ライフサイエンスコーパス: cortical region

1 ave examined communication networks within a cortical region.

2 evoked by a distinct motor task in the same cortical region.

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

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

5 cally thought to be supported by perisylvian cortical regions.

6 ectivity between the right DLPFC and several cortical regions.

7 cular processes involved in specification of cortical regions.

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

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

10 e violations in both auditory and prefrontal cortical regions.

11 s with spindles over anatomically restricted cortical regions.

12 and ESZ groups in several of these posterior cortical regions.

13 d on functional interaction between multiple cortical regions.

14 rdinate the activity of functionally related cortical regions.

15 thought to facilitate communication between cortical regions.

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

17 orebrain, medial temporal lobe, and discrete cortical regions.

18 ion across a network of frontal and parietal cortical regions.

19 area, particularly, for medial and temporal cortical regions.

20 changes in either dimension within the same cortical regions.

21 s to single-pulse stimulation from different cortical regions.

22 cortex and contributes to the segregation of cortical regions.

23 ural activity on a network of interconnected cortical regions.

24 ural connections from atrophic to unaffected cortical regions.

25 investigate functional connectivity between cortical regions.

26 MAP2 is significantly reduced across several cortical regions.

27 ased connectivity between homotopic pairs of cortical regions.

28 scillations that synchronize activity across cortical regions.

29 y display phenotypic variations in different cortical regions.

30 information throughout functionally diverse cortical regions.

31 id not strongly depend on CBF across primary cortical regions.

32 ximately 0.5-0.8, P < 0.0036) across primary cortical regions.

33 6 in the insular cortex and 0.7-1.0 in other cortical regions.

34 translation or anterograde transmission from cortical regions.

35 nal resources by disengaging task-irrelevant cortical regions.

36 al temporoparietal and left occipitotemporal cortical regions.

37 hat generalized across functionally distinct cortical regions.

38 atenin at central and caudal but not rostral cortical regions.

39 tability of neuronal ensembles in respective cortical regions.

40 equently many other functionally specialized cortical regions.

41 poglossal projections arising from the other cortical regions.

42 "importance") were observed in a handful of cortical regions.

43 llial protodomains that fate map to distinct cortical regions.

44 p in the striatal projection zones of nearby cortical regions.

45 anging from 20% in the striatum to 6%-12% in cortical regions.

46 mination of essential (versus participatory) cortical regions.

47 ound additional abnormalities in distributed cortical regions.

48 d significantly with Abeta deposition in all cortical regions.

49 vo data on structural plasticity derive from cortical regions.

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

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

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

53 tonotopic activation across several auditory cortical regions.

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

55 to integrate information processing between cortical regions.

56 the flow of neural signals between different cortical regions.

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

58 nclusions, and other pathological changes in cortical regions.

59 ith activity within a distributed network of cortical regions.

60 lateral core and medial shell arrangement of cortical regions.

61 perties of these neurons differ across these cortical regions.

62 ples resembling those governing other higher cortical regions.

63 ed for unique circuit operations in distinct cortical regions.

64 ly mediated by thinning in the corresponding cortical regions.

65 while remaining more elusive in higher order cortical regions.

66 have not been compared systematically across cortical regions.

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

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

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

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

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

72 ur experiments confirmed that distinct motor cortical regions activate different muscle synergies.

73 rojected predominantly to motor and premotor cortical regions additional to connections to limbic and

74 for a dynamic 0- to 100-min acquisition for cortical regions although other windows (e.g., 75-105 mi

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

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

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

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

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

80 rk showing how myelin density differs across cortical regions and how separate regions can exhibit si

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

82 urons per square millimeter) than many other cortical regions and nonprimate V1s; we also show that V

83 striatum, both in terms of the differential cortical regions and psychological functions associated

84 lbumin (PV) and calbindin (CB) expression in cortical regions and thalamic nuclei of these pathways.

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

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

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

88 lei, and sparse projections go to prefrontal cortical regions and to nucleus accumbens shell and core

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

90 ical implications of HFOs within the frontal cortical region are unclear and should be further invest

91 l to show that LC cells innervating discrete cortical regions are biochemically and electrophysiologi

92 Different olfactory cortical regions are thought to harbor distinct sensory

93 Cortical regions as early as primary visual cortex have

94 al, middle frontal, and medial orbitofrontal cortical regions as well as a greater rate of expansion

95 as infused into prefrontal and orbitofrontal cortical regions as well as into several subcortical lim

96 evoked signals, we found patterns in several cortical regions, as follows: visual cortex, V3/V3A/V7;

97 tional connectivity between several pairs of cortical regions associated with abnormal levels of biom

98 lated to the level of neuronal complexity of cortical regions at the microscale, showing (among sever

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

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

101 ransporter-2 (VGluT2)--project to limbic and cortical regions, but also excite neighboring dopaminerg

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

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

104 In the present study, we asked which cortical regions can exert the greatest influence over o

105 that microstructural degradation of specific cortical regions compromise SW generation and propagatio

106 l during MR imaging that elicits activity in cortical regions consistent with studies of active balan

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

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

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

110 However, in several cortical regions, degraded mnemonic representations reco

111 tant regulator of the age-, experience-, and cortical region-dependent cross-modal response to unilat

112 mily guanosine triphosphatase, Cdc42, to the cortical region destined to become the "front" of the ce

113 e existence of neurons in three multisensory cortical regions, dorsal medial superior temporal area (

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

115 vements, yet unilateral inactivation of this cortical region during movement planning disrupts contra

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

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

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

119 we show that two important medial wall motor cortical regions emerge in relation to these tasks: one

120 Neural responses in many cortical regions encode information relevant to behavior

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

122 in which seizure recruitment of neighboring cortical regions follows a spatially organized pattern c

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

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

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

126 Each cortical region forms recurrent projections, via prefron

127 l change in limbic, striatal, and prefrontal cortical regions from early to mid-adolescence.

128 ed from florbetapir PET images for composite cortical regions (frontal, cingulate, parietal, and temp

129 matter reductions are restricted to specific cortical regions, functional MRI has also shown involvem

130 eterogeneous distribution (globus pallidus > cortical regions > cerebellum) consistent with the repor

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

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

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

134 strate that the anterior and posterior motor cortical regions have significantly different functional

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

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

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

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

139 gene) and amyloid deposition measures among cortical regions (i.e. a major AD hallmark).

140 By tracking area of the cortical region identified in the child sample throughou

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

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

143 tch to temporarily disrupt processing in two cortical regions implicated previously in different form

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

145 the primary visual, limbic and higher order cortical regions in a sequence consistent with the visua

146 au-dependent thinning was found in different cortical regions in Abeta(+) subjects but not in Abeta(-

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

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

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

150 We conclude that specific motor cortical regions in humans provide access to different m

151 phalographic beamformer analyses to localize cortical regions in humans spatially with trial-by-trial

152 density of V1s in nonprimates or many other cortical regions in primates and nonprimates.

153 logically defined axonal connections between cortical regions in rat.

154 e dorsolateral striatum (DLS) and associated cortical regions in the group that received previous res

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

156 e fields (SRFs) in two functionally distinct cortical regions in the pallid bat.

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

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

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

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

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

162 Here, we compare NF efficacy across six cortical regions including: early and high-order visual

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

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

165 Eight patients demonstrated decreased SI in cortical regions, including the left inferior temporal g

166 A set of cortical regions, including the middle intraparietal sul

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

168 ase phenotypes that are related to posterior cortical regions involved in both syndromic variants and

169 s demonstrated that thinning in a network of cortical regions involved in SW generation and propagati

170 ment sleep) was associated with higher CT in cortical regions involved in SW generation surrounding t

171 We identified a wide array of cortical regions involved in visual, auditory, and spati

172 ability in smokers with schizophrenia in the cortical regions is associated with a greater number of

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

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

175 y, particularly in midline and contralateral cortical regions, is an upregulation of activity in inta

176 The CeA receives dense inputs from cortical regions, is the major output region of the amyg

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

178 ly-deafened cats from an extrastriate visual cortical region known to be involved in the processing o

179 123)I-ABC577 demonstrated clear retention in cortical regions known to accumulate amyloid, such as th

180 In all examined cortical regions, many septal GABAergic boutons were in

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

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

183 aneously recorded neuronal activity from six cortical regions [middle temporal area (MT), visual area

184 studies have not measured responses from the cortical regions most implicated in pitch perception in

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

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

187 rage, about half of twin heritability across cortical regions (N=466 twins).

188 Cortical thickness was assessed in 112 cortical regions (nodes) and interregional partial corre

189 from the mean standardized uptake value of 6 cortical regions normalized to a reference region.

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

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

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

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

194 data from electrodes situated over specific cortical regions of interest were fit into linear multiv

195 instability may lead to spurious changes in cortical regions of interest.

196 d images were automatically parcellated into cortical regions of interest.

197 ly opposed influences on CT asymmetry within cortical regions of significant asymmetry in health.

198 icity in neural firing within deep brain and cortical regions of the auditory system.

199 5-HT7R density was found in the thalamus and cortical regions of the pig brain by autoradiography.

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

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

202 er such neural processes are limited to this cortical region or involve the basal ganglia is unclear.

203 ring coefficient, regardless of the analyzed cortical region or, in the case of weighted local effici

204 ., frontal cortex) might be altered, and (3) cortical regions outside of pitch-responsive cortex migh

205 l lesions (P < 10(-5)) and relative to other cortical regions (P < 0.01).

206 lives, but the precise roles that individual cortical regions play in the production of speech are of

207 led that pretrial brain activity in specific cortical regions predicted trial-by-trial changes in par

208 The main outcome was GM volume of cortical regions previously associated with major depres

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

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

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

212 ial attention, an understanding of how these cortical regions process neuronal information at the pop

213 Different cortical regions processing distinct information, such a

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

215 agnetic activity within frontal and parietal cortical regions provides further confirmation of hemody

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

217 i states increased post-learning in the same cortical regions recruited by the task.

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

219 evidence that striosomes receive input from cortical regions related to the control of mood and moti

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

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

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

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

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

225 Although cortical regions responsive to pitch have been identifie

226 Comparing structurally similar cortical regions revealed significant differences in the

227 putamen, globus pallidus, thalamus-and four cortical regions-rostral and dorsal anterior cingulate c

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

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

230 Axo-axonic cells (AACs) in cortical regions selectively innervate the axon initial

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

232 as well as the right amygdala and prefrontal cortical regions, specifically ventromedial prefrontal c

233 ween the lesion location and extent, and the cortical regions standardly implicated in biological mot

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

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

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

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

238 evidence that they might rely on overlapping cortical regions, such as the anterior temporal lobe (AT

239 discrimination across subcortical and visual cortical regions suggests a role for the amygdala in the

240 t information-rich, subset of neurons within cortical regions suggests that this population will play

241 g substantially hypermethylated in two other cortical regions (superior temporal gyrus and prefrontal

242 egarding relations, whereas extrahippocampal cortical regions support representations for single item

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

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

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

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

247 The prefrontal cortex (PFC), a cortical region that was once thought to be functionally

248 of fMRI experiments, we identified a set of cortical regions that are selectively engaged when peopl

249 Cortical regions that demonstrated lower dopamine transm

250 structural backbone of highly interconnected cortical regions that form most of the default mode netw

251 rent increases in low-frequency power across cortical regions that included the prefrontal cortex and

252 e network of association connections between cortical regions that is modulated by inputs from sensor

253 n processing emotion or salience and midline cortical regions that may mediate top-down regulation of

254 es to insular and temporal lobe involvement, cortical regions that modulate cardiac autonomic functio

255 ntegration via interactions with distributed cortical regions that process the individual elements.

256 plies an algorithm to automatically identify cortical regions that satisfy a set of quantifiable crit

257 ng a large-scale anatomical division between cortical regions that support motor-phonological aspects

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

259 resentations are stored in modality-specific cortical regions, that the goal-directed modulation of t

260 s, 2/3 of the STG is occupied by an auditory cortical region, the "parabelt," which is part of a netw

261 ults, with decreases in RSFC between midline cortical regions, the medial prefrontal cortex, and MTL

262 In a network of frontal and parietal cortical regions, the multiple-demand (MD) network, patt

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

264 egrate corticoclaustral input from different cortical regions, these results are consistent with more

265 ugh thalamocortical axons invade appropriate cortical regions, they are unable to organize into prope

266 ng that simple feature values are encoded by cortical regions throughout the visual processing hierar

267 The cortical regions to be investigated were carefully chose

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

269 s extended far beyond circumscribed auditory cortical regions to encompass almost all of auditory cor

270 failure of top-down connections from higher cortical regions to signal predictions to lower regions

271 nique pattern of brain organization and that cortical regions typically involved in perceptual expert

272 y heterogeneous, and the pattern of affected cortical regions varies among subtypes.

273 ecisely timed transmission of information in cortical regions via synchronous oscillations at gamma b

274 An extensive cortical region was identified wherein area related posi

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

276 ess in ventrolateral prefrontal and parietal cortical regions was associated with better declarative

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

278 Structural connectivity between pairs of cortical regions was estimated using a validated techniq

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

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

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

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

283 anatomical scans, and central and peripheral cortical regions were carefully compared between well-ch

284 Six cortical regions were quantified using a standardized re

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

286 nsory-discriminative and emotional-cognitive cortical regions were studied through the transition of

287 thickness measures and empirically localized cortical regions where thickness measures were significa

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

289 be affected on a different level, such as in cortical regions, which cannot be reliably quantified wi

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

291 the interhemispheric coordination among the cortical regions with connections to the caudate nucleus

292 The caudate nucleus and cortical regions with connections to the caudate nucleus

293 This abnormality was specific to cortical regions with connectivity to subcortical hetero

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

295 Cortical regions with overlapping genetic architecture s

296 normative developmental modules composed of cortical regions with similar maturational trajectories

297 ic analysis techniques to spatially localize cortical regions with trial-by-trial temporal activity t

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

299 ack is transmitted to many sensory and motor cortical regions within 25 ms of a mechanical disturbanc

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