ライフサイエンスコーパス: arcuate

1 inferior-fronto-occipital fasciculus or the arcuate.

2 between phonological awareness and the left arcuate.

3 c role of TXNIP activity specifically within arcuate Agrp neurons, we generated Agrp-specific TXNIP g

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 ppocampus, amygdala and the paraventricular, arcuate and dorsomedial nuclei of the hypothalamus.

7 o emanate from this 'seed region': uncinate, arcuate and inferior longitudinal fasciculi.

8 In the left arcuate and left inferior longitudinal fasciculus, child

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

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

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

12 esis and specification of the neurons in the arcuate and ventromedial nuclei.

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

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

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

16 i of the mediobasal hypothalamus, namely the arcuate (ARC) and ventromedial (VMH), tasked with proper

17 Increased levels of H1R were seen in arcuate (Arc) and ventromedial hypothalamus (VMH) as wel

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

19 l premamillary (PMv), dorsomedial (DMH), and arcuate (ARC) nuclei contained the greatest number of ce

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

21 ions including the suprachiasmatic (SCh) and arcuate (Arc) nuclei.

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

23 the ventral medial nucleus (VL VMN) and the arcuate (ARC) respond to hormones and other signals to c

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

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

26 sistance arteries, including renal lobar and arcuate arteries.

27 tic mapping techniques, we have uncovered an arcuate-based circuit that selectively drives energy exp

28 onto the tractographies for the uncinate and arcuate bundles well beyond the rostral temporal lobe; t

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

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

31 perior longitudinal fasciculus including its arcuate component--was strongly associated with deficits

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

33 a Hemifield Test and various combinations of arcuate defects (n = 12), nasal steps (n = 11) and parac

34 The VF arcuate defects extended to within 1 degrees of fixation

35 in healthy controls and were associated with arcuate defects in patients.

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

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

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

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

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

41 hrough the aslant, superior longitudinal and arcuate fasciculi.

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

43 Most researchers agree that the arcuate fasciculus (AF) is the neuroanatomical correlate

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

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

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

47 is of intrahemispheric pathways included the arcuate fasciculus (dorsal language pathway) and uncinat

48 ment was not related to abnormalities of the arcuate fasciculus (or its subsegments), but was associa

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

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

51 0.010] and volume of the long segment of the arcuate fasciculus [beta = 0.730, t(2.732), P = 0.020] w

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

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

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

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

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

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

58 to controls, structural terminations of the arcuate fasciculus in inferior frontal gyrus were indist

59 The arcuate fasciculus is a central connection in this archi

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

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

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

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

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

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

66 as found between language lateralisation and arcuate fasciculus volume.

67 Although fractional anisotropy of the left arcuate fasciculus was decreased in autistic children re

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

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

70 superior longitudinal fasciculus (including arcuate fasciculus) white-matter organization significan

71 thway (the dorsal pathway underpinned by the arcuate fasciculus).

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

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

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

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

76 ly considered language pathways, such as the arcuate fasciculus, are now argued to be domain-general

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

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

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

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

81 ays-the superior longitudinal fasciculus and arcuate fasciculus, the uncinate fasciculus, extreme cap

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

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

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

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

86 Unilateral areas were connected via the arcuate fasciculus.

87 Acute, selective activation of arcuate GABAergic RIP-Cre neurons, which monosynapticall

88 or clusters in the vicinity of the cilium of arcuate hypothalamic neurons in C57BL/6J mice treated wi

89 while bHRs showed greater activation in the arcuate hypothalamic nucleus and in the hippocampus.

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

91 Decreased Fto/Rpgrip1l expression in the arcuate hypothalamus coincides with decreased nuclear en

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

108 ere is substantial postnatal turnover of the arcuate neuronal circuitry in the mouse and reveal the u

109 ry program directing development of multiple arcuate neuronal subpopulations.

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

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

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

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

114 In addition, arcuate NPY neurons exhibited abnormal electrophysiologi

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

116 unlikely to be mediated by leptin action on arcuate NPY/agouti-related protein and proopiomelanocort

117 tic, periventricular, paraventricular (PVN), arcuate nuclei and ventromedial and lateral hypothalamic

118 n infusions reveal that serotonin signals in arcuate nuclei of the hypothalamus through the Htr1a rec

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

120 icular nuclei and energy homeostasis via the arcuate nuclei.

121 Arcuate nucleus (AN) neurons are classically thought to

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

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

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

125 Both are expressed in the arcuate nucleus (Arc) and their synthesis increases with

126 citatory responses through activation of the arcuate nucleus (ARC) and ventrolateral periaqueductal g

127 Kiss1 neurons in the arcuate nucleus (Arc) are also composed of firing and qu

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

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

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

131 The Arcuate nucleus (ARC) in hypothalamus contains antagoniz

132 medial preoptic area (mPOA) and hypothalamic arcuate nucleus (ARC) may operate downstream of the CRF

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

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

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

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

137 MC) neurons to release beta-endorphin in the arcuate nucleus (ARC) of the hypothalamus and the periaq

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

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

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

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

142 aminergic (NEDA) neurons in the hypothalamic arcuate nucleus (ARC) to maintain low levels of serum pr

143 area (MPOA), ventromedial nucleus (VMN), and arcuate nucleus (ARC), all regions critical for kisspept

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

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

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

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

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

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

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

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

152 pothalamic paraventricular nucleus (PVN) and arcuate nucleus (ARC).

153 ority of Kiss1 neurons were localized in the arcuate nucleus (Arc).

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

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

156 luding the lateral hypothalamic area and the arcuate nucleus (ARC)/medial basal hypothalamus, where t

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

158 ar nucleus of the hypothalamus (PVN) and the arcuate nucleus (ArcN) are necessary brain sites and (2)

159 to chemical stimulation of the hypothalamic arcuate nucleus (ARCN) was studied in urethane-anestheti

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

161 signal that promotes axon outgrowth from the arcuate nucleus (ARH) during a discrete developmental cr

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

163 ns to the ventral hypothalamus including the arcuate nucleus (ARH), a center that regulates feeding b

164 The hypothalamic arcuate nucleus (ARH), an important site for modulation

165 In the CNS, the hypothalamic arcuate nucleus (ARN) energy-balance circuit plays a key

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

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

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

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

170 that, in fasted rats, an intact hypothalamic arcuate nucleus and hepatic sympathetic innervation are

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

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

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

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

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

176 Arcuate nucleus glucokinase activation may represent a C

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

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

179 Because the arcuate nucleus in the mediobasal hypothalamus (MBH) pla

180 major impact on the cytoarchitecture of the arcuate nucleus in vulnerable subjects, with changes tha

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

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

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

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

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

186 In addition, deletion of ROCK1 in the arcuate nucleus markedly enhanced food intake, resulting

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

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

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

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

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

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

193 uron injury were evident in the hypothalamic arcuate nucleus of rats and mice within the first week o

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

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

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

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

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

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

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

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

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

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

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

205 neurons have been best characterized in the Arcuate Nucleus of the Hypothalamus (ARH).

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

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

208 melanocortin-expressing cells located in the arcuate nucleus of the hypothalamus and in the pituitary

209 ives dense melanocortinergic inputs from the arcuate nucleus of the hypothalamus and regulates multip

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

211 pression of LEPR only in POMC neurons in the arcuate nucleus of the hypothalamus did not reduce food

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

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

214 tagged neuropeptide Y (NPY) neurons from the arcuate nucleus of the hypothalamus using protocols to i

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

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

217 xigens and are coexpressed in neurons in the arcuate nucleus of the hypothalamus.

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

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

220 s indirectly, by binding to receptors in the arcuate nucleus or ventromedial hypothalamus and regulat

221 nd proopiomelanocortin (POMC) neurons in the arcuate nucleus play central roles in energy homeostasis

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

223 No effect was observed on arcuate nucleus POMC or NPY neurons.

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

225 omelanocortin (POMC) neurons of hypothalamic arcuate nucleus regulate food intake, energy homeostasis

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

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

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

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

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

231 that differences in the accessibility of the arcuate nucleus to prolactin, together with intrinsic di

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

233 e development of neural projections from the arcuate nucleus to the preoptic region, but it does not

234 e development of axonal projections from the arcuate nucleus to the preoptic region.

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

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

237 Regardless of sex, projections from the arcuate nucleus were predominantly from pro-opiomelanoco

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

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

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

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

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

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

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

245 entromedial hypothalamic nucleus, vlVMH; the arcuate nucleus, ARC).

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

247 utamate onto unidentified neurons within the arcuate nucleus, as well as onto other POMC neurons.

248 In the arcuate nucleus, both Neuropeptide Y and proopiomelanoco

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

250 nd that HFD for 3 d rewired the hypothalamic arcuate nucleus, increasing the anorexigenic tone due to

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

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

253 paraventricular nucleus of the hypothalamus, arcuate nucleus, preoptic area, bed nucleus of the stria

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

255 tely body weight.Neurons in the hypothalamic arcuate nucleus, the ventromedial hypothalamic nuclei(VM

256 xpressed in neurons and is detectable in the arcuate nucleus, the ventromedial nucleus, and the dorso

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

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

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

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

261 quence of leptin signaling impairment in the arcuate nucleus.

262 rent projections originating from beyond the arcuate nucleus.

263 g neurons [NK(3)-saporin (SAP)] into the rat arcuate nucleus.

264 itive POMC cells were located in the rostral arcuate nucleus.

265 cated in the medial part of the hypothalamic arcuate nucleus.

266 e (TIDA) neurons located in the hypothalamic arcuate nucleus.

267 co-localized on AgRP neurons located in the arcuate nucleus.

268 omelanocortin (POMC)-expressing cells of the arcuate nucleus.

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

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

271 ularly strong expression in the hypothalamic arcuate nucleus.

272 food intake occur through action within the arcuate nucleus.

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

274 180 subjects (49%) and usually exhibited an arcuate or nasal pattern.

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

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

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

278 are expressed by distinct subpopulations of arcuate POMC neurons and that both 5-HT and leptin exert

279 s a mediator of the diet-induced rewiring of arcuate POMC.

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

281 Arcuate proopiomelanocortin (POMC) neuron-specific delet

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

283 The arcuate RNFL damage, seen in the macular fdOCT scans of

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

285 Thus, GABAergic RIP-Cre neurons in the arcuate selectively drive energy expenditure, contribute

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

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

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

289 is F5a in the posterior bank of the inferior arcuate sulcus, but no functional characterization of F5

290 ion of cortical neurons within rhesus monkey arcuate sulcus, during the execution of a visually guide

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

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.