ライフサイエンスコーパス: intraparietal

1 V3a within caudal PPC, referred to as caudal intraparietal-1 (CIP-1) and CIP-2.

2 Here we report that the anterior intraparietal (AIP) and the rostral ventral premotor are

3 The macaque anterior intraparietal (AIP) area has been implicated in the extr

4 pes using spiking activity from the anterior intraparietal (AIP), ventral premotor (F5), and primary

5 We found long-range intraparietal and frontoparietal correlations that displ

6 (supramarginal gyrus) and superior parietal (intraparietal and superior parietal) regions that show s

7 ted a reproducible set of bilateral frontal, Intraparietal, and ventrolateral temporal regions.

8 The network formed by macaque anterior intraparietal area (AIP) and hand area (F5) of the ventr

9 ediates grasping in primates are in anterior intraparietal area (AIP) and ventral premotor cortex (PM

10 essing of others' actions, with the anterior intraparietal area (AIP) playing a major role in routing

11 or grasping circuit, comprising the anterior intraparietal area (AIP), ventral premotor (PMv), and pr

12 ating single-neuron activity in the anterior intraparietal area (AIP).

13 lates of this property in the macaque caudal intraparietal area (CIP) by measuring slant tuning curve

14 eversible inactivation of the macaque caudal intraparietal area (CIP) during functional magnetic reso

15 nknown, but prior studies suggest the caudal intraparietal area (CIP) may be involved.

16 bpopulation of neurons in the macaque caudal intraparietal area (CIP) visually encodes object tilt in

17 Although the lateral intraparietal area (LIP) and frontal eye field (FEF) are

18 e superior temporal sulcus (FST) and lateral intraparietal area (LIP) and the animals correctly locat

19 motor response tasks, neurons in the lateral intraparietal area (LIP) and the frontal eye fields (FEF

20 after a saccade, gain fields in the lateral intraparietal area (LIP) are unreliable.

21 have shown that some neurons in the lateral intraparietal area (LIP) exhibit anticipatory remapping:

22 The lateral intraparietal area (LIP) has been implicated as a salien

23 The macaque lateral intraparietal area (LIP) has been implicated in both pro

24 lucidate these circuits, the primate lateral intraparietal area (LIP) has been interpreted as a prior

25 neurophysiological responses in the lateral intraparietal area (LIP) have received extensive study f

26 al prefrontal cortex (dlPFC) and the lateral intraparietal area (LIP) in monkeys using a memory sacca

27 The lateral intraparietal area (LIP) in the macaque contains a prior

28 ffects visual salience in the monkey lateral intraparietal area (LIP) in ways that are independent of

29 We tested the hypothesis that the lateral intraparietal area (LIP) integrates disparate task-relev

30 The lateral intraparietal area (LIP) is essential for this process.

31 previously found that neurons in the lateral intraparietal area (LIP) of Macaca mulatta reflect learn

32 in the frontal eye fields (FEFs) and lateral intraparietal area (LIP) of macaques are preferentially

33 It has been suggested that the lateral intraparietal area (LIP) of macaques plays a fundamental

34 n the firing rates of neurons in the lateral intraparietal area (LIP) of rhesus monkeys performing th

35 gest that neural activity in macaque lateral intraparietal area (LIP) provides a useful window into t

36 For example, neurons in the lateral intraparietal area (LIP) reflect learned associations be

37 Firing rates of neurons in the lateral intraparietal area (LIP) reflected the accumulation of l

38 ted by eye movements, neurons in the lateral intraparietal area (LIP) represent the accumulation of e

39 indicate that neural activity in the lateral intraparietal area (LIP) represents the gradual accumula

40 Recordings in the lateral intraparietal area (LIP) reveal that parietal cortex enc

41 appears substantially earlier in the lateral intraparietal area (LIP) than in an anatomically connect

42 that the responses of neurons in the lateral intraparietal area (LIP) to a task-irrelevant distractor

43 fine retinotopic maps in the macaque lateral intraparietal area (LIP) using histological, electrophys

44 from populations of neurons from the lateral intraparietal area (LIP), a cortical node in the NHP sac

45 To answer this, we focus on the lateral intraparietal area (LIP), an area that has been shown to

46 fter cue in frontal eye field (FEF), lateral intraparietal area (LIP), and cuneus support early cover

47 om macaque frontal eye fields (FEF), lateral intraparietal area (LIP), and pulvinar.

48 etal neurons, such as in the macaque lateral intraparietal area (LIP), are strongly influenced by vis

49 ed single-neuron recordings from the lateral intraparietal area (LIP), during a perceptual decision-m

50 (V4), inferior temporal cortex (IT), lateral intraparietal area (LIP), prefrontal cortex (PFC), and f

51 recorded from single neurons in the lateral intraparietal area (LIP), which has been implicated in t

52 nts may be guided by activity in the lateral intraparietal area (LIP), which is thought to represent

53 pharmacological inactivation of the lateral intraparietal area (LIP), which plays a role in the sele

54 neural correlate of decisions in the lateral intraparietal area (LIP).

55 onal category representations in the lateral intraparietal area (LIP).

56 he internal circuitry of the primate lateral intraparietal area (LIP).

57 al bank of the intraparietal sulcus [lateral intraparietal area (LIP)] specifically biased choices ma

58 the posterior parietal cortex [human lateral intraparietal area (LIP)], the anterior cingulate cortex

59 rietal areas by comparing LIP and the medial intraparietal area (MIP) during a visual categorization

60 w that reach-related neurons from the medial intraparietal area (MIP) exhibit a gradual modulation of

61 ved in reach planning, area 5 and the medial intraparietal area (MIP), as animals reached to visual,

62 ecorded at the same electrode in the ventral intraparietal area (VIP) and the lateral prefrontal cort

63 at vestibular heading signals in the ventral intraparietal area (VIP) are represented in body-centere

64 The ventral intraparietal area (VIP) of the macaque monkey brain is

65 nsular vestibular cortex (PIVC), the ventral intraparietal area (VIP), and the dorsal medial superior

66 edial superior temporal area (MSTd), ventral intraparietal area (VIP), and visual posterior sylvian a

67 uperior temporal area (MSTd) and the ventral intraparietal area (VIP), have been shown to integrate v

68 er-level motion areas, including the ventral intraparietal area (VIP), medial superior temporal area,

69 estibular self-motion signals in the ventral intraparietal area (VIP), parietoinsular vestibular cort

70 the anatomical definition of monkey ventral intraparietal area (VIP).

71 ibular and optic flow signals is the ventral intraparietal area (VIP).

72 intraparietal sulcus encompassing the medial intraparietal area and area 5V.

73 y in parietal areas V6, V6A, LIP, and caudal intraparietal area and frontal areas FEF, 45a, 45b, and

74 We suggest medial intraparietal area and V6/V6A as functional counterparts

75 Neural responses in the ventral intraparietal area are modulated by the task reference f

76 Much evidence implicates the lateral intraparietal area as a candidate priority map in the ma

77 d electrical microstimulation in the lateral intraparietal area during a visuospatial discrimination

78 posterior parietal cortex (including lateral intraparietal area LIP) neurons while monkeys learned 7-

79 We demonstrate that decision-related lateral intraparietal area neurons typically undergo gradual cha

80 the frontal eye field (FEF), and the lateral intraparietal area of macaque monkeys during a visuomoto

81 orded from individual neurons in the lateral intraparietal area of monkeys performing a task that inc

82 e in the association areas, PFC, and ventral intraparietal area of rhesus monkeys and found that adja

83 e marmoset frontal eye field-and the lateral intraparietal area of two male marmosets and recorded ne

84 Neuronal responses in the monkey lateral intraparietal area revealed that bound changes are imple

85 This intraparietal area showed stronger responses when the go

86 a better statistical description of lateral intraparietal area spike trains than diffusion-to-bound

87 ccade task while we recorded from the caudal intraparietal area using laminar probes.

88 orded the activity of neurons in the lateral intraparietal area while monkeys performed an intertempo

89 tal eye fields) and parietal cortex (lateral intraparietal area).

90 including the frontal eye field and lateral intraparietal area, and one of their direct, subcortical

91 n-selective dorsal stream areas, the lateral intraparietal area, and the frontal eye fields.

92 s activated parietal areas V6/V6A and medial intraparietal area, caudo-dorsal visual areas, the most

93 It will describe evidence that the lateral intraparietal area, frontal eye field and superior colli

94 acaques (lateral intraparietal area, ventral intraparietal area, middle temporal area, and the medial

95 merosity was encoded earlier in area ventral intraparietal area, suggesting that numerical informatio

96 In the ventral intraparietal area, the choice correlations are also con

97 macaques, the circuit spanning the anterior intraparietal area, the hand area of the ventral premoto

98 l areas of behaving rhesus macaques (lateral intraparietal area, ventral intraparietal area, middle t

99 esentation of heading in the macaque ventral intraparietal area.

100 rea PE to 6DC were particularly dense, while intraparietal areas (especially the putative homolog of

101 f the macaque brain: the lateral and ventral intraparietal areas (LIP; VIP), the middle temporal area

102 Conversely, medial and anterior intraparietal areas (MIP and AIP), and parietal area PEi

103 medial superior temporal (MSTd) and ventral intraparietal areas.

104 -matter in ventral prefrontal, premotor, and intraparietal brain areas.

105 connectivity of human superior parietal and intraparietal clusters with frontal and extrastriate cor

106 ce imaging in humans, we show that the right intraparietal cortex (IPC) and inferior frontal gyrus (I

107 Activity of the neurons in the lateral intraparietal cortex (LIP) displays a mixture of sensory

108 e in oculomotor control, such as the lateral intraparietal cortex (LIP), the frontal eye fields (FEF)

109 s have reported multiple topographic maps in intraparietal cortex and robust responses to ipsilateral

110 e we show that neurons in the monkey lateral intraparietal cortex encode a relative form of saccadic

111 ortant decisions on estimates of number, and intraparietal cortex is thought to provide a crucial sub

112 model of neural responses (e.g., in lateral intraparietal cortex) and reaction time for discriminati

113 in saccade-related neurons in monkey lateral intraparietal cortex.

114 analog of the priority map in monkey lateral intraparietal cortex.

115 ve strategy) are coded in the human anterior intraparietal cortex.

116 lected in neural responses, e.g., in lateral intraparietal cortex.

117 ding and reversibly inactivating the lateral intraparietal (LIP) and middle temporal (MT) areas of rh

118 ly compared neuronal activity in the lateral intraparietal (LIP) area and PFC in monkeys performing a

119 ognitive and spatial encoding in the lateral intraparietal (LIP) area by training monkeys to perform

120 Neurons in the macaque lateral intraparietal (LIP) area exhibit firing rates that appea

121 licated sensorimotor regions such as lateral intraparietal (LIP) area in perceptual decision making.

122 n are combined across neurons in the lateral intraparietal (LIP) area of the posterior parietal corte

123 nses in the middle temporal (MT) and lateral intraparietal (LIP) areas appear to map onto theoretical

124 onclusion that neurons in the monkey lateral intraparietal (LIP) cortical area encode only cue salien

125 Lateral intraparietal (LIP) neurons encode a vast array of senso

126 alternative saccadic eye movements, lateral intraparietal (LIP) neurons representing each saccade fi

127 dings from the middle temporal (MT), lateral intraparietal (LIP), and ventral intraparietal (VIP) are

128 cortical areas (visual area 4 [V4], lateral intraparietal [LIP], posterior parietal area 7A, frontal

129 d (60-80 Hz) that was localized to the right intraparietal lobule and left Brodmann area 9 (BA9).

130 Connections with intraparietal, prefrontal, and temporal areas were very

131 upport to the functional role of the lateral intraparietal region of the brain as a primary area of i

132 work between posterior inferior temporal and intraparietal regions likely linking visual, phonologica

133 orks comprising the visual cortex, bilateral intraparietal sulci, and frontal eye fields.

134 specific to the number task confined to the intraparietal sulci.

135 emonstrate the participation of the anterior intraparietal sulcus (aIPS) and ventral premotor cortex

136 The anterior intraparietal sulcus (aIPS) might support the integratio

137 the superior parietal lobe and the anterior intraparietal sulcus (aIPS), correlated specifically wit

138 biological motion is coded and the anterior intraparietal sulcus (aIPS), where movement information

139 dorsolateral circuit comprising the anterior intraparietal sulcus (aIPS).

140 for both protocols, which included the right intraparietal sulcus (BA 7/40), the right middle frontal

141 y of two regions in this network, the dorsal intraparietal sulcus (DIPS) and the ventral premotor cor

142 dorsolateral prefrontal cortex (dlPFC), and intraparietal sulcus (iPS) - brain regions important for

143 brief TMS bursts (or Sham-TMS) to the dorsal intraparietal sulcus (IPS) 100 ms after visual stimulus

144 cy, based on an interaction between the left intraparietal sulcus (IPS) and a region implicated in vi

145 of the spatial attention network, including intraparietal sulcus (IPS) and frontal eye field (FEF),

146 sustained spatially selective modulations in intraparietal sulcus (IPS) and frontal-eye field (FEF),

147 ated HGP was observed, with activity in left intraparietal sulcus (IPS) and left superior parietal lo

148 We focus on the intraparietal sulcus (IPS) and specifically probe its in

149 orsal frontoparietal network, comprising the intraparietal sulcus (IPS) and the frontal eye fields (F

150 s demonstrate significant activations in the intraparietal sulcus (IPS) and the superior temporal sul

151 eye movement planning can begin, however, an intraparietal sulcus (IPS) area, putative LIP, participa

152 ior frontal junction (IFJ) and over the left intraparietal sulcus (IPS) during task preparation.

153 revealed a distinct activation in the right intraparietal sulcus (IPS) for Flanker interference and

154 ue, or numerosity, have been observed in the intraparietal sulcus (IPS) in monkeys and humans, includ

155 It provides evidence that the superior intraparietal sulcus (IPS) is a critical brain region th

156 The intraparietal sulcus (IPS) is structurally and functiona

157 ivity in the lateral and medial banks of the intraparietal sulcus (IPS) of the posterior parietal cor

158 ventromedial prefrontal cortex (VMPFC), and intraparietal sulcus (IPS) predicted individual differen

159 The intraparietal sulcus (IPS) region is uniquely situated a

160 patches in the anterior part of the macaque intraparietal sulcus (IPS) showing the same depth struct

161 ed with offer quality, while activity in the intraparietal sulcus (IPS) specifically correlated with

162 e revealed a topographic organization in the intraparietal sulcus (IPS) that mirrors the retinotopic

163 Activity in the intraparietal sulcus (IPS) tightly correlates with the n

164 a network of dACC, anterior insula (AI), and intraparietal sulcus (IPS) to be more active when effort

165 We propose a partitioning of the primate intraparietal sulcus (IPS) using immunoarchitectural and

166 Specifically, in superior intraparietal sulcus (IPS), a region previously shown to

167 Neural maturity in the intraparietal sulcus (IPS), a region with a known role i

168 he bottom-up representation is scaled by the intraparietal sulcus (IPS), and that the level of IPS en

169 n activity in this area, especially the left intraparietal sulcus (IPS), and the degree of the crosse

170 te fMRI responses being reported in superior intraparietal sulcus (IPS), but robust multivariate deco

171 spatial attention after rTMS over the right intraparietal sulcus (IPS), but the size of this effect

172 r specific: eye specificity in the posterior intraparietal sulcus (IPS), hand tuning in anterior IPS,

173 ciated with enhanced performance, with right intraparietal sulcus (IPS), left IPS, and right frontal

174 s in primary visual cortex (V1) and superior intraparietal sulcus (IPS), measured during the WM task

175 (V1), the frontal eye fields (FEF), and the intraparietal sulcus (IPS), modulations related to spati

176 We report that a single brain region, the intraparietal sulcus (IPS), shows both elevated neural a

177 In intraparietal sulcus (IPS), we observed the analogous ef

178 ulated by an attention-sensitive region, the intraparietal sulcus (IPS), which sometimes showed a sim

179 on and multiple visual maps exist within the intraparietal sulcus (IPS), with each hemisphere symmetr

180 ow that dorsal parietal cortex-specifically, intraparietal sulcus (IPS)-was engaged during top-down a

181 z bursts of four TMS (or Sham) pulses to the intraparietal sulcus (IPS).

182 , and from the medial bank and fundus of the intraparietal sulcus (IPS).

183 al eye field (FEF) and the cortex within the intraparietal sulcus (IPS).

184 junction (TPJ), and areas near or along the intraparietal sulcus (IPS).

185 n a frontoparietal network that includes the intraparietal sulcus (IPS).

186 onal trial-by-trial variability quarried the intraparietal sulcus (IPS).

187 or cingulate cortex, inferior frontal gyrus, intraparietal sulcus (IPS)].

188 ontrast, the frontal eye field (FEF) and the intraparietal sulcus (IPS0-4) form a circuitry that conc

189 riority map candidates along human posterior intraparietal sulcus (IPS0-IPS3) and two along the prece

190 ), middle frontal gyrus (MFG), LIP, anterior intraparietal sulcus (IPSa)] that may coordinate the tra

191 in the left posterior reading network - left intraparietal sulcus (L.IPS) and left fusiform gyrus (L.

192 r to area V3a and extending into the lateral intraparietal sulcus (LIP) was found.

193 gyrus (LpMTG), left angular gyrus, and left intraparietal sulcus (LIPS), in addition to object- and

194 was no difference between the groups in the intraparietal sulcus (P > 0.574).

195 The right intraparietal sulcus (rIPS) is a key region for the endo

196 cingulate motor areas (CMA), and the ventral intraparietal sulcus (VIP) and compared them to previous

197 maintaining attention to a location [ventral intraparietal sulcus (vIPS)] and a region involved in sh

198 ound that lesions on the lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)]

199 s, whereas lesions on the medial bank of the intraparietal sulcus [parietal reach region (PRR)] speci

200 left posterior temporal cortex, and the left intraparietal sulcus and adjacent regions.

201 arietal grasp regions, namely, left anterior intraparietal sulcus and bilateral superior parietal lob

202 association sensorimotor cortex, in the left intraparietal sulcus and dorsal premotor cortex, as well

203 ces, and two higher-order regions within the intraparietal sulcus and dorsolateral prefrontal cortex.

204 from anterior sectors of the medial bank of intraparietal sulcus and from the ventral premotor corte

205 ers showed greater activity in left anterior intraparietal sulcus and inferior frontal gyrus, regions

206 the right PPC spanning a region between the intraparietal sulcus and inferior parietal lobe were sig

207 found the neural signature of an SPE in the intraparietal sulcus and lateral prefrontal cortex, in a

208 T was significantly greater in the bilateral intraparietal sulcus and left angular gyrus in both adol

209 for the grip component in bilateral anterior intraparietal sulcus and left ventral premotor cortex; n

210 ronger functional connectivity with anterior intraparietal sulcus and LOtv during the haptic than vis

211 between SNPs in CRHR1 and metabolism in the intraparietal sulcus and precuneus.

212 ore, we recorded from neurons in the ventral intraparietal sulcus and the dorsolateral prefrontal cor

213 ntoparietal attention network, including the intraparietal sulcus and the inferior frontal gyrus.

214 ore than participants with ADHD in the right intraparietal sulcus and the left lateral cerebellum in

215 ferior frontal sulcus)] and parietal cortex [intraparietal sulcus areas (IPS1-IPS5) and an area in th

216 hMT+) and frontal and parietal areas (e.g., intraparietal sulcus areas IPS1-IPS4 and frontal eye fie

217 tal gyrus (MFG), inferior frontal gyrus, and intraparietal sulcus correlated with the magnitude of pr

218 , trained on the patterns of activity in the intraparietal sulcus could classify both the type of cue

219 e same time, greater activation in the right intraparietal sulcus during calculation, a region establ

220 the three control-related variables, whereas intraparietal sulcus encoded response complexity and the

221 e macaque, located in the medial bank of the intraparietal sulcus encompassing the medial intrapariet

222 d problems and the horizontal segment of the intraparietal sulcus for the number problems.

223 usal structure the frontal eye field and the intraparietal sulcus form a circuitry that integrates au

224 howed LIMK1 haplotype-related differences in intraparietal sulcus functional connectivity localized t

225 rom the general population, we asked whether intraparietal sulcus functional connectivity patterns si

226 ndrome cohort exhibited opposite patterns of intraparietal sulcus functional connectivity with visual

227 nt for neuronal maturation and migration, on intraparietal sulcus functional connectivity.

228 Stimulation over right ventral intraparietal sulcus impaired target discrimination at c

229 etal cortex locations (frontal eye field and intraparietal sulcus in each hemisphere) to identify reg

230 subsequent analysis, we report that the same intraparietal sulcus neural populations are activated wh

231 vidence of numerical distance effects in the intraparietal sulcus of the developing brain, those effe

232 disruption was used to demonstrate that the intraparietal sulcus played a causal role both in decisi

233 Representations in the intraparietal sulcus reflect actively remembered informa

234 tivations of neuronal populations within the intraparietal sulcus region during an experimental arith

235 ar functional specialization within the left intraparietal sulcus region.

236 there is developmental continuity in how the intraparietal sulcus represents the values of numerositi

237 efined a target brain phenotype by comparing intraparietal sulcus resting functional connectivity in

238 For between-group analyses, differences in intraparietal sulcus resting-state functional connectivi

239 FA), superior temporal sulcus, amygdala, and intraparietal sulcus showed overall reduced neural respo

240 modulates activity in a portion of the left intraparietal sulcus that has previously been shown to b

241 option quantity correlates with areas of the intraparietal sulcus that have previously been associate

242 f motion signals, as well as a region in the intraparietal sulcus thought to be involved in perceptua

243 ariations in two human DLG4 SNPs and reduced intraparietal sulcus volume and abnormal cortico-amygdal

244 Stimulation of the intraparietal sulcus was associated with the occurrence

245 rietal cortex, the horizontal segment of the intraparietal sulcus which is hypothesized to be involve

246 the right middle temporal gyrus and the left intraparietal sulcus with the orbital frontal cortex.

247 rsal attention circuits (frontal eye fields, intraparietal sulcus).

248 Activity in the intraparietal sulcus, a main area in the dorsal frontopa

249 with awareness was found in the banks of the intraparietal sulcus, a region connected to the dorsal a

250 t decision context is represented within the intraparietal sulcus, an area previously shown to be fun

251 ration localized to lateral premotor cortex, intraparietal sulcus, and posterior superior cerebellar

252 f the macaque PRR, in the medial wall of the intraparietal sulcus, and produced the hallmarks of OA,

253 While the frontal eye fields (FEFs), intraparietal sulcus, and temporoparietal junction (TPJ)

254 onse to value in the inferior parietal gyrus/intraparietal sulcus, and that this effect predominated

255 dial and dorsolateral prefrontal cortex, the intraparietal sulcus, and the anterior insula.

256 including the motion-sensitive area MT+, the intraparietal sulcus, and the inferior frontal sulcus.

257 t ventrolateral prefrontal cortex, the right intraparietal sulcus, and the midcingulate/presupplement

258 seeds and by relative hypoconnectivity with intraparietal sulcus, anterior insula, and dACC seeds.

259 rtical areas: early visual cortex, posterior intraparietal sulcus, anterior superior parietal lobule,

260 the left lateral occipital cortex and right intraparietal sulcus, as indicated by psychophysiologica

261 nd premotor cortices as well as the anterior intraparietal sulcus, but also by top-down input from pS

262 ion of interest familywise error corrected), intraparietal sulcus, caudal dorsal premotor cortex, and

263 parietal regions (anterior precuneus, medial intraparietal sulcus, frontal eye fields) that showed th

264 regions of dorsomedial prefrontal cortex and intraparietal sulcus, implementing a comparison process,

265 The intraparietal sulcus, in the dorsal visual processing st

266 ingulate cortex (dACC), anterior insula, and intraparietal sulcus, independent of task specifics.

267 area related to the orienting of attention (intraparietal sulcus, IPS) as well as a region related t

268 rior precuneus (aPCu), extending into medial intraparietal sulcus, is equally active in visual and no

269 At the next stage, in posterior intraparietal sulcus, location is estimated under the as

270 PEc, several areas in the medial bank of the intraparietal sulcus, opercular areas PGop/PFop, and the

271 n superior and lateral frontal cortex and in intraparietal sulcus, pattern classifiers were unable to

272 l attentional control network comprising the intraparietal sulcus, precuneus, and dorsolateral prefro

273 et of cortical regions, including the middle intraparietal sulcus, showed a monotonic variation of th

274 in the lateral prefrontal cortex and ventral intraparietal sulcus, structures critically involved in

275 sustained activity in prefrontal cortex, the intraparietal sulcus, the left angular gyrus and the inf

276 nly at the top of the hierarchy, in anterior intraparietal sulcus, the uncertainty about the causal s

277 e; and, within the dorsal attention network, intraparietal sulcus, which discriminated between traine

278 ntegration of sickness cues was found in the intraparietal sulcus, which was functionally connected t

279 emporal sulcus/temporoparietal junction, and intraparietal sulcus-and were integrated in the dorsal a

280 lutamine (Glx) concentrations from bilateral intraparietal sulcus.

281 rain stimulation protocol delivered over the intraparietal sulcus.

282 cific activity (greater than control) in the intraparietal sulcus.

283 convexity as well as the medial bank of the intraparietal sulcus.

284 ansverse occipital sulci and right posterior intraparietal sulcus.

285 t, in humans, is generated by neurons in the intraparietal sulcus.

286 mpass dorsal regions V3A/B and the posterior intraparietal sulcus.

287 pondences with areas in macaque superior and intraparietal sulcus.

288 ndex) that localize to the visual cortex and intraparietal sulcus.

289 recentral gyrus and the anterior bank of the intraparietal sulcus.

290 s of the left parietal cortex centred on the intraparietal sulcus.

291 ction conflict, whereas TMS of the posterior intraparietal sulcus/inferior parietal lobule interfered

292 In contrast, the posterior intraparietal sulcus/inferior parietal lobule may resolv

293 ial aPFC and the right central precuneus and intraparietal sulcus/inferior parietal lobule.

294 nsistent with oculomotor input) and anterior intraparietal sulcus/superior parietal lobule (consisten

295 signals to update grasp plans in additional intraparietal/superior parietal regions.

296 decision involving a network of ventrocaudal intraparietal, ventral premotor, and inferotemporal cort

297 Neurons in the macaque ventral intraparietal (VIP) area are known to represent heading

298 medial superior temporal (MSTd) and ventral intraparietal (VIP) areas of monkeys during perception o

299 medial superior temporal (MSTd) and ventral intraparietal (VIP) areas of the macaque brain are multi

300 T), lateral intraparietal (LIP), and ventral intraparietal (VIP) areas.