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

1 ations of error magnitude and past errors in posterior parietal cortex.

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

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

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

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

6 ng throughout the dorsal visual pathway into posterior parietal cortex.

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

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

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

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

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

12 rences in functional organization with human posterior parietal cortex.

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

14 7 microA/cm(2), 10 min) to the left or right posterior parietal cortex.

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

16 right orbitofrontal/inferior prefrontal and posterior parietal cortex.

17 contralateral visual hemifield within human posterior parietal cortex.

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

19 to the expansion and areal complexity of the posterior parietal cortex.

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

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

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

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

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

25 due to a disinhibition of the homotopic left posterior parietal cortex.

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

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

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

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

30 al modulation predominantly over ipsilateral posterior-parietal cortex.

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

32 Our work focuses on the posterior parietal cortex, a brain region supporting sho

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

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

35 The posterior parietal cortex and frontal cortical areas to

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

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

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

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

42 poral visual cortex in carnivores, where the posterior parietal cortex and the central temporal regio

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 erstanding the evolution and function of the posterior parietal cortex and the frontoparietal network

46 The posterior parietal cortex and the prefrontal cortex are

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

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

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

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

51 for saccade generation (frontal eye fields, posterior parietal cortex, and higher-level visual areas

52 to 12,000 neurons in mouse auditory cortex, posterior parietal cortex, and hippocampus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

82 The posterior parietal cortex contains neurons that respond

83 Posterior parietal cortex contains several areas defined

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

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

86 eas, nor in PFC, whereas microstimulation in posterior parietal cortex did activate the ITC.

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

88 en described in the medial temporal lobe and posterior parietal cortex, discuss their properties, and

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

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

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

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

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

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

95 Stimulation to the the posterior parietal cortex facilitated numerical learning

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

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

98 Posterior parietal cortex has been traditionally associa

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

100 Thus, posterior parietal cortex has prospective plans for upco

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

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

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

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

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

106 stimulation (cTBS) was applied over the left posterior parietal cortex in a randomized clinical trial

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

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

109 ng long-term calcium imaging recordings from posterior parietal cortex in mice (Mus musculus), we sho

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

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

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

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

114 We recorded the activity of posterior parietal cortex (including lateral intrapariet

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

116 2), (4) dorsal occipital (V3A, V3B), and (5) posterior parietal cortex (IPS-0 to IPS-4).

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

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

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

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

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

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

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

124 The right posterior parietal cortex is part of a broad cortical ne

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

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

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

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

129 y, those with FOG had less activation of the posterior parietal cortex, less deactivation of the dors

130 Thus, posterior parietal cortex links visual and somatosensory

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

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

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

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

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

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

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

138 Coupling among posterior parietal cortex neurons was strong and extende

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

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

141 red excitatory and inhibitory neurons in the posterior parietal cortex of mice judging multisensory s

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

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

144 Posterior parietal cortex of prosimian galagos consists

145 connectional similarities exist between the posterior parietal cortex of the ferret (PPc and PPr) an

146 The two divisions of posterior parietal cortex of the ferret are strongly int

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

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

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

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

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

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

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

154 The posterior parietal cortex plays a central role in spatia

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

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

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

158 Posterior parietal cortex (PPC) activity correlates with

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

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

161 - and maintenance-related impairments in the posterior parietal cortex (PPC) and frontal eye fields (

162 N known from fMRI studies emerged, including posterior parietal cortex (PPC) and hippocampus.

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

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

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

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

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

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

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

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

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

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

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

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

175 Neurons in posterior parietal cortex (PPC) control several effector

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

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

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

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

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

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

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

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

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

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

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

187 t stressors (RMS) on the connectivity of the posterior parietal cortex (PPC) in adolescent male mice.

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

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

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

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

192 The posterior parietal cortex (PPC) in rodents is reciprocal

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

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

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

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

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

198 orimotor behavior.SIGNIFICANCE STATEMENT The posterior parietal cortex (PPC) is thought to merge info

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

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

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

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

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

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

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

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

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

208 This study evaluated the influence of right posterior parietal cortex (PPC) on a direct measure of v

209 The posterior parietal cortex (PPC) performs many functions,

210 The posterior parietal cortex (PPC) receives diverse inputs

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

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

213 ate that interfering with left but not right posterior parietal cortex (PPC) using high-definition ca

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

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

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

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

218 ctrode recording arrays are implanted in the posterior parietal cortex (PPC), a high-level cortical a

219 e properties of L3PNs in monkey DLPFC versus posterior parietal cortex (PPC), a key node in the corti

220 functional connections between PIVC and the posterior parietal cortex (PPC), a major brain region of

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

222 re regions: medial prefrontal cortex (mPFC), posterior parietal cortex (PPC), and the medial parietal

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

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

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

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

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

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

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

230 ptome of L3PNs from macaque monkey DLPFC and posterior parietal cortex (PPC), two key nodes in the co

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

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

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

234 ortex (V1), anterior cingulate cortex (ACC), posterior parietal cortex (PPC), while freely moving rat

235 ut in higher-order sensory areas such as the posterior parietal cortex (PPC).

236 activity in the precentral sulcus (PrCS) and 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 date component of decision circuits, the rat 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 re neurally reflected in the activity of the posterior parietal cortex (PPC): an identical set of vox

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

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

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

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

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

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

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

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

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

257 ch dynamics were revealed within the control posterior parietal cortex region.

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 dorsolateral prefrontal cortex (rDLPFC) and posterior parietal cortex (rPPC).

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

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

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

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

269 c connectivity, cTBS over the contralesional posterior parietal cortex significantly improves and acc

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

271 That activity was followed by similar posterior parietal cortex spectral power increase that d

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

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

274 The neural data suggest that posterior parietal cortex supports serial learning by re

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

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

277 (2017) describe an inhibitory circuit in the posterior parietal cortex that evaluates conflicting aud

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

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

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

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

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

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 tor cortex interrupted the gait cycle, while posterior parietal cortex tracked obstacle location for

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

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

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

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

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

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 nsory and movement signals were strongest in posterior parietal cortex, where gradients of single-fea

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