ライフサイエンスコーパス: parietal cortex

1 regions (dorsolateral prefrontal cortex and parietal cortex).

2 ses is modulated similarly to prefrontal and parietal cortex.

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

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

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

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

7 bstract object identity information in human parietal cortex.

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

9 response for each voxel in human topographic parietal cortex.

10 representation of viewed action in anterior parietal cortex.

11 ual object size in bilateral human posterior parietal cortex.

12 and instead highlight the role of posterior parietal cortex.

13 us is selectively enhanced in prefrontal and parietal cortex.

14 resentation of viewed action in the anterior parietal cortex.

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

16 low reciprocally between primary sensory and parietal cortex.

17 orsolateral prefrontal cortex, and posterior parietal cortex.

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

19 unctional connectivity in lateral and medial parietal cortex.

20 electrode stereotactically implanted in the parietal cortex.

21 psilateral (right) visual hemifield in right parietal cortex.

22 al representation of developing decisions in parietal cortex.

23 the administration of anodal tDCS over right parietal cortex.

24 a cluster of eight electrodes over the right parietal cortex.

25 rasts with that of divisive normalization in parietal cortex.

26 essing by dorsolateral prefrontal cortex and parietal cortex.

27 ulcus, inferior temporal gyrus, and inferior parietal cortex.

28 ght cerebellar lobule VIIb and the posterior parietal cortex.

29 lation to concurrent activity in frontal and parietal cortex.

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

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

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

33 were quantified across AD disease stages in parietal cortex.

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

35 ctions in activity within bilateral inferior parietal cortex.

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

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

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

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

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

41 = .0003), with the largest reductions in the parietal cortex (-37.6%; P < .0001) and precuneus (-31.8

42 rom neural activity in medial prefrontal and parietal cortex 4 s before the participant reports they

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

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

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

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

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

48 y patterns in left (contralateral) motor and parietal cortex and also right (ipsilateral) motor corte

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

50 uced functional connectivity between lateral parietal cortex and dorsal anterior cingulate cortex.

51 ded the firing rates of neurons in posterior parietal cortex and FOF from rats performing a perceptua

52 sity discrimination task known to engage the parietal cortex and in which cue-integration and inhibit

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

54 (bodily self-consciousness [BSC]) in fronto-parietal cortex and more posterior temporo-parietal regi

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

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

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

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

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

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

61 eneral overview of the multiple roles of the parietal cortex and supports its crucial involvement in

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

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

64 so to working memory-related activity in the parietal cortex and the cerebellum.

65 ay, exogenous processing predominates in the parietal cortex and the endogenous control of attention

66 of other somatosensory areas in the anterior parietal cortex and the lateral sulcus, including areas

67 The posterior parietal cortex and the prefrontal cortex are associated

68 or elaborated memory representations in the parietal cortex, and at the same time reducing demands o

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

70 lates of such signals have been found in the parietal cortex, and in separate studies, demonstrated a

71 ventral temporal-occipital cortex, posterior parietal cortex, and medial temporal lobe.

72 ex, posteromedial prefrontal cortex, lateral parietal cortex, and posterior temporal cortex.

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

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

75 t amygdala, the left and right striatum, the parietal cortex, and the posterior cingulate on negative

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

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

78 encoding and nonspatial cognitive signals in parietal cortex, and whether cognitive signals are robus

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

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

81 ther types of functions known to involve the parietal cortex are influenced by a brief exposure to pr

82 Regions of frontal and posterior parietal cortex are known to control the allocation of s

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

84 The prefrontal cortex and posterior parietal cortex are likely to play an active role in the

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

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

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

88 areas that are homologous with the inferior parietal cortex (area PFG) in macaque monkeys.

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

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

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

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

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

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

95 hey further highlight the flexibility of the parietal cortex, because we find it to adapt its functio

96 a functional anatomical distinction in human parietal cortex between regions involved in maintaining

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

98 t between dorsolateral prefrontal cortex and parietal cortex (Brodmann areas 9 and 40) was related to

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

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

101 size that frames of reference for neurons in parietal cortex can depend on the type of sensory stimul

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

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

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

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

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

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

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

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

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

111 The posterior parietal cortex contains neurons that respond to visual

112 Posterior parietal cortex contains several areas defined by topogr

113 dorsal anterior cingulate, and the posterior parietal cortex, correlated positively with expected and

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

115 mance task, notably bilateral prefrontal and parietal cortex, did not show effects of THC.

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

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

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

119 orded spiking activity from macaque inferior parietal cortex during directional manipulation of an is

120 ings quantify the spatiotemporal dynamics of parietal cortex during episodic memory retrieval and pro

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

122 se, that LEC dysfunction could spread to the parietal cortex during preclinical disease and that APP

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

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

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

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

127 ses of the ventral temporal, prefrontal, and parietal cortex enabled decoding of both the type of tas

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

129 ultivoxel ensemble activity in the posterior parietal cortex encodes predicted value and salience in

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

131 ve (insula, caudate, anterior cingulate, and parietal cortex) event information.

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

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

134 tion and tool use, both in part dependent on parietal cortex expansion.

135 Interestingly, the parietal cortex flexibly changes its content of represen

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

137 in humans have emphasized the importance of parietal cortex for spatial navigation, and efforts to i

138 ed that subregions of the medial and lateral parietal cortex form key nodes of a larger brain network

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

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

141 Parietal cortex has long been known to be a site of sens

142 l and postural reference frames in posterior parietal cortex has traditionally been studied during fi

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

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

145 proposed that population-firing patterns in parietal cortex have one-dimensional dynamics on long ti

146 e-sensitive region in the inferior posterior parietal cortex (human 7a), which has connections to bot

147 It has been unclear whether parietal cortex implements target choice at the general

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

149 ngs highlight the importance of the inferior parietal cortex in associating behaviors with their outc

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

151 in bilateral ACC/mPFC, DLPFC, and posterior parietal cortex in both groups.

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

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

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

155 This finding emphasizes a motor role of parietal cortex in spatial choice making and contributes

156 processes are localized to the left lateral parietal cortex in the angular gyrus.

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

158 ng similarities between responses in lateral parietal cortex in the present study and those in a host

159 nal processes are localized to right lateral parietal cortex in the temporoparietal junction and long

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

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

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 ex and in several sub-regions of frontal and parietal cortex, independent of sustained increases in m

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

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

168 ng inferior frontal gyrus (IFG) and inferior parietal cortex (IPC).

169 "multiple-demand" (MD) system of frontal and parietal cortex is active in many different kinds of tas

170 Parietal cortex is central to spatial cognition.

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

172 The parietal cortex is highly multimodal and plays a key rol

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

174 e of gamma-band activity in posterior medial parietal cortex is modulated by the phase of thalamic al

175 Parietal cortex is often implicated in visual processing

176 cortex and hippocampus (dementia), inferior parietal cortex (late mild cognitive impairment and deme

177 e monkey prefrontal (frontal eye fields) and parietal cortex (lateral intraparietal area).

178 synchronization between the frontopolar and -parietal cortex leads to more inaccurate choices between

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

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

181 ssociated with increased activity in lateral parietal cortex (LPC)--"retrieval success effects" that

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

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

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

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

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

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

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

189 significantly more sources localized to the parietal cortex (odds ratio [OR] = 16.7).

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

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

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

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

194 We recorded neural activity in parietal cortex of monkeys in a time reproduction task.

195 Lesions of parietal cortex often lead to hemispatial neglect, an im

196 Anterior parietal cortex, on the other hand, showed clearest modu

197 tween these modules, either within posterior parietal cortex or downstream within frontal cortex, may

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

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

200 Human parietal cortex plays a central role in encoding visuosp

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

202 The posterior parietal cortex plays a central role in spatial function

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

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

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

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

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

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

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

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

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

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

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

214 The posterior parietal cortex (PPC) has traditionally been viewed as c

215 have unexpectedly implicated left posterior parietal cortex (PPC) in episodic retrieval, revealing d

216 tion (rTMS) applied over the right posterior parietal cortex (PPC) in healthy participants has been s

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

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

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

220 g to visual goals that occurs with posterior parietal cortex (PPC) lesions.

221 that populations of neurons in the posterior parietal cortex (PPC) may represent high-level aspects o

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

223 The posterior parietal cortex (PPC) receives diverse inputs and is inv

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

225 idually localized regions of human posterior parietal cortex (PPC) that are putatively involved in at

226 w dissociable contributions of the posterior parietal cortex (PPC) versus lateral occipital (LO) circ

227 athway communication, includes the posterior parietal cortex (PPC) where distinct effector-specific a

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

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

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

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

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

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

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

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

236 y reflected in the activity of the posterior parietal cortex (PPC): an identical set of voxels in thi

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

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

239 ments from the rostral division of posterior parietal cortex (PPCr).

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

241 n children with ADHD, including the inferior parietal cortex, precuneus, and superior temporal cortex

242 teral orbitofrontal cortex, insula, inferior parietal cortex, precuneus, superior temporal cortex, an

243 cingulate, retrosplenial cortex, and medial parietal cortex/precuneus is an epicenter of cortical in

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

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

246 distinct in terms of inputs from the ventral parietal cortex: projections to 6DR originated preferent

247 ived major inputs from the rostral posterior parietal cortex (putative homologs of areas PE, PF, and

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

249 These regions in the posterior parietal cortex required the presence of both brush and

250 ion of neurons suggesting that the posterior parietal cortex retains a constant representation of the

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

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

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

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

257 encoding-related activation in the posterior parietal cortex, selectively for salient objects that we

258 turn-related information from the posterior parietal cortex shift the subset of active hippocampal c

259 y voxels across occipito-temporal and fronto-parietal cortex shifted their tuning toward the attended

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 vidence suggests that neurons in the primate parietal cortex signal salience instead of value.

263 lar lobule VIIb interacts with the posterior parietal cortex, specifically during the late stages of

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

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

266 e at the general cognitive level, or whether parietal cortex subserves the choice of targets of parti

267 However, additional functions of parietal cortex, such as self-action control, may impose

268 c metabolic reductions involving frontal and parietal cortex, thalamus, and caudate nucleus.

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

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

271 itation and coordination within human fronto-parietal cortex that is guided by momentary attentional

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

273 nces in retrieval activity in left posterior parietal cortex, the results provide neural evidence for

274 nated in frontal area 6DR, ventral posterior parietal cortex, the retroinsular cortex, and area TPt.

275 at activity fluctuations in two sites of the parietal cortex, the superior parietal lobe and the ante

276 , particularly in the region of the inferior parietal cortex, there is extensive behavioral evidence

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 or inputs to POR originate in the visual and parietal cortex, thus providing neurons in MEC with a su

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

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

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

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

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

285 er volume of a region in the right posterior parietal cortex was significantly predictive of individu

286 For each voxel in the macaque temporal and parietal cortex we evaluated the similarity of its funct

287 tal cortex, but when we stimulated posterior parietal cortex, we found that stimulation directly affe

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

289 theta phase and amplitude recorded over parietal cortex were consistent when subjects walked thr

290 Although neural responses in frontal and parietal cortex were robust, they were non-specific with

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

292 We compared activity in the frontal and parietal cortex when subjects made visually, aurally, an

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

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

295 ociating simple actions and rewards, and the parietal cortex, which has been shown to represent task

296 ver a locally restricted region of the right parietal cortex, which is known to be involved in visuom

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

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

299 sion of electrical stimulation of the entire parietal cortex with the aim to evaluate the neurophysio

300 frames for reach targets in human posterior parietal cortex, with a gaze-centered reference frame fo