ライフサイエンスコーパス: subregion

1 ffectively across the eastern Greater Mekong subregion.

2 and for attention/memory in the associative subregion.

3 sing neurons within the lateral hypothalamic subregion.

4 re intermingled and never limited to any one subregion.

5 ocampal Formation (HF) presents a homologous subregion.

6 egion and 30.9% (89/288) in the West-Central subregion.

7 pears to be endemic of the Western Indochina Subregion.

8 e selection and spread in the Greater Mekong subregion.

9 utamate and/or Homer2 expression within this subregion.

10 ne maturation in the ventral CA1 hippocampal subregion.

11 lume, but not by the volume of any other MTL subregion.

12 by pregnant young women in countries in this subregion.

13 149 of 2639 (81.4%; 95% CI: 79.3%-83.5%) for subregion.

14 rive visual tuning properties in separate LP subregions.

15 bellum is organized into distinct functional subregions.

16 ficient anatomical sensitivity to resolve SN subregions.

17 cortical, thalamic, and amygdalo-hippocampal subregions.

18 al thalamic, and medial amygdalo-hippocampal subregions.

19 h neural activity in anatomically defined VP subregions.

20 11)C]raclopride binding in selected striatal subregions.

21 rain connectivity patterns of individual OFC subregions.

22 erolateral (alERC) and posteromedial (pmERC) subregions.

23 ely from visual stimulation of individual RF subregions.

24 ibition across the RF is stronger toward OFF subregions.

25 fiable postsynaptic effects that vary across subregions.

26 nal somata, and/or cellular processes in the subregions.

27 % of blindness) as causes in the high-income subregions.

28 -dependent reconfiguration of functional OFC subregions.

29 ula (MHb) that are organized into anatomical subregions.

30 in modern contraceptive use in 2015 between subregions.

31 itectonical receptor fingerprints of the ACC subregions.

32 overall, as well as in the Central and South subregions.

33 the functional specialization of intestinal subregions.

34 its associative and sensorimotor functional subregions.

35 C/pmERC and other medial temporal lobe (MTL) subregions.

36 have been resolved on the scale of striatal subregions.

37 al cortex and dorsolateral prefrontal cortex subregions.

38 fy abnormalities localised to specific tract subregions.

39 -Rs across the hippocampal CA1, CA2, and CA3 subregions.

40 te visual cortex overlying dorsal V3 and V3A subregions.

41 s to gene expression in specific hippocampal subregions.

42 nnections are more evenly distributed across subregions.

43 hern parts of Western and Eastern Palearctic subregions.

44 ogical and molecular differences of striatal subregions.

45 stream within the dentate gyrus (DG) and CA3 subregions.

46 ant tumours such as those containing hypoxic subregions.

47 is a ceramide absent from the viable cancer subregions; (2) the absence of the ion of m/z 391.25 whi

48 spatial encoding and behavioral role of CA3 subregions along the proximodistal axis.

49 large-scale guttae assessment with anatomic subregion analysis in a batch of 40 eyes.

50 The sVlow subregion analysis indicated that some of the reduction

51 Rim-core subregion analysis revealed steep spatial oxygenation gr

52 meningitis: 12.9% (46/357) in the South-East subregion and 30.9% (89/288) in the West-Central subregi

53 g-energy hotspots coincident with the target subregion and capable of broad neutralization.

54 e found to be highest in the hippocampal CA2 subregion and entorhinal cortex, implicating a potential

55 data availability, we aggregated results by subregion and estimated surgical mortality rates.

56 subthalamic nucleus and in its sensorimotor subregion and for attention/memory in the associative su

57 tic resonance imaging in the CA1 hippocampal subregion and from proton magnetic resonance spectroscop

58 motor domains linked to the damaged cortical subregion and that damage encroaching on adjacent region

59 These varied by geographical subregion and year of operation.

60 study tracks changes in separate hippocampal subregions and hippocampal networks in patients with dep

61 s, as well as the associations between these subregions and specific psychiatric disorders (depressio

62 More focused targeting of hippocampal subregions and/or circuits may be a way to improve ECT o

63 We found numerous age (16 subregions) and sex (10 subregions) differences in AVP-i

64 s into other countries of the Greater Mekong subregion, and elucidate the mechanism of piperaquine re

65 tion rates are reportedly high between these subregions, and a lack of linkage has been documented in

66 th gadolinium retention in specific regions, subregions, and layers of cerebral cortex that are criti

67 iors, phase synchrony with other hippocampal subregions, and neural coding properties suggesting that

68 t Fos colocalized with Drd1 and Drd2 in both subregions, and that chemogenetic inhibition of Drd1-, b

69 ate dimeglumine-treated rats showed region-, subregion-, and layer-specific gadolinium retention in t

70 ent in small abundance only in viable cancer subregions; and (3) a slight increase in the relative in

71 mic freshwater fauna, the boundaries of this subregion are still unclear.

72 As these primary somatosensory cortex subregions are distinctly targeted by local versus dista

73 dict them, whereas DA terminals in other NAc subregions are persistently depressed.

74 er, the functional connections between these subregions are poorly understood.

75 ions, while the Indian and Western Indochina subregions are separated by the Naga Hills, Chin Hills,

76 of aging.SIGNIFICANCE STATEMENT Hippocampal subregions are thought to differentially contribute to m

77 ed parcellations of the OFC into two and six subregions based on connectivity patterns with the rest

78 We define three broad LP subregions based on correspondence between connectivity

79 the segregation of structures into discrete subregions based on dichotomies in neurochemical express

80 modality and method detected alterations in subregions belonging to distinct large-scale brain netwo

81 Different striatal subregions belonging to the cortico-striato-thalamic cir

82 This inhibitory OFF-subregion bias has a functional consequence on spatial i

83 ient to explain broad inhibition with an OFF-subregion bias while generating a variety of phase relat

84 differently in the circuitry of hippocampal subregions but become fully integrated within CA1 neuron

85 -advanced connectivity across several insula subregions, but to age-delayed connectivity with the nea

86 s that progressed throughout all hippocampal subregions by 18-20 months of age.

87 we image the activity of large ensembles in subregion CA1 via wide-field fluorescent microscopy duri

88 heta oscillations or activity in hippocampal subregion CA1.

89 ysin immunolabeled puncta in the hippocampal subregion, CA1, in APPSWE /PS1dE9 mice was detected, wit

90 Although striatal subregions collectively share many anatomical and functi

91 e DRN is subdivided into distinct anatomical subregions comprised of multiple cell types, and its com

92 Consequently, excitatory stimuli within a subregion concomitantly drive excitation and inhibition.

93 pective that neurons in multiple hippocampal subregions constitute an important neural substrate link

94 n and symptom end points including total and subregion corneal fluorescein staining, conjunctival sta

95 ere was no sex difference in total influx or subregion-dependent tracer distribution in 17 middle age

96 und numerous age (16 subregions) and sex (10 subregions) differences in AVP-ir fiber fractional areas

97 of standard offers and then inactivating OFC subregions during choices between novel offers of previo

98 oposing specific processing roles for insula subregions during homeostatic inference.

99 allowing preferential neurogenesis in brain subregions during nutrient poor conditions.

100 rns of single neurons in both core and shell subregions during singing correlated with acoustic simil

101 the hippocampus possesses dorsal and ventral subregions, each differing in behavioral, anatomic and g

102 arum malaria increases in the Greater Mekong subregion, emerging resistance to partner drugs in artem

103 Among temporal lobe subregions, episodic memory was most strongly related to

104 in left inferior parietal lobe; and (3) LATL subregions exhibited distinct patterns of functional con

105 ing neurons and also in neurons within alBST subregions expressing GLP1R.

106 s: Gleason score, number of removed LNs, and subregions for lymphadenectomy per patient did not diffe

107 These subregions form corticothalamic loops biased toward vent

108 d network analyses of four prefrontal cortex subregions from postmortem tissue of people with PTSD de

109 developmental changes of the amygdala-vmPFC subregion functional and structural connectivity using r

110 omprehensively understand how this important subregion gates motivated behaviors.

111 Genetic Reconnaissance in the Greater Mekong Subregion (GenRe-Mekong) project.

112 ead of drug resistance in the Greater Mekong Subregion (GMS) have added urgency to accelerate malaria

113 Plasmodium falciparum in the Greater Mekong Subregion (GMS) threatens global malaria elimination eff

114 In the Greater Mekong subregion (GMS), artemisinin resistance is increasingly

115 Plasmodium falciparum in the Greater Mekong Subregion (GMS).

116 nvolved in visual word recognition, distinct subregions harbor slightly different orthographic codes

117 Many primary-tumor subregions have low levels of molecular oxygen, termed h

118 mounting evidence that different hippocampal subregions have specialized roles in other cognitive dom

119 ndochina represents a separate biogeographic subregion having a largely endemic freshwater fauna, the

120 primary tumor and involved lymph nodes into subregions (i.e., habitats) based on (18)F-FDG PET and c

121 heric structural connectivity through the CC subregions II, III and V in patients with ALS.

122 rsion that splits MHC type II genes into two subregions (IIa, IIb).

123 with fractional anisotropy values of the CC subregion III, which structurally connects the bilateral

124 Intrinsic connectivity was assessed by subregion in the amygdala and insula, limbic structures

125 ncreased substantially in the Greater Mekong subregion in the past decade.

126 Here, we calculated relative sizes of 12 HC subregions in a diverse sample of 44 primate species.

127 examined the degree of linkage between these subregions in a wild ruminant.

128 eurons to show distinct causal roles for VTA subregions in distinct forms of relapse.

129 habenular (MHb) and lateral habenular (LHb) subregions in mammals remain undefined.

130 t data recorded from different basal ganglia subregions in rats performing a cued choice task.

131 however, has evaluated the role of these OFC subregions in regulating behavioral responses under thre

132 ted cognitive decline.SIGNIFICANCE STATEMENT Subregions in the human medial temporal lobe are critica

133 tinguish similar events in memory, relies on subregions in the human medial temporal lobes (MTLs).

134 spired by the formation of category-specific subregions in the inferotemporal (IT) cortex.

135 rovide clear evidence for a specific role of subregions in the MPC for the recognition of unique enti

136 reas in the frontal cortex (FC) to different subregions in the rostral anterior cingulate cortex (rAC

137 tem reticular formation, with three discrete subregions in the superior raphe, an intermediate 5-HT-i

138 a high degree of differential innervation of subregions in the VTA and were largely biased toward syn

139 ized by nonoverlapping, spatially restricted subregions in which visual stimuli can either increase o

140 riatal nuclei into pre- and post-commissural subregions, in accordance with previous animal and post-

141 temporal cortex and several lateral parietal subregions, including ANG.

142 myelin distribution, we identified seven Ov subregions, including five neuronal clusters within the

143 Controlling for geographical subregion, income level, and WHO FCTC party status, the

144 mRNA sequencing of hippocampal subregions indicated DEGs in the DG of middle-age rats,

145 ee-plane-assembled approach to segment three subregions individually (three-region model) or to segme

146 ts that while excitation is restricted to RF subregions, inhibition spans the width of simple cell RF

147 hite matter microstructure in the CB and its subregions is associated with subsequent preterm behavio

148 avian and mammalian arcopallial and amygdala subregions is poorly understood.

149 whole imaged field of view and ventro-dorsal subregions, K(i) was linearly correlated with SUR(stat)

150 re-commissural and post-commissural striatal subregions known to receive nigrostriatal projections fr

151 ities were further localized to the gene and subregion levels.

152 defensive responses to threat, with distinct subregions likely playing different roles.

153 Acute vascular damage of this insular subregion might lead to autonomic dysbalance and an upre

154 OapB and found that OapB recognizes a small subregion of OLE RNA, including stem P13, with a dissoci

155 The prelimbic (PL) cortex, a subregion of prefrontal cortex, plays a critical role in

156 We tagged ~1% of neurons in the core subregion of the accumbens (NAcore) activated during cue

157 thin the nucleus basalis of Meynert (NbM), a subregion of the basal forebrain heavily populated by co

158 t a neural subsystem, or 'module' (such as a subregion of the brain, a projection pathway, a neuronal

159 or limb of the anterior commissure (IPAC), a subregion of the extended amygdala.

160 TATEMENT The orbitofrontal cortex (OFC) is a subregion of the frontal cortex that allows organisms to

161 of elevated susceptibility in the posterior subregion of the habenula.

162 ern completion is accomplished in a specific subregion of the hippocampus called CA3, but empirical e

163 eural stem cells (RGLs) in the dentate gyrus subregion of the hippocampus give rise to dentate granul

164 linked to hyperexcitability in the aged CA3 subregion of the hippocampus in rats, monkeys, and human

165 The hippocampus (HC) and prelimbic (PrL) subregion of the medial prefrontal cortex have been link

166 etic diversity was preserved in the southern subregion of the mountains.

167 sed into the infralimbic, but not prelimbic, subregion of the mPFC-reduced binge-like eating.

168 op with M1-projecting TC neurons in a nearby subregion of the PO.

169 op with S1-projecting TC neurons in the same subregion of the PO.

170 s in children aged 3 to 7 years; volume of a subregion of the prefrontal cortex, the inferior frontal

171 cial interactions is strongest in a specific subregion of the pSTS but extends to a lesser extent int

172 ed T1-weighted MRI can depict a hyperintense subregion of the substantia nigra involved in the degene

173 ients had decreased volumes of the accumbens subregion of the ventral striatum.

174 Here we focused on one subregion of this heterogeneous structure, the ventrolat

175 1-projecting thalamocortical (TC) neurons in subregions of both the ventral posterior lateral and pos

176 deep learning method consistently segmented subregions of brain glioma with high accuracy, efficienc

177 inated a fundamental distinction between two subregions of Broca's area that likely play computationa

178 g for each subtype varied within and between subregions of CA1 and dentate gyrus.

179 at hypoxic conditions, as are often found in subregions of cervical and head and neck cancers, enable

180 ty (FC) of alEC and posteromedial EC (pmEC), subregions of EC that differ in functional specializatio

181 Although subregions of frontal and parietal cortex both contribut

182 5 binding potentials at a voxel level within subregions of frontal, parietal and temporal cortices.

183 ses via alternative splicing within specific subregions of functional domains.

184 Three subregions of glioma-the necrotic and nonenhancing tumor

185 ly inactivating individual, millimeter-scale subregions of IT while monkeys performed several core ob

186 y beyond the specific case of face-selective subregions of IT.

187 ) within cortical, striatal, and hippocampal subregions of male adult rat offspring.

188 ormation was organized in category-selective subregions of medial left anterior temporal lobe (LATL);

189 ned whether people with damage restricted to subregions of prefrontal cortex showed the patterns of i

190 ssociable whole-brain networks formed by the subregions of primary olfactory cortex.

191 that neurons in a network of interconnected subregions of primate anterior cingulate cortex and basa

192 an oversampling and undersampling of certain subregions of rat OFC for study, and this will be demons

193 exibility of network-level topology in eight subregions of the ACC (spanning three task-positive netw

194 ross ventral (A25, A24a) and dorsal (A24b,c) subregions of the ACC, while amygdalar connections are m

195 temporal sulcus (STS) projecting into dorsal subregions of the amygdala, but whether this same pathwa

196 ects of fear memory in the basal and lateral subregions of the amygdala.

197 lthough the anxiety-related role of distinct subregions of the anterior BNST was recently reported, l

198 us, and localized increases and decreases in subregions of the caudate, putamen, and hippocampus in 2

199 estigated spiking activity in core and shell subregions of the cortical nucleus LMAN during developme

200 contributions of map-like representations in subregions of the default mode network and sentence-like

201 gulator of fear memory formation in multiple subregions of the fear circuit.

202 AVP- and OT-ir fibers and cell bodies in 22 subregions of the forebrain SBNN in juvenile and adult,

203 tional areas or cell bodies in any of the 22 subregions of the forebrain SBNN.

204 he entire scanning region, as well as in the subregions of the grids.

205 DAC3, has a role in fear memory formation in subregions of the hippocampus and amygdala.

206 hosphorylation causes neuronal cell death in subregions of the hippocampus and cortex.

207 efferent neuroanatomical connectivity of the subregions of the hippocampus is reviewed with regard to

208 istributed code in the dentate gyrus and CA1 subregions of the hippocampus.

209 al information is dynamically reactivated in subregions of the human MTL and how this reactivation gu

210 f alpha(1) receptor-encoding mRNA across the subregions of the IC, alpha(2A) and beta(2) receptor-enc

211 )] dynamics were coordinated within distinct subregions of the islet, invariant with islet size.

212 r heterogeneity can be elucidated by mapping subregions of the lesion with differential imaging chara

213 in the cingulate and medial secondary motor subregions of the medial prefrontal cortex have heteroge

214 ese results indicate that TAAR1 in different subregions of the mesocorticolimbic system distinctly co

215 hod, we demonstrated that TAAR1 in different subregions of the mesocorticolimbic system distinctly co

216 However, the specific role of TAAR1 in subregions of the mesocorticolimbic system in drug addic

217 that TAAR1 mRNA is expressed throughout the subregions of the mesocorticolimbic system.

218 od, we assessed the role of TAAR1 within the subregions of the mesocorticolimbic system: that is, the

219 blazer gene expression in cells within other subregions of the migratory stream.

220 receptor expression and co-expression in the subregions of the mouse auditory midbrain.

221 that the prelimbic (PL) and infralimbic (IL) subregions of the mPFC had elevated c-Fos immunolabeling

222 hat activation of GluA1-containing AMPARs in subregions of the nucleus accumbens reinstates cocaine s

223 the ventral mPFC and interact with distinct subregions of the nucleus accumbens.

224 specialized roles for the medial and lateral subregions of the OFC in mediating specific symptoms of

225 llular actions of mu-opioids within distinct subregions of the OFC.

226 However, the role of TAAR1 in specific subregions of the reward system in drug addiction is unk

227 n distributed across micturition loci (e.g., subregions of the salience, sensorimotor, and default ne

228 We also found that the distinct subregions of the same ICN had a frequency specific cont

229 tegration is frequency specific and distinct subregions of the same ICN have functionally distinct ro

230 integration with other ICNs of the distinct subregions of the same ICN were different at 2 frequency

231 novel insights on how cholinergic inputs to subregions of the SNc regulate the excitability of DA ne

232 ect connectivity with anterior and posterior subregions of the subthalamic nucleus.

233 distinct clusters corresponding to specific subregions of the urban area.

234 al cells spread across functionally distinct subregions of the visual thalamus.

235 totemporal sulcus (OTS) of both hemispheres (subregions of the visual word form area, VWFA).

236 bilateral nucleus accumbens core and shell (subregions of the VS) during limited access to palatable

237 he WHO Mortality Database (2000-15) covering subregions of the WHO European Region: Eastern Europe, N

238 aled lower thickness and surface area across subregions of these structures.

239 s to experimentally control sensory input to subregions of visual cortex while internal models contin

240 combination therapies in the Greater Mekong subregion poses a major threat to malaria control and el

241 que functional connectivity profiles of each subregion, producing a map of the large-scale processing

242 successfully identified distinct functional subregions, providing significant improvements over exis

243 d a map of spatial heterogeneity within each subregion, reconciling previously contradictory descript

244 tal cortex, but the causal roles of specific subregions remain unidentified.

245 Moreover, inactivating different IT subregions resulted in different patterns of subtask def

246 terns of subtask deficits, predicted by each subregion's neuronal object discriminability.

247 These findings identify a mechanism of subregion-selective death of 5HT neurons in the dorsal r

248 Some of these subregions showed further subnuclei and each region of t

249 ithin each category-selective area, distinct subregions showed significant genetic influence.

250 Crucially, the subregion showing the highest reward-related asymmetry (

251 ingitis cases were analyzed by age group and subregion (South-East and West-Central).

252 Though subregion-specific anomalies in amygdala function have b

253 ic stress causes NMDA-receptor-dependent and subregion-specific cell death of 5HT neurons in the dors

254 gical blockade of the orexin-1 receptor, and subregion-specific knockdown of orexin cell populations.

255 rewards and increase their consumption in a subregion-specific manner.

256 t, in a behaviorally dynamic manner, through subregion-specific synchronization of neuronal oscillati

257 connectivity, and location (both layer- and subregion-specific).

258 cocaine-mediated induction of DeltaFosB was subregion-specific, and that DeltaFosB transcriptional a

259 content of the CEA-DA path; and (3) striatal subregions specifically involved in CEA-DA-striatal loop

260 on module in our study also suggest striatum subregion specificity.

261 Priming with a conserved subregion, such as FP, can thus induce Abs with binding-

262 itofrontal cortex (OFC), a critical cortical subregion that controls learning, decision-making, and p

263 tral hypothalamic arcuate nucleus (ARC), the subregion that has received the most attention in the pa

264 The MTL subregions that are known to be affected early by tau pa

265 levels are elevated in all three hippocampal subregions that becomes more pronounced at the oldest ag

266 .96; 95% CI, 0.95-0.97), best combination of subregions that discriminates a binary outcome based on

267 iple brain regions, and is also divided into subregions that innervate one another.

268 sion was also significantly reduced in sVlow subregions that were hyperoxic under 80% O2 conditions.

269 It is comprised of cytologically distinct subregions that, in concert, give rise to successful enc

270 ariable logistic regression) across striatal subregions, the association between the multivariate str

271 opallium/amygdala complex into the following subregions: the arcopallium anterius (AA), the arcopalli

272 ology was highest in two hippocampal-related subregions: the CA2 subfield and the entorhinal cortex (

273 er drug resistance across the Greater Mekong subregion, threatens regional malaria control and elimin

274 ining transcriptomes of multiple hippocampal subregions to link age-related impairments associated wi

275 and compare the receptor architecture of the subregions to their possible mammalian counterparts.

276 a displayed widespread patterns of primarily subregion-uniform intrinsic connectivity change, includi

277 ons, for example, in experiments that bleach subregions versus the entire condensate, two commonly em

278 othalamic neurons to the ventral hippocampus subregion (vHP).

279 nd between PwMS and PwCIS for all lobules in subregions VI and left crus I (p<0.05).

280 -PF-striatum organization that allow each PF subregion, via its precise connectivity with cortex, to

281 edial (Nucleus Accumbens Shell, VS) striatal subregions was examined by ex vivo real-time dual-record

282 e right hemisphere, in particular its dorsal subregion, was significantly associated with the relativ

283 determine functional connectivity among MTL subregions, we had 131 subjects fitted with indwelling e

284 , we assessed whether volumes of hippocampal subregions were related to cumulative glucocorticoid lev

285 However, in the MISO North subregion where wind provides 22.5% of grid generation,

286 In the Greater Mekong Subregion, where artemisinin-resistant Plasmodium falcip

287 ndependent origins across the Greater Mekong subregion, which has motivated a regional malaria elimin

288 aunas of the Western Indochina and Sundaland subregions, while the Indian and Western Indochina subre

289 The second subregion with 10 species covers the Amur Basin, rivers

290 al, viscerosensory NTS, focusing on a medial subregion with aldosterone-sensitive HSD2 neurons.

291 e estimated high average COI in a peri-urban subregion with lower transmission intensity, suggesting

292 The first subregion with six species encompasses a huge area from

293 ymphadenectomies conducted in small anatomic subregions, with 1 LNM (condition 1) or 1-2 LNM (conditi

294 regulation in specific cortical and striatal subregions, with additional deficits in somatostatin-rel

295 avior ascribe distinct functions to striatal subregions, with the dorsolateral striatum (DLS) especia

296 generated abnormality heatmap, highlighting subregions within each input fundus image for further cl

297 In all cases, subregions within each network showed heritable function

298 By computational modeling we delineate subregions within promoters that are relevant for their

299 resent meta-analytic data revealing distinct subregions within the vmPFC that correspond to each of t

300 incided with local hypotrophy of BLA and CMA subregions (without being statistically correlated) and