ライフサイエンスコーパス: preoptic area

1 paraventricular nucleus and the ventromedial preoptic area.

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

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

4 to the thermoregulatory command center, the preoptic area.

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

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

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

8 throughout the hypothalamus and towards the 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 except for equivalent input from the medial preoptic area.

15 uclei also receive descending input from the preoptic area.

16 thalamus and a sleep-promoting region in the preoptic area.

17 ot seen in the PGE(2) sensitive parts of the preoptic area.

18 90 min after their infusions into the medial preoptic area.

19 xpression in the hypothalamic neuroendocrine preoptic area.

20 vicinity of GnRH neurons within the rostral preoptic area.

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

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

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

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

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

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

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

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

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

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

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

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

33 synthesis in thermoregulatory regions of the preoptic area and anterior hypothalamus (POA/AH).

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

35 hypothalamic tissue slices, primarily in the preoptic area and anterior hypothalamus, a thermoregulat

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

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

38 erminals descend almost exclusively from the preoptic area and are found in two primary candidate sit

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

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

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

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

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

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

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

46 se (GAD) 65 mRNA was increased in the medial preoptic area and posteromedial bed nucleus of the stria

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 Given the putative role of the lateral preoptic area as a primary contributor of the cell bodie

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

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

76 IV-VI of the cerebral cortex, medial septum, preoptic area, bed nucleus of the stria terminalis, supr

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

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

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

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

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

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

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

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

85 The preoptic area, dorsal thalamus, tuberal and hypothalamic

86 r retrograde tracer injections in the medial preoptic area, dorsomedial and paraventricular hypothala

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

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

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

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

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

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

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

94 ital, ethanol and adenosine, into the medial preoptic area has been shown to increase sleep, suggesti

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

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

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

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

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

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

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

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

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

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

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

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

107 y distributed within the basal forebrain and preoptic area, infundibular region, central hypothalamus

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

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

110 The preoptic area is implicated in both sleep generation and

111 The parvocellular preoptic area itself is also vocally active, although th

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

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

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

115 FO), median preoptic nucleus (MnPO), lateral preoptic area (LPO), or lateral hypothalamus (LH) on the

116 PS erectile control include both the lateral preoptic area (LPOA) and ventral division of the bed nuc

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

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

119 medial cell group of the sexually dimorphic preoptic area (medial SDA), and the parvicellular part o

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

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

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

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

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

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

126 it mRNA was prominent in the lateral septum, preoptic area, mediobasal hypothalamus, and tuberomammil

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

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

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

130 uce sleep when microinjected into the medial preoptic area (MPA) of the anterior hypothalamus.

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

132 ase sleep when microinjected into the medial preoptic area (MPA) of the rat.

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

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

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

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

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

138 on GnRH-GABA interactions within the medial preoptic area (mPOA) across pubertal development (experi

139 Neurotoxic lesions involving the medial preoptic area (MPOA) and anterior hypothalamus (n = 5) h

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

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

142 c-Fos and Fos B within neurons of the medial preoptic area (MPOA) and ventral bed nucleus of the stri

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

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

145 Increased dopamine (DA) in the medial preoptic area (MPOA) facilitates male sexual behavior.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

164 and ibotenic acid (IA) lesions of the medial preoptic area (MPOA) on the temporal pattern of female s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

195 5, on thermoregulatory neurons in the medial preoptic area of the hypothalamus (mPOA) of rats while s

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

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

198 5) were found in the dorsomedial nucleus and preoptic area of the hypothalamus and also the medial am

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

235 at estrogen acts on GABAergic neurons in the preoptic area (POA) to elicit a biphasic profile of lute

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

280 hanism via which estrogen acts in the medial preoptic area to prevent the display of female reproduct

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 ve positive cells than females in the medial preoptic area, ventromedial nucleus of the hypothalamus,

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

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

288 anisms may be localized to the ventrolateral preoptic area (VLPO) and that this region sends inhibito

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

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

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

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

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

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

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

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

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

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

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

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