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 IPS5 is located at the intersection of the intraparietal and postcentral sulcus; SPL1 branches off

7 addition to the precuneus, medial, anterior intraparietal, and superior parietal cortex were also ac

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

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

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

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

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

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

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

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

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

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

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

19 n that single neurons in the macaque lateral intraparietal area (LIP) can predict the amount of time

20 t evidence shows that neurons in the lateral intraparietal area (LIP) carry both spatial and nonspati

21 Neurons in the lateral intraparietal area (LIP) encoded these attentional biase

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

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

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

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

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

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

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

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

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

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

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

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

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

35 he activity of single neurons in the lateral intraparietal area (LIP) of rhesus macaques to determine

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

37 in the middle temporal area (MT) and lateral intraparietal area (LIP) of two macaque monkeys.

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

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

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

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

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

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

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

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

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

47 we show that neurons in the primate lateral intraparietal area (LIP), a cortical area previously lin

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

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

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

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

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

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

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

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

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

57 that is used to solve the task, and lateral intraparietal area (LIP), which represents the transform

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

76 superior temporal area (MST) and the ventral intraparietal area (VIP).

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

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

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

80 For both tasks, firing rates in the lateral intraparietal area appeared to reflect the accumulation

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

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

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

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

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

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

87 This intraparietal area showed stronger responses when the go

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

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

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

91 of activity were not observed in the lateral intraparietal area, an area linked to the frontoparietal

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

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

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

95 The lateral intraparietal area, for example, responds preferentially

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

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

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

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

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

101 esentation of heading in the macaque ventral intraparietal area.

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

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

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

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

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

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

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

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

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

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

112 del predicts that the neurons in the lateral intraparietal cortex involved in evidence accumulation e

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

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

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

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

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

118 ed in the activity of neurons in the lateral intraparietal cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

133 fields (SMA/SEFs), prefrontal cortex (PFC), intraparietal sulci (IPS), and the areas of the visual c

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

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

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

137 that a region in the anterior portion of the intraparietal sulcus (aIPS) is involved in prehensile mo

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

139 magnetic stimulation to either the anterior intraparietal sulcus (aIPS) or superior parietal lobule

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

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

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

143 m responses in either left or right anterior intraparietal sulcus (aIPS).

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

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

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

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

148 ime series, that frontal eye field (FEF) and intraparietal sulcus (IPS) activity predicts visual occi

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

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

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

152 eared to be left lateralized, including left intraparietal sulcus (IPS) and left MFG/IFG.

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

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

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

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

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

158 Previous imaging studies determined the intraparietal sulcus (IPS) as a central area for numeric

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

160 responses than ungrouped shapes in inferior intraparietal sulcus (IPS) even when grouping was task-i

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

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

163 es have highlighted the role of the superior intraparietal sulcus (IPS) in storing single object feat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 ds (FEF), superior parietal lobule (SPL) and intraparietal sulcus (IPS).

187 inferior frontal sulcus (IFS) but not in the intraparietal sulcus (IPS).

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

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

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

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

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

193 ur topographically organized areas along the intraparietal sulcus (IPS1-IPS4).

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

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

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

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

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

199 dial parietal cortical foci [right posterior intraparietal sulcus (pIPS) and right precuneus] signifi

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

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

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

203 ed regions in the human PPC [visual area V7, intraparietal sulcus 1 (IPS1), and IPS2].

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

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

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

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

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

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

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

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

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

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

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

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

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

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

218 In contrast, the anterior temporal lobe and intraparietal sulcus are activated by changes in acousti

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

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

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

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

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

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

225 crostructure, in white matter underlying the intraparietal sulcus following training of a complex vis

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

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

228 These results suggest that the left intraparietal sulcus is involved in subword reading proc

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

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

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

232 cale, whereas the anterior temporal lobe and intraparietal sulcus process auditory size information i

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

234 ar functional specialization within the left intraparietal sulcus region.

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

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

237 syndrome had bilateral abnormalities in the intraparietal sulcus that correlated with age, intellige

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

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

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

241 In control subjects, a region in the left intraparietal sulcus was activated for reading pseudowor

242 Stimulation of the intraparietal sulcus was associated with the occurrence

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

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

245 ior parietal cortices (i.e. areas within the intraparietal sulcus), SMA and primary motor cortex were

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

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

248 were associated with activation in the left intraparietal sulcus, a region associated with receptivi

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

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

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

264 s to the supramarginal gyrus (SMG), anterior intraparietal sulcus, inferior frontal gyrus opercularis

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

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

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

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

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

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

271 e gyrus, right superior parietal lobe, right intraparietal sulcus, right precuneus, and right cuneus.

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

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

274 t resulted in enhanced activity of bilateral intraparietal sulcus, supporting the idea of featural-le

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 lts show that this role may be served by the intraparietal sulcus, which additively integrated a spat

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

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

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

281 lutamine (Glx) concentrations from bilateral intraparietal sulcus.

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

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

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

285 ansverse occipital sulci and right posterior intraparietal sulcus.

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

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

288 pondences with areas in macaque superior and intraparietal sulcus.

289 ror and anticipatory value correlates in the intraparietal sulcus.

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

291 ons in dorsal visual areas in and around the intraparietal sulcus.

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

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

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

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

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.