ライフサイエンスコーパス: parietal cortex

1 regions (dorsolateral prefrontal cortex and parietal cortex).

2 that creates the inhibitory tagging seen in parietal cortex.

3 with lesions in left dorsal premotor but not parietal cortex.

4 ses is modulated similarly to prefrontal and parietal cortex.

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

6 us is selectively enhanced in prefrontal and parietal cortex.

7 oss-regional dynamics in the hippocampus and parietal cortex.

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

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

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

11 were quantified across AD disease stages in parietal cortex.

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

13 ctions in activity within bilateral inferior parietal cortex.

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

15 mation about others' actions to the inferior parietal cortex.

16 e onset of hand movement in both frontal and parietal cortex.

17 eas including dmFC, precuneus, and posterior parietal cortex.

18 rection, two functions that both localize to parietal cortex.

19 isinhibition of the homotopic left posterior parietal cortex.

20 t the prodromal stage, involving the temporo-parietal cortex.

21 across monkey premotor, motor, and posterior parietal cortex.

22 yrus (ANG), a subregion of posterior lateral parietal cortex.

23 bstract object identity information in human parietal cortex.

24 the prefrontal, medial temporal, and medial parietal cortex.

25 al selection throughout posterior visual and parietal cortex.

26 response for each voxel in human topographic parietal cortex.

27 representation of viewed action in anterior parietal cortex.

28 ual object size in bilateral human posterior parietal cortex.

29 and instead highlight the role of posterior parietal cortex.

30 resentation of viewed action in the anterior parietal cortex.

31 al intraparietal (LIP) area of the posterior parietal cortex.

32 low reciprocally between primary sensory and parietal cortex.

33 orsolateral prefrontal cortex, and posterior parietal cortex.

34 P and the parietal reach region (PRR) of the parietal cortex.

35 ar to recent observations in hippocampus and parietal cortex.

36 io of alpha power over the left versus right parietal cortex.

37 error magnitude and past errors in posterior parietal cortex.

38 ated activity, and motor-related activity in parietal cortex.

39 ported by parahippocampal cortex and lateral parietal cortex.

40 mplars in inferior frontal gyrus and lateral parietal cortex.

41 out the dorsal visual pathway into posterior parietal cortex.

42 e tract strength between parahippocampus and parietal cortex.

43 four cell classes across primate frontal and parietal cortex.

44 also found in frontal eye fields and dorsal parietal cortex.

45 ansion and areal complexity of the posterior parietal cortex.

46 and temporal cortical areas but increased in parietal cortex.

47 ion predominantly over ipsilateral posterior-parietal cortex.

48 een linked to alpha oscillations in occipito-parietal cortex [3,11].

49 = .0003), with the largest reductions in the parietal cortex (-37.6%; P < .0001) and precuneus (-31.8

50 Our work focuses on the posterior parietal cortex, a brain region supporting short-term me

51 cognition paradigm that the lateral inferior parietal cortex, a region that has previously been assoc

52 t through the altered engagement of inferior parietal cortex; a region implicated in sensorimotor int

53 k as a shared feature of the organization of parietal cortex across Euarchontoglires and Laurasiather

54 MRI pattern analysis to test whether lateral parietal cortex actively represents the contents of memo

55 Although parietal cortex activity is thought to represent accumul

56 ralized alpha (8-14 Hz) oscillatory power in parietal cortex: alpha increases in the hemisphere ipsil

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

58 FC in the cingulum, precuneus, and bilateral parietal cortex and a lower FC in the cerebellum and in

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

60 citatory projections from auditory cortex to parietal cortex and found this was sufficient to increas

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

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

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

64 al position discrimination in right inferior parietal cortex and precuneus, respectively.

65 ral prefrontal cortex and the right superior parietal cortex and precuneus.

66 encoding of decision variables in posterior parietal cortex and prefrontal cortex (frontal orienting

67 anslation direction and rotation velocity in parietal cortex and show that rotation velocity can be r

68 f visual salience, we reversibly inactivated parietal cortex and simultaneously recorded salience sig

69 howed increased connectivity in the superior parietal cortex and striatum in their global network.

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

71 nces specifically engaged the right inferior parietal cortex and the anterior insula.

72 the layer IV and V pyramidal neurons of the parietal cortex and the CA1 basilar tree of the hippocam

73 al cortex in carnivores, where the posterior parietal cortex and the central temporal region (PMLS) p

74 is linked to altered activity in the lateral parietal cortex and the connectivity between the hippoca

75 the evolution and function of the posterior parietal cortex and the frontoparietal network across ma

76 n 10% in most large cortical regions (14% in parietal cortex) and ranged from 14% (cerebellum) to 51%

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

78 de generation (frontal eye fields, posterior parietal cortex, and higher-level visual areas).

79 neurons in mouse auditory cortex, posterior parietal cortex, and hippocampus.

80 n the left superior frontal gyrus, bilateral-parietal cortex, and left precuneus, and negatively with

81 d significant regional variation, highest in parietal cortex, and lowest in cerebellum.

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

83 anterior cingulate, precuneus region of the parietal cortex, and striatum-findings similar to those

84 poral occipital cortex (VTOC), the posterior parietal cortex, and the prefrontal cortex, predicted lo

85 of the medial occipital cortex, the lateral parietal cortex, and the superior precentral sulcus (tho

86 osterior cingulate, calcarine, and occipital-parietal cortex; and right rostral anterior cingulate co

87 Multiple-demand (MD) regions of frontal and parietal cortex appear essential for the orchestration o

88 Evolutionary adaptations of temporo-parietal cortex are considered to be a critical speciali

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

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

91 the somatosensory functions of the anterior parietal cortex are well established, the posterior pari

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

93 om other somatosensory areas of the anterior parietal cortex (areas 1, 3b, and 3a), the second somato

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

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

96 dence that the X-chromosome affects not only parietal cortex, as described in previous studies, but a

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

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

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

100 bundles innervating posterior cingulate and parietal cortex, basal ganglia, and temporal cortex.

101 (at 16 Hz), recorded in superior frontal and parietal cortex, became significantly coupled with high

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

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

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

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

106 esponse patterns, that a region in the human parietal cortex can robustly represent task-relevant obj

107 s primarily arising from lesions of the left parietal cortex centred on the intraparietal sulcus.

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

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

110 We studied how the posterior parietal cortex combines new information with ongoing ac

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

112 de attempt showed bilateral abnormalities in parietal cortex compared to nonsuicidal depressed patien

113 Parietal cortex compensates for this by updating reach g

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

115 Posterior parietal cortex contains several areas defined by topogr

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

117 n PFC, whereas microstimulation in posterior parietal cortex did activate the ITC.

118 ed in the medial temporal lobe and posterior parietal cortex, discuss their properties, and reflect o

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

120 g working memory load, including frontal and parietal cortex, dorsal cingulate, supplementary motor a

121 The dorsal circuit, that includes inferior parietal cortex, dorsal lateral prefrontal cortex, and t

122 elected (internally vs externally driven) in parietal cortex, dorsal premotor cortex, and primary mot

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

124 We recorded from parietal cortex during flexible switching between catego

125 nto oscillatory bursts in bilateral inferior parietal cortex during multiple-object processing.

126 parietal lesion; and (3) fMRI activation of parietal cortex during object manipulation requiring con

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

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

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

130 ntrahemispheric connectivity between FEF and parietal cortex, emphasizing the relevance of interhemis

131 rve assays revealed that while the posterior parietal cortex encodes a graded value of the accumulati

132 lateral intraparietal area (LIP) reveal that parietal cortex encodes variables related to spatial dec

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

134 Thus, attention effects in topographic parietal cortex exhibit hemispheric asymmetries similar

135 plicating PMLS as a potential gateway to the parietal cortex for dorsal stream processing.

136 light on the roles of inferior and superior parietal cortex for internally directed cognition.

137 rrences of alpha-oscillatory burst events in parietal cortex for processing objects versus ensembles

138 These results support the general role of parietal cortex for the integration of visuospatial pert

139 sly rewarded stimuli in posterior visual and parietal cortex from ~260 ms after stimulus onset.

140 Stimulation to parietal cortex had no significant impact on the dynamic

141 l cortex are well established, the posterior parietal cortex has a relevant role in processing the se

142 Conversely, the left parietal cortex has been linked to retrieval of vivid me

143 trosplenial complex (RSC), located in medial parietal cortex, has been implicated in numerous cogniti

144 egions such as precuneus and lateral temporo-parietal cortex have been shown to be more vulnerable to

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

146 icipants' peak of activation within the left parietal cortex impaired their ability to generalize lea

147 n (cTBS) was applied over the left posterior parietal cortex in a randomized clinical trial, either i

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

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

150 studies have consistently implicated lateral parietal cortex in episodic remembering, but the functio

151 rm calcium imaging recordings from posterior parietal cortex in mice (Mus musculus), we show that dri

152 right dorsolateral prefrontal cortex and the parietal cortex in non-relapsers.

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

154 se observations demonstrate a causal role of parietal cortex in regulating salience signals within th

155 es at 1 week in the fasting state and in the parietal cortex in response to any food cues at 4 weeks

156 (fMRI) reduced fMRI activations in posterior parietal cortex in the dorsal stream and, surprisingly,

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

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

159 We recorded the activity of posterior parietal cortex (including lateral intraparietal area LI

160 ns of several white matter tracts in temporo-parietal cortex, including the middle and superior longi

161 Direct pharmacological inactivation of parietal cortex increased minimum integration times, sug

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

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

164 spatial activation patterns in the inferior parietal cortex indeed represent task-reward association

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

166 nae VII and IX, the added effect of adjacent parietal cortex injury to the frontal motor lesion (F2P2

167 Here, we asked whether the parietal cortex integrates acoustic features from audito

168 10 Hz) but not theta (6 Hz) HD-tACS of right parietal cortex interfered with attending left but not r

169 prefrontal cortex (dlPFC) and left inferior parietal cortex (IPC) in the Tenacity group.

170 Concurrent damage to the lateral frontal and parietal cortex is common following middle cerebral arte

171 It has been unclear whether parietal cortex is involved in spatial decision-making i

172 The right posterior parietal cortex is part of a broad cortical network invo

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

174 ith FOG had less activation of the posterior parietal cortex, less deactivation of the dorsolateral p

175 Brain areas within the lateral parietal cortex (LPC) and ventral temporal cortex (VTC)

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

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

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

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

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

181 cohort of patients (n = 50), from the medial parietal cortex (MPC) and the medial temporal lobe (MTL)

182 Human medial parietal cortex (MPC) is implicated in multiple cognitiv

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

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

185 speech conditions < baseline) in the temporo-parietal cortex, neutral > angry in the anterior superio

186 Inactivation of parietal cortex not only caused pronounced and selective

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

188 that lateral prefrontal cortex and posterior parietal cortex of high-capacity individuals are more de

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

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

191 tory and inhibitory neurons in the posterior parietal cortex of mice judging multisensory stimuli.

192 nal similarities exist between the posterior parietal cortex of the ferret (PPc and PPr) and the cat

193 The two divisions of posterior parietal cortex of the ferret are strongly interconnecte

194 By contrast, carbachol delivery to parietal cortex, or noradrenaline delivery to either pre

195 Overall, we show that human parietal cortex, part of the dorsal visual processing pa

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

197 ted over the prefrontal cortex (PFC) and the parietal cortex (PC).

198 happy > neutral response within the temporo-parietal cortex, peaking in the anterior temporal cortex

199 Our results demonstrate that the parietal cortex plays a central role in representing ass

200 r, our findings provide causal evidence that parietal cortex plays a role in the network that integra

201 ere focused on regions of the prefrontal and parietal cortex potentially implicated in delusion proce

202 Posterior parietal cortex (PPC) activity correlates with monkeys'

203 auses activity changes in the left posterior parietal cortex (PPC) and an assessment of tactile tempo

204 tenance-related impairments in the posterior parietal cortex (PPC) and frontal eye fields (FEF).

205 om fMRI studies emerged, including posterior parietal cortex (PPC) and hippocampus.

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

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

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

209 Here, we found that the posterior parietal cortex (PPC) contributes to combining position

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

211 Neurons in posterior parietal cortex (PPC) control several effectors (e.g., e

212 The posterior parietal cortex (PPC) controls allocation of attention a

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

214 ated visual target location, while posterior parietal cortex (PPC) exhibited chance-level decoding ac

215 olution, both largely dependent on posterior parietal cortex (PPC) expansion.

216 The posterior parietal cortex (PPC) has traditionally been considered

217 s (RMS) on the connectivity of the posterior parietal cortex (PPC) in adolescent male mice.

218 The posterior parietal cortex (PPC) in rodents is reciprocally connect

219 Posterior parietal cortex (PPC) is an extensive region of the huma

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

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

222 ehavior.SIGNIFICANCE STATEMENT The posterior parietal cortex (PPC) is thought to merge information on

223 The posterior parietal cortex (PPC) of primates integrates sensory inf

224 y evaluated the influence of right posterior parietal cortex (PPC) on a direct measure of visual proc

225 The posterior parietal cortex (PPC) performs many functions, including

226 n an ongoing debate on whether the posterior parietal cortex (PPC) represents only spatial awareness,

227 nterfering with left but not right posterior parietal cortex (PPC) using high-definition cathodal tra

228 ording arrays are implanted in the posterior parietal cortex (PPC), a high-level cortical area in bot

229 es of L3PNs in monkey DLPFC versus posterior parietal cortex (PPC), a key node in the cortical workin

230 l connections between PIVC and the posterior parietal cortex (PPC), a major brain region of the corti

231 : medial prefrontal cortex (mPFC), posterior parietal cortex (PPC), and the medial parietal and poste

232 in a key decision-making node, the posterior parietal cortex (PPC), depends on the temporal structure

233 3PNs from macaque monkey DLPFC and posterior parietal cortex (PPC), two key nodes in the cortical wor

234 ecognize three subdivisions of the posterior parietal cortex (PPC), which are architectonically disti

235 , anterior cingulate cortex (ACC), posterior parietal cortex (PPC), while freely moving rats performe

236 er-order sensory areas such as the posterior parietal cortex (PPC).

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

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

239 ng the prefrontal cortex (PFC) and posterior parietal cortex (PPC).

240 a stiffness estimator in the human posterior parietal cortex (PPC).

241 s can be derived from cells in the posterior parietal cortex (PPC).

242 n the precentral sulcus (PrCS) and posterior parietal cortex (PPC).

243 ary motor cortex (MI, area 4), and posterior parietal cortex (PPC, area 5) while monkeys made either

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

245 e medial prefrontal cortex, lateral inferior parietal cortex, precuneus, and medial and lateral tempo

246 Moreover, deactivation of the left inferior parietal cortex predicted both inter- and intra-individu

247 d inferior portions of neighboring posterior parietal cortex, predominantly in the left hemisphere.

248 tive to Sham-TMS increased activation in the parietal cortex regardless of sensory stimulation, confi

249 s were revealed within the control posterior parietal cortex region.

250 prefrontal cortex and alpha oscillations in parietal cortex, respectively.

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

252 uotopic activity in visual (areas V1-V4) and parietal cortex revealed that directing attention to one

253 Parietal cortex RNA-sequencing (RNA-seq) data were gener

254 matter volume in a region of right posterior parietal cortex (rPPC) is predictive of preferences for

255 ral prefrontal cortex (rDLPFC) and posterior parietal cortex (rPPC).

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

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

258 sessment was performed on immune-staining of parietal cortex sections.

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

260 gle-cell recordings from macaque frontal and parietal cortex show some similar properties to human MD

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

262 vity, cTBS over the contralesional posterior parietal cortex significantly improves and accelerates n

263 al experiment, we hypothesized that inferior parietal cortex (specifically supramarginal gyrus [SMG])

264 t activity was followed by similar posterior parietal cortex spectral power increase that decreased i

265 Neuronal counts in parietal cortex, striatum, and hippocampus were higher i

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

267 the left lateral prefrontal cortex and right parietal cortex, suggesting that dopamine facilitates as

268 The study of the evolution of the parietal cortex supplies an interesting case-study in wh

269 onnectivity between regions in occipital and parietal cortex supported enhanced decoding of the curre

270 The neural data suggest that posterior parietal cortex supports serial learning by representing

271 s in the basal ganglia, anterior frontal and parietal cortex, thalamus, basal ganglia and cerebellum.

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

273 activity patterns in a subregion of lateral parietal cortex, the angular gyrus, supported successful

274 ems to elicit more activation in the temporo-parietal cortex, thereby suggesting enhanced sensitivity

275 In vivo, in the rat parietal cortex, these electrodes could detect brain NO

276 Within parietal cortex, this decreased branching was most evide

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

278 Human parietal cortex thus participates in the moment-to-momen

279 but the functional contributions of lateral parietal cortex to memory remain a topic of debate.

280 y suggesting enhanced sensitivity of temporo-parietal cortex to positive emotional stimuli at this st

281 interrupted the gait cycle, while posterior parietal cortex tracked obstacle location for planning f

282 networks, whereby prefrontal regions inhibit parietal cortex under internal implicit control.SIGNIFIC

283 tex (M1) and a small portion of premotor and parietal cortex using intracortical microstimulation in

284 orded simultaneously from medial and lateral parietal cortex using intracranial electrodes in three h

285 ispheric asymmetries have been identified in parietal cortex ventrolateral to visuotopic IPS.

286 The ventral lateral parietal cortex (VLPC) shows robust activation during ep

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

288 A BOLD signal change in right superior parietal cortex was associated with subsequent memory on

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

290 ht striatum, post-central gyrus and superior parietal cortex were observed when participants were hyp

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

292 suppression) is triggered and in the lateral parietal cortex when control is exerted, with the latter

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

294 e source of the inhibitory tagging signal to parietal cortex, where a neuronal instantiation of inhib

295 movement signals were strongest in posterior parietal cortex, where gradients of single-feature repre

296 field desynchronizations in sensorimotor and parietal cortex, whereas a number of cognitive task stud

297 ontal cortex, precentral gyrus, and inferior parietal cortex, whereas activation was higher in alcoho

298 ted how delay-period activity in frontal and parietal cortex, which is known to correlate with the de

299 is of single-neuron activity from the monkey parietal cortex, which reveals a mixture of directional

300 intraparietal sulcus (IPS) of the posterior parietal cortex while monkeys made choices about where t