ライフサイエンスコーパス: posterior parietal cortex

1 the neural substrate of that linkage in the posterior parietal cortex.

2 network of several brain regions, including posterior parietal cortex.

3 ng a higher-level homunculus in the superior posterior parietal cortex.

4 rformance is associated with activity in the posterior parietal cortex.

5 acquired from area V6A of the monkey medial posterior parietal cortex.

6 ng from circumscribed lesions of frontal and posterior parietal cortex.

7 rences in functional organization with human posterior parietal cortex.

8 cuits for attention and eye movements in the posterior parietal cortex.

9 7 microA/cm(2), 10 min) to the left or right posterior parietal cortex.

10 ior cingulate cortex, prefrontal cortex, and posterior parietal cortex.

11 right orbitofrontal/inferior prefrontal and posterior parietal cortex.

12 contralateral visual hemifield within human posterior parietal cortex.

13 n of visual and proprioceptive inputs in the posterior parietal cortex.

14 ity between the dorsal prefrontal cortex and posterior parietal cortex.

15 reas, somatosensory areas S2 and PV, and the posterior parietal cortex.

16 ns of current pulses at rostral locations in posterior parietal cortex.

17 er connections from the lateral temporal and posterior parietal cortex.

18 sory areas 3a and 1, and the rostral half of posterior parietal cortex.

19 or regions, the somatosensory cortex and the posterior parietal cortex.

20 a), left premotor cortex, and left and right posterior parietal cortex.

21 was associated with activation in the right posterior parietal cortex.

22 s more likely to arise from connections with posterior parietal cortex.

23 rimotor areas including dmFC, precuneus, and posterior parietal cortex.

24 intention across monkey premotor, motor, and posterior parietal cortex.

25 ses to visual object size in bilateral human posterior parietal cortex.

26 s studies, and instead highlight the role of posterior parietal cortex.

27 the lateral intraparietal (LIP) area of the posterior parietal cortex.

28 cortex, dorsolateral prefrontal cortex, and posterior parietal cortex.

29 between right cerebellar lobule VIIb and the posterior parietal cortex.

30 trial types); (3) gamma power (35-60 Hz) in posterior parietal cortex 100 ms before cue onset (great

31 However, damage to the posterior parietal cortex, a critical brain region along

32 campal cortex projects preferentially to the posterior parietal cortex and area V4.

33 We recorded the firing rates of neurons in posterior parietal cortex and FOF from rats performing a

34 The posterior parietal cortex and frontal cortical areas to

35 Larger regions of posterior parietal cortex and frontal motor cortex are p

36 nt influence of DA over neuronal activity in posterior parietal cortex and in certain regions of the

37 as were more active during match delays, and posterior parietal cortex and inferior frontal cortex we

38 wed sustained alpha/micro suppression in the Posterior Parietal Cortex and Inferior Parietal Lobe, in

39 ereas the dorsal stream is directed into the posterior parietal cortex and is concerned with visuospa

40 nguish the encoding of decision variables in posterior parietal cortex and prefrontal cortex (frontal

41 jections from visuomotor areas including the posterior parietal cortex and premotor cortex.

42 from the dorsally directed activation of the posterior parietal cortex and right dorsolateral prefron

43 rent stimulation applied over the unlesioned posterior parietal cortex and the facilitatory effect of

44 ts from visuomotor cortical areas within the posterior parietal cortex and the frontal eye fields.

45 The posterior parietal cortex and the prefrontal cortex are

46 ate the short-latency connection between the posterior parietal cortex and the primary motor cortex (

47 al pattern of old > new activity in the left posterior parietal cortex and then right prefrontal cort

48 This relationship was apparent only in posterior-parietal cortex and not in other motor system

49 tion was stronger in auditory cortex than in posterior parietal cortex, and both regions contained ch

50 rea, cingulate motor areas, premotor cortex, posterior parietal cortex, and cerebellum.

51 lexity in ventral temporal-occipital cortex, posterior parietal cortex, and medial temporal lobe.

52 ant for the visuomotor processing within the posterior parietal cortex, and neuropsychological and ps

53 r area, somatosensory cortex, temporal lobe, posterior parietal cortex, and occipital lobe.

54 fferentially activated middle frontal gyrus, posterior parietal cortex, and posterior cingulate gyrus

55 rtex SI, secondary somatosensory cortex SII, posterior parietal cortex, and premotor cortex.

56 ventrotemporal occipital cortex (VTOC), the posterior parietal cortex, and the prefrontal cortex, pr

57 arietal rostroventral area, premotor cortex, posterior parietal cortex, and with the medial auditory

58 regions of the lateral prefrontal cortex and posterior parietal cortex are engaged uniformly by inter

59 Regions of frontal and posterior parietal cortex are known to control the alloc

60 The prefrontal cortex and posterior parietal cortex are likely to play an active r

61 hat backwards modulatory influences from the posterior parietal cortex are sufficient to account for

62 the signals measured from the monkey medial posterior parietal cortex are valid for correctly decodi

63 terior cortical areas, the retrosplenial and posterior parietal cortex, are involved in path integrat

64 y somatosensory cortex (S1, areas 3a and 2), posterior parietal cortex (area 5) and the deep cerebell

65 Here we show that neurons in the posterior parietal cortex (area LIP) represent elapsed t

66 transformed into decision-related signals in posterior parietal cortex (area LIP).

67 n in prefrontal cortex, premotor cortex, and posterior parietal cortex, areas that have previously be

68 d behavioural choices in auditory cortex and posterior parietal cortex as mice performed a sound loca

69 ascicle adjacent to primary sensorimotor and posterior parietal cortex, as well as grey matter volume

70 tor cortex, primary motor cortex, insula and posterior parietal cortex, as well as in contralateral p

71 ultiple nonmotor areas in the prefrontal and posterior parietal cortex, as well as the cortical motor

72 ted a robust topographic separation in human posterior parietal cortex associated with searching for

73 The findings suggest that the posterior parietal cortex automatically detects and enco

74 ranscranial magnetic stimulation to the left posterior parietal cortex biases this competitive proces

75 comparisons) were observed only in superior posterior parietal cortex bilaterally as a main effect o

76 ct cortical excitability in occipital versus posterior parietal cortex, calling into question the bro

77 direct current stimulation applied over the posterior parietal cortex can be used to modulate visuos

78 Lesions in human posterior parietal cortex can cause optic ataxia (OA), i

79 tic stimulation (TMS) of human occipital and posterior parietal cortex can give rise to visual sensat

80 al premotor cortex (PMV), the caudal half of posterior parietal cortex, cingulate cortex, visual area

81 SMA connections were with medial posterior parietal cortex, cingulate motor cortex, PMD,

82 p of the seen limb, whereas remapping in the posterior parietal cortex closely reflects changes in th

83 Although auditory cortex and posterior parietal cortex coded information by tiling in

84 We studied how the posterior parietal cortex combines new information with

85 Patients with lesions of the left posterior parietal cortex commonly fail in identifying t

86 Mountcastle and colleagues proposed that the posterior parietal cortex contains a "command apparatus"

87 The posterior parietal cortex contains neurons that respond

88 Posterior parietal cortex contains several areas defined

89 traparietal sulcus (area CIP), a part of the posterior parietal cortex, contribute to short-term memo

90 ns of the medial temporal lobe (MTL) and the posterior parietal cortex, contribute to source memory s

91 We investigated whether posterior parietal cortex controls attentional switching

92 sula, the dorsal anterior cingulate, and the posterior parietal cortex, correlated positively with ex

93 axons were present in certain regions (e.g., posterior parietal cortex, dentate gyrus) not previously

94 Stimulation of the right posterior parietal cortex did not alter hand choice, sug

95 ch cellular resolution imaging data from the posterior parietal cortex during a virtual memory-guided

96 vity in posterior inferior frontal gyrus and posterior parietal cortex during outcome anticipation.

97 into anatomically reorganized motor, but not posterior parietal, cortex eliminated behavioral gains f

98 tuning curve assays revealed that while the posterior parietal cortex encodes a graded value of the

99 how that multivoxel ensemble activity in the posterior parietal cortex encodes predicted value and sa

100 abeled neurons across a mediolateral belt of posterior parietal cortex extending from the medial wall

101 Stimulation to the the posterior parietal cortex facilitated numerical learning

102 It is widely agreed that the right posterior parietal cortex has a preeminent role in visuo

103 or parietal cortex are well established, the posterior parietal cortex has a relevant role in process

104 The primate posterior parietal cortex has been implicated in a large

105 Posterior parietal cortex has been traditionally associa

106 Specifically, we asked whether human posterior parietal cortex has prospective planning activ

107 Thus, posterior parietal cortex has prospective plans for upco

108 of spatial and postural reference frames in posterior parietal cortex has traditionally been studied

109 ing regions in the inferotemporal cortex and posterior parietal cortex, higher-order auditory and pol

110 ond saccade-sensitive region in the inferior posterior parietal cortex (human 7a), which has connecti

111 ction times, as well as with activity in the posterior parietal cortex [human lateral intraparietal a

112 whereas lesions of cholinergic afferents of posterior parietal cortex impaired the latter effects bu

113 in the primary sensorimotor, prefrontal, or posterior parietal cortex in an additional control monke

114 ller fALFF in bilateral ACC/mPFC, DLPFC, and posterior parietal cortex in both groups.

115 consecutive days on the contralesional, left posterior parietal cortex in patients suffering from sub

116 e imaging (fMRI) reduced fMRI activations in posterior parietal cortex in the dorsal stream and, surp

117 ty of experiments highlights a role of human posterior parietal cortex in visual working memory and a

118 etwork of cortical regions in prefrontal and posterior parietal cortex, include voluntary shifts of a

119 lls were also distributed more widely in the posterior parietal cortex, including areas 7a, 7m, LIP,

120 Recent studies show that activity in the posterior parietal cortex increases with working memory

121 elp place many recent findings regarding the posterior parietal cortex into a common conceptual frame

122 2), (4) dorsal occipital (V3A, V3B), and (5) posterior parietal cortex (IPS-0 to IPS-4).

123 Second, left FEF and left posterior parietal cortex (IPS1/2) generated stronger co

124 These results suggest that the posterior parietal cortex is a common hub for the contro

125 These results suggest that the posterior parietal cortex is a key neural locus of our i

126 results support the hypothesis that superior posterior parietal cortex is a supramodal area implicate

127 The posterior parietal cortex is centrally involved in this

128 The posterior parietal cortex is critical for on-line contro

129 unique in providing causal evidence that the posterior parietal cortex is involved in decisions of ha

130 The results indicate that the posterior parietal cortex is involved in the spatial pla

131 Therefore, we find evidence that the posterior parietal cortex is involved in transforming mu

132 l projection to the superior colliculus from posterior parietal cortex is not a characteristic of tre

133 in one node of this network: activity in the posterior parietal cortex is tightly correlated with the

134 basalis region, and their innervation of the posterior parietal cortex, is critical to these surprise

135 However, when tDCS was applied to the posterior parietal cortex, it had no effects on learning

136 Stronger coupling in posterior parietal cortex led to a population code with

137 ion in the left visual cortex, the bilateral posterior parietal cortex (left > right), and the fronta

138 Thus, posterior parietal cortex links visual and somatosensory

139 higher-order areas in lateral occipital and posterior parietal cortex (LOC, IPS1 and IPS2) responded

140 Posterior parietal cortex, located at the junction of mu

141 support for the hypothesis that the MTL and posterior parietal cortex make material-general contribu

142 To test whether the posterior parietal cortex may be a necessary source of s

143 esses and include lateral prefrontal cortex, posterior parietal cortex, medial prefrontal cortex, ros

144 Thus, the posterior parietal cortex might be a part of the network

145 n contrast, AL has stronger connections with posterior parietal cortex, motor cortex, and the spatial

146 to stimulate microelectrode sites throughout posterior parietal cortex, movements were elicited only

147 We tracked the activity of posterior parietal cortex neurons for a month as mice st

148 Coupling among posterior parietal cortex neurons was strong and extende

149 f activity in neurons of the LIP area of the posterior parietal cortex of alert behaving monkeys perf

150 es showed that lateral prefrontal cortex and posterior parietal cortex of high-capacity individuals a

151 ls in the parietal reach region (PRR) of the posterior parietal cortex of macaque monkeys have tempor

152 oups of single neurons within prefrontal and posterior parietal cortex of monkeys performing a task t

153 ty with the cortex of the lateral sulcus and posterior parietal cortex of owl monkeys, galagos, and m

154 Posterior parietal cortex of prosimian galagos consists

155 ections using the activity of neurons in the posterior parietal cortex of two monkeys.

156 Cortical fMRI variability in the posterior-parietal cortex of individual subjects explain

157 in two ways: (i) by cooling deactivation of posterior parietal cortex or (ii) in conjunction with br

158 actions between these modules, either within posterior parietal cortex or downstream within frontal c

159 elled by cooling of either the contralateral posterior parietal cortex or the contralateral superior

160 umerical notation while receiving TES to the posterior parietal cortex or the dorsolateral prefrontal

161 Magnetic stimulation of the right posterior parietal cortex or the right ventral occipital

162 tions labeled neurons across a large zone of posterior parietal cortex, overlapping the region projec

163 The posterior parietal cortex plays a central role in spatia

164 g between visual input and motor output, the posterior parietal cortex plays an important role in int

165 The parietal reach region (PRR) in the posterior parietal cortex plays an important role in the

166 rculum/inferior parietal cortex (PO/IP), and posterior parietal cortex (PP), areas that consistently

167 A key finding was that the multimodal posterior parietal cortex (PPC) also contributes substan

168 stimuli causes activity changes in the left posterior parietal cortex (PPC) and an assessment of tac

169 fMRI research suggests that both the posterior parietal cortex (PPC) and dorsolateral prefron

170 -with dorsal visual stream regions including posterior parietal cortex (PPC) and left secondary visua

171 mon, domain-independent transient signal [in posterior parietal cortex (PPC) and prefrontal cortex] t

172 er interconnected cortical areas such as the posterior parietal cortex (PPC) and the primary motor co

173 Previous work on monkeys suggests that the posterior parietal cortex (PPC) and ventral premotor cor

174 sal forebrain cholinergic projections to the posterior parietal cortex (PPC) are involved in regulati

175 The retrosplenial cortex (RSP) and the posterior parietal cortex (PPC) are the primary sources

176 r temporal gyrus (STG), and not in the right posterior parietal cortex (PPC) as conventionally though

177 s neuronal representations, we recorded from posterior parietal cortex (PPC) before and after trainin

178 cortical areas, whereas neural activity from posterior parietal cortex (PPC) can be used to decode co

179 We report that a subset of neurons in the posterior parietal cortex (PPC) closely reflect the choi

180 nt imaging studies have shown that the human posterior parietal cortex (PPC) contains four topographi

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

182 We test the hypothesis that the posterior parietal cortex (PPC) contributes to the contr

183 The posterior parietal cortex (PPC) controls allocation of a

184 patterned, coherent spiking activity in the posterior parietal cortex (PPC) coordinates the timing o

185 Our results show that the posterior parietal cortex (PPC) encodes memories for spa

186 to the rotated visual target location, while posterior parietal cortex (PPC) exhibited chance-level d

187 primate evolution, both largely dependent on posterior parietal cortex (PPC) expansion.

188 Current theories of posterior parietal cortex (PPC) function emphasize space

189 The posterior parietal cortex (PPC) has an important role in

190 The posterior parietal cortex (PPC) has traditionally been c

191 The posterior parietal cortex (PPC) has traditionally been v

192 High-level cognitive signals in the posterior parietal cortex (PPC) have previously been use

193 Single-cell studies of monkey posterior parietal cortex (PPC) have revealed the extens

194 Recent models of human posterior parietal cortex (PPC) have variously emphasize

195 aging data have unexpectedly implicated left posterior parietal cortex (PPC) in episodic retrieval, r

196 functionally distinct movement zones of the posterior parietal cortex (PPC) in galagos identified by

197 ic stimulation (rTMS) applied over the right posterior parietal cortex (PPC) in healthy participants

198 e implicated the prefrontal cortex (PFC) and posterior parietal cortex (PPC) in numerical judgments.

199 to study the functional organization of the posterior parietal cortex (PPC) in prosimian galagos.

200 Hypometabolism in the posterior parietal cortex (PPC) is among the first in vi

201 Posterior parietal cortex (PPC) is an extensive region o

202 The posterior parietal cortex (PPC) is believed to be involv

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

204 Posterior parietal cortex (PPC) is thought to be importa

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

206 The posterior parietal cortex (PPC) is thought to have a fun

207 The posterior parietal cortex (PPC) is thought to play an im

208 The human posterior parietal cortex (PPC) is widely believed to su

209 Because animals with posterior parietal cortex (PPC) lesions exhibit spatial

210 in reaching to visual goals that occurs with posterior parietal cortex (PPC) lesions.

211 suggested that populations of neurons in the posterior parietal cortex (PPC) may represent high-level

212 The posterior parietal cortex (PPC) of monkeys and prosimian

213 The posterior parietal cortex (PPC) of primates integrates s

214 The posterior parietal cortex (PPC) of rhesus monkeys has be

215 cues are used for spatial processing in the posterior parietal cortex (PPC) of the mammalian brain.

216 The posterior parietal cortex (PPC) receives diverse inputs

217 re has been an ongoing debate on whether the posterior parietal cortex (PPC) represents only spatial

218 y in individually localized regions of human posterior parietal cortex (PPC) that are putatively invo

219 st, we show dissociable contributions of the posterior parietal cortex (PPC) versus lateral occipital

220 Here, we report that ACC and posterior parietal cortex (PPC) were sensitive to distin

221 sm, interpathway communication, includes the posterior parietal cortex (PPC) where distinct effector-

222 ion (PRR) and dorsal area 5 (area 5d) in the posterior parietal cortex (PPC) while monkeys performed

223 n in dorsolateral prefrontal cortex (DLPFC), posterior parietal cortex (PPC), and inferior frontal gy

224 eas including medial agranular cortex (AGm), posterior parietal cortex (PPC), and visual association

225 eral agranular cortex (AGl), orbital cortex, posterior parietal cortex (PPC), and visual association

226 Posterior parietal cortex (PPC), BA 39, was non-modality

227 visuomotor transformations performed by the posterior parietal cortex (PPC), but to date there are f

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

229 l during decision making at sites within the posterior parietal cortex (PPC), dorsal prefrontal corte

230 table among these were subregions within the posterior parietal cortex (PPC), dorsal premotor cortex

231 The posterior parietal cortex (PPC), historically believed t

232 The primate posterior parietal cortex (PPC), part of the dorsal visu

233 hese include lateral agranular cortex (AGl), posterior parietal cortex (PPC), ventrolateral orbital c

234 To study online control mechanisms in the posterior parietal cortex (PPC), we recorded from single

235 We recognize three subdivisions of the posterior parietal cortex (PPC), which are architectonic

236 date component of decision circuits, the rat posterior parietal cortex (PPC).

237 chored in dorsolateral prefrontal cortex and posterior parietal cortex (PPC).

238 udies have revealed multiple visual areas in posterior parietal cortex (PPC).

239 ed representations for reach planning in the posterior parietal cortex (PPC).

240 e identified effector-related regions in the posterior parietal cortex (PPC).

241 of the input is selected, is mediated by the posterior parietal cortex (PPC).

242 tic ataxia" is caused by damage to the human posterior parietal cortex (PPC).

243 are consistent with those observed in monkey posterior parietal cortex (PPC).

244 n, including the prefrontal cortex (PFC) and posterior parietal cortex (PPC).

245 stence of a stiffness estimator in the human posterior parietal cortex (PPC).

246 for grasps can be derived from cells in the posterior parietal cortex (PPC).

247 activity in the precentral sulcus (PrCS) and posterior parietal cortex (PPC).

248 re neurally reflected in the activity of the posterior parietal cortex (PPC): an identical set of vox

249 a 6), primary motor cortex (MI, area 4), and posterior parietal cortex (PPC, area 5) while monkeys ma

250 /hMT+, primary somatosensory cortex (SI) and posterior parietal cortex (PPC; Brodmann areas 7/40).

251 evoke movements from the rostral division of posterior parietal cortex (PPCr).

252 uperior and inferior portions of neighboring posterior parietal cortex, predominantly in the left hem

253 attention (inferior temporal visual cortex, posterior parietal cortex, premotor cortex, and hippocam

254 n macaques and had connections restricted to posterior parietal cortex primarily associated with visu

255 he idea of two segregated populations in the posterior parietal cortex, PRR and LIP, that are involve

256 nd 8C received major inputs from the rostral posterior parietal cortex (putative homologs of areas PE

257 urrent stimulation applied over the lesioned posterior parietal cortex reduced symptoms of visuospati

258 e parietal reach region (PRR) located in the posterior parietal cortex represents targets for reachin

259 These regions in the posterior parietal cortex required the presence of both

260 s, whereas the lateral prefrontal cortex and posterior parietal cortex responded similarly whether ch

261 he population of neurons suggesting that the posterior parietal cortex retains a constant representat

262 Injections in posterior parietal cortex revealed that the rostral half

263 Grey matter volume in a region of right posterior parietal cortex (rPPC) is predictive of prefer

264 ctions, disynaptic connections were made via posterior parietal cortex (RSC-->PPC-->M2) and anteromed

265 cranial magnetic stimulation impulses to the posterior parietal cortex selectively disrupted the cont

266 revealed encoding-related activation in the posterior parietal cortex, selectively for salient objec

267 motion and turn-related information from the posterior parietal cortex shift the subset of active hip

268 ht cerebellar lobule VIIb interacts with the posterior parietal cortex, specifically during the late

269 es in the motor cortex, prefrontal cortices, posterior parietal cortex, striatum, and thalamus after

270 bserved in the inferior frontal junction and posterior parietal cortex, suggesting core roles for the

271 tions, displayed increased activation of the posterior parietal cortex, supporting the view that pari

272 A localized cluster of neurons in macaque posterior parietal cortex, termed the parietal reach reg

273 refrontal cortex, anterior cingulate cortex, posterior parietal cortex, thalamus, and caudate are eng

274 teral sulcus and more medial portions of the posterior parietal cortex than the PMV.

275 (2017) describe an inhibitory circuit in the posterior parietal cortex that evaluates conflicting aud

276 we identified three cortical areas in human posterior parietal cortex that exhibited topographic res

277 r problem-solving that includes the superior posterior parietal cortex, the horizontal segment of the

278 d by a neuroanatomical network involving the posterior parietal cortex, the posterior cingulate, and

279 ed differences in retrieval activity in left posterior parietal cortex, the results provide neural ev

280 puts originated in frontal area 6DR, ventral posterior parietal cortex, the retroinsular cortex, and

281 d by a restricted network involving the left posterior parietal cortex, the right anterior intermedia

282 ndition, they were stimulated over the right posterior parietal cortex, the right or left dorsal occi

283 decoding reach trajectories from the medial posterior parietal cortex, this highlights the medial pa

284 ections were placed in frontal cortex and in posterior parietal cortex to define the connections of m

285 tomical tracers into M1, M2, 3a, 3b, SC, and posterior parietal cortex to establish the ipsilateral c

286 g reduced cytochrome oxidase activity in the posterior parietal cortex, ventral tegmental area, and s

287 al network, interhemispheric connectivity in posterior parietal cortex was acutely disrupted but full

288 In contrast, activation of the posterior parietal cortex was predicted by risk preferen

289 ty between the ventral prefrontal cortex and posterior parietal cortex was relatively greater in pati

290 gray matter volume of a region in the right posterior parietal cortex was significantly predictive o

291 ffective connectivity between MT/MST and the posterior parietal cortex was stronger in deaf than in h

292 edial-frontal cortex, but when we stimulated posterior parietal cortex, we found that stimulation dir

293 the organization of motor representations in posterior parietal cortex, we test how three motor varia

294 Finally, ventrolateral PFC and posterior parietal cortex were more active during both u

295 ual areas, we also discovered an area in the posterior parietal cortex where activity patterns allowe

296 e of activity was substantially different in posterior parietal cortex, where transient increases in

297 significant interaction effects in bilateral posterior parietal cortex, which is compatible with evid

298 nks of the intraparietal sulcus (IPS) of the posterior parietal cortex while monkeys made choices abo

299 ble coding frames for reach targets in human posterior parietal cortex, with a gaze-centered referenc

300 ory cortex to both motor cortex and inferior posterior parietal cortex, with the latter area also exe