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1 evoked activity in auditory cortex (superior temporal gyrus).
2 nt of the superior frontal gyrus, and middle temporal gyrus).
3 age to the posterior half of the left middle temporal gyrus.
4 as in the right Heschl's gyrus and superior temporal gyrus.
5 rial transit time (ATT) in the left superior temporal gyrus.
6 erior occipital gyrus and posterior inferior temporal gyrus.
7 uperior temporal sulcus and posterior middle temporal gyrus.
8 ior frontal gyrus and contralateral superior temporal gyrus.
9 us, planum temporale, and posterior superior temporal gyrus.
10 region and instead activated right superior temporal gyrus.
11 ite matter underlying the posterior superior temporal gyrus.
12 etworks, was strongest in the right superior temporal gyrus.
13 al gyrus, inferior parietal lobe, and middle temporal gyrus.
14 imary auditory cortex and bilateral superior temporal gyrus.
15 cus, the left angular gyrus and the inferior temporal gyrus.
16 uence on the evoked response in the superior temporal gyrus.
17 al lobe and Brodmann's area 21 of the middle temporal gyrus.
18 ft hemisphere, especially along the superior temporal gyrus.
19 lower-level sensory regions of the superior temporal gyrus.
20 ietal lobule, precentral gyrus, and superior temporal gyrus.
21 related with activation in the left superior temporal gyrus.
22 lated with atrophy in the posterior superior temporal gyrus.
23 re Brodmann areas 45/47 and posterior middle temporal gyrus.
24 at probably index activity from the superior temporal gyrus.
25 ly organized in the human posterior superior temporal gyrus.
26 arietal cortices, as well as the left middle temporal gyrus.
27 ann areas 45/47 bilaterally and right middle temporal gyrus.
28 ifference in the volume of the left superior temporal gyrus.
29 ngulate, precuneus, left insula and superior temporal gyrus.
30 right middle fusiform gyrus and the inferior temporal gyrus.
31 lus the right middle fusiform gyrus/inferior temporal gyrus.
32 ere found in the left anterior to mid middle temporal gyrus.
33 nd limbic lobes and decrease in the superior temporal gyrus.
34 xternal speech, the opposite of the superior temporal gyrus.
35 men, and larger surface of the left inferior temporal gyrus.
36 frontal cortex (DLPFC), and bilateral middle temporal gyrus.
37 ly captured activity in the posterior middle 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 (-12)), cortical thickness of the transverse temporal gyrus (0.90[0.86; 0.96]; p = 5 x 10(-4)), educa
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 insula, anterior cingulate cortex, superior temporal gyrus, amygdala, parahippocampal gyrus, and pre
48 In contrast, activity in posterior superior temporal gyrus, an area associated with the processing o
49 ined, left cingulate gyrus and left superior temporal gyrus and a fewer NODs in the right superior te
50 rly-course schizophrenia, including superior temporal gyrus and anterior cingulate cortex, were most
51 e was consistently localized in the inferior temporal gyrus and anterior to the temporo-occipital inc
52 nts (at 100 ms after W2 onset in left middle temporal gyrus and at 140 ms in left Heschl's gyrus) wer
54 es in supplementary motor area (SMA), middle temporal gyrus and cerebellum in EP, but not CHR-SZ pati
55 tivity of the precuneus with the left middle temporal gyrus and connectivity of the dACC with the par
56 us, but it was less predictive in the middle temporal gyrus and failed to be predictive in the primar
57 nsula, superior temporal sulcus and superior temporal gyrus and happy < baseline in the anterior insu
58 the primary auditory cortex (i.e., superior temporal gyrus and Heschl's gyrus) correlated with reduc
59 ese neural representations past the superior temporal gyrus and how they engage higher-level language
60 reater decreases in activation in the middle temporal gyrus and increases in cuneus activation in res
61 the response time courses along the superior temporal gyrus and inferior frontal gyrus were remarkabl
64 with lesioned voxels in the posterior middle temporal gyrus and inferior parietal lobule, respectivel
66 tion of ventral stream areas, such as middle temporal gyrus and lateral occipital complex, with both
67 results confirm that both the left inferior temporal gyrus and left inferior frontal gyrus are invol
68 decreased thickness was seen in the superior temporal gyrus and posterior cingulate cortex in 22q11DS
69 sulcus (STS), happy > angry in the superior temporal gyrus and posterior superior temporal sulcus, a
70 greater [18F]AV-1451 uptake in the inferior temporal gyrus and precuneus was associated with increas
71 creased [18F]AV-1451 binding in the inferior temporal gyrus and precuneus were also evident in PD-imp
74 ated in two other cortical regions (superior temporal gyrus and prefrontal cortex), but not in the ce
76 dle frontal gyrus (bilaterally), left middle temporal gyrus and right posterior cingulate prior to tr
77 rus, left anterior cingulate, right superior temporal gyrus and right precentral gyrus during psychog
78 egrity of a posterior region of the superior temporal gyrus and sulcus predicted auditory short-term
79 ice areas (TVAs) are regions of the superior temporal gyrus and sulcus that respond more to vocal sou
80 erior parietal lobule and posterior inferior temporal gyrus and sulcus was positively correlated with
81 ural activity in bilateral anterior superior temporal gyrus and supratemporal plane was correlated wi
83 area 37, and unilaterally in the left middle temporal gyrus and the dorsal portion of Broca's area.
85 ere was hypometabolism in the right superior temporal gyrus and the left inferior parietal lobule.
86 ty of the right insula with the right middle temporal gyrus and the left intraparietal sulcus with th
90 gnificantly smaller GMV in the left superior temporal gyrus and widespread frontal, frontolimbic, and
91 modulation was mainly detected in the Middle Temporal Gyrus and within regions related to the mirror
92 ion of neural networks in the right superior temporal gyrus and, to a lesser extent, other areas dist
93 ft superior temporal gyrus to right superior temporal gyrus), and positive correlation between semant
94 ocampus, parahippocampal gyrus, and superior temporal gyrus, and an increase in white matter volume i
95 ictive disorders, including insula, superior temporal gyrus, and anterior/mid-cingulate cortex among
96 tions to the middle temporal gyrus, inferior temporal gyrus, and cingulate cortex, was associated wit
97 ilateral middle frontal gyrus, left superior temporal gyrus, and cingulate gyrus/anterior cingulate c
98 poral gyrus, middle temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encodin
99 l efficiency in the left superior and middle temporal gyrus, and individuals with psychotic BD did no
101 bilateral primary auditory cortex, superior temporal gyrus, and lateral prefrontal cortex for deviat
103 prefrontal cortex, left temporal pole/middle temporal gyrus, and left hippocampus in PTSD patients co
104 tofrontal cortex, ventral striatum, inferior temporal gyrus, and occipital cortex in both depression
105 central and postcentral gyri, right superior temporal gyrus, and opercula, which differentiated betwe
110 ral orbitofrontal gyri (LOFG), left superior temporal gyrus, and right insular, lingual and superior
111 right middle occipital gyrus, right inferior temporal gyrus, and right occipital lobe white matter.
112 nucleus, globus pallidus, putamen, superior temporal gyrus, and substructures within thalamus (later
113 in the posterior cingulate/precuneus, middle temporal gyrus, and superior occipital cortex during the
114 twork (dorsomedial prefrontal cortex, middle temporal gyrus, and temporal pole), and c) emotion-relat
115 ferior frontal gyrus, the posterior superior temporal gyrus, and the inferior parietal lobule, while
117 gyrus and a fewer NODs in the right superior temporal gyrus as compared to those born preterm at low
118 anguage areas, right precentral and superior temporal gyrus, as well as left caudate and anterior cin
119 owed significant activations in the inferior temporal gyrus at the previously proposed location of th
120 odel was used to identify right ITG inferior temporal gyrus atrophy (odds ratio, 0.83; 95% confidence
121 f the left and right middle latency superior temporal gyrus auditory ~50ms response (M50)(1) was meas
122 frontal gyrus (BA 9/46), the right superior temporal gyrus (BA 22), the right insula (BA 13), and th
124 from multiple positions within the superior temporal gyrus (BA21), dorsolateral frontal lobe (BA9),
125 d (posterior cingulate) and bilateral middle temporal gyrus (beta = 0.67 vs. 0.43), the right inferio
126 language processing, including the superior temporal gyrus (beta=-88.8 muL per risk allele, p=7.64x1
128 insular was active coincident with superior temporal gyrus but was more active for self-generated sp
130 the planum temporale and posterior superior temporal gyrus contralateral to the direction of stimula
131 hat anterior cingulate, insula, and superior temporal gyrus correlated with emotional appraisals, whe
132 CAP in the superior frontal gyrus and middle temporal gyrus correlated with the Stroop Color-Word Int
133 pole, inferior parietal lobule, and superior temporal gyrus) corresponded to regions associated with
134 segment of the AF that terminates in middle temporal gyrus corresponds to the ventral stream, and th
135 cept the rostral inferotemporal and superior temporal gyrus cortices) are components of the medial te
137 terestingly, we also found that the superior temporal gyrus demonstrated a consistent ability to impr
138 the DPFC connects with the rostral superior temporal gyrus, dorsal bank of the superior temporal sul
140 ng Brodmann areas 45/47 and posterior middle temporal gyrus during syntactic processing, patients act
141 us and putamen, and left insula and superior temporal gyrus during these tasks was significantly lowe
142 ive response in the human posterior superior temporal gyrus, enhancing the efficiency of auditory spe
143 In contrast, lesions within the superior temporal gyrus extending into the supramarginal gyrus, a
144 volumes in the right orbitofrontal/superior temporal gyrus extending to the amygdala, insula, and pa
146 ht primary auditory cortex to right superior temporal gyrus (feed-forward) and from left primary audi
147 is revealed additional decreases in superior temporal gyrus for the hearing loss group compared to th
150 tive to normal controls in the left superior temporal gyrus, frontal regions, cerebellum and caudate.
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 ulate cortex, and positively in the inferior temporal gyrus; (ii) abnormal CSF amyloid-beta42 (<1098)
156 r frontal gyrus and left middle and superior temporal gyrus in a pattern that is consistent with regi
157 inferior parietal lobe and posterior middle temporal gyrus in action recognition, driven in part by
158 een left inferior frontal gyrus and superior temporal gyrus in autism, and large-scale connectivity s
160 volumetric alterations in the right superior temporal gyrus in children and adolescents with autism,
161 d to show reduced recruitment of left middle temporal gyrus in response to orthographic input, within
164 tical areas, mostly located along the middle temporal gyrus, in which local fMRI patterns resulted in
166 lateral prefrontal cortex and right inferior temporal gyrus; increased grey matter in right insula, r
167 who had preservation of the posterior middle temporal gyrus, inferior fronto-occipital fasciculus and
168 eft dorsolateral prefrontal cortex, inferior temporal gyrus, inferior parietal gyrus, and cerebellum
169 analyses showed more activity in left middle temporal gyrus, inferior parietal lobule, and inferior f
170 ral region and its connections to the middle temporal gyrus, inferior temporal gyrus, and cingulate c
171 ontal cortex, and uncus, and in the superior temporal gyrus, insula, and anterior cingulate cortex.
172 of the posterior cingulate cortex, superior temporal gyrus, insula, fusiform gyrus, and caudate nucl
173 , we found that increased posterior superior temporal gyrus interhemispheric functional connectivity
174 - 0.09 in fatigued patients), right inferior temporal gyrus ( ITG inferior temporal gyrus ) (Montreal
175 s, right orbitofrontal gyrus, right inferior temporal gyrus (ITG), left postcentral gyrus/precuneus,
176 s within two primary brain regions (inferior temporal gyrus [ITG] and middle frontal gyrus [MFG]), we
177 ntal cortex and inferiorly into the superior temporal gyrus), left medial superior frontal gyrus (SDM
178 n in left supramarginal gyrus, left superior temporal gyrus, left middle temporal gyrus (MTG), and le
179 s significantly increased in the left middle temporal gyrus, left parahippocampal gyrus and left fusi
180 zed network, including left posterior middle temporal gyrus (LpMTG), left angular gyrus, and left int
182 ow gamma modulations in the ACC and Superior Temporal Gyrus may associate with increases of voluntary
183 rrors, and suggest that the posterior middle temporal gyrus may compute an intermediate representatio
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 c landscapes, stronger activations of middle temporal gyrus (MT/V5), and hippocampus were found in th
189 ula, inferior frontal junction (IFJ), middle temporal gyrus (MTG) and fusiform gyrus (FG) are active
191 tive PCR, respectively, in postmortem middle temporal gyrus (MTG) of Alzheimer disease (AD) and Hunti
192 , the ventral ATL (vATL) and anterior middle temporal gyrus (MTG) were shown to connect to areas resp
193 euronal spiking activity in the human middle temporal gyrus (MTG), a cortical region supporting the s
194 s, left superior temporal gyrus, left middle temporal gyrus (MTG), and left inferior frontal gyrus (I
196 N and temporal cortices including the middle temporal gyrus (MTG), paracingulate gyrus, amygdala, hip
197 right superior temporal sulcus (STS)/middle temporal gyrus (MTG), while directing attention to biolo
199 uning to individual vowels, whereas superior temporal gyrus neurons have nonspecific, sinusoidally mo
200 the causal relationship between (i) superior-temporal gyrus of either hemisphere and auditory halluci
201 atau314 proteins are present in the inferior temporal gyrus of human brains; (2) Deltatau314 proteins
205 ocampus/parahippocampus, inferior and middle temporal gyrus, olfactory gyrus and caudate are all rela
208 MT+/V5+ and implicate the posterior superior temporal gyrus/planum temporale in auditory motion proce
209 lly, IA participants recruited left superior temporal gyrus/planum temporale, matching the pattern ob
210 in the left superior temporal sulcus/middle temporal gyrus plus the right middle fusiform gyrus/infe
212 tex, angular gyrus (AG) and posterior middle temporal gyrus (pMTG), are thought to be crucial to sema
213 ntic similarity in posterior middle/inferior temporal gyrus (pMTG/ITG) and precuneus (PC) and additio
214 ere located in the posterior middle/inferior temporal gyrus (pMTG/ITG), angular gyrus, ventral tempor
215 eater activation in the precuneus and middle temporal gyrus predicted lower weight variability.From o
216 or cingulate, precuneus, insula and superior temporal gyrus preferentially differentiates tool-object
217 ized primarily to lateral posterior superior temporal gyrus (pSTG) and modulated binaural-cue respons
219 male and female) over the posterior superior temporal gyrus (pSTG), a brain area known to be importan
220 edictive contexts in left posterior superior temporal gyrus (pSTG), an area previously associated wit
221 , composed of functional fields in posterior temporal gyrus (pSTG), inferior parietal lobule (IPL), a
222 ft posterior superior temporal sulcus/middle temporal gyrus (pSTS/MTG) in crossmodal integration, whi
223 s in the superior frontal gyrus and superior temporal gyrus, regions previously linked to schizophren
226 nia (N=14) and comparison (N=14) of superior temporal gyrus revealed a smaller molecular mass of imma
227 sks, the bilateral fusiform gyrus and middle temporal gyrus, right inferior, middle, and superior fro
228 at single electrodes over the human superior temporal gyrus selectively represented intonation contou
230 n the left AI/FO and left posterior superior temporal gyrus (STG) and between the left AI/FO and dors
232 in speech processing, including the superior temporal gyrus (STG) and the posterior inferior frontal
233 MRI method show that defects in the superior temporal gyrus (STG) in response to language are early e
235 8] suggest that the right posterior superior temporal gyrus (STG) in the human brain is specialized f
240 phalographic brain responses in the superior temporal gyrus (STG) is uniquely consistent with a segme
241 trypsin-, and caspase-like) in the superior temporal gyrus (STG) of 25 SZ and 25 comparison subjects
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
254 ential at Cz, M50 at left and right superior temporal gyrus [STG]) and 100 msec (N100 at Cz, M100 at
255 with task performance in posterior superior temporal gyrus (STGp) that was observed in healthy subje
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
263 uding somatosensory cortex, insula, superior temporal gyrus, supramarginal gyrus, striatum, amygdala,
265 e in neurotransmission in the right Superior Temporal Gyrus (t=1.403, p=0.00780), Fusiform Gyrus (t=1
266 izing principle of information in the middle temporal gyrus, taking into consideration the input-moda
267 rain regions (medial frontal gyrus, superior temporal gyrus, thalamus, and subventricular zone).
269 es, most notably in right posterior superior temporal gyrus, than an identical shift that occurred fa
270 even to language, and voxels in left middle temporal gyrus that were responsive to language and imag
271 gyrus, the paracentral lobule, the superior temporal gyrus, the middle cingulate gyrus, the putamen
272 posterior superior temporal sulcus/superior temporal gyrus, the right medial anterior temporal lobe,
273 ns (sensorimotor, Broca's area, and superior temporal gyrus), these behavior- and location-dependent
274 within these pathways: the posterior middle temporal gyrus, thought to serve as a lexical interface
275 rior cingulate and bilateral middle/inferior temporal gyrus to capitalize on the salient categorical
276 rimary auditory cortex in the human superior temporal gyrus to determine what acoustic information in
278 inter-hemispheric connection (left superior temporal gyrus to right superior temporal gyrus), and po
279 egions pre-training (left middle frontal and temporal gyrus) to insight problem-solving regions post-
280 We observed that damage to the inferior temporal gyrus, to the fusiform gyrus and to a white mat
281 c features of speech from posterior superior temporal gyrus toward anterior superior temporal gyrus i
283 rtex, inferior frontal gyrus, right superior temporal gyrus, ventral posterior cingulate cortex, glob
284 )F T807 binding particularly in the inferior temporal gyrus was associated with clinical impairment.
285 arginal gyrus and supramarginal gyrus/middle temporal gyrus was associated with response to sertralin
286 acentral lobule, fusiform gyrus and inferior temporal gyrus was lowest in patients, intermediate in t
288 cortex, parahippocampal cortex, and inferior temporal gyrus) was associated with how well the test qu
289 , the superior frontal gyrus, and the middle temporal gyrus were inversely related to dementia severi
291 n left Brodmann area 45 and posterior middle temporal gyrus-were correlated with preserved syntactic
292 sing occurred in the left posterior superior temporal gyrus (Wernicke's area) and motor production pr
293 severe Alzheimer's hippocampus and superior temporal gyrus when normalized to expression of a neuron
294 coupling within the left posterior superior temporal gyrus, whereas perceptually equivalent nonspeec
295 terface areas (e.g., left posterior superior temporal gyrus), which was reliable only when the noise
296 ves afferents from the superior and inferior temporal gyrus, which provide complex auditory and visua
297 e human nonprimary auditory cortex (superior temporal gyrus) while subjects listened to speech syllab
298 th the medial prefrontal cortex and superior temporal gyrus, while aberrant limbic connectivity predi
299 ators of the auditory MMN along the superior temporal gyrus with no evidence of a somatosensory MMN i