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1 evoked activity in auditory cortex (superior temporal gyrus).
2 us, planum temporale, and posterior superior temporal gyrus.
3 region and instead activated right superior temporal gyrus.
4 ite matter underlying the posterior superior temporal gyrus.
5 etworks, was strongest in the right superior temporal gyrus.
6 al gyrus, inferior parietal lobe, and middle temporal gyrus.
7 imary auditory cortex and bilateral superior temporal gyrus.
8 cus, the left angular gyrus and the inferior temporal gyrus.
9 uence on the evoked response in the superior temporal gyrus.
10 al lobe and Brodmann's area 21 of the middle temporal gyrus.
11 ft hemisphere, especially along the superior temporal gyrus.
12 lower-level sensory regions of the superior temporal gyrus.
13 ietal lobule, precentral gyrus, and superior temporal gyrus.
14 related with activation in the left superior temporal gyrus.
15 lated with atrophy in the posterior superior temporal gyrus.
16 re Brodmann areas 45/47 and posterior middle temporal gyrus.
17 at probably index activity from the superior temporal gyrus.
18 ly organized in the human posterior superior temporal gyrus.
19 ann areas 45/47 bilaterally and right middle temporal gyrus.
20 ifference in the volume of the left superior temporal gyrus.
21 ngulate, precuneus, left insula and superior temporal gyrus.
22 right middle fusiform gyrus and the inferior temporal gyrus.
23 lus the right middle fusiform gyrus/inferior temporal gyrus.
24 ere found in the left anterior to mid middle temporal gyrus.
25 utamen, lateral prefrontal gyrus, and middle temporal gyrus.
26 ultisensory association area of the superior temporal gyrus.
27 th rCBF in the occipital cortex and inferior temporal gyrus.
28 or the upper bank of the posterior superior temporal gyrus.
29 is differentially processed in the superior temporal gyrus.
30 ly captured activity in the posterior middle temporal gyrus.
31 age to the posterior half of the left middle temporal gyrus.
32 as in the right Heschl's gyrus and superior temporal gyrus.
33 frontal cortex (DLPFC), and bilateral middle temporal gyrus.
34 rial transit time (ATT) in the left superior temporal gyrus.
35 erior occipital gyrus and posterior inferior temporal gyrus.
36 uperior temporal sulcus and posterior middle temporal gyrus.
37 ior frontal gyrus and contralateral superior temporal gyrus.
38 m gyrus (0.036 vs 0.041; p<0.0001), inferior temporal gyrus (0.035 vs 0.041; p<0.0001), and middle te
40 cingulate cortex, 65% of those in the middle temporal gyrus, 61% of those in hippocampal CA1, 23% of
41 Here, we recorded from the human superior temporal gyrus, a high-order auditory cortex, and studie
43 een the anterior hippocampus and left middle temporal gyrus, a region important for the retrieval of
44 more precisely to the left anterior superior temporal gyrus, a region previously implicated in semant
45 the Val/Val COMT genotype showed less middle temporal gyrus activation and those with the DRD4-L vers
47 In contrast, activity in posterior superior temporal gyrus, an area associated with the processing o
48 ined, left cingulate gyrus and left superior temporal gyrus and a fewer NODs in the right superior te
49 e was consistently localized in the inferior temporal gyrus and anterior to the temporo-occipital inc
51 tivity of the precuneus with the left middle temporal gyrus and connectivity of the dACC with the par
52 us, but it was less predictive in the middle temporal gyrus and failed to be predictive in the primar
53 the primary auditory cortex (i.e., superior temporal gyrus and Heschl's gyrus) correlated with reduc
54 ese neural representations past the superior temporal gyrus and how they engage higher-level language
55 ides evidence that areas within the superior temporal gyrus and inferior frontal gyrus are heavily re
56 the response time courses along the superior temporal gyrus and inferior frontal gyrus were remarkabl
58 with lesioned voxels in the posterior middle temporal gyrus and inferior parietal lobule, respectivel
60 tion of ventral stream areas, such as middle temporal gyrus and lateral occipital complex, with both
61 results confirm that both the left inferior temporal gyrus and left inferior frontal gyrus are invol
62 decreased thickness was seen in the superior temporal gyrus and posterior cingulate cortex in 22q11DS
63 greater [18F]AV-1451 uptake in the inferior temporal gyrus and precuneus was associated with increas
64 creased [18F]AV-1451 binding in the inferior temporal gyrus and precuneus were also evident in PD-imp
66 ated in two other cortical regions (superior temporal gyrus and prefrontal cortex), but not in the ce
68 dle frontal gyrus (bilaterally), left middle temporal gyrus and right posterior cingulate prior to tr
69 rus, left anterior cingulate, right superior temporal gyrus and right precentral gyrus during psychog
70 egrity of a posterior region of the superior temporal gyrus and sulcus predicted auditory short-term
71 ice areas (TVAs) are regions of the superior temporal gyrus and sulcus that respond more to vocal sou
72 erior parietal lobule and posterior inferior temporal gyrus and sulcus was positively correlated with
73 ural activity in bilateral anterior superior temporal gyrus and supratemporal plane was correlated wi
74 ructural brain abnormalities in the superior temporal gyrus and the amygdala-hippocampal complex.
76 area 37, and unilaterally in the left middle temporal gyrus and the dorsal portion of Broca's area.
78 ty of the right insula with the right middle temporal gyrus and the left intraparietal sulcus with th
82 gnificantly smaller GMV in the left superior temporal gyrus and widespread frontal, frontolimbic, and
83 modulation was mainly detected in the Middle Temporal Gyrus and within regions related to the mirror
84 ion of neural networks in the right superior temporal gyrus and, to a lesser extent, other areas dist
85 ft superior temporal gyrus to right superior temporal gyrus), and positive correlation between semant
86 ocampus, parahippocampal gyrus, and superior temporal gyrus, and an increase in white matter volume i
87 ictive disorders, including insula, superior temporal gyrus, and anterior/mid-cingulate cortex among
88 tions to the middle temporal gyrus, inferior temporal gyrus, and cingulate cortex, was associated wit
89 ilateral middle frontal gyrus, left superior temporal gyrus, and cingulate gyrus/anterior cingulate c
90 temporal lobes spread to include the middle temporal gyrus, and extended into more posterior regions
91 poral gyrus, middle temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encodin
93 bilateral primary auditory cortex, superior temporal gyrus, and lateral prefrontal cortex for deviat
95 prefrontal cortex, left temporal pole/middle temporal gyrus, and left hippocampus in PTSD patients co
96 ns in left and right angular gyrus, left mid-temporal gyrus, and left middle frontal gyrus that predi
98 tofrontal cortex, ventral striatum, inferior temporal gyrus, and occipital cortex in both depression
99 central and postcentral gyri, right superior temporal gyrus, and opercula, which differentiated betwe
100 nation of right middle frontal gyrus, middle temporal gyrus, and posterior cingulate activation best
101 erolateral Heschl's gyrus, anterior superior temporal gyrus, and posterior planum polare) and posteri
104 right middle occipital gyrus, right inferior temporal gyrus, and right occipital lobe white matter.
105 ulate cortex, medial parietal cortex, middle temporal gyrus, and superior frontal gyrus, whereas peop
106 in the posterior cingulate/precuneus, middle temporal gyrus, and superior occipital cortex during the
107 twork (dorsomedial prefrontal cortex, middle temporal gyrus, and temporal pole), and c) emotion-relat
108 ferior frontal gyrus, the posterior superior temporal gyrus, and the inferior parietal lobule, while
109 include the parahippocampal gyrus, superior temporal gyrus, anterior temporal poles, and the tempora
111 gyrus and a fewer NODs in the right superior temporal gyrus as compared to those born preterm at low
112 anguage areas, right precentral and superior temporal gyrus, as well as left caudate and anterior cin
113 inference; and (2) within the left superior temporal gyrus at the coherence break or when participan
114 owed significant activations in the inferior temporal gyrus at the previously proposed location of th
115 odel was used to identify right ITG inferior temporal gyrus atrophy (odds ratio, 0.83; 95% confidence
116 f the left and right middle latency superior temporal gyrus auditory ~50ms response (M50)(1) was meas
117 frontal gyrus (BA 9/46), the right superior temporal gyrus (BA 22), the right insula (BA 13), and th
120 from multiple positions within the superior temporal gyrus (BA21), dorsolateral frontal lobe (BA9),
122 d (posterior cingulate) and bilateral middle temporal gyrus (beta = 0.67 vs. 0.43), the right inferio
123 language processing, including the superior temporal gyrus (beta=-88.8 muL per risk allele, p=7.64x1
124 17/18), left hippocampus, bilateral superior temporal gyrus, bilateral lenticular nuclei and the righ
127 the planum temporale and posterior superior temporal gyrus contralateral to the direction of stimula
128 hat anterior cingulate, insula, and superior temporal gyrus correlated with emotional appraisals, whe
129 CAP in the superior frontal gyrus and middle temporal gyrus correlated with the Stroop Color-Word Int
130 pole, inferior parietal lobule, and superior temporal gyrus) corresponded to regions associated with
131 segment of the AF that terminates in middle temporal gyrus corresponds to the ventral stream, and th
132 cept the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial te
134 terestingly, we also found that the superior temporal gyrus demonstrated a consistent ability to impr
135 the DPFC connects with the rostral superior temporal gyrus, dorsal bank of the superior temporal sul
137 ng Brodmann areas 45/47 and posterior middle temporal gyrus during syntactic processing, patients act
138 us and putamen, and left insula and superior temporal gyrus during these tasks was significantly lowe
139 In contrast, lesions within the superior temporal gyrus extending into the supramarginal gyrus, a
140 volumes in the right orbitofrontal/superior temporal gyrus extending to the amygdala, insula, and pa
141 ior and posterior cingulate, superior/middle temporal gyrus extending to the hippocampus, precuneus,
142 ht primary auditory cortex to right superior temporal gyrus (feed-forward) and from left primary audi
143 ociated with hypoperfusion of right superior temporal gyrus (Fisher's exact test; p < 0.0001), wherea
144 tion areas - from Heschl's gyrus to superior temporal gyrus for the auditory spelling task and from c
145 is revealed additional decreases in superior temporal gyrus for the hearing loss group compared to th
147 tive to normal controls in the left superior temporal gyrus, frontal regions, cerebellum and caudate.
148 r temporal gyri, the left posterior superior temporal gyrus gray matter in the schizophrenia group ha
149 ntrast, smaller bilateral posterior inferior temporal gyrus gray matter volume is present in both sch
150 ophrenia, whereas smaller posterior inferior temporal gyrus gray matter volumes may be related to pat
152 d with a lesion area comprising the superior temporal gyrus, Heschl's gyrus, insula, and striatum in
153 An anteromedial Heschl's gyrus/superior temporal gyrus (HG/STG) region, engaged by the word reco
154 rtex and surrounding regions of the superior temporal gyrus; however, the manner in which these regio
155 r frontal gyrus and left middle and superior temporal gyrus in a pattern that is consistent with regi
156 inferior parietal lobe and posterior middle temporal gyrus in action recognition, driven in part by
157 een left inferior frontal gyrus and superior temporal gyrus in autism, and large-scale connectivity s
159 volumetric alterations in the right superior temporal gyrus in children and adolescents with autism,
162 tical areas, mostly located along the middle temporal gyrus, in which local fMRI patterns resulted in
163 lateral prefrontal cortex and right inferior temporal gyrus; increased grey matter in right insula, r
164 eft dorsolateral prefrontal cortex, inferior temporal gyrus, inferior parietal gyrus, and cerebellum
165 analyses showed more activity in left middle temporal gyrus, inferior parietal lobule, and inferior f
166 ral region and its connections to the middle temporal gyrus, inferior temporal gyrus, and cingulate c
167 ontal cortex, and uncus, and in the superior temporal gyrus, insula, and anterior cingulate cortex.
168 of the posterior cingulate cortex, superior temporal gyrus, insula, fusiform gyrus, and caudate nucl
169 , we found that increased posterior superior temporal gyrus interhemispheric functional connectivity
170 ent with the suggestion that the left middle temporal gyrus is involved in representing semantic info
171 a suggest that the right hemisphere superior temporal gyrus is particularly involved during early inf
172 essing, whereas the left hemisphere superior temporal gyrus is particularly involved during later inf
173 - 0.09 in fatigued patients), right inferior temporal gyrus ( ITG inferior temporal gyrus ) (Montreal
174 s, right orbitofrontal gyrus, right inferior temporal gyrus (ITG), left postcentral gyrus/precuneus,
175 ntal cortex and inferiorly into the superior temporal gyrus), left medial superior frontal gyrus (SDM
176 n in left supramarginal gyrus, left superior temporal gyrus, left middle temporal gyrus (MTG), and le
177 s significantly increased in the left middle temporal gyrus, left parahippocampal gyrus and left fusi
178 ior cingulate cortex (ACC), insula, superior temporal gyrus; left frontal and parietal operculum, med
180 zed network, including left posterior middle temporal gyrus (LpMTG), left angular gyrus, and left int
181 ow gamma modulations in the ACC and Superior Temporal Gyrus may associate with increases of voluntary
182 rrors, and suggest that the posterior middle temporal gyrus may compute an intermediate representatio
184 activity in the anterior portion of superior temporal gyrus, middle temporal gyrus, right occipital c
185 In addition, spikes in the left inferior temporal gyrus, middle temporal gyrus, superior temporal
186 right inferior temporal gyrus ( ITG inferior temporal gyrus ) (Montreal Neurological Institute [ MNI
187 vestibular processing areas including middle temporal gyrus, motion sensitive area MT/V5, superior pa
188 ula, inferior frontal junction (IFJ), middle temporal gyrus (MTG) and fusiform gyrus (FG) are active
189 tive PCR, respectively, in postmortem middle temporal gyrus (MTG) of Alzheimer disease (AD) and Hunti
190 , the ventral ATL (vATL) and anterior middle temporal gyrus (MTG) were shown to connect to areas resp
191 euronal spiking activity in the human middle temporal gyrus (MTG), a cortical region supporting the s
192 s, left superior temporal gyrus, left middle temporal gyrus (MTG), and left inferior frontal gyrus (I
194 emantic priming in five regions: left middle temporal gyrus (MTG), bilateral anterior cingulate, ante
195 right superior temporal sulcus (STS)/middle temporal gyrus (MTG), while directing attention to biolo
196 uning to individual vowels, whereas superior temporal gyrus neurons have nonspecific, sinusoidally mo
197 ral lobe (right hippocampus and right middle temporal gyrus), occipital lobe (left lingual gyrus), an
198 the causal relationship between (i) superior-temporal gyrus of either hemisphere and auditory halluci
201 ived from microelectrode penetrations in the temporal gyrus of the common marmoset (Callithrix jacchu
202 ocampus/parahippocampus, inferior and middle temporal gyrus, olfactory gyrus and caudate are all rela
205 (in planum temporale and posterior superior temporal gyrus) pathways as early as approximately 70-15
206 MT+/V5+ and implicate the posterior superior temporal gyrus/planum temporale in auditory motion proce
207 lly, IA participants recruited left superior temporal gyrus/planum temporale, matching the pattern ob
208 in the left superior temporal sulcus/middle temporal gyrus plus the right middle fusiform gyrus/infe
210 tex, angular gyrus (AG) and posterior middle temporal gyrus (pMTG), are thought to be crucial to sema
211 ere located in the posterior middle/inferior temporal gyrus (pMTG/ITG), angular gyrus, ventral tempor
212 eater activation in the precuneus and middle temporal gyrus predicted lower weight variability.From o
213 or cingulate, precuneus, insula and superior temporal gyrus preferentially differentiates tool-object
214 ized primarily to lateral posterior superior temporal gyrus (pSTG) and modulated binaural-cue respons
215 edictive contexts in left posterior superior temporal gyrus (pSTG), an area previously associated wit
216 , composed of functional fields in posterior temporal gyrus (pSTG), inferior parietal lobule (IPL), a
217 ft posterior superior temporal sulcus/middle temporal gyrus (pSTS/MTG) in crossmodal integration, whi
218 s in the superior frontal gyrus and superior temporal gyrus, regions previously linked to schizophren
220 nia (N=14) and comparison (N=14) of superior temporal gyrus revealed a smaller molecular mass of imma
221 sks, the bilateral fusiform gyrus and middle temporal gyrus, right inferior, middle, and superior fro
222 r portion of superior temporal gyrus, middle temporal gyrus, right occipital cortex, and inferior fro
223 at single electrodes over the human superior temporal gyrus selectively represented intonation contou
224 ustained delay-period activity, the superior temporal gyrus (STG) activated more vigorously when the
226 n the left AI/FO and left posterior superior temporal gyrus (STG) and between the left AI/FO and dors
227 ted with the dorsal TG, the rostral superior temporal gyrus (STG) and dorsal bank of STS, and the ret
229 in speech processing, including the superior temporal gyrus (STG) and the posterior inferior frontal
230 as differentially expressed between superior temporal gyrus (STG) and the remaining cerebral cortex.
231 MRI method show that defects in the superior temporal gyrus (STG) in response to language are early e
233 8] suggest that the right posterior superior temporal gyrus (STG) in the human brain is specialized f
237 phalographic brain responses in the superior temporal gyrus (STG) is uniquely consistent with a segme
240 ous studies revealed that posterior superior temporal gyrus (STG) responds to acoustic scale in human
241 ions on the supratemporal plane and superior temporal gyrus (STG) were investigated using Granger cau
242 rior frontal gyrus (IFG), posterior superior temporal gyrus (STG), and inferior parietal lobule (IPL)
243 s, as in monkeys, is located on the superior temporal gyrus (STG), and is functionally and structural
244 he inferior frontal gyrus (IFG) and superior temporal gyrus (STG), the sensory and visual cortices, a
245 consistently localized to left mid-superior temporal gyrus (STG), whereas activation associated with
253 inferior parietal lobule [IPL], and superior temporal gyrus (STG]) were drawn on the MRI scans of all
254 ential at Cz, M50 at left and right superior temporal gyrus [STG]) and 100 msec (N100 at Cz, M100 at
256 It is connected with the rostral superior temporal gyrus (STGr) and the dorsal bank of the superio
257 odmann area 45 and the left posterior middle temporal gyrus, suggesting that when this relationship b
258 ic activation increase in the right superior temporal gyrus/sulcus (STG/STS) during speaker categoriz
259 ft supramarginal gyrus, and right transverse temporal gyrus, superior parietal lobule, and paracentra
260 in the left inferior temporal gyrus, middle temporal gyrus, superior temporal gyrus, and fusiform gy
261 We identified a key system in the middle temporal gyrus/superior temporal sulcus region that has
262 onger decreases for patients in right middle temporal gyrus/superior temporal sulcus, bilateral precu
264 e in neurotransmission in the right Superior Temporal Gyrus (t=1.403, p=0.00780), Fusiform Gyrus (t=1
265 es, most notably in right posterior superior temporal gyrus, than an identical shift that occurred fa
266 even to language, and voxels in left middle temporal gyrus that were responsive to language and imag
267 gyrus, the paracentral lobule, the superior temporal gyrus, the middle cingulate gyrus, the putamen
268 posterior superior temporal sulcus/superior temporal gyrus, the right medial anterior temporal lobe,
269 ns (sensorimotor, Broca's area, and superior temporal gyrus), these behavior- and location-dependent
270 within these pathways: the posterior middle temporal gyrus, thought to serve as a lexical interface
271 rior cingulate and bilateral middle/inferior temporal gyrus to capitalize on the salient categorical
272 rimary auditory cortex in the human superior temporal gyrus to determine what acoustic information in
274 inter-hemispheric connection (left superior temporal gyrus to right superior temporal gyrus), and po
275 We observed that damage to the inferior temporal gyrus, to the fusiform gyrus and to a white mat
276 c features of speech from posterior superior temporal gyrus toward anterior superior temporal gyrus i
278 )F T807 binding particularly in the inferior temporal gyrus was associated with clinical impairment.
279 acentral lobule, fusiform gyrus and inferior temporal gyrus was lowest in patients, intermediate in t
281 medial prefrontal cortex and right superior temporal gyrus was observed in children with ASD relativ
282 Posterior gray matter volume in the inferior temporal gyrus was smaller bilaterally in both patient g
284 ual spelling task from calcarine to superior temporal gyrus was stronger than all other effects from
285 cortex, parahippocampal cortex, and inferior temporal gyrus) was associated with how well the test qu
286 , the superior frontal gyrus, and the middle temporal gyrus were inversely related to dementia severi
287 le temporal gyri and left posterior superior temporal gyrus were present in schizophrenia but not in
289 n left Brodmann area 45 and posterior middle temporal gyrus-were correlated with preserved syntactic
290 sing occurred in the left posterior superior temporal gyrus (Wernicke's area) and motor production pr
291 g the stories: (1) within the right superior temporal gyrus when a verb in the text implied the infer
292 severe Alzheimer's hippocampus and superior temporal gyrus when normalized to expression of a neuron
293 coupling within the left posterior superior temporal gyrus, whereas perceptually equivalent nonspeec
294 terface areas (e.g., left posterior superior temporal gyrus), which was reliable only when the noise
296 x, and the posterior portion of the superior temporal gyrus, which is known as a region involved in o
297 ves afferents from the superior and inferior temporal gyrus, which provide complex auditory and visua
298 e human nonprimary auditory cortex (superior temporal gyrus) while subjects listened to speech syllab
299 ators of the auditory MMN along the superior temporal gyrus with no evidence of a somatosensory MMN i
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