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1 circuits (frontal eye fields, intraparietal sulcus).
2 that enables the enlargement of the gingival sulcus.
3 medial orbital sulcus and transverse orbital sulcus.
4 in the rostral portion of the medial orbital sulcus.
5 ded along the crest of the superior temporal sulcus.
6 rior temporal plane including Heschl's gyrus/sulcus.
7 ontal gyrus, and posterior superior temporal sulcus.
8 in the dorsal bank and fundus of the rhinal sulcus.
9 respectively; P = .01) in the proximal ulnar sulcus.
10 the arcuate sulcus and the caudal principal sulcus.
11 tered in the fundus of the superior limiting sulcus.
12 the posterior half of the superior limiting sulcus.
13 refrontal cortex (LPFC) lining the principal sulcus.
14 concentrations from bilateral intraparietal sulcus.
15 network, with overlaps around the principal sulcus.
16 (AF) face patch within the superior temporal sulcus.
17 ontal cortex, and the left superior temporal sulcus.
18 r and loop protrusion/erosion in the ciliary sulcus.
19 (greater than control) in the intraparietal sulcus.
20 well as the medial bank of the intraparietal sulcus.
21 e areas within hMT+/V5 and superior temporal sulcus.
22 e epithelial gap junction layer to the outer sulcus.
23 alize to the visual cortex and intraparietal sulcus.
24 s and the anterior bank of the intraparietal sulcus.
25 extending along the right superior temporal sulcus.
26 with the iris implant placed in the ciliary sulcus.
27 y that tracked the fusiform gyrus/collateral sulcus.
28 parietal cortex centred on the intraparietal sulcus.
29 iate fMRI in the posterior superior temporal sulcus.
30 in the superficial tissues lining the labial sulcus.
31 depth of the ascending branch of the central sulcus (14 of 23, 61%) or in its immediate vicinity (nin
32 region located near the transverse occipital sulcus [16], might provide this perceptual source by ext
33 work (VLPFC) in and ventral to the principal sulcus; 2) a dorsal network (DPFC) in and dorsal to the
34 morphology differences in the paracingulate sulcus, a fold in the medial prefrontal cortex, with a 1
35 was found in the banks of the intraparietal sulcus, a region connected to the dorsal attention netwo
36 olume in the left anterior superior temporal sulcus, a region in the functionally defined theory of m
37 confined to the posterior superior temporal sulcus, a region previously associated with perception o
39 -brain analysis, increased superior temporal sulcus activity was also associated with nonresponse to
40 participation of the anterior intraparietal sulcus (aIPS) and ventral premotor cortex (PMv) in visua
41 parietal lobe and the anterior intraparietal sulcus (aIPS), correlated specifically with the percepti
42 tion is coded and the anterior intraparietal sulcus (aIPS), where movement information is elaborated
44 fusiform face area (FFA), superior temporal sulcus, amygdala, and intraparietal sulcus showed overal
45 text is represented within the intraparietal sulcus, an area previously shown to be functionally netw
46 specimens showed a significantly smaller AV sulcus and a severely underdeveloped annulus fibrosus.
47 ocated in the left lateral occipito-temporal sulcus and adjacent fusiform gyrus shows maximal selecti
49 cortex, comprising the midsuperior temporal sulcus and anterior and dorsal prefrontal cortex, covari
50 as in the anterior upper bank of the lateral sulcus and anterior insula that may include the primary
51 with pain localized ventral to the cingulate sulcus and cognitive effects localized more dorsally wit
53 sectors of the medial bank of intraparietal sulcus and from the ventral premotor cortex, whereas med
54 etwork (DPFC) in and dorsal to the principal sulcus and in the frontal pole; 3) a caudolateral networ
55 activity in the posterior superior temporal sulcus and inferior parietal lobe during nonimitative ac
57 nal connectivity with anterior intraparietal sulcus and LOtv during the haptic than visual exploratio
58 ulation of a cortical area in the collateral sulcus and medial fusiform gyrus, which was place-select
59 recentral sulcal segment between the central sulcus and one of its hook-shaped anterior ascending bra
63 regional changes with right inferior frontal sulcus and right anterior insula occupying more central
64 f attention, including the inferior parietal sulcus and superior parietal lobule, the frontal eye-mov
66 trongly connected with the superior temporal sulcus and the cortex on the adjacent superior and middl
67 ed from neurons in the ventral intraparietal sulcus and the dorsolateral prefrontal cortex of numeric
69 long the upper bank of the superior temporal sulcus and the lateral bank of the superior temporal gyr
72 is located in the dorsal bank of the rhinal sulcus, and is divided into the medial orbital area, ven
73 accumbens, left posterior superior temporal sulcus, and left premotor cortex, OT increased activity
74 ed to lateral premotor cortex, intraparietal sulcus, and posterior superior cerebellar cortex are mod
75 ampal place area (PPA), transverse occipital sulcus, and retrosplenial cortex (RSC), key regions asso
77 f the organ of Corti, cells lining the inner sulcus, and supporting cells distributed along the epith
78 the frontal eye fields (FEFs), intraparietal sulcus, and temporoparietal junction (TPJ) of both hemis
79 in the inferior parietal gyrus/intraparietal sulcus, and that this effect predominated toward the end
81 l prefrontal cortex, the right intraparietal sulcus, and the midcingulate/presupplementary motor area
82 eterm birth on the insula, superior temporal sulcus, and ventral portions of the pre- and postcentral
83 /temporoparietal junction, and intraparietal sulcus-and were integrated in the dorsal anterior cingul
84 Insall-Salvati ratio), trochlear morphology (sulcus angle, lateral and medial trochlear inclination,
85 regulate the contribution of EPDCs to the AV sulcus, annulus fibrosus, and the parietal leaflets of t
87 early visual cortex, posterior intraparietal sulcus, anterior superior parietal lobule, and the ventr
88 of neurons in the rostral bank of the ansate sulcus (areas 1-2) in 2 cats while the cats walked on a
89 relation (P = .01) with NCV slowing over the sulcus as an electrophysiologic indicator of myelin shea
90 in the anterior bank and lip of the central sulcus as monkeys performed more naturalistic movements,
91 ral occipital cortex and right intraparietal sulcus, as indicated by psychophysiological interaction
92 superior temporal gyri and superior temporal sulcus, as well as the white matter underlying the poste
93 ncluded the right anterior superior temporal sulcus associated with the perception of human voices as
94 le lavage samples collected from the coronal sulcus at baseline and 4 weekly visits after MC were ass
96 ight middle temporal gyrus/superior temporal sulcus, bilateral precuneus as well as left anterior cin
98 d 3, 6, and 9 months; they included modified sulcus bleeding index (mSBI), plaque index (PI), probing
100 s; they included plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), and cl
101 They included plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), and cl
102 eters, including plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), clinic
103 as site-specific plaque index (PI), modified sulcus bleeding index (mSBI), probing depth (PD), relati
104 gery were: 1) plaque index (PI); 2) modified sulcus bleeding index (mSBI); 3) probing depth (PD); 4)
109 : 1) site-specific plaque index; 2) modified sulcus bleeding index; 3) probing depth (PD); 4) relativ
110 tials (LFPs) in the middle superior temporal sulcus body patch, defined by fMRI in the same rhesus mo
111 y higher bacterial loads in the peri-implant sulcus but significantly lower bacterial loads at the in
112 t familywise error corrected), intraparietal sulcus, caudal dorsal premotor cortex, and cerebellar lo
113 rt, infusion of 1 ml of clotted blood into a sulcus caused spreading depolarizations in 5/6 animals (
114 ubset of hemispheres only a single cingulate sulcus (cgs) is present, a majority of hemispheres exhib
117 clerotomy, pars plana, pars plicata, ciliary sulcus, ciliary body, or peripheral lens, and complex an
118 ions: (1) U-fibres running in the precentral sulcus, connecting the precentral gyrus and the SMA; (2)
119 e SMA; (2) U-fibres running in the cingulate sulcus, connecting the SMA with the cingulate gyrus; (3)
120 stance, tooth surfaces close to the gingival sulcus contact serum proteins that emanate via this sulc
121 he patterns of activity in the intraparietal sulcus could classify both the type of cue used for targ
123 unds show significant differences in central sulcus (CS) morphology, particularly in the inferior reg
124 nges in cortical organization of the central sulcus (CS) were associated with AG sound production.
126 s indicated that the caudal superior frontal sulcus (cSFS), in the vicinity of the frontal eye fields
127 ion, the gingival thickness and the gingival sulcus depth can be non-invasively measured, varying fro
128 Gingival samples were grouped by adjacent sulcus depth: 1 to 3 mm (normal), 3 mm with bleeding on
129 ns in this network, the dorsal intraparietal sulcus (DIPS) and the ventral premotor cortex (PMv).
130 reater activation in the right intraparietal sulcus during calculation, a region established to be in
132 activity in the posterior superior temporal sulcus during imitation and greater activity in the post
133 ic intraocular lens (SPA-IOL) in the ciliary sulcus during phacoemulsification complicated with poste
134 gned SPA-IOL may be implanted in the ciliary sulcus during phacoemulsification with PCT rather than s
135 sociated malformations include bottom-of-the-sulcus dysplasia (3 members from 2 families), and focal
136 ated in the medial bank of the intraparietal sulcus encompassing the medial intraparietal area and ar
137 e cochlea, as well as to Deiters' cells, the sulcus epithelium, the basilar membrane, and the surface
138 e auditory field of the anterior ectosylvian sulcus (fAES), and no area involved in somatosensory ori
143 , above and anterior to the anterior frontal sulcus, from which saccadic eye movements were evoked wi
144 face areas outside of the superior temporal sulcus fundus responded more to facial motion than gener
145 eye-movement field, and the inferior frontal sulcus/gyrus, and these regions functionally colateraliz
146 udy was to report the efficacy and safety of sulcus implantation of a SPA-IOL, designed for both in-t
148 o underwent phacoemulsification with PCT and sulcus implantation of SPA-IOL designed for both in-the-
150 arietal lobe and posterior superior temporal sulcus in imitation and social cognition, impaired imita
151 r grey matter volume in the right collateral sulcus, in a region lying between the fusiform and lingu
152 the anterior parietal cortex and the lateral sulcus, including areas 3a, 1, 2, the second somatosenso
153 ventral bank/fundus of the superior temporal sulcus, inferior temporal gyrus, and inferior parietal c
154 , whereas TMS of the posterior intraparietal sulcus/inferior parietal lobule interfered with perceptu
155 In contrast, the posterior intraparietal sulcus/inferior parietal lobule may resolve perceptual c
157 itrectomy (odds ratio [OR] 1.8, P = .03) and sulcus intraocular lens placement (OR 1.65, P = .03) dur
160 entral sulcus (sPCS) and inferior precentral sulcus (iPCS), anatomically interdigitated with two audi
161 entral sulcus (sPCS) and inferior precentral sulcus (iPCS), interleaved with two bilateral regions th
162 prefrontal cortex (dlPFC), and intraparietal sulcus (iPS) - brain regions important for cognitive exe
164 bserved, with activity in left intraparietal sulcus (IPS) and left superior parietal lobule (SPL) dif
166 lanning can begin, however, an intraparietal sulcus (IPS) area, putative LIP, participates in motor d
168 stinct activation in the right intraparietal sulcus (IPS) for Flanker interference and in the right m
169 ity, have been observed in the intraparietal sulcus (IPS) in monkeys and humans, including children.
170 des evidence that the superior intraparietal sulcus (IPS) is a critical brain region that influences
171 ateral and medial banks of the intraparietal sulcus (IPS) of the posterior parietal cortex while monk
172 e anterior part of the macaque intraparietal sulcus (IPS) showing the same depth structure selectivit
175 epresentation is scaled by the intraparietal sulcus (IPS), and that the level of IPS engagement refle
176 this area, especially the left intraparietal sulcus (IPS), and the degree of the crossed-hand illusio
177 ses being reported in superior intraparietal sulcus (IPS), but robust multivariate decoding being rep
178 tion after rTMS over the right intraparietal sulcus (IPS), but the size of this effect varied largely
179 e specificity in the posterior intraparietal sulcus (IPS), hand tuning in anterior IPS, and a foot bi
180 isual cortex (V1) and superior intraparietal sulcus (IPS), measured during the WM task at 2-4 s after
181 hat a single brain region, the intraparietal sulcus (IPS), shows both elevated neural activity and gl
182 e visual maps exist within the intraparietal sulcus (IPS), with each hemisphere symmetrically represe
186 to the orienting of attention (intraparietal sulcus, IPS) as well as a region related to scene proces
187 eased activity in the left superior temporal sulcus (L. STS), a key site for the integration of real
189 femoral neck, obliteration of the paralabral sulcus, labral defects, and defects of the hip capsule i
190 ons on the lateral bank of the intraparietal sulcus [lateral intraparietal area (LIP)] specifically b
192 , left angular gyrus, and left intraparietal sulcus (LIPS), in addition to object- and word-specific
193 t the next stage, in posterior intraparietal sulcus, location is estimated under the assumption that
196 ocalization within the left occipitotemporal sulcus maps onto a peak of connectivity with language ar
197 8.1 [441.9]; P = .05), and superior temporal sulcus (mean [SEM], 4697.8 [192.0] vs 5446.0 [159.6]; P
198 lly includes the posterior superior temporal sulcus, medial parietal, and dorsomedial prefrontal cort
199 s of single macaque middle superior temporal sulcus (midSTS) body patch neurons to reveal the image f
201 FA) is a region in the left occipitotemporal sulcus of literate individuals that is purportedly speci
203 We show that, although activation in the sulcus of the ACC signaled the costs on all trials, gyra
204 erical distance effects in the intraparietal sulcus of the developing brain, those effects could be e
206 potential from microbes in the oral gingival sulcus of two bottlenose dolphins (Tursiops truncatus).
207 reas in the medial bank of the intraparietal sulcus, opercular areas PGop/PFop, and the retroinsular
210 traddles the fundus of the superior limiting sulcus over its entire posterior-to-anterior extent is c
212 more frequently connected to the precentral sulcus (P < .001) in patients with FCD2 than in control
213 gyrus, dorsal bank of the superior temporal sulcus, parahippocampal cortex, and posterior cingulate
214 ions on the medial bank of the intraparietal sulcus [parietal reach region (PRR)] specifically biased
218 of SPA-IOL designed for both in-the-bag and sulcus positioning (Seelens AF, Hanita, Israel) between
222 control network comprising the intraparietal sulcus, precuneus, and dorsolateral prefrontal cortex is
223 and a region around the transverse occipital sulcus (previously known as "TOS"), here renamed the "oc
224 lied MVPD to the posterior superior temporal sulcus (pSTS) and to the fusiform face area (FFA), using
225 FFA, and EVC to posterior superior temporal sulcus (pSTS) best explained how face selectivity arises
226 around the human posterior superior temporal sulcus (pSTS) is known to be critical for speech percept
227 response in the posterior superior temporal sulcus (pSTS) to stimuli depicting social interactions b
229 , but not in the posterior superior temporal sulcus (pSTS), carried cue invariant information about t
230 uch as the right posterior superior temporal sulcus (pSTS), implicated in visual perception of biolog
231 cal regions, the posterior superior temporal sulcus (pSTS), where biological motion is coded and the
232 to higher-order posterior superior temporal sulcus (pSTS), which is selectively activated by animate
235 ajority of hemispheres exhibit an additional sulcus referred to as the paracingulate sulcus (pcgs).
236 euronal populations within the intraparietal sulcus region during an experimental arithmetic conditio
237 the middle temporal gyrus/superior temporal sulcus region that has reduced cortical functional conne
239 areas in the fundus of the superior temporal sulcus responded to general object motion; face areas ou
240 ion in the right posterior superior temporal sulcus (rpSTS) that responds more strongly during facial
244 temporal sulcus, amygdala, and intraparietal sulcus showed overall reduced neural responses when part
245 or frontal gyrus, and left superior temporal sulcus showed similar patterns of diagnosticity and sens
246 n the presence or absence of a paracingulate sulcus showed that PE effects extended across the dorsal
247 regions, including the middle intraparietal sulcus, showed a monotonic variation of the fMRI BOLD si
248 lateral frontal cortex, superior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), ana
249 ed for visual attention, superior precentral sulcus (sPCS) and inferior precentral sulcus (iPCS), int
250 that includes the superior parieto-occipital sulcus (sPOS) and a dorsolateral circuit comprising the
251 ncrease in the right superior temporal gyrus/sulcus (STG/STS) during speaker categorization and in th
253 ingulate cortex (ACC), and superior temporal sulcus (STS) are linked to basic social cognitive proces
254 ongside high activation of superior temporal sulcus (STS) comparable to SC-Fathers, and functional co
255 macaque monkeys to map the superior temporal sulcus (STS) for BOLD modulation associated with visuall
257 ntral lip of the posterior superior temporal sulcus (STS) in area TEO, and an anterior curvature-bias
258 cortical pathway from the superior temporal sulcus (STS) projecting into dorsal subregions of the am
259 aled a region in the right superior temporal sulcus (STS) that lies within the auditory cortex, and i
260 d bilateral regions of the superior temporal sulcus (STS) whose responses varied with segment length.
261 ced cortical volume in the superior temporal sulcus (STS), a region implicated in schizophrenia.
263 nd cortex; voice-selective superior temporal sulcus (STS); the amygdala, which is crucial for process
264 channels, through ventral superior temporal sulcus (STSv) and dorsal/ventral inferotemporal gyrus (T
265 donations in the posterior superior temporal sulcus, suggesting that domain-general attention shifts
266 gyrus, the right posterior superior temporal sulcus/superior temporal gyrus, the right medial anterio
267 found that penile (glans, foreskin, coronal sulcus) T cells and, to a lesser extent, macrophages and
268 efrontal cortex, posterior superior temporal sulcus/temporoparietal junction, and intraparietal sulcu
269 ns, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal sulcus (cIFS)
270 on, transverse gyrus intersecting precentral sulcus (tgPCS) and caudal inferior frontal sulcus (cIFS)
271 ivity in a portion of the left intraparietal sulcus that has previously been shown to be involved in
272 leading to formation of a deepened gingival sulcus that is highly prone to pathologic changes and, u
273 e regions of the superior temporal gyrus and sulcus that respond more to vocal sounds than a range of
274 zed a region in the macaque occipitotemporal sulcus that responds preferentially to images of scenes.
275 EPDCs contribute to the mesenchyme of the AV sulcus, the annulus fibrosus, and the parietal leaflets
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 ls, as well as a region in the intraparietal sulcus thought to be involved in perceptual decision-mak
279 parietal cortex, and the superior precentral sulcus (thought to contain the human homolog of the maca
282 show that activity in the superior temporal sulcus varies with the contextual familiarity in the mod
283 tention to a location [ventral intraparietal sulcus (vIPS)] and a region involved in shifting attenti
284 rtex (PIVC), areas V6 and V6A, and cingulate sulcus visual area, have been identified in humans by pa
286 erior temporal gyrus (STG)/superior temporal sulcus was connected to a distinct set of auditory and l
288 le and posterior inferior temporal gyrus and sulcus was positively correlated with noun manipulabilit
290 Conclusion Obliteration of the paralabral sulcus was the most frequent finding after arthroscopic
294 ation within the posterior superior temporal sulcus, which conveys visual information about others' a
295 the dorsal attention network, intraparietal sulcus, which discriminated between trained and novel vi
296 contact serum proteins that emanate via this sulcus, which may impact pellicle composition locally.
297 sickness cues was found in the intraparietal sulcus, which was functionally connected to core areas o
298 the upper and lower banks of the postlateral sulcus, while the elephant seal visual cortex extends fa
300 cal alpha power around the parieto-occipital sulcus within the first second after the emergence of a
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