ライフサイエンスコーパス: subregion

1 er level of species richness in the southern subregion.

2 tion and inhibition within a given On or Off subregion.

3 o 20-year chronosequences identified in each subregion.

4 ort the specialized function of the targeted subregion.

5 low transmission foci in the Greater Mekong Subregion.

6 posterior subregion but not in the anterior subregion.

7 ppocampal circuit than either the CA1 or CA3 subregion.

8 th-East Asia and the Eastern Mediterranean D subregion.

9 s could coexist and interact within the same subregion.

10 e selection and spread in the Greater Mekong subregion.

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

12 by pregnant young women in countries in this subregion.

13 utamate and/or Homer2 expression within this subregion.

14 al cortex and dorsolateral prefrontal cortex subregions.

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

16 fy abnormalities localised to specific tract subregions.

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

18 ntensity (HG) and low-grazing intensity (LG) subregions.

19 e less overlapping than those in neighboring subregions.

20 ely from visual stimulation of individual RF subregions.

21 ng across five mouse tissues and three brain subregions.

22 t within known DMN subsystems and across DMN subregions.

23 were prominent in the oval and juxtacapsular subregions.

24 is organized into transcriptionally distinct subregions.

25 VTA (aVTA) and CRF tone is increased in both subregions.

26 ic dissection and functional studies of BNST subregions.

27 mechanistic contributions for its different subregions.

28 icuculline (to activate) to these amygdaloid subregions.

29 ct nAChR function and output of cells in MHb subregions.

30 it?" and "To whom was it done?") in distinct subregions.

31 and motivation in medial and lateral frontal subregions.

32 es that are not captured by the larger eGRID subregions.

33 beling of Fos with Drd1 and Drd2 in three DS subregions.

34 t the functional contributions of perirhinal subregions.

35 ns) strikingly varies between core and shell subregions.

36 based on state boundaries and multiple-state subregions.

37 curin-like-1 (Obsl1)-in different sarcomeric subregions.

38 ibition across the RF is stronger toward OFF subregions.

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

40 % of blindness) as causes in the high-income subregions.

41 -dependent reconfiguration of functional OFC subregions.

42 in modern contraceptive use in 2015 between subregions.

43 itectonical receptor fingerprints of the ACC subregions.

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

45 the functional specialization of intestinal subregions.

46 its associative and sensorimotor functional subregions.

47 rain connectivity patterns of individual OFC subregions.

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

49 have been resolved on the scale of striatal subregions.

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

51 vely associated with brain volume in several subregions affected by AD, in particular the left subicu

52 t for the existence of functionally distinct subregions along the parahippocampal longitudinal axis a

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

54 The sVlow subregion analysis indicated that some of the reduction

55 Using RNAscope to determine striatal subregion and cell-type specificity of the activated neu

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

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

58 and map it to elements of both the A32-like subregion and the seven-layered beta-sheet of the gp41-i

59 fields with primarily overlapping ON and OFF subregions and are highly direction selective.

60 etween the neural activity in IT face neuron subregions and face gender-discrimination behavior.

61 toarchitectonic probability maps of amygdala subregions and Granger causality methods to evaluate tas

62 N stocks were generally similar in both subregions and soil N stock changes during pasture estab

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

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

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

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

67 of DA release can strikingly differ between subregions, and as such, it is possible that these patte

68 y within soybean (Glycine max) seed regions, subregions, and tissues during development.

69 of mPFC-to-amygdala projection neurons in a subregion- and cell-type-specific manner, which is also

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

71 e enhanced apical EPSC responses in all mPFC subregions, anterior cingulate (AC), prelimbic (PL), and

72 diated by anatomically distinct frontal lobe subregions are both critical for adaptive choice in more

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

74 Cerebellar subregions are part of these networks, but how the cereb

75 file of high gamma power (HGP) in dorsal PPC subregions as participants made old/new recognition memo

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

77 These results disassociate the frontal subregions based on their dynamics, and suggest a tempor

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

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

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

81 ioral relevance was evident in its posterior subregion but not in the anterior subregion.

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

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

84 in the expression profiles of the lead three subregions compared with newly emerged cells.

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

86 ctivity but the influence of ELS on amygdala subregion connectivity and modulation of emotion is uncl

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

88 resentations in LATL into spatially distinct subregions, continuing the lateral-medial segregation of

89 the medial versus orbitofrontal cortex (OFC) subregions contributing differentially to processes such

90 ultiple brain functions: specific cerebellar subregions control the temporal dynamics of the networks

91 regions functionally connected to 6 striatal subregions defined a priori.

92 The 14 subregions, defined on the basis of child and adult mort

93 Warpgroup adds peak subregion detection, consensus integration bound detecti

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

95 n, are also present in CA2, but that the CA2 subregion differs substantially from the other CA subreg

96 acial refugia mainly located in the southern subregion during the LIG and rapidly expanded during the

97 aling expected memory effects in PFC and MTL subregions during encoding and retrieval.

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

99 tional mechanisms supported by different MTL subregions during mental time travel, we developed a com

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

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

102 the recruitment of functionally distinct AnG subregions during the retrieval of episodic and semantic

103 a rostrocaudal axis composed of 2-4 smaller subregions each.

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

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

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

107 have suggested that dorsal and ventral mPFC subregions exert opposing effects on fear, as do subregi

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

109 l premotor cortex, indicating that each LATL subregion exhibits distinct patterns of connectivity.

110 ferior (MHbVI) and ventrolateral MHb (MHbVL) subregions expressed functional nAChRs with different ph

111 w that these ventrolateral anterior temporal subregions form part of a network responsible for semant

112 ased, and (2) it allows random querying of a subregion from a BAM-like file in an encrypted form.

113 a transition in the engaged dorsal striatal subregion, from dorsomedial to dorsolateral, as skill pe

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

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

116 The hippocampal CA2 subregion has a different anatomical connectivity patter

117 k of regions functionally connected to these subregions has not been demarcated.

118 y patterns of CA2 compared with the other CA subregions have not been reported.

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

120 tains just VC (termed IC3), or both of these subregions (IC2 + IC3).

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

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

123 e critical involvement of human frontal lobe subregions in a probabilistic, multidimensional learning

124 ens of FBD, with the greatest falling on the subregions in Africa, followed by the subregions in Sout

125 the necessary contributions of frontal lobe subregions in attributing feedback to relevant and irrel

126 gion differs substantially from the other CA subregions in its population coding.

127 nsively map psychological states to discrete subregions in medial frontal cortex using relatively unb

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

129 on the subregions in Africa, followed by the subregions in South-East Asia and the Eastern Mediterran

130 gests a model where the size of two distinct subregions in the active site determines PRMT7 product s

131 of DA neurons that target distinct striatal subregions in the context of an instrumental reversal le

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

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

134 These EC subregions, in turn, exhibited differential connectivity

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

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

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

138 ble in the infralimbic but not the prelimbic subregion induced excessive alcohol seeking.

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

140 o presented, which reveals that the thalamic subregions innervated by the basal ganglia preferentiall

141 H3-groove of Bcl-xL, although lacking the h1-subregion interaction.

142 ue-induced craving were specific to striatal subregions involved in habitual responding to rewarding

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

144 r, application of nicotine to cells in these subregions led to different action potential firing patt

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

146 These neighboring subregions lie along the upper bank of the superior temp

147 Our data suggest that each PFC subregion may be capable of generating distinct patterns

148 Evidence suggests that core and shell subregions may play dissociable roles in guiding motivat

149 ariation in the patterns of activity between subregions may reflect distinct functional roles.

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

151 in c-Fos in the NAcc, specifically the shell subregion (NAccSh).

152 ions split the "QTL-hotspot" region into two subregions namely "QTL-hotspot_a" (15 genes) and "QTL-ho

153 Fos expression was neither subregion nor cell-type specific (52.5 and 39.2% of Fos

154 and cingulate of the salience network; and a subregion of fusiform gyrus associated with face percept

155 rol carrier protein 2 (SCP2) occupies only a subregion of larger peroxisomes, highlighting the hetero

156 We show that activity patterns in a subregion of lateral parietal cortex, the angular gyrus,

157 n be decoded from the angular gyrus (ANG), a subregion of posterior lateral parietal cortex.

158 ocaine-specific effect was detected within a subregion of the amygdala-frontal network.

159 Here, we show that a subregion of the anterior cingulate cortex in the gyrus

160 disrupted function of the dentate gyrus (DG) subregion of the brain, and they improve with treatment

161 melanocytes migrates and incorporates into a subregion of the cochlear epithelium, forming the interm

162 These results identify the necessary subregion of the frontal cortex for WM and specify how t

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

164 The dentate gyrus (DG) subregion of the hippocampus is widely viewed to realize

165 in the interpeduncular intermediate (IPI), a subregion of the interpeduncular nucleus (IPN).

166 studies have implicated the infralimbic (IL) subregion of the medial prefrontal cortex in extinction

167 neuronal ensemble located in the infralimbic subregion of the medial prefrontal cortex that controls

168 Neurons in the dorsal subregion of the medial superior temporal (MSTd) area of

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

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

171 the dorsal anterior cingulate cortex (dACC) subregion of the mPFC.

172 may modulate neuronal activity in the shell subregion of the nucleus accumbens (NASh).

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

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

175 d activation within the nucleus accumbens, a subregion of the striatum.

176 show that neurons in the olfactory tubercle subregion of the ventral striatum robustly encode the on

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

178 ." The medial orbitofrontal cortex (mOFC), a subregion of the ventromedial prefrontal cortex, is uniq

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

180 provide evidence that functionally distinct subregions of angular gyrus (AnG) contribute to the retr

181 We also examined subregions of basal amygdala nuclei- rostral basolateral

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

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

184 ese results show previously unknown discrete subregions of dynorphin-containing cells in the NAc shel

185 Although subregions of frontal and parietal cortex both contribut

186 5 binding potentials at a voxel level within subregions of frontal, parietal and temporal cortices.

187 ibly suppressed the neural activity in small subregions of IT cortex of macaque monkeys performing a

188 brief neural suppression of specific spatial subregions of IT induces behavioral effects opens the do

189 2 then identifies distinct, but neighboring, subregions of lmSTC whose activity patterns carry inform

190 vely map specific psychological functions to subregions of medial frontal anatomy.

191 by multiple psychological states, suggesting subregions of medial frontal cortex are functionally het

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

193 egions exert opposing effects on fear, as do subregions of other structures.

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

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

196 Finally, specific subregions of sensorimotor cortex were identified in whi

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

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

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

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

201 ss may be performed and the role of distinct subregions of the anterior temporal cortex.

202 ave shown that semantic cognition depends on subregions of the anterior temporal lobe (ATL).

203 In addition, subregions of the ATL have distinct functional propertie

204 on these findings, we propose that different subregions of the BF could support action and learning u

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

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

207 Therefore, we analyzed subregions of the DR and MR by their afferent input.

208 l and tissue dynamics in vein and inter-vein subregions of the Drosophila pupal wing.

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

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

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

212 Subregions of the frontal cortex including the orbitofro

213 ion is differentially passed on to different subregions of the hippocampal formation.

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

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

216 n whether adult neurogenesis within specific subregions of the hippocampus contributes to these disti

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

218 ells showed marked differences in entorhinal subregions of the human brain.

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

220 based on fMRI activity in spatially distinct subregions of the left medial anterior temporal lobe (LA

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

222 uscarinic and kainate receptors in different subregions of the medial prefrontal cortex (mPFC).

223 Multiple subregions of the medial prefrontal cortex are known to

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

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

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

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

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

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

230 Immunoblotting was employed on tissue from subregions of the nucleus accumbens (NAc) and the amygda

231 le AMPA receptors (CP-AMPARs) to synapses in subregions of the nucleus accumbens promotes cocaine see

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

233 Different subregions of the prefrontal cortex (PFC) contribute to

234 g uncertainty about rewards within different subregions of the primate basal forebrain (BF).

235 Domains map subregions of the receptive field, such that multiple co

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

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

238 low-frequency MRI signal variations between subregions of the spinal cord at rest in humans, similar

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

240 ation, and thymic selection can be mapped to subregions of the thymus.

241 es the dynamic interaction between different subregions of the ventral temporal cortex.

242 with DBS electrodes in the dorsal or ventral subregions of the VS and trained to the morphine conditi

243 typically in the form of isolated patches in subregions of these dendrites.

244 ng of associated proteins to subsets or even subregions of these polymers.

245 hundreds of LSVs that are specific to brain subregions or altered in Alzheimer's patients.

246 dge in LATL is organized in category-related subregions, providing evidence for the existence of mult

247 n our model, case fatality rate estimates by subregion ranged from 0.7 (central Europe) to 13.9 (cent

248 Perioperative mortality estimates by subregion ranged from 2.8 (South Asia) to 50.2 (East Asi

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

250 o determine whether the IC and its different subregions regulate relapse to cocaine-seeking behavior

251 tial differential connectivity between these subregions requires investigation.

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

253 Although isolated subregions show a preference for high rates of amplitude

254 The tool-selective LATL subregion showed greater functional connectivity with le

255 Within each zone, the more fine-grained subregions showed distinct, but subtler, variations in p

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

257 All five subregions showed significantly high familiality.

258 n of hippocampal neurons, located in the CA2 subregion, signals current location during immobility, a

259 Though subregion-specific anomalies in amygdala function have b

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

261 Optogenetic experiments show the subregion-specific heterogeneity in the synaptic propert

262 s to provide compelling evidence that the DG subregion specifically sustains representations of simil

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

264 Across disparate methods, subregion specificity in the left medial frontal pole vo

265 t the dentate gyrus (DG) and CA3 hippocampal subregions support pattern separation by inferring the n

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

267 primates suggest that EC can be divided into subregions that connect differentially with perirhinal c

268 e VII or right lateral cerebellar Crus I/II, subregions that prominently couple to the dorsal-attenti

269 ich were further subdivided into 2-4 smaller subregions that showed additional functional variation.

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

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

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

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

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

275 We aggregated mortality results by subregion to account for variability in data availabilit

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

277 e Greater Mekong-an exceptionally biodiverse subregion undergoing rapid development-we combined maps

278 enerational families and the heritability of subregions using advanced shape analysis.

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

280 We examined the corpus callosum and its subregion volumes and their relationship to cognition, p

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

282 tes of functional connectivity between these subregions, we recorded simultaneously from medial and l

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

284 neuron excitability only within one striatal subregion, whereas all training produces widespread chan

285 ively suppresses serotonin removal in septal subregions, whereas both fluoxetine and a dopamine trans

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

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

288 e interval [CI]: 3.96, 68.76), more than two subregions with bone marrow lesions (OR, 4.00; 95% CI: 1

289 years of forest-to-pasture conversion in two subregions with different management practices during pa

290 creased for knees that exhibited two or more subregions with severe cartilage loss (odds ratio [OR],

291 cm depth in the forest were similar for both subregions, with an average of 47.1 +/- 1.8 Mg C ha(-1)

292 at many proteins localize to highly specific subregions within bacterial cells.

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

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

295 The relative roles of distinct subregions within frontal cortex are poorly understood.

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

297 o previous reports, discovered that distinct subregions within the CA1 and CA3 are composed of unique

298 The presence of multiple functional subregions within the small volume of BNST raises signif

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