ライフサイエンスコーパス: parietal

1 ous tACS during the verbal WM task increased parietal activity, which correlated with behavioral perf

2 nce that somatosensory perception depends on parietal alpha activity.SIGNIFICANCE STATEMENT Artificia

3 ontal lobe regions, as well as left inferior-parietal and cingulate regions, maximally around questio

4 wed enhanced functional connectivity between parietal and frontal regions in the crossed versus uncro

5 showed lower T1/T2-weighted ratio values in parietal and occipital areas.

6 In patients, thinner cortex in parietal and occipital cortical regions was associated w

7 data, GBA carriers showed reduced posterior parietal and occipital cortical synaptic activity and ni

8 Parietal and occipital cortical thickness were related t

9 Parietal and occipital cortices contain, respectively, t

10 ress this, we studied how the GABA levels of parietal and occipital cortices related to interindividu

11 ed within and across the subcortex, frontal, parietal and occipital lobes.

12 l as with extended deactivations of superior parietal and occipital regions representing parts of the

13 ates, in the medial-frontal, orbito-frontal, parietal and occipital regions.

14 educed cortical thickness in frontal, medial parietal and occipital regions.

15 specific connections (in particular, between parietal and posterior temporal areas) for preserving sp

16 le categorical representations in downstream parietal and prefrontal areas.

17 lation of choice-encoding pattern signals in parietal and prefrontal cortex and (ii) predicted by pha

18 ve been found during perceptual decisions in parietal and prefrontal cortex; however the source of su

19 eurons in higher cortical areas, such as the parietal and prefrontal cortices, mnemonically encode th

20 of cortical thickness) of the right inferior parietal and right fusiform areas was shown to play a ke

21 regions during encoding and between temporo-parietal and right-frontal regions during recognition of

22 during fetal development and in the temporal-parietal and sub-cortex during infancy through adulthood

23 results suggest that disruptions of temporal parietal and sub-cortical neurogenesis during infancy ar

24 Results indicated diminished inferior parietal and temporal cerebral blood flow for patients w

25 in measuring brain activity from prefrontal, parietal and temporal cortices of healthy adults (n = 19

26 a voxel level within subregions of frontal, parietal and temporal cortices.

27 ted with reduced FDG metabolism in posterior parietal and temporal regions, while attentional perform

28 ssociated with lesions in the right occipito-parietal and thalamic areas integrating visual and somat

29 ling (effective connectivity) between fronto-parietal and visual areas during perception and imagery.

30 , representations of mean reward are seen in parietal and visual areas, and later in frontal regions

31 % for frontal, 1.98% for temporal, 2.28% for parietal, and 3.27% for occipital VOIs.

32 cerebral cortex, including visual, posterior parietal, and dorsolateral prefrontal regions.

33 identified in dorsal extrastriate, posterior parietal, and frontal cortex as well as the thalamus, in

34 network spanning the early visual, temporal, parietal, and frontal cortices.

35 greater task-related activation in frontal, parietal, and hippocampal regions compared with controls

36 f studies report that neurons in prefrontal, parietal, and inferotemporal association cortices show r

37 onnectivity within the default mode, frontal-parietal, and motor control networks.

38 les are predominately associated with motor, parietal, and occipital regions, while interhemispheric

39 tem that includes left-hemispheric premotor, parietal, and posterior temporal cortices is activated e

40 tem that includes left-hemispheric premotor, parietal, and posterior temporal cortices.

41 ficulty was represented in anterior insular, parietal, and prefrontal cortices.

42 olume ratio of frontal, lateral temporal and parietal, and retrosplenial PiB-PET tracer uptake.

43 microECoG) arrays positioned over occipital, parietal, and temporal cortical regions.

44 ent subjects than controls in the occipital, parietal, and temporal cortices as well as the posterior

45 e network of brain areas, including frontal, parietal, and visual areas.

46 ning that beta-band top-down influences from parietal area 7a to visual area V1 are correlated with b

47 limbic, right inferior frontal, and inferior parietal areas during imitation of emotional faces corre

48 l as in the left insula and adjacent temporo-parietal areas.

49 ens had the highest abundance of omental and parietal arteriolar C1q, C3d, terminal complement comple

50 Findings were validated in omental and parietal arterioles from independent pediatric control (

51 effector of TGF-beta Furthermore, in the PD parietal arterioles, C1q and terminal complement complex

52 damaged by stroke, in particular within the parietal association and the primary somatosensory corte

53 occipital and thalamic region, and the left parietal association area.

54 with lesions of the right occipital and left parietal association areas after adjusting for confoundi

55 4 patients with idiopathic VA origins in the parietal band among 294 consecutive patients with VA ori

56 The parietal band is one of the muscle bands in the right ve

57 The catheter ablation of the parietal band VAs was always challenging, requiring a la

58 The QRS morphologies of the parietal band VAs were characterized by a left bundle br

59 During parietal band VAs, a far-field ventricular electrogram w

60 cular arrhythmias (VAs) originating from the parietal band.

61 Idiopathic VAs rarely originated from the parietal band.

62 across visual formats in bilateral inferior parietal, bilateral occipitotemporal, left premotor, and

63 anial remains, particularly in occipital and parietal bones.

64 uding auditory sensory, but also frontal and parietal brain regions involved in controlling auditory

65 reases in delta connectivity were evident in parietal but not frontal regions.

66 Experiment 2 revealed that prestimulus parietal, but no occipital, alpha EEG phase and power, a

67 thin-subject, the phase and power of ongoing parietal, but not occipital, alpha-band oscillations at

68 ion induced lateralization of alpha power in parietal, but notably also in auditory cortical regions.

69 of E-cadherin (Cdh1) and p53 in the gastric parietal cell lineage.

70 Parietal cells (PCs), whose function is to pump acid int

71 c, transgenic overexpression of ML1 in mouse parietal cells induced constitutive acid secretion.

72 Gastric acid secretion by parietal cells requires trafficking and exocytosis of H/

73 ocalize initially to the precursor secondary parietal cells then predominantly to daughter tapetal ce

74 aling with Ca(2+)-dependent TV exocytosis in parietal cells, providing a regulatory mechanism that co

75 types, including chief cells and functional parietal cells.

76 ond network consisting of bilateral frontal, parietal, cingulate, and insular regions.

77 cture consisted of a high-frequency occipito-parietal component of the AR (ARC1) and a low-frequency

78 However, the evolution of enhanced LMC-parietal connections likely allowed for more complex syn

79 us, and no priming-related changes in fronto-parietal connectivity.

80 y visual area V1, higher visual area V4, and parietal control area 7a during attentional task perform

81 tter fiber bundles, which connect the fronto-parietal control network and the fronto-temporal network

82 nf either from the amygdala (N=19) or from a parietal control region not involved in emotional proces

83 d into decision-related signals in posterior parietal cortex (area LIP).

84 gocentric neural coding has been observed in parietal cortex (PC), but its topographical and laminar

85 work on monkeys suggests that the posterior parietal cortex (PPC) and ventral premotor cortex (PMv)

86 representations, we recorded from posterior parietal cortex (PPC) before and after training on a vis

87 rt that a subset of neurons in the posterior parietal cortex (PPC) closely reflect the choice-outcome

88 We test the hypothesis that the posterior parietal cortex (PPC) contributes to the control of visu

89 Our results show that the posterior parietal cortex (PPC) encodes memories for spatial locat

90 Here, we tested whether rat posterior parietal cortex (PPC) is causal for processing visual se

91 The human posterior parietal cortex (PPC) is thought to contribute to memory

92 nent of decision circuits, the rat posterior parietal cortex (PPC).

93 tent with those observed in monkey posterior parietal cortex (PPC).

94 mary somatosensory cortex (SI) and posterior parietal cortex (PPC; Brodmann areas 7/40).

95 synaptic connections were made via posterior parietal cortex (RSC-->PPC-->M2) and anteromedial thalam

96 Hz) beta band power decreases in central and parietal cortex and (14-20 Hz) beta band power increases

97 es in activation in regions of occipital and parietal cortex and bilateral insula during sustained in

98 ned alpha/micro suppression in the Posterior Parietal Cortex and Inferior Parietal Lobe, indicating i

99 relationship was apparent only in posterior-parietal cortex and not in other motor system areas, the

100 excitability directly in human occipital and parietal cortex and observed that, whereas alpha-band dy

101 ction and lesion sites in the right occipito-parietal cortex and thalamus, as well as in the left ins

102 erefore, task representations in frontal and parietal cortex are largely switch independent.

103 ls measured from the monkey medial posterior parietal cortex are valid for correctly decoding informa

104 parietal cortex, this highlights the medial parietal cortex as a target site for transforming neural

105 ral choices in auditory cortex and posterior parietal cortex as mice performed a sound localization t

106 Although subregions of frontal and parietal cortex both contribute and coordinate to suppor

107 ation (TMS) of human occipital and posterior parietal cortex can give rise to visual sensations calle

108 Although auditory cortex and posterior parietal cortex coded information by tiling in time neur

109 Patients with lesions of the left posterior parietal cortex commonly fail in identifying their finge

110 e and colleagues proposed that the posterior parietal cortex contains a "command apparatus" for the o

111 re fibers connecting homologous areas of the parietal cortex course.

112 We show that right parietal cortex distinguishes between fearful and neutra

113 r resolution imaging data from the posterior parietal cortex during a virtual memory-guided two-alter

114 group-by-abstinence interaction in occipital/parietal cortex during sustained inhibition, with greate

115 topographically organized human frontal and parietal cortex during WM maintenance cause distinct but

116 s, beta-band activity was most predictive of parietal cortex excitability.

117 l activity from nonhuman primate frontal and parietal cortex have led to the development of methods o

118 interaction is represented in prefrontal and parietal cortex in a task-dependent manner.

119 against a "content-poor" view of the role of parietal cortex in attention.

120 increased sustained activity in auditory and parietal cortex in REG relative to RAND scenes, emerging

121 The exposed surface of the primate superior parietal cortex includes two cytoarchitectonically defin

122 Low-frequency TMS to left parietal cortex increases low-frequency oscillations and

123 ld stimulation (tSMS) over the somatosensory parietal cortex increases oscillatory power specifically

124 Stronger coupling in posterior parietal cortex led to a population code with long times

125 distortions supports theories positing that parietal cortex mainly codes for retrospective sensory i

126 sory responses distributed across the fronto-parietal cortex may support working memory on behavioral

127 ctivations in the prefrontal, cingulate, and parietal cortex measured during cocaine-cue responding w

128 According to current theorizing, the parietal cortex mediates this system [4].

129 We tracked the activity of posterior parietal cortex neurons for a month as mice stably perfo

130 Coupling among posterior parietal cortex neurons was strong and extended over lon

131 ified microglia isolated at autopsy from the parietal cortex of 39 human subjects with intact cogniti

132 Cortical fMRI variability in the posterior-parietal cortex of individual subjects explained their m

133 y, we find that cortical fMRI variability in parietal cortex of individual subjects explained their m

134 Representations in parietal cortex reveal a notable exception to this patte

135 prefrontal cortex-bilateral inferior lateral parietal cortex RSFC was predictive of treatment respons

136 Instead, the human parietal cortex seems to be "content rich" and capable o

137 tend to two adjacent stimuli, prefrontal and parietal cortex shows a selective enhancement of only th

138 cribe an inhibitory circuit in the posterior parietal cortex that evaluates conflicting auditory and

139 ivity between left sensorimotor and inferior parietal cortex was also found during illusory hand owne

140 contrast, regions of the inferotemporal and parietal cortex were selectively tuned to faces and acti

141 analyses also revealed a greater reliance on parietal cortex when using the learned S-R versus S-C as

142 attention areas (eg, occipital and superior parietal cortex) may be associated with inhibitory contr

143 tronger in auditory cortex than in posterior parietal cortex, and both regions contained choice infor

144 buted network of regions such as the insula, parietal cortex, and somatosensory areas, which are also

145 pre- to post-treatment) in the left inferior parietal cortex, as well as a positive partial correlati

146 , primary motor cortex, insula and posterior parietal cortex, as well as in contralateral prefrontal

147 d with grey matter density in prefrontal and parietal cortex, as well as the hippocampus.

148 on about task representations in frontal and parietal cortex, but there was no difference in the deco

149 l excitability in occipital versus posterior parietal cortex, calling into question the broader assum

150 r cortex (PMV), the caudal half of posterior parietal cortex, cingulate cortex, visual areas within t

151 ence to sign is strongest over occipital and parietal cortex, in contrast to speech, where coherence

152 uneus, medial prefrontal cortex, and lateral parietal cortex, indicating that reduced activity may no

153 motor cortex, prefrontal cortices, posterior parietal cortex, striatum, and thalamus after overdrinki

154 reach trajectories from the medial posterior parietal cortex, this highlights the medial parietal cor

155 zation of motor representations in posterior parietal cortex, we test how three motor variables (body

156 ses is modulated similarly to prefrontal and parietal cortex.

157 l frontal, insular, dorsomedial frontal, and parietal cortex.

158 from area V6A of the monkey medial posterior parietal cortex.

159 rhinal, inferior temporal (IT), and inferior parietal cortex.

160 e left) as well as in frontal, temporal, and parietal cortex.

161 were quantified across AD disease stages in parietal cortex.

162 tion, which occurs in different areas of the parietal cortex.

163 ctions in activity within bilateral inferior parietal cortex.

164 as not previously been reported in the human parietal cortex.

165 us is selectively enhanced in prefrontal and parietal cortex.

166 mically reorganized motor, but not posterior parietal, cortex eliminated behavioral gains from rehabi

167 he premotor cortex (PM) receives inputs from parietal cortical areas representing processed visuospat

168 Here we show that parietal cortical neurons involved in oculomotor decisio

169 trolateral, orbital), anterior cingulate and parietal cortical regions.

170 ngulate cortex and the superior and inferior parietal cortices (P = 0.0006, 0.0015, and 0.0023, respe

171 CBF change in the bilateral parietal cortices also correlated with motor function im

172 ntral striatum and the medial prefrontal and parietal cortices and between the dorsal striatum and th

173 ularly affected the primary sensorimotor and parietal cortices and thalamus.

174 ined the responses of neurons in frontal and parietal cortices during a pulse-based accumulation of e

175 prefrontal, superior temporal, and superior parietal cortices, when the subjects believed that the s

176 tion is unlikely to be inherited from fronto-parietal cortices, which do not project to SCs, but may

177 ith no change in the middle frontal gyrus or parietal cortices.

178 tal and prefrontal, and superior and lateral parietal cortices.

179 odes and specific regions within frontal and parietal cortices.

180 domain-general regions of the prefrontal and parietal cortices.

181 ithin bilateral medial frontal and posterior parietal cortices.

182 communication between lateral prefrontal and parietal cortices.

183 dorsolateral prefrontal and lateral temporo-parietal cortices.

184 Parietal DAP and DMP exhibited egocentric spatial maps c

185 lts suggest that ZIKV spreads from basal and parietal decidua to chorionic villi and amniochorionic m

186 rigin of the pathogenic signal that triggers parietal epithelial cell recruitment remains elusive.

187 the aberrant proliferation and migration of parietal epithelial cells (PECs)/progenitor cells, and t

188 ticoids act directly on activated glomerular parietal epithelial cells in crescentic nephritis.

189 and genetic tracing studies have shown that parietal epithelial cells participate in the formation o

190 e each acted directly on primary cultures of parietal epithelial cells, inhibiting cellular outgrowth

191 of podocytes triggers a focal activation of parietal epithelial cells, which subsequently form cellu

192 ol, characterized by less robust frontal and parietal ERP distributions across the response selection

193 antly differentiated on the presence of left parietal features and AOS, and amnestic AD could be diff

194 .05, kE=2198, x=-30, y=52, z=14) and temporo-parietal functional connectivity (t=5.07, PFDR<0.05, kE=

195 Specifically, parietal GABA level correlated with size illusion magnit

196 docyte lesions and recruitment of pathogenic parietal glomerular epithelial cells.

197 icroscopy confirmed the presence of a 3.8 mm parietal granuloma with a few calcifications in the left

198 of N-acetylaspartate to creatinine levels in parietal gray matter (r = -0.352 and P < .001 at baselin

199 ecentral gyrus, Rolandic operculum, superior parietal gyrus, angular gyrus, and middle temporal pole.

200 < .001) in the posterior cingulate, lateral parietal, hippocampal, and parahippocampal cortices and

201 Critically, these parietal identity representations were behaviorally rele

202 ight in the 4-repeat-tau group, with greater parietal involvement in the TDP43A group.

203 The Presenilin-1 group had similar parietal involvement to the early-onset group with local

204 ed by an increased activation in the temporo-parietal junction (TPJ) during decision making in OB and

205 Generous decisions engage the temporo-parietal junction (TPJ) in the experimental more than in

206 ammatic variant, and within the left temporo-parietal junction in patients with the semantic variant.

207 level-dependent (BOLD) signal in the temporo-parietal junction is modulated by adviser's current leve

208 ral prefrontal cortex and the right temporal-parietal junction) included the ventral attention networ

209 e hierarchy, such as the precuneus, temporal parietal junction, and medial frontal cortices, there we

210 margins of sieve elements where it lines the parietal layer and colocalizes in spherical bodies aroun

211 ed activation in the right anterior inferior parietal lobe (aIPL), bilateral lingual gyrus and the cu

212 l prefrontal cortex (RLPFC) and the inferior parietal lobe (IPL).

213 metabolism was most commonly observed in the parietal lobe followed by the occipital lobe.

214 increased in CD vs HC in the right inferior parietal lobe post-cocaine and in the left superior fron

215 timodal associative areas in the frontal and parietal lobe than primary regions of sensorimotor and v

216 y from associative areas in the temporal and parietal lobe toward functional connectivity with the fr

217 The right parietal lobe was compressed by the mass.

218 ugar foods causes adaptions in the striatum, parietal lobe, and prefrontal and visual cortices in the

219 n the Posterior Parietal Cortex and Inferior Parietal Lobe, indicating increases of cortical involvem

220 us, precuneus, posterior cingulate, inferior parietal lobe, supramarginal gyrus, striatum, and thalam

221 , with the largest decreases observed in the parietal lobe.

222 ro-parieto-occipital junction and the medial parietal lobe.

223 in the left thalamus and bilateral inferior parietal lobe.

224 t not animals, were encoded in left inferior parietal lobe; and (3) LATL subregions exhibited distinc

225 ose metabolism in the occipital and inferior parietal lobes relative to controls.

226 neonatal brain in the frontal, temporal, and parietal lobes.

227 ly between inferior prefrontal and occipital/parietal lobes.

228 refrontal cortex and both the right superior parietal lobule and the left lateral occipital cortex) i

229 he primary somatosensory cortex and superior parietal lobule influences brain networks associated wit

230 Atypical RCrusI-inferior parietal lobule structural connectivity was also evident

231 We identified a region in the right superior parietal lobule that responded to both types of visuomot

232 eft IFG and the right IFG and right inferior parietal lobule was also significantly correlated with a

233 tivity in the postcentral gyrus and superior parietal lobule was sensitive to dot periodicity.

234 ed functional connectivity with the inferior parietal lobule, and children with ASD showed atypical f

235 with higher metabolic values in the inferior parietal lobule, anterior cingulate, inferior temporal l

236 ion contrast map included bilateral superior parietal lobule, bilateral dorsolateral prefrontal corte

237 or superior temporal gyrus, and the inferior parietal lobule, while those of patients with atypical l

238 of the right frontal pole, the right lateral parietal lobules, and the left posterior cingulate corte

239 ingulate gyrus, the putamen and the superior parietal lobules.

240 cture memory test preferentially engaged the parietal memory network as well as portions of the front

241 A reduced baseline parietal metabolism is associated with risk of cognitive

242 Parietal, midline, and prefrontal, but not primary corti

243 ional expressions activates the human fronto-parietal mirror network.

244 ifferences in engagement of a fronto-cingulo-parietal network, involving decreased engagement in IGD

245 wide-spread bilateral frontal, temporal, and parietal network.

246 nal phase synchronization within a posterior parietal network.

247 y identified, specific frontal, striatal and parietal networks we suggest that these structures are i

248 making within specific frontal, striatal and parietal networks; we conclude that manual tracking util

249 Group differences in cerebellar and parietal neuronal activity occurred during the time wind

250 l function at baseline, cortical thinning in parietal, occipital and frontal cortex and reduced hippo

251 ved spectroscopy data were acquired from the parietal-occipital cortex and supplementary motor area i

252 Using fMRI, we identified several areas of parietal, occipitotemporal, and frontal cortex that exhi

253 ht-frontal region and subsequently the right-parietal ones.

254 odulated functional connectivity between the parietal operculum (related to speed) and postcentral gy

255 Parietal operculum, corona radiata, and internal capsule

256 Activity in the parietal operculum, insula, and inferior and superior fr

257 ted with infarcts involving posterior areas (parietal P = 0.046, temporal P < 0.001) independently of

258 ing, there was a significant increase in the parietal P3 amplitude with MPH, indicative of enhanced p

259 ral studies of the phloem and shows that the parietal phloem layer plays an important role in plant r

260 ) posterior negativity and a later (>300 ms) parietal positivity in the time domain and an increase i

261 amining population recordings from posterior parietal (PPC) and prefrontal (PFC) cortices in two male

262 ortical (right inferior frontal and inferior parietal/precuneus) and cerebellar regions.

263 entify a core cortical network of occipital, parietal, premotor, and prefrontal areas maximally activ

264 The parietal region showed significantly greater left latera

265 he first trimester (eyes, midface, chin, and parietal region), and binge-level exposure in the first

266 e CMRglc of the conscious brain (e.g., right parietal region, 99.6 +/- 10.2 mumol/100 g/min; n = 6) w

267 ness, delta waves propagated from frontal to parietal regions as a traveling wave.

268 First, visual and parietal regions coordinated with sensorimotor and premo

269 differential connectivity with occipital and parietal regions implicated in the processing of low-lev

270 EG theta activity over frontal, temporal and parietal regions in response to negative stimuli in SAD

271 nently in the inferior temporal and inferior parietal regions in the full cohort, with florbetapir po

272 matter was thinner in frontal, temporal and parietal regions of both brain hemispheres.

273 eas connections originating from frontal and parietal regions peaked at beta frequency.

274 ferior-frontal, middle-frontal, and inferior-parietal regions preceded by high-gamma attenuation in t

275 -temporal regions and decreases in posterior-parietal regions that largely recovered by two weeks pos

276 fferences in the topological organization of parietal regions were found between phenotypically diffe

277 ocampus, along with cerebellar, temporal and parietal regions were more substantial in major depressi

278 nnectivity was reduced between S1 and fronto-parietal regions, in both the TMSR and non-TMSR patients

279 and S1 and of both these regions with fronto-parietal regions, known to be important for multisensory

280 ct category decoding in occipitotemporal and parietal regions.

281 the left-temporal, right-temporal, and right-parietal regions.

282 th the largest effects in frontotemporal and parietal regions; psychotic bipolar probands had small r

283 ved amygdalar rtfMRI-nf, 16 received control parietal rtfMRI-nf).

284 related EEG responses were found in a centro-parietal scalp location, whose slope depended on change

285 reward variability emerges simultaneously in parietal/sensory and frontal sources and later than mean

286 on of predicted mean reward emerges early in parietal/sensory regions and later in frontal cortex.

287 y shown to form projections to the posterior parietal, somatosensory, visual, and motor cortex.

288 nalysis (MVPA) decoding of task in occipital-parietal sources remained above chance for almost 1 s, a

289 but not for strangers, localized to temporal-parietal structures and expressed in gamma rhythms.

290 occipitotemporal cortex and several lateral parietal subregions, including ANG.

291 bjects, in the hippocampus and in occipital, parietal, temporal, and frontal cortices (t's > 2.2, P's

292 cortical VOI composed of average values from parietal, temporal, and occipital areas.

293 beling atlas) volumes of interest (VOIs) for parietal, temporal, occipital, anterior, and posterior h

294 d (13-20 Hz) power (but not phase) predicted parietal TMS phosphenes.

295 perception of phosphenes after occipital and parietal TMS.

296 Baseline parietal to cerebellum FDG metabolism ratios predicted M

297 Critically, we next show that parietal tSMS enhances the detection of near-threshold s

298 Inferior parietal volume reduction was characteristic of schizoph

299 yzed revealed significantly reduced inferior parietal volume relative to controls (F3,113 = 9.7, P <

300 ecifically in trophoblast giant cells in the parietal yolk sac.