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1 rsal attention circuits (frontal eye fields, intraparietal sulcus).
2 rain stimulation protocol delivered over the intraparietal sulcus.
3 cific activity (greater than control) in the intraparietal sulcus.
4 convexity as well as the medial bank of the intraparietal sulcus.
5 ansverse occipital sulci and right posterior intraparietal sulcus.
6 t, in humans, is generated by neurons in the intraparietal sulcus.
7 mpass dorsal regions V3A/B and the posterior intraparietal sulcus.
8 pondences with areas in macaque superior and intraparietal sulcus.
9 ror and anticipatory value correlates in the intraparietal sulcus.
10 ons in dorsal visual areas in and around the intraparietal sulcus.
11 luded the dorsolateral prefrontal cortex and intraparietal sulcus.
12 ependent response in two regions of the left intraparietal sulcus.
13 nding from the medial wall to lateral to the intraparietal sulcus.
14 An FEF injection labeled neurons in the intraparietal sulcus.
15 ch as the angular gyrus and the banks of the intraparietal sulcus.
16 ed in cortices along the lateral fissure and intraparietal sulcus.
17 ile the converse pattern was observed in the intraparietal sulcus.
18 ion in those with symptoms were found in the intraparietal sulcus.
19 ntral premotor cortex (Brodmann area 44) and intraparietal sulcus.
20 ns of target and distractor coherence in the intraparietal sulcus.
21 dle temporal, and gamma activity in the left intraparietal sulcus.
22 univariate responses, as well as in the left intraparietal sulcus.
23 ociated with decreased activity in bilateral intraparietal sulcus.
24 hub areas, notably middle frontal gyrus and intraparietal sulcus.
25 us, the postcentral sulcus, and the anterior intraparietal sulcus.
26 ndex) that localize to the visual cortex and intraparietal sulcus.
27 recentral gyrus and the anterior bank of the intraparietal sulcus.
28 s of the left parietal cortex centred on the intraparietal sulcus.
29 lutamine (Glx) concentrations from bilateral intraparietal sulcus.
30 memory-guided saccades [visual area 7 (V7), intraparietal sulcus 1 (IPS1), and IPS2], which are cand
33 were associated with activation in the left intraparietal sulcus, a region associated with receptivi
34 with awareness was found in the banks of the intraparietal sulcus, a region connected to the dorsal a
35 ith increased functional connectivity of the intraparietal sulcus, a region involved in numerosity pr
36 with reduced engagement of the left anterior intraparietal sulcus, a region involved in visual workin
37 of normal height with greater left anterior intraparietal sulcus activation showed higher problem-so
38 emonstrate the participation of the anterior intraparietal sulcus (aIPS) and ventral premotor cortex
39 ion of cortical activity within the anterior intraparietal sulcus (aIPS) by transcranial magnetic sti
40 that a region in the anterior portion of the intraparietal sulcus (aIPS) is involved in prehensile mo
42 magnetic stimulation to either the anterior intraparietal sulcus (aIPS) or superior parietal lobule
43 PMv), dorsal premotor cortex (PMd), anterior intraparietal sulcus (aIPS), and anterior superior parie
44 the superior parietal lobe and the anterior intraparietal sulcus (aIPS), correlated specifically wit
45 biological motion is coded and the anterior intraparietal sulcus (aIPS), where movement information
49 t decision context is represented within the intraparietal sulcus, an area previously shown to be fun
51 ed functional connectivity between the right intraparietal sulcus and an extended network (bilateral
52 arietal grasp regions, namely, left anterior intraparietal sulcus and bilateral superior parietal lob
53 association sensorimotor cortex, in the left intraparietal sulcus and dorsal premotor cortex, as well
54 ces, and two higher-order regions within the intraparietal sulcus and dorsolateral prefrontal cortex.
55 from anterior sectors of the medial bank of intraparietal sulcus and from the ventral premotor corte
56 ers showed greater activity in left anterior intraparietal sulcus and inferior frontal gyrus, regions
57 the right PPC spanning a region between the intraparietal sulcus and inferior parietal lobe were sig
58 found the neural signature of an SPE in the intraparietal sulcus and lateral prefrontal cortex, in a
59 T was significantly greater in the bilateral intraparietal sulcus and left angular gyrus in both adol
60 for the grip component in bilateral anterior intraparietal sulcus and left ventral premotor cortex; n
61 ronger functional connectivity with anterior intraparietal sulcus and LOtv during the haptic than vis
62 PPC, concentrated in the lateral bank of the intraparietal sulcus and on the angular gyrus, responds
63 ppocampus (mood alteration, mental fatigue), intraparietal sulcus and precuneus (physical fatigue), c
65 hat the basic functional organization of the intraparietal sulcus and surrounding regions is similar
66 ore, we recorded from neurons in the ventral intraparietal sulcus and the dorsolateral prefrontal cor
67 ntoparietal attention network, including the intraparietal sulcus and the inferior frontal gyrus.
68 tion-insensitive areas such as the posterior intraparietal sulcus and the junction of the left medial
69 f the white matter between the fundus of the intraparietal sulcus and the lateral ventricle (n = 3).
70 ore than participants with ADHD in the right intraparietal sulcus and the left lateral cerebellum in
71 e importance of cortical regions such as the intraparietal sulcus and the middle frontal gyrus for su
76 ration localized to lateral premotor cortex, intraparietal sulcus, and posterior superior cerebellar
78 f the macaque PRR, in the medial wall of the intraparietal sulcus, and produced the hallmarks of OA,
81 onse to value in the inferior parietal gyrus/intraparietal sulcus, and that this effect predominated
83 including the motion-sensitive area MT+, the intraparietal sulcus, and the inferior frontal sulcus.
84 uding Broca's area, the premotor region, the intraparietal sulcus, and the inferior parietal region),
85 t ventrolateral prefrontal cortex, the right intraparietal sulcus, and the midcingulate/presupplement
87 emporal sulcus/temporoparietal junction, and intraparietal sulcus-and were integrated in the dorsal a
88 cortex, the caudal IPL and lower rim of the intraparietal sulcus; and in dorsal prearcuate cortex an
89 seeds and by relative hypoconnectivity with intraparietal sulcus, anterior insula, and dACC seeds.
90 precentral sulcus, inferior frontal sulcus, intraparietal sulcus, anterior insula, and presupplement
91 rtical areas: early visual cortex, posterior intraparietal sulcus, anterior superior parietal lobule,
92 In contrast, the anterior temporal lobe and intraparietal sulcus are activated by changes in acousti
93 ging to show that the frontopolar cortex and intraparietal sulcus are preferentially active during ex
94 ther neurons in the caudolateral part of the intraparietal sulcus (area CIP), a part of the posterior
95 ferior frontal sulcus)] and parietal cortex [intraparietal sulcus areas (IPS1-IPS5) and an area in th
96 hMT+) and frontal and parietal areas (e.g., intraparietal sulcus areas IPS1-IPS4 and frontal eye fie
97 the left lateral occipital cortex and right intraparietal sulcus, as indicated by psychophysiologica
98 tive areas such as left MT+ and the anterior intraparietal sulcus, as well as motion-insensitive area
99 for both protocols, which included the right intraparietal sulcus (BA 7/40), the right middle frontal
100 nd premotor cortices as well as the anterior intraparietal sulcus, but also by top-down input from pS
101 ion of interest familywise error corrected), intraparietal sulcus, caudal dorsal premotor cortex, and
103 en shifts in the frontal eye field (FEF) and intraparietal sulcus, core regions of the dorsal frontop
104 tal gyrus (MFG), inferior frontal gyrus, and intraparietal sulcus correlated with the magnitude of pr
105 , trained on the patterns of activity in the intraparietal sulcus could classify both the type of cue
106 y of two regions in this network, the dorsal intraparietal sulcus (DIPS) and the ventral premotor cor
107 l premotor cortex, supplementary motor area, intraparietal sulcus, dorsolateral prefrontal cortex and
108 e same time, greater activation in the right intraparietal sulcus during calculation, a region establ
109 h as faces, along with hypoactivation of the intraparietal sulcus during visuospatial processing.
110 the three control-related variables, whereas intraparietal sulcus encoded response complexity and the
111 e macaque, located in the medial bank of the intraparietal sulcus encompassing the medial intrapariet
112 sity) to show that glutamate and GABA in the intraparietal sulcus explain unique variance both in cur
113 crostructure, in white matter underlying the intraparietal sulcus following training of a complex vis
115 usal structure the frontal eye field and the intraparietal sulcus form a circuitry that integrates au
116 parietal regions (anterior precuneus, medial intraparietal sulcus, frontal eye fields) that showed th
117 howed LIMK1 haplotype-related differences in intraparietal sulcus functional connectivity localized t
118 rom the general population, we asked whether intraparietal sulcus functional connectivity patterns si
119 ndrome cohort exhibited opposite patterns of intraparietal sulcus functional connectivity with visual
121 ge = 7.08, sd = 0.38) in subdivisions of the intraparietal sulcus (hIP1, hIP2, and hIP3) and the angu
124 regions of dorsomedial prefrontal cortex and intraparietal sulcus, implementing a comparison process,
125 etal cortex locations (frontal eye field and intraparietal sulcus in each hemisphere) to identify reg
127 ingulate cortex (dACC), anterior insula, and intraparietal sulcus, independent of task specifics.
129 s to the supramarginal gyrus (SMG), anterior intraparietal sulcus, inferior frontal gyrus opercularis
130 ction conflict, whereas TMS of the posterior intraparietal sulcus/inferior parietal lobule interfered
133 al premotor cortex, caudal cingulate sulcus, intraparietal sulcus, insula, frontal operculum and cere
134 l medial cortices, as well as temporal lobe, intraparietal sulcus, insula, parietal operculum, precun
135 dorsolateral prefrontal cortex (dlPFC), and intraparietal sulcus (iPS) - brain regions important for
136 brief TMS bursts (or Sham-TMS) to the dorsal intraparietal sulcus (IPS) 100 ms after visual stimulus
137 ime series, that frontal eye field (FEF) and intraparietal sulcus (IPS) activity predicts visual occi
138 induced learning engaged increased bilateral intraparietal sulcus (IPS) activity relative to repetiti
139 cy, based on an interaction between the left intraparietal sulcus (IPS) and a region implicated in vi
140 aps are located along the medial bank of the intraparietal sulcus (IPS) and are revealed by direct vi
141 of the spatial attention network, including intraparietal sulcus (IPS) and frontal eye field (FEF),
142 sustained spatially selective modulations in intraparietal sulcus (IPS) and frontal-eye field (FEF),
144 ated HGP was observed, with activity in left intraparietal sulcus (IPS) and left superior parietal lo
146 etween parietal brain regions, including the intraparietal sulcus (IPS) and the angular gyrus (AG), a
147 orsal frontoparietal network, comprising the intraparietal sulcus (IPS) and the frontal eye fields (F
148 s demonstrate significant activations in the intraparietal sulcus (IPS) and the superior temporal sul
149 ventrolateral prefrontal cortex (VLPFC), and intraparietal sulcus (IPS) are involved in orienting att
150 have revealed that regions in and around the intraparietal sulcus (IPS) are parametrically modulated
151 eye movement planning can begin, however, an intraparietal sulcus (IPS) area, putative LIP, participa
152 Previous imaging studies determined the intraparietal sulcus (IPS) as a central area for numeric
153 ior frontal junction (IFJ) and over the left intraparietal sulcus (IPS) during task preparation.
154 responses than ungrouped shapes in inferior intraparietal sulcus (IPS) even when grouping was task-i
155 We found that glutamate and GABA within the intraparietal sulcus (IPS) explained unique variance in
156 revealed a distinct activation in the right intraparietal sulcus (IPS) for Flanker interference and
159 ue, or numerosity, have been observed in the intraparietal sulcus (IPS) in monkeys and humans, includ
160 es have highlighted the role of the superior intraparietal sulcus (IPS) in storing single object feat
167 ivity in the lateral and medial banks of the intraparietal sulcus (IPS) of the posterior parietal cor
168 ndom noise stimulation (tRNS) applied to the intraparietal sulcus (IPS) or dorsolateral prefrontal co
169 ventromedial prefrontal cortex (VMPFC), and intraparietal sulcus (IPS) predicted individual differen
171 tional connectivity between the SMA and left intraparietal sulcus (IPS) region was lower in CD patien
172 aled a posterior-to-anterior gradient in the intraparietal sulcus (IPS) showing that the dominant fac
173 patches in the anterior part of the macaque intraparietal sulcus (IPS) showing the same depth struct
174 ed with offer quality, while activity in the intraparietal sulcus (IPS) specifically correlated with
175 rietal cortex, with emphasis on areas in the intraparietal sulcus (IPS) that are implicated in visual
176 e revealed a topographic organization in the intraparietal sulcus (IPS) that mirrors the retinotopic
177 les and males), we discovered regions in the intraparietal sulcus (IPS) that were selectively involve
179 a network of dACC, anterior insula (AI), and intraparietal sulcus (IPS) to be more active when effort
180 e comprising cortical layers V1, V2, V3, and intraparietal sulcus (IPS) to investigate how neural rep
181 We propose a partitioning of the primate intraparietal sulcus (IPS) using immunoarchitectural and
182 daptation effects have been localized to the intraparietal sulcus (IPS), a higher-level region of the
183 esting concentration of GABA within the left intraparietal sulcus (IPS), a key region supporting nume
186 he bottom-up representation is scaled by the intraparietal sulcus (IPS), and that the level of IPS en
187 n activity in this area, especially the left intraparietal sulcus (IPS), and the degree of the crosse
188 te fMRI responses being reported in superior intraparietal sulcus (IPS), but robust multivariate deco
189 spatial attention after rTMS over the right intraparietal sulcus (IPS), but the size of this effect
190 een the inferior frontal gyrus (IFG) and the intraparietal sulcus (IPS), dictates the recruitment of
191 ed with the attentional network, namely, the intraparietal sulcus (IPS), frontal eye field (FEF), and
192 r specific: eye specificity in the posterior intraparietal sulcus (IPS), hand tuning in anterior IPS,
193 ciated with enhanced performance, with right intraparietal sulcus (IPS), left IPS, and right frontal
194 s in primary visual cortex (V1) and superior intraparietal sulcus (IPS), measured during the WM task
195 (V1), the frontal eye fields (FEF), and the intraparietal sulcus (IPS), modulations related to spati
196 We report that a single brain region, the intraparietal sulcus (IPS), shows both elevated neural a
198 ulated by an attention-sensitive region, the intraparietal sulcus (IPS), which sometimes showed a sim
199 on and multiple visual maps exist within the intraparietal sulcus (IPS), with each hemisphere symmetr
200 ow that dorsal parietal cortex-specifically, intraparietal sulcus (IPS)-was engaged during top-down a
213 owever, revealed that decoding accuracies in intraparietal sulcus (IPS)/superior parietal lobe (SPL)
215 area related to the orienting of attention (intraparietal sulcus, IPS) as well as a region related t
216 ontrast, the frontal eye field (FEF) and the intraparietal sulcus (IPS0-4) form a circuitry that conc
217 riority map candidates along human posterior intraparietal sulcus (IPS0-IPS3) and two along the prece
219 ), middle frontal gyrus (MFG), LIP, anterior intraparietal sulcus (IPSa)] that may coordinate the tra
221 rior precuneus (aPCu), extending into medial intraparietal sulcus, is equally active in visual and no
222 in the left posterior reading network - left intraparietal sulcus (L.IPS) and left fusiform gyrus (L.
223 ound that lesions on the lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)]
224 resentations in the medial temporal lobe and intraparietal sulcus, learning in children with ASD was
226 gyrus (LpMTG), left angular gyrus, and left intraparietal sulcus (LIPS), in addition to object- and
228 subsequent analysis, we report that the same intraparietal sulcus neural populations are activated wh
229 r cingulate gyrus (Brodmann area 24), in the intraparietal sulcus of right posterior parietal cortex,
230 vidence of numerical distance effects in the intraparietal sulcus of the developing brain, those effe
231 ive neurons was highest in the fundus of the intraparietal sulcus; only few numerosity-selective neur
232 PEc, several areas in the medial bank of the intraparietal sulcus, opercular areas PGop/PFop, and the
234 s, whereas lesions on the medial bank of the intraparietal sulcus [parietal reach region (PRR)] speci
235 n superior and lateral frontal cortex and in intraparietal sulcus, pattern classifiers were unable to
236 dial parietal cortical foci [right posterior intraparietal sulcus (pIPS) and right precuneus] signifi
237 disruption was used to demonstrate that the intraparietal sulcus played a causal role both in decisi
238 l attentional control network comprising the intraparietal sulcus, precuneus, and dorsolateral prefro
239 hese regions, only activity within the right intraparietal sulcus predicts the accuracy with which ob
240 cale, whereas the anterior temporal lobe and intraparietal sulcus process auditory size information i
241 ions in the anterior and lateral bank of the intraparietal sulcus produced impaired finger scaling re
243 tivations of neuronal populations within the intraparietal sulcus region during an experimental arith
245 This result demonstrates that the anterior intraparietal sulcus represents the goal of an observed
246 there is developmental continuity in how the intraparietal sulcus represents the values of numerositi
248 efined a target brain phenotype by comparing intraparietal sulcus resting functional connectivity in
249 For between-group analyses, differences in intraparietal sulcus resting-state functional connectivi
250 e gyrus, right superior parietal lobe, right intraparietal sulcus, right precuneus, and right cuneus.
252 FA), superior temporal sulcus, amygdala, and intraparietal sulcus showed overall reduced neural respo
253 et of cortical regions, including the middle intraparietal sulcus, showed a monotonic variation of th
254 ior parietal cortices (i.e. areas within the intraparietal sulcus), SMA and primary motor cortex were
255 In the immediately adjacent parietooccipital/intraparietal sulcus, structural neuroimaging showed a g
256 in the lateral prefrontal cortex and ventral intraparietal sulcus, structures critically involved in
257 nsistent with oculomotor input) and anterior intraparietal sulcus/superior parietal lobule (consisten
258 t resulted in enhanced activity of bilateral intraparietal sulcus, supporting the idea of featural-le
259 the superior parietal gyrus and the anterior intraparietal sulcus that activated independently of bot
260 syndrome had bilateral abnormalities in the intraparietal sulcus that correlated with age, intellige
261 modulates activity in a portion of the left intraparietal sulcus that has previously been shown to b
262 option quantity correlates with areas of the intraparietal sulcus that have previously been associate
263 sustained activity in prefrontal cortex, the intraparietal sulcus, the left angular gyrus and the inf
264 nly at the top of the hierarchy, in anterior intraparietal sulcus, the uncertainty about the causal s
265 f motion signals, as well as a region in the intraparietal sulcus thought to be involved in perceptua
266 recruit the spatial cognition system in the intraparietal sulcus to encode the direction of another'
267 s applied to a more caudal region within the intraparietal sulcus, to the parieto-occipital complex (
268 -defined superior precentral sulcus, but not intraparietal sulcus, unbalanced the prioritization of r
269 ifying medial precuneus, left angular gyrus, intraparietal sulcus, ventral occipitotemporal cortex, a
270 cingulate motor areas (CMA), and the ventral intraparietal sulcus (VIP) and compared them to previous
271 maintaining attention to a location [ventral intraparietal sulcus (vIPS)] and a region involved in sh
272 ariations in two human DLG4 SNPs and reduced intraparietal sulcus volume and abnormal cortico-amygdal
273 In control subjects, a region in the left intraparietal sulcus was activated for reading pseudowor
276 al eye field and two separate regions in the intraparietal sulcus were similarly recruited in all con
277 or colliculus, anterior insula, and anterior intraparietal sulcus, were more involved with evaluating
278 ortical activation occurred primarily in the intraparietal sulcus when a location was attended before
279 iscrimination selectively activated the left intraparietal sulcus, whereas grating location discrimin
280 rietal cortex, the horizontal segment of the intraparietal sulcus which is hypothesized to be involve
281 lts show that this role may be served by the intraparietal sulcus, which additively integrated a spat
282 e; and, within the dorsal attention network, intraparietal sulcus, which discriminated between traine
283 ntegration of sickness cues was found in the intraparietal sulcus, which was functionally connected t
284 the right middle temporal gyrus and the left intraparietal sulcus with the orbital frontal cortex.
285 lateral occipital areas, extending into the intraparietal sulcus, with a limited version of the same