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1 oral cortex, hippocampus, and the precentral sulcus).
2 alize to the visual cortex and intraparietal sulcus.
3 ctivation in the posterior superior temporal sulcus.
4 rosplenial complex, and transverse occipital sulcus.
5 s and the anterior bank of the intraparietal sulcus.
6 extending along the right superior temporal sulcus.
7 with the iris implant placed in the ciliary sulcus.
8 y that tracked the fusiform gyrus/collateral sulcus.
9 parietal cortex centred on the intraparietal sulcus.
10 iate fMRI in the posterior superior temporal sulcus.
11 in the superficial tissues lining the labial sulcus.
12 that enables the enlargement of the gingival sulcus.
13 medial orbital sulcus and transverse orbital sulcus.
14 in the rostral portion of the medial orbital sulcus.
15 ded along the crest of the superior temporal sulcus.
16 rior temporal plane including Heschl's gyrus/sulcus.
17 ontal gyrus, and posterior superior temporal sulcus.
18 in the dorsal bank and fundus of the rhinal sulcus.
19 superior temporal gyrus and inferior frontal sulcus.
20 ly and face recognition in right subparietal sulcus.
21 respectively; P = .01) in the proximal ulnar sulcus.
22 the arcuate sulcus and the caudal principal sulcus.
23 d in rodents, Layer 4 is thin in the nostril sulcus.
24 on protocol delivered over the intraparietal sulcus.
25 ed in the posterior bank of the suprasylvian sulcus.
26 mediated by the posterior superior temporal sulcus.
27 o >60 degrees in the parietooccipital medial sulcus.
28 l lobule X), and the right superior temporal sulcus.
29 unctional asymmetry of the superior temporal sulcus.
30 depth of the ascending branch of the central sulcus (14 of 23, 61%) or in its immediate vicinity (nin
31 region located near the transverse occipital sulcus [16], might provide this perceptual source by ext
32 work (VLPFC) in and ventral to the principal sulcus; 2) a dorsal network (DPFC) in and dorsal to the
33 morphology differences in the paracingulate sulcus, a fold in the medial prefrontal cortex, with a 1
34 was found in the banks of the intraparietal sulcus, a region connected to the dorsal attention netwo
35 olume in the left anterior superior temporal sulcus, a region in the functionally defined theory of m
36 -brain analysis, increased superior temporal sulcus activity was also associated with nonresponse to
37 participation of the anterior intraparietal sulcus (aIPS) and ventral premotor cortex (PMv) in visua
38 tion is coded and the anterior intraparietal sulcus (aIPS), where movement information is elaborated
39 pocampus and the posterior superior temporal sulcus) also showed face-preference, and much of the vis
40 fusiform face area (FFA), superior temporal sulcus, amygdala, and intraparietal sulcus showed overal
41 specimens showed a significantly smaller AV sulcus and a severely underdeveloped annulus fibrosus.
43 regions, namely, left anterior intraparietal sulcus and bilateral superior parietal lobule, met our c
44 with pain localized ventral to the cingulate sulcus and cognitive effects localized more dorsally wit
46 nsorimotor cortex, in the left intraparietal sulcus and dorsal premotor cortex, as well as in the bas
48 etwork (DPFC) in and dorsal to the principal sulcus and in the frontal pole; 3) a caudolateral networ
49 activity in the posterior superior temporal sulcus and inferior parietal lobe during nonimitative ac
50 commonly used model, it is embedded within a sulcus and is inaccessible to modern electrophysiologica
51 antly greater in the bilateral intraparietal sulcus and left angular gyrus in both adolescents and ad
53 nal connectivity with anterior intraparietal sulcus and LOtv during the haptic than visual exploratio
54 recentral sulcal segment between the central sulcus and one of its hook-shaped anterior ascending bra
57 regional changes with right inferior frontal sulcus and right anterior insula occupying more central
58 < baseline in the insula, superior temporal sulcus and superior temporal gyrus and happy < baseline
61 long the upper bank of the superior temporal sulcus and the lateral bank of the superior temporal gyr
62 the presence/absence of the inferior rostral sulcus and the subgenual intralimbic sulcus influences s
64 xtended into the posterior superior temporal sulcus), and hypo-connectivity between the rTPJ and medi
66 is located in the dorsal bank of the rhinal sulcus, and is divided into the medial orbital area, ven
67 ed to lateral premotor cortex, intraparietal sulcus, and posterior superior cerebellar cortex are mod
68 ampal place area (PPA), transverse occipital sulcus, and retrosplenial cortex (RSC), key regions asso
71 the frontal eye fields (FEFs), intraparietal sulcus, and temporoparietal junction (TPJ) of both hemis
72 in the inferior parietal gyrus/intraparietal sulcus, and that this effect predominated toward the end
74 l prefrontal cortex, the right intraparietal sulcus, and the midcingulate/presupplementary motor area
75 eterm birth on the insula, superior temporal sulcus, and ventral portions of the pre- and postcentral
76 /temporoparietal junction, and intraparietal sulcus-and were integrated in the dorsal anterior cingul
77 ochlear facet asymmetry, trochlear depth and sulcus angle, and the Insall-Salvati ratio were evaluate
78 Insall-Salvati ratio), trochlear morphology (sulcus angle, lateral and medial trochlear inclination,
79 mporal gyrus and posterior superior temporal sulcus, angry < baseline in the insula, superior tempora
81 early visual cortex, posterior intraparietal sulcus, anterior superior parietal lobule, and the ventr
82 long the lower bank of the superior temporal sulcus are predictive of the location of face-selective
83 of neurons in the rostral bank of the ansate sulcus (areas 1-2) in 2 cats while the cats walked on a
84 ight (1) the fundus of the parieto-occipital sulcus as a landmark for the transition between these re
85 identify the fundus of the parieto-occipital sulcus as a potential location for the crossover from pe
86 in the anterior bank and lip of the central sulcus as monkeys performed more naturalistic movements,
87 , (2) the anterior bank of parieto-occipital sulcus as the point of maximal separation between these
88 ncluded the right anterior superior temporal sulcus associated with the perception of human voices as
89 le lavage samples collected from the coronal sulcus at baseline and 4 weekly visits after MC were ass
90 lated brain activity in the left midfusiform sulcus, at a site medial to the classical visual word fo
91 ight middle temporal gyrus/superior temporal sulcus, bilateral precuneus as well as left anterior cin
92 th (PD) at 1- and 2-week as well as modified sulcus bleeding index (mSBI) at 1-, 4-, and 6-week (P <
94 d 3, 6, and 9 months; they included modified sulcus bleeding index (mSBI), plaque index (PI), probing
95 They included plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), and cl
97 eters, including plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), clinic
98 as site-specific plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), relati
99 gery were: 1) plaque index (PI); 2) modified sulcus bleeding index (mSBI); 3) probing depth (PD); 4)
103 al parameters (plaque index, gingival index, sulcus bleeding index, probing depth, and clinical attac
104 : 1) site-specific plaque index; 2) modified sulcus bleeding index; 3) probing depth (PD); 4) relativ
105 tials (LFPs) in the middle superior temporal sulcus body patch, defined by fMRI in the same rhesus mo
106 y higher bacterial loads in the peri-implant sulcus but significantly lower bacterial loads at the in
107 rtices as well as the anterior intraparietal sulcus, but also by top-down input from pSTS and DLPFC.S
109 t familywise error corrected), intraparietal sulcus, caudal dorsal premotor cortex, and cerebellar lo
110 rt, infusion of 1 ml of clotted blood into a sulcus caused spreading depolarizations in 5/6 animals (
113 isocortex, which gives rise to the cingulate sulcus (CiS) and the lateral fissure (LF), is conserved
114 ions: (1) U-fibres running in the precentral sulcus, connecting the precentral gyrus and the SMA; (2)
115 e SMA; (2) U-fibres running in the cingulate sulcus, connecting the SMA with the cingulate gyrus; (3)
116 stance, tooth surfaces close to the gingival sulcus contact serum proteins that emanate via this sulc
117 interactions with the left superior temporal sulcus, contributes to incidental acquisition of sound c
118 unds show significant differences in central sulcus (CS) morphology, particularly in the inferior reg
119 nges in cortical organization of the central sulcus (CS) were associated with AG sound production.
120 ion, the gingival thickness and the gingival sulcus depth can be non-invasively measured, varying fro
121 ns in this network, the dorsal intraparietal sulcus (DIPS) and the ventral premotor cortex (PMv).
123 activity in the posterior superior temporal sulcus during imitation and greater activity in the post
124 sociated malformations include bottom-of-the-sulcus dysplasia (3 members from 2 families), and focal
125 rol-related variables, whereas intraparietal sulcus encoded response complexity and the fusiform gyru
126 ated in the medial bank of the intraparietal sulcus encompassing the medial intraparietal area and ar
127 e auditory field of the anterior ectosylvian sulcus (fAES), and no area involved in somatosensory ori
128 nts (100 with periodontitis, 25 healthy) two sulcus fluid samples each were collected and pooled for
131 the frontal eye field and the intraparietal sulcus form a circuitry that integrates auditory and vis
132 , above and anterior to the anterior frontal sulcus, from which saccadic eye movements were evoked wi
133 re called the floor of the superior temporal sulcus (fSTS), as the primary cortical target of superio
134 plotype-related differences in intraparietal sulcus functional connectivity localized to the fusiform
135 l population, we asked whether intraparietal sulcus functional connectivity patterns similar to those
136 exhibited opposite patterns of intraparietal sulcus functional connectivity with visual processing re
138 er eyelid ptosis (n = 14, 52%), and superior sulcus hollowing (n = 15, 52%) were the most frequently
139 tasias), and (3) periorbital (e.g., superior sulcus hollowing, proptosis, enophthalmos, hypoglobus, a
141 cations (frontal eye field and intraparietal sulcus in each hemisphere) to identify regions of the do
143 arietal lobe and posterior superior temporal sulcus in imitation and social cognition, impaired imita
144 Tube-shunt implantation through the ciliary sulcus in pseudophakic eyes appears relatively safe to t
145 r grey matter volume in the right collateral sulcus, in a region lying between the fusiform and lingu
147 ial iris had been implanted into the ciliary sulcus; in 2 eyes it had been sutured to the sclera.
148 the anterior parietal cortex and the lateral sulcus, including areas 3a, 1, 2, the second somatosenso
150 rostral sulcus and the subgenual intralimbic sulcus influences significantly the sulcal organization
151 itrectomy (odds ratio [OR] 1.8, P = .03) and sulcus intraocular lens placement (OR 1.65, P = .03) dur
153 duced with reverse (anterior) optic capture, sulcus IOL placement, piggyback IOLs, and neodymium:yttr
154 entral sulcus (sPCS) and inferior precentral sulcus (iPCS), anatomically interdigitated with two audi
155 entral sulcus (sPCS) and inferior precentral sulcus (iPCS), interleaved with two bilateral regions th
156 prefrontal cortex (dlPFC), and intraparietal sulcus (iPS) - brain regions important for cognitive exe
158 bserved, with activity in left intraparietal sulcus (IPS) and left superior parietal lobule (SPL) dif
160 stinct activation in the right intraparietal sulcus (IPS) for Flanker interference and in the right m
161 ity, have been observed in the intraparietal sulcus (IPS) in monkeys and humans, including children.
162 des evidence that the superior intraparietal sulcus (IPS) is a critical brain region that influences
164 ateral and medial banks of the intraparietal sulcus (IPS) of the posterior parietal cortex while monk
165 prefrontal cortex (VMPFC), and intraparietal sulcus (IPS) predicted individual differences in context
166 e anterior part of the macaque intraparietal sulcus (IPS) showing the same depth structure selectivit
167 quality, while activity in the intraparietal sulcus (IPS) specifically correlated with offer quantity
168 ACC, anterior insula (AI), and intraparietal sulcus (IPS) to be more active when effort demand was hi
169 a partitioning of the primate intraparietal sulcus (IPS) using immunoarchitectural and connectivity
171 epresentation is scaled by the intraparietal sulcus (IPS), and that the level of IPS engagement refle
172 this area, especially the left intraparietal sulcus (IPS), and the degree of the crossed-hand illusio
173 ses being reported in superior intraparietal sulcus (IPS), but robust multivariate decoding being rep
174 tion after rTMS over the right intraparietal sulcus (IPS), but the size of this effect varied largely
175 e specificity in the posterior intraparietal sulcus (IPS), hand tuning in anterior IPS, and a foot bi
176 isual cortex (V1) and superior intraparietal sulcus (IPS), measured during the WM task at 2-4 s after
177 hat a single brain region, the intraparietal sulcus (IPS), shows both elevated neural activity and gl
179 e visual maps exist within the intraparietal sulcus (IPS), with each hemisphere symmetrically represe
184 rontal eye field (FEF) and the intraparietal sulcus (IPS0-4) form a circuitry that concurrently encod
185 riorly directed ciliary body, absent ciliary sulcus, iris angulation, flat iris plane, and iridotrabe
186 eased activity in the left superior temporal sulcus (L. STS), a key site for the integration of real
187 femoral neck, obliteration of the paralabral sulcus, labral defects, and defects of the hip capsule i
188 ons on the lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)] specifically b
189 t the next stage, in posterior intraparietal sulcus, location is estimated under the assumption that
192 ocalization within the left occipitotemporal sulcus maps onto a peak of connectivity with language ar
193 8.1 [441.9]; P = .05), and superior temporal sulcus (mean [SEM], 4697.8 [192.0] vs 5446.0 [159.6]; P
194 lly includes the posterior superior temporal sulcus, medial parietal, and dorsomedial prefrontal cort
195 tertiary, longitudinal sulcus (mid-fusiform sulcus, MFS) that bisects the FG into lateral and medial
196 cognition, contains a tertiary, longitudinal sulcus (mid-fusiform sulcus, MFS) that bisects the FG in
197 s of single macaque middle superior temporal sulcus (midSTS) body patch neurons to reveal the image f
198 Neurons in the middle superior temporal sulcus (mSTS)-previously implicated in social perception
200 FA) is a region in the left occipitotemporal sulcus of literate individuals that is purportedly speci
202 We show that, although activation in the sulcus of the ACC signaled the costs on all trials, gyra
203 erical distance effects in the intraparietal sulcus of the developing brain, those effects could be e
204 potential from microbes in the oral gingival sulcus of two bottlenose dolphins (Tursiops truncatus).
206 selective regions along the occipitotemporal sulcus (OTS) of both hemispheres (subregions of the visu
209 more frequently connected to the precentral sulcus (P < .001) in patients with FCD2 than in control
210 ions on the medial bank of the intraparietal sulcus [parietal reach region (PRR)] specifically biased
212 surgery, were implanted with a ring-shaped, sulcus-placed, foldable IOP sensor in a single procedure
215 control network comprising the intraparietal sulcus, precuneus, and dorsolateral prefrontal cortex is
216 response in the posterior superior temporal sulcus (pSTS) and its connectivity with the fusiform fac
217 lied MVPD to the posterior superior temporal sulcus (pSTS) and to the fusiform face area (FFA), using
218 FFA, and EVC to posterior superior temporal sulcus (pSTS) best explained how face selectivity arises
220 around the human posterior superior temporal sulcus (pSTS) is known to be critical for speech percept
221 s" to either the posterior superior temporal sulcus (pSTS) or dorsolateral prefrontal cortex (DLPFC)
222 response in the posterior superior temporal sulcus (pSTS) to stimuli depicting social interactions b
224 uch as the right posterior superior temporal sulcus (pSTS), implicated in visual perception of biolog
225 cal regions, the posterior superior temporal sulcus (pSTS), where biological motion is coded and the
228 ocial attention (posterior superior temporal sulcus, pSTS) and interoception (somatosensory cortex).
230 the middle temporal gyrus/superior temporal sulcus region that has reduced cortical functional conne
231 he LPMCv CSP originated from the postarcuate sulcus region, was bilateral, sparse, and primarily targ
232 rectangular, whereas the side of the nostril sulcus representing the lateral wall is funnel-like.
235 t brain phenotype by comparing intraparietal sulcus resting functional connectivity in individuals wi
236 group analyses, differences in intraparietal sulcus resting-state functional connectivity were calcul
237 ion in the right posterior superior temporal sulcus (rpSTS) that responds more strongly during facial
240 utative nostril representation is an oblique sulcus running from lateral (surface) to medial (inside)
242 temporal sulcus, amygdala, and intraparietal sulcus showed overall reduced neural responses when part
243 n the presence or absence of a paracingulate sulcus showed that PE effects extended across the dorsal
244 region on the floor of the superior temporal sulcus; smaller reductions were also found in frontal ey
245 lateral frontal cortex, superior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), ana
246 ed for visual attention, superior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), int
247 , a site at the rostral end of the cingulate sulcus stood out as having strong inputs from many areas
249 ongside high activation of superior temporal sulcus (STS) comparable to SC-Fathers, and functional co
250 ct inactivation of the mid-superior temporal sulcus (STS) cortical region identified by fMRI caused s
251 macaque monkeys to map the superior temporal sulcus (STS) for BOLD modulation associated with visuall
253 cortical pathway from the superior temporal sulcus (STS) projecting into dorsal subregions of the am
254 aled a region in the right superior temporal sulcus (STS) that lies within the auditory cortex, and i
255 d bilateral regions of the superior temporal sulcus (STS) whose responses varied with segment length.
256 al > angry in the anterior superior temporal sulcus (STS), happy > angry in the superior temporal gyr
257 the posterior and anterior superior temporal sulcus (STS), the extrastriate body area (EBA) and the o
258 e-selective patches of the superior temporal sulcus (STS), we found a double dissociation of areas pr
261 nd cortex; voice-selective superior temporal sulcus (STS); the amygdala, which is crucial for process
262 donations in the posterior superior temporal sulcus, suggesting that domain-general attention shifts
263 oculomotor input) and anterior intraparietal sulcus/superior parietal lobule (consistent with sensori
264 gyrus, the right posterior superior temporal sulcus/superior temporal gyrus, the right medial anterio
265 found that penile (glans, foreskin, coronal sulcus) T cells and, to a lesser extent, macrophages and
266 M network regions, such as superior temporal sulcus/temporoparietal junction (TPJ) and precuneus acro
267 efrontal cortex, posterior superior temporal sulcus/temporoparietal junction, and intraparietal sulcu
268 on, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal sulcus (cIFS)
269 ns, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal sulcus (cIFS)
270 y correlates with areas of the intraparietal sulcus that have previously been associated with numeric
271 leading to formation of a deepened gingival sulcus that is highly prone to pathologic changes and, u
272 e regions of the superior temporal gyrus and sulcus that respond more to vocal sounds than a range of
273 e views, located in the posterior collateral sulcus, the inferior parietal sulcus, and superior parie
274 ngs of the FEF, due to its location within a sulcus, the macaque FEF is virtually inaccessible to ele
275 eral prefrontal areas, the superior temporal sulcus, the posterior insula, and orbitofrontal cortex.
276 of the hierarchy, in anterior intraparietal sulcus, the uncertainty about the causal structure of th
277 of serum proteins emanate from the gingival sulcus, their ability to participate in dental pellicle
278 parietal cortex, and the superior precentral sulcus (thought to contain the human homolog of the maca
279 a were collected before and after unilateral sulcus tube-shunt implantation from the surgical and the
281 tention to a location [ventral intraparietal sulcus (vIPS)] and a region involved in shifting attenti
282 rtex (PIVC), areas V6 and V6A, and cingulate sulcus visual area, have been identified in humans by pa
284 erior temporal gyrus (STG)/superior temporal sulcus was connected to a distinct set of auditory and l
286 le and posterior inferior temporal gyrus and sulcus was positively correlated with noun manipulabilit
287 Conclusion Obliteration of the paralabral sulcus was the most frequent finding after arthroscopic
291 ation within the posterior superior temporal sulcus, which conveys visual information about others' a
292 the dorsal attention network, intraparietal sulcus, which discriminated between trained and novel vi
293 contact serum proteins that emanate via this sulcus, which may impact pellicle composition locally.
294 sickness cues was found in the intraparietal sulcus, which was functionally connected to core areas o
295 that both Hominoidea possess a paracingulate sulcus, which was previously thought to be unique to the
296 the upper and lower banks of the postlateral sulcus, while the elephant seal visual cortex extends fa
297 tside the eye was implanted into the ciliary sulcus with or without trans-scleral suture fixation.
299 cal alpha power around the parieto-occipital sulcus within the first second after the emergence of a