ライフサイエンスコーパス: arcuate

1 between phonological awareness and the left arcuate.

2 inferior-fronto-occipital fasciculus or the arcuate.

3 ated to be mediated by kisspeptin neurons in arcuate and anteroventral periventricular (AVPV) nuclei,

4 alpha [ERalpha]); kisspeptin neurons in the arcuate and anteroventral periventricular nuclei are pos

5 Imaging of single cells from the arcuate and dorsomedial hypothalamic nuclei revealed thi

6 y were more dorsally situated, including the arcuate and middle longitudinal fasciculi.

7 arly as E9.5 in the lateral hypothalamic and arcuate and rapidly expands to dorsomedial and ventromed

8 degree of microstructural alteration of the arcuate and uncinate fasciculi was associated with sever

9 and microglia, as well as in micropunches of arcuate and ventromedial hypothalamic nuclei (VMN).

10 come into close contact with neurons in the arcuate and ventromedial hypothalamic nuclei.

11 ) and in the anterior periventricular (PVa), arcuate, and dorsomedial hypothalamic nuclei.

12 ria; anterior hypothalamus; paraventricular, arcuate, and dorsomedial hypothalamic nuclei; lateral hy

13 ression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the hypothalamus, reg

14 on RNA extracted from laser micro-dissected arcuate (ARC) and paraventricular (PVN) hypothalamic nuc

15 genetics to investigate whether hypothalamic arcuate (ARC) dopamine/tyrosine hydroxylase (TH) neurons

16 optic area (POA), suprachiasmatic (SCN), and arcuate (ARC) nuclei, and that RFRP-3 neurons are presen

17 mic anteroventral periventricular (AVPV) and arcuate (ARC) nuclei, while the region-specific role of

18 hypothalamic area/zona incerta (LH) and the arcuate (Arc) nucleus.

19 on sector of VF progression was the superior arcuate area (65%).

20 ventricular (PVH) and dorsomedial (DMH), the arcuate (ARH) nuclei and the lateral hypothalamic areas

21 r, whereas the diameters of interlobular and arcuate arteries declined to 50%+/-12% and 68%+/-6% of t

22 sistance arteries, including renal lobar and arcuate arteries.

23 raesophageal mass (brain), as well as in the arcuate body, a region of the brain thought to receive v

24 der visual neuropils project directly to the arcuate body, suggesting that the posterior median eyes

25 s of the principal eyes are connected to the arcuate body, whereas the second-order neuropils of the

26 In arcuate, but not AVPV, kisspeptin neurons, estradiol red

27 sical data collected in 2006 reveal a large, arcuate, complex grounding zone sediment system at the f

28 led correspondence map that demonstrates the arcuate course of the NFL in the macula.

29 wn feeding-related brain regions such as the arcuate, dorsomedial, and paraventricular hypothalamic n

30 d cortical thickness increased in both right arcuate end points, the middle temporal (T = 4.25) and p

31 leptin, IL-6, and MCP-1 in WT and increased arcuate expression of Kiss1 and Esr1 (ERalpha) and liver

32 In patients with CFS, right anterior arcuate FA increased with disease severity (r = 0.649, P

33 Right anterior arcuate FA may serve as a biomarker for CFS.

34 ding, and that the superior longitudinal and arcuate fascicles are shared across the math and reading

35 hrough the aslant, superior longitudinal and arcuate fasciculi.

36 We focused on the arcuate fasciculus (AF) and inferior longitudinal fascic

37 has been demonstrated in the strength of the arcuate fasciculus (AF), a fiber pathway interlinking th

38 rnix (FF), parahippocampal WM bundle (PWMB), arcuate fasciculus (AF), inferior longitudinal fasciculu

39 (frontal and temporal cortex) by way of the arcuate fasciculus (AF).

40 , we detected white matter reductions in the arcuate fasciculus (dorsal language stream) bilaterally,

41 FS population, FA was increased in the right arcuate fasciculus (P = .0015), and in right-handers, FA

42 l additionally introduced the left and right arcuate fasciculus (separate analysis for each segment).

43 0.010] and volume of the long segment of the arcuate fasciculus [beta = 0.730, t(2.732), P = 0.020] w

44 yelin that were observed throughout the left arcuate fasciculus and associated with age-related diffe

45 rietal (anterior segment) connections of the arcuate fasciculus are left and right lateralized, respe

46 Using the arcuate fasciculus as an example of discontinuity in the

47 lume measures from the three segments of the arcuate fasciculus connecting Wernicke's to Broca's regi

48 propose that developmental sculpting of the arcuate fasciculus determines acquisition, storage, and

49 The left arcuate fasciculus had decreased fractional anisotropy,

50 d in understanding how lateralization of the arcuate fasciculus impacts on severity of symptoms and t

51 ual-stream accounts that deny a role for the arcuate fasciculus in semantic processing, and for ventr

52 The arcuate fasciculus is a central connection in this archi

53 nalysis suggested that lateralization of the arcuate fasciculus is a heterogeneous process that depen

54 es in vocabulary knowledge are influenced by arcuate fasciculus macrostructure (i.e., shape and volum

55 However, atypical patterns of arcuate fasciculus morphology or macrostructure were ass

56 We tested the hypothesis that arcuate fasciculus morphology, which supports the develo

57 suggest that deterioration of tissue in the arcuate fasciculus occurs with normal aging, while havin

58 The human arcuate fasciculus pathway is crucial for language, inte

59 ndices from fMRI(LI) and optic radiation and arcuate fasciculus probabilistic tractography was perfor

60 This demonstrates that the arcuate fasciculus underwent additional evolutionary mod

61 as found between language lateralisation and arcuate fasciculus volume.

62 Fractional anisotropy in the left arcuate fasciculus was significantly related to individu

63 aslant tract and the anterior segment of the arcuate fasciculus were particularly engaged with the qu

64 cingulum, and the anterior part of the left arcuate fasciculus when controlling for age, sex, and ac

65 alyses indicated that both dorsally located (arcuate fasciculus) and ventrally located (inferior fron

66 PFC) as well as on the integrity of the left arcuate fasciculus, a fiber bundle linking the posterior

67 Our study focused on the arcuate fasciculus, a language pathway composed of three

68 uggest that the anterior segment of the left arcuate fasciculus, a white matter tract that lies deep

69 inferior longitudinal fasciculus, the right arcuate fasciculus, and the left uncinate fasciculus.

70 positively correlated with the volume of the arcuate fasciculus, but not with other tracts.

71 nes in the anterior and long segments of the arcuate fasciculus, cingulum and uncinate--predominantly

72 The arcuate fasciculus, connecting both of them, was most se

73 cingulum, superior longitudinal fasciculus, arcuate fasciculus, inferior fronto-occipital fasciculus

74 slexia and white matter organization in left arcuate fasciculus, inferior longitudinal fasciculus, an

75 blishes a primate auditory prototype for the arcuate fasciculus, reveals an earlier phylogenetic orig

76 phonological word forms is supported by the arcuate fasciculus, these findings demonstrate that lear

77 w phonological word forms is mediated by the arcuate fasciculus, these findings show that the tempora

78 These findings indicate that the left arcuate fasciculus, which connects anterior and posterio

79 bstrates of g and working memory include the arcuate fasciculus.

80 o determine the fractional anisotropy of the arcuate fasciculus.

81 uperior longitudinal fasciculus, but not the arcuate fasciculus.

82 y damage to the anterior segment of the left arcuate fasciculus.

83 de connected by the white matter of the left arcuate fasciculus.

84 of g/Gwm were primarily associated with the arcuate fasciculus.

85 The RNFL was seen as arcuate hyperreflective bundles.

86 in the periventricular, paraventricular, and arcuate hypothalamic nuclei and locus ceruleus of mice e

87 ostrema -> nucleus of the solitary tract and arcuate hypothalamic nucleus -> paraventricular nucleus

88 hamsters and mice increased AgRP within the arcuate hypothalamic nucleus with concomitant increases

89 cleus, paraventricular hypothalamic nucleus, arcuate hypothalamic nucleus, primary and secondary soma

90 ow that kisspeptin-expressing neurons in the arcuate hypothalamus (Kiss1(ARH)) of female mice control

91 riventricular hypothalamus, Kiss1(AVPV), and arcuate hypothalamus, Kiss1(ARH)), which drive the pulsa

92 ing-induced activation of neurons within the arcuate hypothalamus.

93 id feedback was found to act specifically on arcuate Kiss1 expression.

94 itters GABA and glutamate rapidly depolarize arcuate kisspeptin neurons and estradiol increases this

95 rvations support the hypothesis that PSPs in arcuate kisspeptin neurons are regulated by estradiol-se

96 The hypothalamic arcuate kisspeptin neurons are thought to represent the

97 Whole-cell recordings of arcuate kisspeptin neurons in brain slices from ovariect

98 ted as we increase the basal activity of the arcuate kisspeptin neurons in vivo using continuous opto

99 roperties by estradiol feedback thus renders arcuate kisspeptin neurons more sensitive to fast synapt

100 Mice with ERalpha knocked down in arcuate kisspeptin neurons showed disrupted cyclicity, a

101 Vglut2-ires-Cre lines, approximately 70% of arcuate kisspeptin neurons were targeted in Vglut2-ires-

102 tion and maintain cyclicity through AVPV and arcuate kisspeptin neurons, respectively, independent fr

103 to AVPV neurons and markedly increased it to arcuate kisspeptin neurons, which also exhibited increas

104 gic transmission to AVPV and increased it to arcuate kisspeptin neurons; positive feedback had the op

105 Median arcuate ligament (MAL) syndrome is a rare disease result

106 5) was conducted, using the key terms median arcuate ligament syndrome and celiac artery compression

107 Median arcuate ligament syndrome is rare, and as a diagnosis of

108 ments of the diaphragmatic crura, the median arcuate ligament.

109 ave visual field defects, with predominantly arcuate loss and enlarged blind spots that require forma

110 t not vocabulary, from (2) relatively stable arcuate macrostructure (shape/volume) that explained sig

111 The hypothalamic arcuate-median eminence complex (Arc-ME) controls energy

112 n the hypothalamic neuronal populations, the arcuate melanocortin system plays a major role in contro

113 Whereas bilateral intra-arcuate microinjection of saline vehicle was without eff

114 d (1) the effects of age-related declines in arcuate microstructure (mean diffusivity; myelin content

115 receptor apparent affinity, the decrease in arcuate miniature postsynaptic current amplitude was att

116 vated key appetite-regulating neurons in the arcuate, namely proopiomelanocortin neurons.

117 ry program directing development of multiple arcuate neuronal subpopulations.

118 ssed in several subpopulations of developing arcuate neurons and plays crucial roles in their fate sp

119 neuropeptide Y (NPY)-expressing hypothalamic arcuate neurons before plaque formation.

120 GABA depolarized the membrane potential of arcuate neurons from OVX+E mice; this response was blunt

121 ed protein (AgRP) from discrete hypothalamic arcuate neurons onto common target sites in the central

122 We further demonstrated that some of these arcuate neurons were also targets of leptin action.

123 hreshold activated L-type Ca(2+) currents in arcuate neuropeptide Y neurons.

124 this study, we examined whether Abeta causes arcuate NPY neuronal dysfunction by disrupting intracell

125 A high-fat diet did not alter arcuate NPY neuronal InsR expression in males or females

126 ferences were not associated with changes in arcuate NPY neuronal insulin receptor expression.

127 In addition, arcuate NPY neurons exhibited abnormal electrophysiologi

128 nd reduce the intracellular Ca(2+) levels in arcuate NPY neurons from Tg2576 brain slices.

129 s Abeta can potentially disrupt hypothalamic arcuate NPY neurons leading to weight loss and a patholo

130 es and prevents acyl-ghrelin from activating arcuate NPY neurons.

131 prised of the dorsomedial, ventromedial, and arcuate nuclei, as well as parts of the lateral hypothal

132 the anteroventral periventricular (AVPV) and arcuate nuclei, providing homeostatic feedback on episod

133 icular nuclei and energy homeostasis via the arcuate nuclei.

134 Arcuate nucleus (AN) neurons are classically thought to

135 high tdTomato expression in the hypothalamic arcuate nucleus (Arc) (i.e., within parts of the neural

136 ind that kisspeptin-producing neurons in the arcuate nucleus (ARC) already communicate with a specifi

137 labeled liraglutide bound neurons within the arcuate nucleus (ARC) and other discrete sites in the hy

138 Neurons within the hypothalamic arcuate nucleus (ARC) are important regulators of energy

139 In the hypothalamus, ACBP is enriched in arcuate nucleus (ARC) astrocytes, ependymocytes and tany

140 ted peptide (AgRP)-expressing neurons in the arcuate nucleus (ARC) at the base of the hypothalamus ar

141 xpenditure, and within the hypothalamus, the arcuate nucleus (ARC) functions as a gateway for hormona

142 The Arcuate nucleus (ARC) in hypothalamus contains antagoniz

143 /FoxO1 signaling pathway in the hypothalamic arcuate nucleus (ARC) mediates MCH-induced feeding, adip

144 Arcuate nucleus (ARC) neurons sense the fed or fasted st

145 hat the great majority of mouse hypothalamic arcuate nucleus (ARC) neurons that synthesize TH in the

146 evaluated the hypothesis that destruction of arcuate nucleus (ARC) neurons, in concert with dampening

147 n of reactive oxygen species (ROS) levels in arcuate nucleus (ARC) neurons.

148 The arcuate nucleus (ARC) of the hypothalamus comprises neur

149 owed an increased number of microglia in the arcuate nucleus (ARC) of the hypothalamus.

150 primarily through activation of hypothalamic arcuate nucleus (ARC) pro-opiomelanocortin (POMC) neuron

151 ctive Ca(2+) activation of glia in the mouse arcuate nucleus (ARC) reversibly induces increased food

152 Neurons in the hypothalamic arcuate nucleus (ARC) that co-express kisspeptin, neurok

153 ss of excitatory neurons in the hypothalamic arcuate nucleus (ARC) that utilizes glutamate as a fast

154 Dopamine neurons of the hypothalamic arcuate nucleus (ARC) tonically inhibit the release of t

155 thesized that, not only the SCN but also the arcuate nucleus (ARC), are involved in the Tb setting th

156 The hypothalamic arcuate nucleus (Arc), containing pro-opoiomelanocortin

157 In the hypothalamic arcuate nucleus (ARC), proopiomelanocortin (POMC) neuron

158 sses governed by neurons in the hypothalamic arcuate nucleus (ARC), such as growth, reproduction and

159 the tyrosine hydroxylase (TH) neuron of the arcuate nucleus (ARC), that we show makes an orexigenic

160 urons are sparse in the rostral hypothalamic arcuate nucleus (ARC), the subregion that has received t

161 We found that the hypothalamic arcuate nucleus (ARC), ventromedial nucleus (VMN), and l

162 ood pressure (BP) through its actions in the arcuate nucleus (ARC).

163 with insulin receptors, in the hypothalamic arcuate nucleus (ARC).

164 MC and GABAergic-neurons in the hypothalamic arcuate nucleus (ARC).

165 lized with proopiomelanocortin (POMC) in the arcuate nucleus (ARC).

166 d afferent projections from the hypothalamic arcuate nucleus (Arc).

167 unique presence of RFRP-3 cell bodies in the arcuate nucleus (Arc).

168 We show that hypothalamic arcuate nucleus (Arc)POMC-deficient mice, which develop

169 vation of proopiomelanocortin neurons in the arcuate nucleus (ArcN), and this action requires simulta

170 The hypothalamic arcuate nucleus (ARH) is a brain region critical for reg

171 d that the kisspeptin neurons located in the arcuate nucleus (ARN) may be involved.

172 Kisspeptin neurons in the hypothalamic arcuate nucleus (Kiss1(ARH)) co-express Kiss1, NKB, dyno

173 specific activation of this receptor in the arcuate nucleus affected adipocyte metabolism.

174 Arcuate nucleus agouti-related peptide (AgRP) neurons pl

175 Kisspeptin neurons of the arcuate nucleus and anteroventral-periventricular region

176 inputs from the canonical feeding regions of arcuate nucleus and parabrachial nucleus.

177 d in Kiss1 neurons of the mouse hypothalamic arcuate nucleus and that MKRN3 repressed promoter activi

178 also observed in the ventral subiculum, the arcuate nucleus and the ventrolateral subdivision of the

179 Agouti-related peptide (AgRP) neurons in the arcuate nucleus are GABAergic, express leptin receptors

180 Moreover, NPY neurons in the arcuate nucleus became resistant to the inhibitory effec

181 e activity was specifically increased in the arcuate nucleus but not other regions of the hypothalamu

182 Only Npy gene expression in the arcuate nucleus displayed no significant variations betw

183 Consistent with these results, their arcuate nucleus fails to express key fate markers of Isl

184 Arcuate nucleus glucokinase activation may represent a C

185 increased glucose ingestion, while decreased arcuate nucleus glucokinase activity reduced glucose int

186 Kisspeptin neurons in the hypothalamic arcuate nucleus help convey homeostatic estradiol feedba

187 actor (BDNF) further directed the cells into arcuate nucleus hypothalamic-like neurons that express h

188 tereotaxic guided deletion of ERalpha in the arcuate nucleus increases bone mass in intact and ovarie

189 asmatic area and the mediobasal hypothalamic arcuate nucleus independently generate ultradian rhythms

190 Blockade of arcuate nucleus insulin receptors did not lower SNA in p

191 glucokinase activity within the hypothalamic arcuate nucleus is involved in regulation of dietary glu

192 hat axonal dynorphin immunoreactivity in the arcuate nucleus is strong, and that a large number of dy

193 rexigenic proopiomelanocortin neurons in the arcuate nucleus is unclear, leptin resistance and elevat

194 ly behaving mice to evaluate the role of the arcuate nucleus kisspeptin (ARN(KISS)) neurons in LH pul

195 agouti-related protein (AgRP) neurons in the arcuate nucleus made few direct synapses onto VTA MC3R n

196 hypothalamic inflammation and activation of arcuate nucleus microglia, resulting in altered input or

197 ain homeostasis, hypothalamic neurons in the arcuate nucleus must dynamically sense and integrate a m

198 signaling, including the poor development of arcuate nucleus neural projections, were recovered by Le

199 weaker direct inhibitory effect of Dyn-A on arcuate nucleus neuropeptide Y (NPY) neurons mediated by

200 er, Acb enkephalin neurons expressed Y1R and arcuate nucleus NPY neurons projected to the Acb.

201 oups in hypothalamic energy-sensing systems (arcuate nucleus NPY was upregulated, and cocaine- and am

202 at a subpopulation of ERalpha neurons in the arcuate nucleus of female mice undergoes a shift in phen

203 Levels of Mkrn3 mRNA were high in the arcuate nucleus of prepubertal mice, decreased immediate

204 and genetic activation of glucokinase in the arcuate nucleus of rodent models increased glucose inges

205 Proopiomelanocortin (POMC) neurons in the arcuate nucleus of the hypothalamus (ARC) also regulate

206 ted peptide (AgRP)-expressing neurons of the arcuate nucleus of the hypothalamus (ARC) are oppositely

207 Agouti-related peptide (AgRP) neurons of the arcuate nucleus of the hypothalamus (ARC) promote homeos

208 (AgRP) neurons-interoceptive neurons in the arcuate nucleus of the hypothalamus (ARC)-are both neces

209 onociceptin (PNOC)-expressing neurons in the arcuate nucleus of the hypothalamus (ARC).

210 Neuropeptide Y (NPY) neurons in both the arcuate nucleus of the hypothalamus (ARH) and the dorsom

211 ood intake, POMC and NPY/AgRP neurons in the arcuate nucleus of the hypothalamus (ARH) are derived fr

212 The arcuate nucleus of the hypothalamus (ARH) is critical fo

213 tional profiling in neuronal nuclei from the arcuate nucleus of the hypothalamus (ARH) reveal differe

214 In the arcuate nucleus of the hypothalamus (ARH) satiety signal

215 receive synaptic inputs from neurons of the arcuate nucleus of the hypothalamus (ARH) that contains

216 ptin stimulates the growth of axons from the arcuate nucleus of the hypothalamus (ARH) to other regio

217 en only after the second week of life in the arcuate nucleus of the hypothalamus (ARH).

218 ite through interactions with neurons in the arcuate nucleus of the hypothalamus (ARH).

219 tivity of NPY/AgRP/GABA neurons (NAG) in the arcuate nucleus of the hypothalamus (ARH).

220 rogesterone receptor-expressing cells in the arcuate nucleus of the hypothalamus (ARN).

221 preferentially project to the medioposterior arcuate nucleus of the hypothalamus (mpARH) and GE-ERalp

222 ivity of pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus (POMC(ARH) neurons)

223 Proopiomelanocortin (POMC) neurons in the arcuate nucleus of the hypothalamus are activated by ene

224 Agouti-related peptide (AgRP) neurons in the arcuate nucleus of the hypothalamus are critical for hom

225 ghrelin mediates neural fiber growth in the arcuate nucleus of the hypothalamus during the neonatal

226 elanocortin (POMC)-expressing neurons in the arcuate nucleus of the hypothalamus play a pivotal role

227 Our tracing experiments showed that the arcuate nucleus of the hypothalamus, as a major site for

228 companied by an inflammatory response in the arcuate nucleus of the hypothalamus, evidenced by increa

229 stimulate appetite-modulating neurons in the arcuate nucleus of the hypothalamus, exerting an orexige

230 In the arcuate nucleus of the hypothalamus, these changes are n

231 gulated by a group of neurons present in the arcuate nucleus of the hypothalamus, which release Pomc-

232 in ingestive behavior and are located in the arcuate nucleus of the hypothalamus.

233 to date were enriched for expression in the arcuate nucleus of the hypothalamus.

234 i-related protein (AgRP) is expressed in the arcuate nucleus of the mammalian hypothalamus and plays

235 yn-A) directly and dose-dependently inhibits arcuate nucleus POMC neurons.

236 cing, we examined whether NPY neurons in the arcuate nucleus projected to the Acb.

237 ted peptide (AgRP)-expressing neurons in the arcuate nucleus regulate hunger.

238 Neurons in the hypothalamic arcuate nucleus relay and translate important cues from

239 population, the dopamine/GABA neurons in the arcuate nucleus represent a subpopulation with a functio

240 lts suggest that glucokinase activity in the arcuate nucleus specifically regulates glucose intake an

241 a subset of GLP-1R-expressing neurons in the arcuate nucleus to produce weight loss.

242 tion may function as interneurons within the arcuate nucleus to regulate other aspects of hypothalami

243 mus and Kiss1, Pomc, and Somatostatin in the arcuate nucleus was observed in jerboas captured in spri

244 oximately 50% of dopamine neurons within the arcuate nucleus were labeled with a GABA-specific report

245 ypothalamus (the equivalent of the mammalian arcuate nucleus), projecting throughout the hypothalamus

246 gf10(+) tanycytes predominantly populate the arcuate nucleus, a subset of which express the orexigeni

247 d levels of Kiss1 (but not Tac2) mRNA in the arcuate nucleus, and a reduced compensatory luteinizing

248 thway in neuropeptide-Y-ergic neurons of the arcuate nucleus, and are accompanied by CB1-mediated enh

249 ally born cells in the medial preoptic area, arcuate nucleus, and medial amygdala differentiate into

250 he paraventricular hypothalamic nucleus, the arcuate nucleus, and the preoptic area.

251 entral forebrain (the anterior hypothalamus, arcuate nucleus, anteroventral periventricular nucleus,

252 ck and from a metabolic sensory organ as the arcuate nucleus, are essential for an adequate temperatu

253 In the arcuate nucleus, both Neuropeptide Y and proopiomelanoco

254 enular nucleus, zona incerta, neurosecretory arcuate nucleus, cranial motor nuclei III and IV, Edinge

255 ons expressing agouti-related protein in the arcuate nucleus, indicating that DMH(TrkB) neurons are d

256 lly inhibited this pathway in neurons of the arcuate nucleus, one key center for control of energy ho

257 nt cells were abundant in the area postrema, arcuate nucleus, paraventricular nucleus, and ventromedi

258 grative function of FoxO1 extends beyond the arcuate nucleus, suggesting that central nervous system

259 kade of insulin receptors (with S961) in the arcuate nucleus, the site of action of insulin, did not

260 ir cell bodies, they send processes into the arcuate nucleus, the ventromedial nucleus, and the dorso

261 est whether they can activate neurons of the arcuate nucleus, we targeted expression of a Ca(2+)-perm

262 everal hypothalamic nuclei, particularly the arcuate nucleus, where robust GHSR mRNA expression has b

263 ard to meal-related gut control of appetite, arcuate nucleus-based hypothalamic circuits linking ener

264 ted primarily in two hypothalamic areas: the arcuate nucleus-median eminence (ARC-ME) and the paraven

265 ion of BigLEN containing AgRP neurons in the arcuate nucleus.

266 opiomelanocortin neurons in the hypothalamic arcuate nucleus.

267 ularly strong expression in the hypothalamic arcuate nucleus.

268 food intake occur through action within the arcuate nucleus.

269 d, also release GABA within the hypothalamic arcuate nucleus.

270 ypothalamic parenchyma, in particular in the arcuate nucleus.

271 oinfundibular dopamine (TIDA) neurons of the arcuate nucleus.

272 a novel isoform of rat beta-endorphin in the arcuate nucleus.

273 quence of leptin signaling impairment in the arcuate nucleus.

274 nd in particular NPY and POMC neurons in the arcuate nucleus.

275 rent projections originating from beyond the arcuate nucleus.

276 (NLT), the putative homolog of the mammalian arcuate nucleus.

277 stage 2b (inferior altitudinal with superior arcuate) occurred in 6 of 234 VFs (2.6%), and stage 3 (t

278 180 subjects (49%) and usually exhibited an arcuate or nasal pattern.

279 significant correlations were found for the arcuate or the inferior-fronto-occipital fasciculus.

280 on of prodynorphin-expressing neurons in the arcuate or the parabrachial nucleus lowered T(b).

281 terminal stria; anterior hypothalamic area; arcuate, paraventricular, and dorsomedial hypothalamic n

282 lyses, IPFS in the superior hemifield had an arcuate pattern initially that later deepened approximat

283 The arcuate pro-opiomelanocortin (POMC) neurons in particula

284 Arcuate proopiomelanocortin (POMC) neuron-specific delet

285 and to receive input from leptin-responsive arcuate proopiomelanocortin neurons, the physiological f

286 We found that the long and anterior arcuate segments are lateralized before adolescence and

287 volume and fractional anisotropy of the left arcuate showed a particularly strong positive correlatio

288 the Victoriapithecus brain has principal and arcuate sulci of the frontal lobe not seen in the stem c

289 ateral network (CLPFC) in and rostral to the arcuate sulcus and the caudal principal sulcus.

290 n, increased energy expenditure, and reduced arcuate suppressor of cytokine signaling 3 expression, i

291 neurons disrupted their projections from the arcuate to the paraventricular nucleus, reduced energy e

292 are caused by lateral rollback of a tightly arcuate trench migrating parallel to the plate boundary

293 The arcuate, uncinate, inferior-fronto-occipital and inferio

294 In this work, we dissected language-related (arcuate, uncinate, inferior-fronto-occipital, and inferi

295 mpus, and hypothalamic regions including the arcuate, ventromedial, and paraventricular nuclei.

296 A partial arcuate visual field defect with an enlarged blind spot

297 ptor substrate-1 (IRS-1) in the hypothalamic arcuate was determined.

298 The superior arcuate was the most common sector of progression.

299 M integrity in interhemispheric, limbic, and arcuate WM tracts.

300 nd inferior-nasal) all in the 5.0- to 7.0-mm arcuate zone.