caudally at the medial preoptic area.

8 tegmental nuclei, dorsal raphe, and lateral preoptic area.

9 activity of nitric oxide (NO) in the medial preoptic area.

10 passing the ventral retina, optic stalks and preoptic area.

11 jection were combined, but not in the medial preoptic area.

12 ing hormone (LHRH)-containing neurons in the preoptic area.

13 gf-, signals to induce Vax expression in the preoptic area.

14 potentially synapse with tac3a cells in the preoptic area.

15 throughout the hypothalamus and towards the preoptic area.

16 xpression in the hypothalamic neuroendocrine preoptic area.

17 vicinity of GnRH neurons within the rostral preoptic area.

18 alamic nucleus, the arcuate nucleus, and the preoptic area.

19 llular, and gigantocellular AVT cells in the preoptic area.

20 d [14C]2-fluoro-2-deoxyglucose (2-DG) in the preoptic area (25%) and significantly lower uptake in th

21 calizes with isotocin-producing cells in the preoptic area, a critical node in the highly conserved v

22 revealed abundant expression throughout the preoptic area, a vocal-acoustic site in the hypothalamus

23 ast, c-Fos was absent from the ventrolateral preoptic area (active during sleep).

24 RESEARCH DESIGN AND The effect of preoptic area administration of insulin on CBT in mice w

25 O) was of interest because its levels in the preoptic area affect ejaculation, and it could synchroni

26 Suppression of ERalpha in the preoptic area almost completely abolished maternal care,

27 ne vasopressin (AVP)-positive neurons in the preoptic area, an increase in the size of magnocellular

28 bitory stimulation of neurons in the lateral preoptic area and (2) by return of rats to an environmen

29 that outputs from the rdAcbSh to the lateral preoptic area and anterior and lateral hypothalamic area

30 ly 85-90% of GnRH cell bodies throughout the preoptic area and anterior hypothalamic area in the rat.

31 y identified vocal regions of the forebrain (preoptic area and anterior hypothalamus) and of the midb

32 leptin resistance development in the medial preoptic area and anteroventral periventricular nucleus,

33 ed by increased Fos expression in the medial preoptic area and arcuate nucleus--two reproductive cont

34 sleep regulation, such as the ventrolateral preoptic area and dorsal median preoptic nucleus.

35 e brain, with the highest density within the preoptic area and hypothalamus.

36 the medial zone of the dorsal telencephalon, preoptic area and hypothalamus.

37 rosencephalic neuron groups were seen in the preoptic area and in rostral and caudal periventricular

38 y organizing the synaptic development of the preoptic area and leading to male-typical sexual behavio

39 thalamic nuclei, including the ventrolateral preoptic area and median preoptic nucleus.

40 eoptic area, especially in the ventrolateral preoptic area and median preoptic nucleus.

41 amus, irNPB cells were present in the medial preoptic area and nucleus, ventromedial preoptic nucleus

42 ss decreased GAD65 mRNA levels in the medial preoptic area and posteromedial BST of aged rats.

43 v3.1 and -3.2, but not Cav3.3, in the medial preoptic area and the arcuate nucleus.

44 nding projections of Dl are primarily to the preoptic area and the caudal hypothalamus, whereas desce

45 Two brain regions are highlighted: the preoptic area and the cerebellum.

46 band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA),

47 ndle along the base of the brain between the preoptic area and the pituitary stalk, and neurons of th

48 sleep-promoting neurons in the ventrolateral preoptic area and the superior colliculus.

49 nuclei, and some scattered cells lie in the preoptic area and ventral part of the ventral telencepha

50 and vocal-acoustic integration sites in the preoptic area and ventral telencephalon.

51 H labeling and was limited to regions of the preoptic area and ventral thalamus, which is consistent

52 othalamic and lateral preoptic areas, medial preoptic area, and certain other hypothalamic regions, a

53 bens, septum, substantia innominata, lateral preoptic area, and diagonal band nuclei of the basal for

54 us semicircularis); and (4) basal forebrain, preoptic area, and hypothalamic nuclei.

55 rs were distributed throughout the thalamus, preoptic area, and hypothalamus.

56 for E(2) signaling pathways in cells of the preoptic area, and it may thereby mediate E(2) negative

57 ehavior, both centrally, particularly in the preoptic area, and peripherally, notably through its rol

58 aviest input coming from the lateral septum, preoptic area, and posterior hypothalamus.

59 (medial septum, diagonal band, magnocellular preoptic area, and substantia innominata).

60 locus coeruleus, medial septal area, medial preoptic area, and substantia innominata.

61 rons in the medial septum, the magnocellular preoptic area, and the substantia innominata.

62 ompassing the medial septal area, the medial preoptic area, and the substantia innominata.

63 an amygdalar complex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypot

64 an amygdalar complex, hippocampus, striatum, preoptic area, anterior hypothalamus, ventromedial hypot

65 ics, show that galanin is upregulated in the preoptic area-anterior hypothalamus (POA-AH) of nest-hol

66 Electrophysiological experiments on preoptic area/anterior hypothalamic neurons show that C2

67 The preoptic area/anterior hypothalamus, a region that conta

68 rtion of pubertally born cells in the medial preoptic area, arcuate nucleus, and medial amygdala diff

69 ls in the basal ganglia, amygdaloid complex, preoptic area, basal hypothalamus, mesencephalic tectum

70 entral medial ganglionic eminence and dorsal preoptic area based on fate mapping using an Shh-Cre all

71 ucleus of the hypothalamus, arcuate nucleus, preoptic area, bed nucleus of the stria terminalis, para

72 re consistently detected at the level of the preoptic area, but the main kiss2 mRNA-positive populati

73 of the lateral geniculate nucleus (LGv), and preoptic area, but the overall projections were more wid

74 substantia innominata (SI) and magnocellular preoptic area, but there was no innervation by the choli

75 d putative glutamatergic cells in the caudal preoptic area, caudal BST, and medial amygdala of male g

76 lpha cell number in the rat hypothalamus and preoptic area changes with aging in a region-specific ma

77 increased activity in the lateral septum and preoptic area, demonstrating recruitment of shared brain

78 ian preoptic nucleus (MnPO) and dorsolateral preoptic area (DLPO) and in the A7 noradrenergic cell gr

79 erminal nerve, ventral telencephalon, caudal preoptic area, dorsal mesencephalic tegmentum, and rostr

80 factory bulbs, ventral telencephalon, caudal preoptic area, dorsal tegmentum and rostral rhombencepha

81 The preoptic area, dorsal thalamus, tuberal and hypothalamic

82 d in many hypothalamic regions including the preoptic area, dorsomedial nucleus, lateral hypothalamus

83 GL-efferent projections to the ventrolateral preoptic area, dorsomedial, and medial tuberal hypothala

84 ent study is a quantitative investigation of preoptic area efferents to these monoaminergic groups.

85 the existence of sleep-active neurons in the preoptic area, especially in the ventrolateral preoptic

86 ion, and optrode recording, we show that the preoptic area GABAergic neurons projecting to the tubero

87 atures of AVT neurons in the gigantocellular preoptic area (gPOA) and axon varicosities within the ve

88 The medial preoptic area has been shown to be intricately involved

89 pecific and not reflective of differences in preoptic area height or brain size.

90 We isolated mRNA from the hypothalamus-preoptic area (HPOA), amygdala (AMYG), medulla (MD), fro

91 t brain, the dorsal telencephalon, habenula, preoptic area, hypothalamus, and cerebellum.

92 Key neuroendocrine centers, like the preoptic area, hypothalamus, and pituitary, conspicuousl

93 e sbLPXRFa-ir cells profusely innervated the preoptic area, hypothalamus, optic tectum, semicircular

94 ptum, nucleus of the diagonal band of Broca, preoptic area, hypothalamus, rostral pallium, nucleus ac

95 including the olfactory bulb, telencephalon, preoptic area, hypothalamus, thalamus, midbrain, optic t

96 phin-releasing hormone (GnRH) neurons in the preoptic area/hypothalamus that control the onset of pub

97 impairment, indicating a crucial role of the preoptic area in sleep generation.

98 s and astrocytes and appears specific to the preoptic area in that hippocampal neurons responded with

99 neuronal spine plasticity in the developing preoptic area in which estradiol induces prostaglandin-E

100 in magnocellular neurons of the hypothalamic preoptic area including those expressing vasopressin and

101 ssociated with AVT-ir neurons throughout the preoptic area, indicating the potential for functional i

102 dotropin-releasing hormone-II neurons in the preoptic area, IPe, arcuate nucleus of hypothalamus, and

103 ng paced mating behavior, whereas the medial preoptic area is a critical component of the neural circ

104 rginine-vasopressin (AVP) on the activity of preoptic area kisspeptin neurons.

105 mygdala, septal territories, medial pallium, preoptic area, lateral hypothalamus, thalamus, and preth

106 re found in forebrain regions, including the preoptic area, lateral septal nucleus, ventral subiculum

107 expression in the medial amygdala and medial preoptic area may fully mediate the effects of genotype

108 ith the highest density in the magnocellular preoptic area (MCPO).

109 nucleus accumbens, ventral pallidum, medial preoptic area, medial amygdala, and the supraoptic nucle

110 ade tracing from the locus coeruleus, medial preoptic area, medial septal area, and substantia innomi

111 etween PnNOS and PIN was found in the medial preoptic area, medial septum, and cortex, and less in th

112 ic nucleus, lateral hypothalamic and lateral preoptic areas, medial preoptic area, and certain other

113 n in both the preoptic area (POA) and medial preoptic area/medial bed nucleus of the stria terminalis

114 nucleus, anterior hypothalamic area, medial preoptic area, median preoptic nucleus, anteroventral pe

115 d to profile gene expression patterns in the preoptic area/mediobasal hypothalamus (POA/MBH) of male

116 ntral periventricular nucleus [AVPV], median preoptic area [MePO], and medial preoptic nucleus [MPN])

117 Inhibition of median preoptic area (MnPO) neurons blocked the BAT thermogenic

118 anted with a push-pull cannula in the medial preoptic area (MPA) and ovariectomized bilaterally.

119 Recent advances have revealed the medial preoptic area (MPA) as a key site for the regulation of

120 in norepinephrine (NE) levels in the medial preoptic area (MPA) of the hypothalamus.

121 the stria terminals (BNST, 59%), and medial preoptic area (MPA, 53%).

122 he hypothalamic nuclei, including the medial preoptic area (MPO) and the suprachiasmatic nucleus (SCN

123 in the medial preoptic nucleus (MPN), medial preoptic area (MPO), lateral hypothalamus (LH), central

124 antagonizing GABA(A) receptors in the medial preoptic area (MPO), which is thought to contain neurons

125 fferences were observed in the caudal medial preoptic area (MPO), with significantly more FG+ cells o

126 on, and opioids and kisspeptin in the medial preoptic area (mPOA) and hypothalamic arcuate nucleus (A

127 sal forebrain region encompassing the medial preoptic area (MPOA) and the substantia innominata (SI).

128 udies have emphasized the role of the medial preoptic area (MPOA) as an important site for the regula

129 Dopamine in the medial preoptic area (MPOA) facilitates copulation in male rats

130 l nitric oxide synthase (nNOS) in the medial preoptic area (MPOA) has been implicated in various phys

131 f LS and in cingulate cortex (Cg) and medial preoptic area (MPOA) in female mice.

132 Dopamine (DA) released from the medial preoptic area (MPOA) in response to a receptive female o

133 acilitative neurotransmitter, and the medial preoptic area (MPOA) is a critical integrative site for

134 The medial preoptic area (MPOA) is a critical integrative site for

135 The medial preoptic area (MPOA) is a critical regulatory site for t

136 The medial preoptic area (mPOA) is a key site for the dopaminergic

137 Finally, because the medial preoptic area (MPOA) is also important for maternal beha

138 The medial preoptic area (MPOA) is an integral site for male sexual

139 The medial preoptic area (MPOA) is critical for male sexual behavio

140 role of dopamine (DA) release in the medial preoptic area (mPOA) is for the activation of male sexua

141 Nitric oxide in the medial preoptic area (MPOA) is important for the expression and

142 While the medial preoptic area (MPOA) is known to be critical for materna

143 on potential frequency in neighboring medial preoptic area (mPOA) neurons and GABAA receptor-mediated

144 ing PGE(2) (3 fmol/1 microl) into the medial preoptic area (mPOA) of conscious, unrestrained rats.

145 The medial preoptic area (mPOA) of the hypothalamus is involved in

146 fects of ibotenic acid lesions of the medial preoptic area (mPOA) on the display of partner preferenc

147 ffect of ibotenic acid lesions of the medial preoptic area (mPOA) on the expression of a conditioned

148 rogen receptor 1 (ESR1) in either the medial preoptic area (MPOA) or the ventromedial hypothalamus, v

149 of galanin-expressing neurons in the medial preoptic area (MPOA) that are specifically activated dur

150 The medial preoptic area (mPOA), a region in the hypothalamus, is a

151 The medial preoptic area (mPOA), an essential node for social behav

152 he dorsomedial hypothalamus (DMH) and median preoptic area (mPOA), both critical sites to regulate sy

153 cleus of the stria terminalis (BNST), medial preoptic area (MPOA), paraventricular nucleus (PVN), ant

154 The medial preoptic area (MPOA), ventral pallidum (VP), and nucleus

155 ntral periventricular nucleus (AVPV), medial preoptic area (MPOA), ventromedial nucleus (VMN), and ar

156 ptors may contribute to mating is the medial preoptic area (MPOA), which is vital for male sexual beh

157 BAergic synaptic current decay in the medial preoptic area (mPOA).

158 LPH) and adjacent lateral part of the medial preoptic area (MPOA).

159 nucleus of the stria terminalis, and medial preoptic area (MPOA).

160 pus (areas important for memory), and medial preoptic area (mPOA, an area important in display of mat

161 o express Fos in response to VCS (the medial preoptic area, MPOA; the ventrolateral portion of the ve

162 medial cell group of the sexually dimorphic preoptic area (mSDA) contain cells that are activated sp

163 ovide easy genetic access to sleep-promoting preoptic area neurons and a valuable entry point for dis

164 s a promising tool to explore whether medial preoptic area neurons interact with VTA neurons to contr

165 Stimulation of glutamatergic median preoptic area neurons produced a profound hypothermia du

166 ptor-alpha (ERalpha) protein is expressed in preoptic area neurons, and a very dense immunoreactive f

167 escribed in adult fish as the neurosecretory preoptic area (NPO), this region has not been clearly de

168 T peptide distribution, including the medial preoptic area, nucleus accumbens, central amygdala, late

169 arvocellular and magnocellular nuclei of the preoptic area, nucleus preglomerulosus, and posterior, v

170 brain regions such as the lateral and medial preoptic areas, nucleus of the diagonal band, nucleus ac

171 mammals, thermoregulation is mediated by the preoptic area of anterior hypothalamus (POA), with ~30%

172 lence ERalpha expression specifically in the preoptic area of female mice and measured a variety of b

173 Instead, a connection of the bursa with the preoptic area of Martegiani or its extension, Cloquet's

174 ursa fused broadly with the extension of the preoptic area of Martegiani, namely Cloquet's canal, or

175 ould alter the sexual differentiation of the preoptic area of offspring and resulting sociosexual beh

176 ulation of kisspeptin neurons appears in the preoptic area of only the male between E19 and P1.

177 The medial preoptic area of the adult sheep contains an ovine sexua

178 Thermoregulatory neurons in the preoptic area of the anterior hypothalamus (POA) form sy

179 t to be initiated via vagal afferents to the preoptic area of the anterior hypothalamus (POAH), an im

180 bcl-2 and bax mRNA expression in the medial preoptic area of the developing lamb fetus decreased dur

181 5, on thermoregulatory neurons in the medial preoptic area of the hypothalamus (mPOA) of rats while s

182 Activating PAG-projecting neurons in the preoptic area of the hypothalamus (POA(PAG) neurons) eli

183 r and killed to examine AVT phenotype in the preoptic area of the hypothalamus (POA), an area importa

184 is displayed by neurons in the ventromedial preoptic area of the hypothalamus (VMPO).

185 eurons reveals both known dimorphisms in the preoptic area of the hypothalamus and the bed nucleus of

186 and other mammalian species, lesions in the preoptic area of the hypothalamus cause profound sleep i

187 Injection of insulin into the preoptic area of the hypothalamus induced a specific and

188 Microdialysis experiments in the medial preoptic area of the hypothalamus showed that DVS (30 mg

189 dentify a negative feedback circuit in mouse preoptic area of the hypothalamus that regulates body te

190 in the dorsal and ventral telencephalon, the preoptic area of the hypothalamus, and the lateral reces

191 c inputs from sleep-promoting regions in the preoptic area of the hypothalamus.

192 gulated by neurons in the medial and lateral preoptic area of the hypothalamus.

193 observed in the olfactory bulb, pallium, and preoptic area of the telencephalon, and the subpallium i

194 erved in the olfactory bulb, subpallium, and preoptic area of the telencephalon.

195 matic nucleus, islands of Calleja and medial preoptic area, olfactory bulb, nucleus accumbens shell,

196 cleus of the stria terminalis and the medial preoptic area on the display of paced mating behavior in

197 njection of prostaglandin E2 into the medial preoptic area or by disinhibition of neurones in the rap

198 pathways, such as the lateral septum, medial preoptic area or dorsomedial hypothalamus.

199 cold-related signals, comprised the lateral preoptic area, parastrial nucleus, dorsomedial hypothala

200 us, paraventricular nucleus of the thalamus, preoptic area, paraventricular nucleus of the hypothalam

201 areas such as somatosensory/insular cortex, preoptic area, paraventricular nucleus, dorsomedial nucl

202 taining was present in neurons of the medial preoptic area, paraventricular nucleus, medial septum, a

203 gion were heavily concentrated in the medial preoptic area, paraventricular thalamic nucleus, the sub

204 ular thalamic nucleus), hypothalamus (medial preoptic area, perifornical, arcuate, dorsomedial, paras

205 tor potentiation of cAMP accumulation in the preoptic area (POA) and hypothalamus (HYP).

206 t levels of aromatase expression in both the preoptic area (POA) and medial preoptic area/medial bed

207 DA) and serotonin (5-HT) activity within the preoptic area (POA) and striatum, neural sites important

208 activity in forebrain regions, including the preoptic area (POA) and ventromedial nucleus of the amyg

209 At a neuroanatomical level, the preoptic area (POA) and ventromedial nucleus of the hypo

210 The preoptic area (POA) controls body temperature by modulat

211 in the medial ganglionic eminence (MGE) and preoptic area (PoA) give rise to GABAergic inhibitory in

212 The preoptic area (POA) is a key site for estrogenic regulat

213 The preoptic area (POA) is critical for maternal behavior in

214 al steroids in the highly sexually dimorphic preoptic area (POA) is to reduce activity of DNA methylt

215 Hypothalamic preoptic area (POA) neurons are intimately involved in m

216 ntral part of the ventral telencephalon, the preoptic area (POA) of the hypothalamus and the ventral

217 Several lines of evidence show that the preoptic area (POA) of the hypothalamus is critically im

218 In the present study, the preoptic area (POA) of the hypothalamus was investigated

219 ate the mechanism of cold sensitivity in the preoptic area (POA) of the hypothalamus, a critical ther

220 m individual warm-sensitive neurons from the preoptic area (POA) of the hypothalamus, a region involv

221 gonadal inputs on the AVP/AVT system in the preoptic area (POA) of the hypothalamus, we conducted th

222 of PGE2 (200 pmol in 70 nl) into the medial preoptic area (POA) or microinjection of the GABAA antag

223 sity did not differ between the sexes in the preoptic area (POA) or ventromedial nucleus of the amygd

224 es demonstrating that galanin neurons in the preoptic area (POA) promote mating and parental care in

225 he demonstration that galanin neurons in the preoptic area (POA) promote mating and parental care in

226 The preoptic area (POA) regulates body temperature, but is n

227 more abundant sbGnRH mRNA expression in the preoptic area (POA) than in other brain regions.

228 with females had smaller TH-ir cells in the preoptic area (POA) than vigorous males housed in isolat

229 Activation of the preoptic area (POA) warm sensitive neurons is known to p

230 n warm sensitive neurons of the hypothalamic preoptic area (POA) which play a critical role in the re

231 4) but is also expressed in the hypothalamic preoptic area (POA)(5).

232 n from the skin to a median subregion of the preoptic area (POA), a thermoregulatory centre.

233 nown migratory stream that emanates from the preoptic area (POA), a ventral telencephalic domain adja

234 sis (IncT) and age affect CO activity in the preoptic area (POA), an area that modulates copulatory b

235 evelopment, estradiol differentiates the rat preoptic area (POA), an essential brain region in the ma

236 cal and auditory networks in the subpallium, preoptic area (POA), anterior hypothalamus, dorsal thala

237 AR-ir cells in the nucleus accumbens (Acb), preoptic area (POA), bed nucleus of the stria terminalis

238 frontal cortex (CX), striatum, hypothalamus, preoptic area (POA), cerebellum, and ventral tegmental a

239 In the female rat preoptic area (POA), containing the gonadotropin-releasi

240 In the preoptic area (POA), estradiol aromatized from testoster

241 fibers in the olfactory bulb, telencephalon, preoptic area (POA), hypothalamus, midbrain, hindbrain,

242 we found that Kp neurons are present in the preoptic area (POA), suprachiasmatic (SCN), and arcuate

243 ductive social behavior in this species, the preoptic area (POA), the anterior hypothalamus (AH), sep

244 to the thermoregulatory command center, the preoptic area (POA).

245 he density of dendritic spines in the medial preoptic area (POA).

246 ir nuclear receptors in the hypothalamus and preoptic area (POA).

247 losum lamina terminalis (OVLT) region of the preoptic area (POA).

248 osum of the lamina terminalis (OVLT) and the preoptic area (POA).

249 mammalian hippocampus), accumbens, anterior preoptic area (POA; homolog of the mammalian paraventric

250 Medial and lateral septum (SM, SL), medial preoptic area (POM), and n. intercollicularis (ICo) were

251 PnNOS was found in the media preoptic area, posterior magnocellular, and the parvocel

252 VT-ir neuronal features in the parvocellular preoptic area (pPOA) should have a negative relationship

253 the embryonic medial ganglionic eminence and preoptic area preferentially develop electrical, but not

254 emales exhibited increased metabolism in the preoptic area, primary motor cortex, and the amygdala, a

255 nhibition of KOR neurons in the hypothalamic preoptic area reduced the CR-induced hypothermia, wherea

256 nscriptomes of brain sections containing the preoptic area (region involved in regulating aggressive

257 nd neural circuitry through which the medial preoptic area regulates this responsivity is described.

258 on of the boundary between the telencephalic preoptic area, rich in Nkx2.1 expression, and the pretha

259 sular cortex, lateral septal nucleus, medial preoptic area, rostral linear nucleus, and in the Edinge

260 he paraventricular nucleus (PVN) and rostral preoptic area (rPOA).

261 to each other and to the sexually dimorphic preoptic area (SDA), but those projections involve less

262 The sexually dimorphic nucleus of the preoptic area (SDN-POA) has received increased attention

263 ume of the sexually dimorphic nucleus of the preoptic area (SDN-POA) in Long-Evans rats.

264 sed in the sexually dimorphic nucleus of the preoptic area (SDN-POA), a nucleus in which apoptosis is

265 superior colliculus homologs, hypothalamus, preoptic area, septum, nucleus of the diagonal band of B

266 The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1-

267 In contrast, lesions of the medial preoptic area significantly lengthen contact-return late

268 thalamic paraventricular nucleus, and medial preoptic area, sites strongly implicated in the control

269 Here we identify a population of preoptic area sleep neurons on the basis of their projec

270 lic regions, and diencephalic regions of the preoptic area, thalamus, and hypothalamus, but was also

271 expressed in a small group of neurons in the preoptic area that project directly towards the pituitar

272 ct to a subset of the regions, including the preoptic area, that are innervated by the PMv as a whole

273 different diencephalic regions including the preoptic area, the bed nuclei stria terminalis, the para

274 bed nucleus of stria terminalis, the lateral preoptic area, the entopeduncular nucleus, and the later

275 he medial preoptic area, the periventricular preoptic area, the external nucleus of the amygdala, the

276 RC), the paraventricular nucleus, the medial preoptic area, the lateral septum, and nucleus of the so

277 ar group in the lateral aspect of the medial preoptic area, the magnocellular subdivision of the medi

278 tory nucleus, the lateral septum, the medial preoptic area, the periventricular preoptic area, the ex

279 the ventrolateral subdivision of the medial preoptic area ('thermoregulatory center'), and the retic

280 nections previously observed (e.g., anterior preoptic area to DTAM) were not confirmed.

281 d nucleus of the stria terminalis, amygdala, preoptic area, ventral hypothalamus, nucleus isthmus, te

282 d in groups of neurons in the telencephalon, preoptic area, ventral hypothalamus, thalamus, and pitui

283 not in surrounding sites (thalamus, lateral preoptic area, ventral tegmental area, dorsomedial hypot

284 areas controlling reproductive behaviors-the preoptic area, ventromedial amygdala (AMY), and ventrome

285 g less ERalpha-IR than females in the medial preoptic area, ventromedial nucleus, ventrolateral porti

286 c input to the sleep-promoting ventrolateral preoptic area (VLPO) [1] arises from the lateral hypotha

287 ve neurons in the hypothalamic ventrolateral preoptic area (VLPO) and the wake-active monoaminergic b

288 ld after E(2) treatment in the ventrolateral preoptic area (VLPO), the suspected site of action for t

289 ompared to the sleep-promoting ventrolateral preoptic area (VLPO), whereas green light produced great

290 (LH), and ventrolateral, medial, and median preoptic areas (VLPO, MPA, and MnPO, respectively).

291 reoptic nucleus (MnPN) and the ventrolateral preoptic area (vlPOA) contain putative sleep-regulatory

292 reoptic nucleus (MnPN) and the ventrolateral preoptic area (vlPOA) express immunoreactivity for c-Fos

293 optic nucleus (MnPN) and the ventral lateral preoptic area (vlPOA) of the hypothalamus express sleep-

294 ound in cells localized in the ventrolateral preoptic area (vlPOA).

295 tes downstream neurons in the ventral medial preoptic area (vMPO) that mediates body temperature decr

296 ume of the sexually dimorphic nucleus of the preoptic area was unaffected by the tfm allele, soma siz

297 POINTS: Glutamatergic neurons in the median preoptic area were stimulated using genetically targeted

298 nd anatomical deficiency in the diencephalic preoptic area, where the optic chiasm normally forms.

299 posterior ventricular nucleus of the caudal preoptic area, whereas LPXRFa-R-immunoreactive cells are

300 r and elevated neural activity in the medial preoptic area, whereas sexual behavior remains normal.