ライフサイエンスコーパス: cortical region

1 ave examined communication networks within a cortical region.

2 ake in all disease groups, across widespread cortical regions.

3 ty (dedifferentiation) in category-selective cortical regions.

4 roception, including insula and sensorimotor cortical regions.

5 n relaying sensory information to downstream cortical regions.

6 ther than falling into functionally discrete cortical regions.

7 NC(W)) in superior frontal and supramarginal cortical regions.

8 d MR-driven methods showed high agreement in cortical regions.

9 buting to coordination within one or several cortical regions.

10 r modules projecting to functionally related cortical regions.

11 al studies is limited in localized and small cortical regions.

12 ha power emerged from more anterior, frontal cortical regions.

13 nisotropy (FA) were heterogeneous across the cortical regions.

14 ual areas (V1-V3) versus downstream parietal cortical regions.

15 and perturbing neural activity from multiple cortical regions.

16 ectivity between the right DLPFC and several cortical regions.

17 and dorsal endopiriform nucleus, but not in cortical regions.

18 changes in either dimension within the same cortical regions.

19 y display phenotypic variations in different cortical regions.

20 as in broader emotion and sensory processing cortical regions.

21 equently many other functionally specialized cortical regions.

22 ivity, with a composite SUVR averaged over 6 cortical regions.

23 rconnects somesthetic-motor and visual-motor cortical regions.

24 ioned over occipital, parietal, and temporal cortical regions.

25 tonotopic activation across several auditory cortical regions.

26 levels of GABA in M1, but not in three other cortical regions.

27 to integrate information processing between cortical regions.

28 the flow of neural signals between different cortical regions.

29 eases in low-frequency activity in posterior cortical regions.

30 nclusions, and other pathological changes in cortical regions.

31 ith activity within a distributed network of cortical regions.

32 lateral core and medial shell arrangement of cortical regions.

33 perties of these neurons differ across these cortical regions.

34 ples resembling those governing other higher cortical regions.

35 ed for unique circuit operations in distinct cortical regions.

36 ly mediated by thinning in the corresponding cortical regions.

37 while remaining more elusive in higher order cortical regions.

38 have not been compared systematically across cortical regions.

39 he receptive fields in human depth-sensitive cortical regions.

40 osis, mood state, age and sex differences on cortical regions.

41 l, orbital), anterior cingulate and parietal cortical regions.

42 er in parietal, but notably also in auditory cortical regions.

43 cally thought to be supported by perisylvian cortical regions.

44 cular processes involved in specification of cortical regions.

45 tinotopy and ON-OFF polarity in neighbouring cortical regions.

46 linearly decreased with age for most of the cortical regions.

47 ptor-mediated high-frequency oscillations in cortical regions.

48 migrate along vessels as they are colonizing cortical regions.

49 patients with ASD and controls in postmortem cortical regions.

50 el claustrocortical connections to different cortical regions.

51 MN consists of preferentially interconnected cortical regions.

52 rocyte layer patterns diverged between mouse cortical regions.

53 target stimuli in multiple sensory and motor cortical regions.

54 emory representations across hippocampal and cortical regions.

55 mpairments across individuals only in select cortical regions.

56 olving virtually all white matter tracts and cortical regions.

57 emories and interactions between the HPC and cortical regions.

58 known about cholinergic influences on motor cortical regions.

59 hanism for PFC to communicate with posterior cortical regions [13], independently subserve communicat

60 V (T) values was less than 10% in most large cortical regions (14% in parietal cortex) and ranged fro

61 ow was decreased in AD compared with aMCI in cortical regions (-5% +/- 1%) and in the reference regio

62 r, more recent work has implicated posterior cortical regions [9-12], suggesting that PFC engagement

63 prosimian primates was identified as a small cortical region, above and anterior to the anterior fron

64 ls of the superior temporal cortex and other cortical regions acquired with the resting-state functio

65 group aggregated regional volumes data of 68 cortical regions across both hemispheres from 1379 PTSD

66 hesis that the amygdala engages with distant cortical regions after encoding in a manner that predict

67 We identify an orofacial motor cortical region and, via a series of perturbation experi

68 ting-state oscillations between pairs of 330 cortical regions and 16 subcortical regions in 298 healt

69 (18)F-AV-1451, with poor fits in 33%-53% of cortical regions and 80% in subcortical areas.

70 Knowledge about the precise cortical regions and connections supporting this control

71 s undergo specific modifications in distinct cortical regions and display "regional variants." It is

72 medial SN connects with limbic striatal and cortical regions and encodes value (greater response to

73 Recent data showed deficit extending to most cortical regions and even to other extrastriatal subcort

74 ramidal neurons (n = 2,238) across all three cortical regions and gigantopyramidal neurons (n = 1,189

75 These maps revealed distinct cortical regions and large-scale networks associated wit

76 ues, but to different degrees, with multiple cortical regions and neostriatum tending to have the gre

77 hese included subcortical, white matter, and cortical regions and nonventricular cerebrospinal fluid

78 ter connectivity between the hippocampus and cortical regions and that intrinsic hippocampal function

79 curves and kinetic parameters were equal for cortical regions and the cerebellum in control subjects

80 f white matter tracts connecting ipsilateral cortical regions and the corpus callosum were significan

81 The total distribution volumes for multiple cortical regions and the hippocampus showed statisticall

82 ygdala and the medial and orbital prefrontal cortical regions and their functional interactions.

83 ed evidence on the involvement of widespread cortical regions and their white matter connections.

84 For example, several cortical regions and white-matter tracts have been desig

85 tter density in areas involved in executive (cortical regions) and integrative (bilateral thalamus an

86 in synaptophysin in hippocampus and frontal cortical regions, and a tendency for reductions in other

87 ocular dominance, involving subcortical and cortical regions, and connections between cortical inhib

88 ll varieties of cortical sleep waves, in all cortical regions, and in all stages of NREM sleep, but w

89 e oriented from white matter toward multiple cortical regions, and persistent SCGN-expressing cells w

90 processing or excitability in task-relevant cortical regions, and reflect enhanced cortical prioriti

91 ccurring simultaneously in multiple cerebral cortical regions are critical for mediating behaviors.

92 l pathology, and in PET-only studies, medial cortical regions are seen to accumulate amyloid earlier

93 In primates, specific visual cortical regions are specialized for processing of coher

94 Different olfactory cortical regions are thought to harbor distinct sensory

95 -down cortical neurons projecting to sensory cortical regions are well-positioned to integrate long-r

96 ry visual cortex (V1) to a downstream visual cortical region (area LL) that previous work has implica

97 e interactions changed significantly between cortical regions as a function of frequencies (i.e. beta

98 also be applicable to other hippocampal and cortical regions as dopaminergic fibres innervate wide b

99 eive communication asymmetry to characterize cortical regions as senders, receivers or neutral, based

100 igate the molecular-functional properties of cortical regions associated with educational attainment,

101 processing and gray matter structure in all cortical regions at baseline, were used to predict futur

102 We propose a classification of cortical regions based on the vascular topology.

103 likely to be different from that in sensory cortical regions because the OB lacks an obvious topogra

104 cal pharmacological inactivations of several cortical regions before retrieval of an aversive memory

105 e African wild dog compared to other canids, cortical regions beyond the primary sensory areas will n

106 oach, in available brain tissue from up to 8 cortical regions bilaterally.

107 tinct functional activation abnormalities in cortical regions but not in the cerebellum.

108 ncentration of amyloid-beta42 in the frontal cortical region, but not amyloid-beta40.

109 regions send convergent information to each cortical region, but the organizational logic of thalami

110 n DEn revealed labeled terminals in the same cortical regions, but only in the ipsilateral hemisphere

111 eption are subserved by strongly overlapping cortical regions, but reveal that attention to one or ot

112 n can lead to reorganization of the deprived cortical regions by another sensory system.

113 rietal (P = 0.026) and occipital (P = 0.047) cortical regions compared with healthy controls.

114 a normalization mechanism that operates in a cortical region composed of neighboring category-selecti

115 ivariate patterns of activity in a number of cortical regions contain representations that change mor

116 The fMRI activity in visual cortical regions contralateral to the cued direction of

117 nderstanding how neural activity in specific cortical regions contributes to behavior.

118 Remarkably, cortical regions contributing heavily to the prediction

119 rmance have receptive fields that cluster in cortical regions corresponding to the retinotopic locati

120 ontrast, fMRI activity in ipsilateral visual cortical regions covaried inversely with occipital alpha

121 rocally connected with functionally distinct cortical regions, differentially innervate striatal neur

122 By contrast, striatal and cortical regions differentiated between craving food and

123 erexcitable bursts in vivo were present in a cortical region distal to (>0.7 mm) freeze-lesion-induce

124 and inhibition and was more prominent in the cortical region distal to the microgyrus.

125 Next, we report new cortical regions downstream of whisker-evoked sensory pr

126 of population firing peaks across widespread cortical regions during complete waking periods.

127 arvalbumin (PV) has been observed in several cortical regions during development in a temporal patter

128 led to higher task correlations in relevant cortical regions during functional MRI language mapping

129 stablishes a baseline for human sleep in all cortical regions during the first sleep cycle.

130 ty of multivoxel fMRI patterns in visuomotor cortical regions during unilateral reaching movements wi

131 Classic theories suggest that cortical regions either reflect stimulus intensity or ad

132 converging glutamate inputs from limbic and cortical regions, encoding contextual and emotional info

133 Similar effects were observed in other cortical regions examined in an exploratory analysis.

134 Together, our results demonstrate that cortical regions exhibit functional relationships with w

135 ce, the evaluation being limited to a single cortical region for epigenetic and transcriptomic data,

136 NT The frontal eye field (FEF) is a critical cortical region for overt and covert spatial attention.

137 ng by the medial frontal cortex (MFC), a key cortical region for reward-guided learning and decision-

138 h regional proteome data identifies the same cortical region for smoking behavior as found with fMRI

139 onal MRI voxel activation in left hemisphere cortical regions for verb generation (from 3.8 +/- 1.0 t

140 that neurons in frontal cortex, as in other cortical regions, form a sparse and overcomplete represe

141 lity, and direction of communication between cortical regions has not been fully addressed.

142 Canonical IN types conserved across distinct cortical regions have been defined by their morphologica

143 Individual neurons in many cortical regions have been found to encode specific, ide

144 with human studies, where sex differences in cortical regions have been reported but are characterize

145 tion or whether the GABA levels of different cortical regions have selective influence on perception

146 These two cortical regions have the highest density in alpha4beta2

147 Depending on the subsecond timing and cortical region, HFB indexed semantic interference (i.e.

148 ies of the olfactory bulb, granular zones of cortical regions, hippocampus, amygdala, lateral septal

149 Consistent binding of (18) F-Mefway in cortical regions, hippocampus, and raphe was observed ac

150 connections between hierarchically arranged cortical regions, how are increases in sensory response

151 on of the mid-superior temporal sulcus (STS) cortical region identified by fMRI caused similar neglec

152 bilateral inactivation of only a few dorsal cortical regions impaired performance.

153 ue monkeys in the functional organization of cortical regions implicated in pitch perception.

154 ly distinct, albeit overlapping, networks of cortical regions implicated in specific aspects of speec

155 sations from adults or infants in a range of cortical regions implicated in the processing of affecti

156 midal neurons in the primary motor cortex, a cortical region important for the acquisition and extinc

157 strated a significant neuroprotection in the cortical region in the galectin-3 knockout animals in re

158 rumental to the functional repertoire of the cortical region in which they reside.

159 direct electrical stimulation across several cortical regions in 14 human subjects (6 males) implante

160 ess and surface area measures of 34 cerebral cortical regions in 2,256 individuals with major depress

161 atio with the largest effects within frontal cortical regions in 980 older individuals across the dis

162 A mega-analysis investigating all cortical regions in a large sample of PTSD and control s

163 focally lowered the temperature of distinct cortical regions in awake neurosurgical patients, and we

164 al frontal with striatal and lateral frontal cortical regions in BDD, by sparser bottom-up striatum-m

165 Local slow waves can appear in various cortical regions in both awake humans [2] and rodents [3

166 DeltaBP(P)) were significantly lower in the cortical regions in CDSs compared with healthy control s

167 sing 3-D electron microscopy applied to four cortical regions in mouse.

168 rch in primates to studies of medial frontal cortical regions in rodents.

169 rimotor network and widespread engagement of cortical regions in the activated network.

170 ctro-acupuncture group, and those of several cortical regions in the moxibustion group, were correlat

171 ole for presupplementary/supplementary motor cortical regions in the pathology and treatment of compu

172 while ICV-normalized results showed thicker cortical regions in the right temporal lobe (FDRq = 0.05

173 otransmission selectively in layer 3 of four cortical regions in the vsWM network from 20 matched pai

174 stribution of the tau pathology to selective cortical regions in these preclinical cases implies phen

175 ical microstructure is differentiated across cortical regions in this critical period is unknown.

176 tions primarily decrease across a variety of cortical regions in two highly distinct data sets: non-h

177 on both invasive and noninvasive analyses in cortical regions in which paired helical filament tau ac

178 ne reduced NAcc functional connectivity with cortical regions including the anterior cingulate cortex

179 responses within distributed subcortical and cortical regions including the striatum, insula, lateral

180 ern was not observed in other memory-related cortical regions, including DLPFC, thus supporting a spe

181 In most other cortical regions, including dorsolateral prefrontal and

182 (P < 0.05) between dACC and several frontal cortical regions, including left superior frontal gyrus

183 quantify anatomical connectivity between six cortical regions, including PFC, and the thalamus.

184 relatively stable, with some subcortical and cortical regions increasing while others reduced.

185 vidence that the midventrolateral prefrontal cortical region interacts with specific posterior cortic

186 revealed the existence of a large network of cortical regions involved in the regulation of heart rat

187 hesis that, within the left occipitotemporal cortical regions involved in visual word recognition, di

188 omprehension, a broad network of perisylvian cortical regions is involved in sound and language proce

189 ns beyond relaying information to or between cortical regions is unknown.

190 tern here described is not observed in other cortical regions; it is proposed to rely on the peculiar

191 nal connectivity between the hippocampus and cortical regions known to be involved during memory enco

192 reveals that, across this diverse series of cortical regions, L5 commonly projects to multiple thala

193 This study provides evidence for a precise cortical region (lateral frontal pole) and a structural

194 a but were also found in three other frontal cortical regions: lateral orbitofrontal cortex (orbital

195 that tau preferentially spreads to specific cortical regions, likely through functional connections,

196 glutamate and GABA neurotransmission across cortical regions may contribute to vsWM deficits in schi

197 terior cingulate cortex and other prefrontal cortical regions may represent neural mechanisms of OCD.

198 These data suggest that the cerebral cortical regions mediating vestibular-motion ('am I movi

199 yzing multihuman ECoG recordings to identify cortical regions most relevant to processing lexical inf

200 patial extent, region, and laterality of the cortical regions most responsive to variations in pitch

201 ay be influenced early in song learning by a cortical region (NIf) at the interface between auditory

202 also the first time that the activity of sub-cortical regions, normally considered "invisible" to EEG

203 For each of 48 white matter tracts and 68 cortical regions, normative percentiles of variation in

204 allowed induction of ischemia in a specific cortical region of conscious mice of any postnatal age,

205 In contrast, ANI infusion in the equivalent cortical region of intact animals had no effect on reach

206 med to study functional connectivity between cortical region of interest and striatum.

207 ed input to avBST from the rostral prelimbic cortical region of mPFC and observed concurrent increase

208 mine early postnatal changes in this initial cortical region of the olfactory system.

209 ied from extracellular recordings in several cortical regions of awake behaving monkeys.

210 educed dendritic spine densities in selected cortical regions of developing brains.

211 relative size or reorganization of adjacent cortical regions of fossil hominins.

212 id cores were generally similar in all three cortical regions of individual patients.

213 measure D(2/3) receptor binding potential in cortical regions of interest in recently abstinent CDSs

214 Furthermore, within 68 cortical regions of interest measured from each patient,

215 ll subcortical reference regions and for all cortical regions of interest, except cingulum.

216 eneration in a priori NbM and the entorhinal cortical regions of interest.

217 uclei diffusively project to subcortical and cortical regions of RSNs.

218 increase of 3-nitrotyrosine was found in the cortical regions of the adult mutant, signaling both oxi

219 ll-type heterogeneity in one of the simplest cortical regions of the mammalian brain, the rodent hipp

220 to decrease, from caudal to rostral, across cortical regions of the vsWM network.

221 At least five cortical regions on the medial and lateral aspects of ea

222 as well as neural ensembles within multiple cortical regions over two hemispheres of the awake mouse

223 ller regional brain volumes in most cerebral cortical regions (P<0.05).

224 natomical variation within a subset of these cortical regions partially mediates the positive associa

225 exts corresponded to increased activation in cortical regions previously shown to respond to social c

226 Our work identifies a cortical region primarily, if not exclusively, centred o

227 We constructed a cellular taxonomy of one cortical region, primary visual cortex, in adult mice on

228 Different cortical regions processing distinct information, such a

229 y in the brain stem, but also in medial wall cortical regions projecting to the adrenal medulla, posi

230 onsistently observed with aducanumab only in cortical regions prone to amyloid plaque deposition, reg

231 both subcortical (R = 0.769, p < 0.0001) and cortical regions (R = 0.836, p < 0.0001).

232 Anatomically connected cortical regions receive common input from a subset of c

233 ure is observed to decay sharply outside the cortical region receiving the thalamocortical projection

234 that local cellular environment in distinct cortical regions regulates these terminal phenotypes.

235 e cortex and demonstrate that face-selective cortical regions represent multiple distinct types of in

236 amma-band EEG, consistent with activation of cortical regions representing attended locations in spac

237 ng activity that was strictly drawn out from cortical regions representing the darkened location.

238 Beyond the separation according to cortical region, response latency in each neuronal clust

239 ter meaningfulness by increasing activity in cortical regions responsible for processing personal att

240 ear anatomical distinctions between auditory cortical regions responsive to changes in either pitch o

241 Although cortical regions responsive to pitch have been identifie

242 Comparing structurally similar cortical regions revealed significant differences in the

243 aneous single unit recordings from all these cortical regions revealed statistically significant neur

244 Our findings suggest that GABA level of a cortical region selectively influences perception of vis

245 tion or whether the GABA levels of different cortical regions selectively influence perception of dif

246 heterotopic than homotopic projections; all cortical regions send more association than commissural

247 t reporter mice (Otr(venus/+)) and find that cortical regions show temporally and spatially heterogen

248 We also report that cortical regions showing asymmetries in task-evoked acti

249 y for image backgrounds were associated with cortical regions showing peripheral preference (e.g. par

250 c mice, we examined the connectivity of four cortical regions (somatosensory, visual, motor and prefr

251 rkinson's disease, loss of 11C-BU99008 VT in cortical regions, striatum, thalamus and brainstem corre

252 number of association connections from each cortical region strongly correlates with the number of i

253 d, recurrent interactions between widespread cortical regions, subcortical regions, including the str

254 ippocampus, as well as their connectivity to cortical regions such as dorsal medial and lateral prefr

255 rneuron (IN) types conserved across distinct cortical regions such as the hippocampus and the neocort

256 demonstrated that seizures can occur in deep cortical regions such as the mesial temporal lobes witho

257 in the human middle temporal gyrus (MTG), a cortical region supporting the semantic representation o

258 igh-fidelity information relay to or between cortical regions, thalamic circuits shift and sustain fu

259 more extensive tests of the function of each cortical region than had been possible before in humans

260 ed the circuit anatomy of zebra finch HVC, a cortical region that generates sequences underlying the

261 spots of dopaminergic drive notably include cortical regions that are associated with both limbic an

262 Cortical regions that are damaged by insults, such as is

263 "temporal receptive windows" are longest in cortical regions that are distant from sensory input.

264 to amyloid beta (Abeta) plaque deposition in cortical regions that are functionally associated with E

265 u, facilitated by Abeta, transits from EC to cortical regions that are most closely associated with t

266 Neuroimaging studies have identified three cortical regions that respond selectively to scenes: par

267 ontoparietal network" refers to a network of cortical regions that support sustained attention and wo

268 ASD (iASD), with consistent signals in both cortical regions that were distinct to those observed in

269 ure, the amygdala (experiment 1), and a deep cortical region, the anterior cingulate cortex (ACC, exp

270 cortical network that comprises, among other cortical regions, the posterior superior temporal sulcus

271 esults show modulation of extensive auditory cortical regions throughout primary and non-primary regi

272 ters activity in the BG and downstream motor cortical regions to cause these disorganized movements r

273 rain activity patterns in arbitrary pairs of cortical regions to guide a visual cursor to a target lo

274 urons (LRNs) innervated similar or different cortical regions to high-rhythmic-firing neurons (HRNs)

275 d the differential contributions of specific cortical regions to reading pseudowords (ventral precent

276 dependency in the contribution of prefrontal cortical regions to rule-guided behaviour.

277 y mid-level regions, while some higher-order cortical regions took more than 10 seconds to align.

278 onal activity from motor, visual, and memory cortical regions using stimulus-induced tasks.

279 An extensive cortical region was identified wherein area related posi

280 ver, activation of pyramidal neurons in this cortical region was sufficient to induce MIA-associated

281 s pattern of coupling with the other frontal cortical regions was assessed.

282 ts, thinner cortex in parietal and occipital cortical regions was associated with worse treatment res

283 t, the heritability of connectivity among 39 cortical regions was estimated.

284 le the connectivity between the IC and other cortical regions was highly bidirectional, the IC connec

285 ower and spatially nonuniform clearance from cortical regions was observed as compared with the contr

286 tural connectivity strength between pairs of cortical regions was quantified with structural covarian

287 expression profile of SCZ risk genes across cortical regions was significantly correlated with the r

288 nses in the prefrontal and superior temporal cortical regions were assessed during a working memory t

289 al morphology and microstructure showed that cortical regions were ordered along a principal axis, wi

290 Six cortical regions were quantified using a standardized re

291 (iii) ReHo changes in multiple cortical regions were significantly correlated with CDAI

292 re projects predominantly to frontal-midline cortical regions, whereas the dorsal and ventral shell p

293 both the anterior and the posterior auditory cortical regions, whereas, at late time intervals, memor

294 le network communication between distributed cortical regions while allowing for modular specializati

295 e-selective (PPA) and object-selective (LOC) cortical regions while participants studied images for a

296 ted with cortical thinning across the entire cortical regions while presence of CSS was independently

297 The growing inventory of cortical regions with distinctive and often very specifi

298 e (t(977) = 2.992, p = 0.003) and five other cortical regions, with no significant effect in the hipp

299 ake and Centiloid scores in disease-specific cortical regions, with several reference regions: cerebe

300 lamus is globally connected with distributed cortical regions, yet the functional significance of thi