ライフサイエンスコーパス: superior temporal gyrus

1 odifying evoked activity in auditory cortex (superior temporal gyrus).

2 neural networks, was strongest in the right superior temporal gyrus.

3 n left primary auditory cortex and bilateral superior temporal gyrus.

4 site influence on the evoked response in the superior temporal gyrus.

5 in the left hemisphere, especially along the superior temporal gyrus.

6 tivity in lower-level sensory regions of the superior temporal gyrus.

7 neus, parietal lobule, precentral gyrus, and superior temporal gyrus.

8 ively correlated with activation in the left superior temporal gyrus.

9 was correlated with atrophy in the posterior superior temporal gyrus.

10 sites that probably index activity from the superior temporal gyrus.

11 ch than external speech, the opposite of the superior temporal gyrus.

12 tegorically organized in the human posterior superior temporal gyrus.

13 ificant difference in the volume of the left superior temporal gyrus.

14 terior cingulate, precuneus, left insula and superior temporal gyrus.

15 nt in a multisensory association area of the superior temporal gyrus.

16 n fissure or the upper bank of the posterior superior temporal gyrus.

17 structure is differentially processed in the superior temporal gyrus.

18 gulate, periaqueductal grey matter (PAG) and superior temporal gyrus.

19 ces, anterior cingulate, insular cortex, and superior temporal gyrus.

20 ea 36 projects only to rostral levels of the superior temporal gyrus.

21 s in the entorhinal cortex, area TE, and the superior temporal gyrus.

22 s in temporal lobe structures, including the superior temporal gyrus.

23 gyrus, left medial parietal cortex and right superior temporal gyrus.

24 rder and tissue volume in the right anterior superior temporal gyrus.

25 ied the frontoparietal operculum, insula and superior temporal gyrus.

26 emporal and limbic lobes and decrease in the superior temporal gyrus.

27 , as well as in the right Heschl's gyrus and superior temporal gyrus.

28 nged arterial transit time (ATT) in the left superior temporal gyrus.

29 ral inferior frontal gyrus and contralateral superior temporal gyrus.

30 gular gyrus, planum temporale, and posterior superior temporal gyrus.

31 ruit this region and instead activated right superior temporal gyrus.

32 as the white matter underlying the posterior superior temporal gyrus.

33 ed gray matter volume reductions in the left superior temporal gyrus (13% difference) and bilateral f

34 smaller gray matter volumes in the posterior superior temporal gyrus (16% smaller on the right, 15% s

35 ter reductions were found bilaterally in the superior temporal gyrus (6.0%), but not in the hippocamp

36 The superior temporal gyrus, a heteromodal auditory and lang

37 Here, we recorded from the human superior temporal gyrus, a high-order auditory cortex, a

38 In posterior superior temporal gyrus, a proportion of sites had suppr

39 e effect more precisely to the left anterior superior temporal gyrus, a region previously implicated

40 These findings provide new evidence that superior temporal gyrus abnormalities may result from ge

41 of the planum temporale, Heschl's gyrus, and superior temporal gyrus, additionally controlled for han

42 c and/or neurodevelopmental underpinnings of superior temporal gyrus alterations are unknown.

43 vation in insula, anterior cingulate cortex, superior temporal gyrus, amygdala, parahippocampal gyrus

44 In contrast, activity in posterior superior temporal gyrus, an area associated with the pro

45 n in matched comparison subjects in the left superior temporal gyrus, an area important for language

46 reas combined, left cingulate gyrus and left superior temporal gyrus and a fewer NODs in the right su

47 temporal lobe (excluding the volumes of the superior temporal gyrus and amygdala/hippocampal complex

48 ted in early-course schizophrenia, including superior temporal gyrus and anterior cingulate cortex, w

49 I volumes were calculated for gray matter of superior temporal gyrus and for the amygdala-hippocampal

50 For comparison, superior temporal gyrus and fusiform gyrus gray matter v

51 in the insula, superior temporal sulcus and superior temporal gyrus and happy < baseline in the ante

52 reases in the primary auditory cortex (i.e., superior temporal gyrus and Heschl's gyrus) correlated w

53 ens to these neural representations past the superior temporal gyrus and how they engage higher-level

54 tudy provides evidence that areas within the superior temporal gyrus and inferior frontal gyrus are h

55 ontrast, the response time courses along the superior temporal gyrus and inferior frontal gyrus were

56 previously implicated in ASD, including the superior temporal gyrus and inferior frontal sulcus.

57 lly, the activated areas included the entire superior temporal gyrus and large portions of the pariet

58 previously reported abnormality in the left superior temporal gyrus and may be a vulnerability marke

59 with smaller left hemisphere volumes in the superior temporal gyrus and middle temporal gyrus.

60 Focally decreased thickness was seen in the superior temporal gyrus and posterior cingulate cortex i

61 temporal sulcus (STS), happy > angry in the superior temporal gyrus and posterior superior temporal

62 permethylated in two other cortical regions (superior temporal gyrus and prefrontal cortex), but not

63 am that originates in the caudal part of the superior temporal gyrus and projects to the parietal cor

64 ipital gyrus, left anterior cingulate, right superior temporal gyrus and right precentral gyrus durin

65 tural integrity of a posterior region of the superior temporal gyrus and sulcus predicted auditory sh

66 mporal voice areas (TVAs) are regions of the superior temporal gyrus and sulcus that respond more to

67 Neural activity in bilateral anterior superior temporal gyrus and supratemporal plane was corr

68 ampus and amygdala) and neocortical regions (superior temporal gyrus and temporal pole) were examined

69 l lobe structural brain abnormalities in the superior temporal gyrus and the amygdala-hippocampal com

70 y of temporal lobe structures, including the superior temporal gyrus and the amygdala/hippocampal com

71 significant main effect of diagnosis in the superior temporal gyrus and the amygdala/hippocampal com

72 past risk modulated with the activity in the superior temporal gyrus and the angular gyrus, respectiv

73 In addition, the anterior third of the superior temporal gyrus and the dorsal bank of the super

74 There was hypometabolism in the right superior temporal gyrus and the left inferior parietal l

75 cortical gray matter volume loss in the left superior temporal gyrus and thus may not be developmenta

76 PD had significantly smaller GMV in the left superior temporal gyrus and widespread frontal, frontoli

77 ecorrelation of neural networks in the right superior temporal gyrus and, to a lesser extent, other a

78 ction (left superior temporal gyrus to right superior temporal gyrus), and positive correlation betwe

79 rior hippocampus, parahippocampal gyrus, and superior temporal gyrus, and an increase in white matter

80 ed in addictive disorders, including insula, superior temporal gyrus, and anterior/mid-cingulate cort

81 campus, bilateral middle frontal gyrus, left superior temporal gyrus, and cingulate gyrus/anterior ci

82 erior temporal gyrus, middle temporal gyrus, superior temporal gyrus, and fusiform gyrus during memor

83 significantly smaller average temporal lobe, superior temporal gyrus, and hippocampal volumes than no

84 ponses in bilateral primary auditory cortex, superior temporal gyrus, and lateral prefrontal cortex f

85 heres, bilateral sensorimotor cortices, left superior temporal gyrus, and left cingulate cortex.

86 measuring the volumes of the temporal lobe, superior temporal gyrus, and mesial temporal structures

87 f the precentral and postcentral gyri, right superior temporal gyrus, and opercula, which differentia

88 lateral prefrontal cortex, ventral striatum, superior temporal gyrus, and parahippocampal region.

89 " (in anterolateral Heschl's gyrus, anterior superior temporal gyrus, and posterior planum polare) an

90 ortical gray matter nuclei, corpus callosum, superior temporal gyrus, and pre- and postcentral gyri.

91 ight lateral orbitofrontal gyri (LOFG), left superior temporal gyrus, and right insular, lingual and

92 g caudate nucleus, globus pallidus, putamen, superior temporal gyrus, and substructures within thalam

93 primarily in dorsolateral prefrontal cortex, superior temporal gyrus, and superior parietal lobule.

94 in the right dorsolateral prefrontal cortex, superior temporal gyrus, and supplementary motor area, a

95 f the inferotemporal cortex, portions of the superior temporal gyrus, and the granular region of the

96 as the inferior frontal gyrus, the posterior superior temporal gyrus, and the inferior parietal lobul

97 maller volume on the right side of the total superior temporal gyrus; and 3) a positive correlation b

98 e regions include the parahippocampal gyrus, superior temporal gyrus, anterior temporal poles, and th

99 temporal gyrus and a fewer NODs in the right superior temporal gyrus as compared to those born preter

100 isphere language areas, right precentral and superior temporal gyrus, as well as left caudate and ant

101 plied the inference; and (2) within the left superior temporal gyrus at the coherence break or when p

102 latency of the left and right middle latency superior temporal gyrus auditory ~50ms response (M50)(1)

103 ht middle frontal gyrus (BA 9/46), the right superior temporal gyrus (BA 22), the right insula (BA 13

104 rior parietal lobe (BA 7), and the bilateral superior temporal gyrus (BA 22).

105 acquired from multiple positions within the superior temporal gyrus (BA21), dorsolateral frontal lob

106 supratemporal plane (core), and areas on the superior temporal gyrus (belt).

107 rtant for language processing, including the superior temporal gyrus (beta=-88.8 muL per risk allele,

108 tter volume differences in the left or right superior temporal gyrus between the subjects with schizo

109 rtex (BA 17/18), left hippocampus, bilateral superior temporal gyrus, bilateral lenticular nuclei and

110 Posterior insular was active coincident with superior temporal gyrus but was more active for self-gen

111 atter-white matter ratios in the rest of the superior temporal gyrus, but this pattern was not observ

112 ontal cortex and aberrant recruitment of the superior temporal gyrus, caudate nucleus, and thalamus.

113 in gray matter volume over time in the left superior temporal gyrus compared with patients with firs

114 reased in the planum temporale and posterior superior temporal gyrus contralateral to the direction o

115 e found that anterior cingulate, insula, and superior temporal gyrus correlated with emotional apprai

116 temporal pole, inferior parietal lobule, and superior temporal gyrus) corresponded to regions associa

117 them (except the rostral inferotemporal and superior temporal gyrus cortices) are components of the

118 nal, inferotemporal, and anterior tip of the superior temporal gyrus cortices.

119 Interestingly, we also found that the superior temporal gyrus demonstrated a consistent abilit

120 M50 dipoles localizing to superior temporal gyrus demonstrated gating similar to t

121 ry gating would be evident in M50 sources in superior temporal gyrus, demonstrating ratios similar to

122 eases in regional cerebral blood flow in the superior temporal gyrus, dorsal anterior and posterior c

123 contrast, the DPFC connects with the rostral superior temporal gyrus, dorsal bank of the superior tem

124 inferior frontal gyrus, premotor cortex, and superior temporal gyrus during a picture description tas

125 al thalamus and putamen, and left insula and superior temporal gyrus during these tasks was significa

126 s a positive response in the human posterior superior temporal gyrus, enhancing the efficiency of aud

127 In contrast, lesions within the superior temporal gyrus extending into the supramarginal

128 ay matter volumes in the right orbitofrontal/superior temporal gyrus extending to the amygdala, insul

129 from right primary auditory cortex to right superior temporal gyrus (feed-forward) and from left pri

130 ongly associated with hypoperfusion of right superior temporal gyrus (Fisher's exact test; p < 0.0001

131 l association areas - from Heschl's gyrus to superior temporal gyrus for the auditory spelling task a

132 st analysis revealed additional decreases in superior temporal gyrus for the hearing loss group compa

133 isphere auditory regions, particularly right superior temporal gyrus, for processing speech.

134 Prefrontal cortex and superior temporal gyrus from postmortem brains of indivi

135 umes relative to normal controls in the left superior temporal gyrus, frontal regions, cerebellum and

136 ssive volume reduction of the left posterior superior temporal gyrus gray matter in patients with fir

137 d inferior temporal gyri, the left posterior superior temporal gyrus gray matter in the schizophrenia

138 between left temporal pole and left anterior superior temporal gyrus gray matter volumes.

139 The superior temporal gyrus has been implicated in language

140 An abnormal superior temporal gyrus has figured prominently in schiz

141 ical gray matter volumes, including the left superior temporal gyrus, have been reported in magnetic

142 lumes were determined for the temporal lobe, superior temporal gyrus, Heschl's gyrus (HG), and the pl

143 associated with a lesion area comprising the superior temporal gyrus, Heschl's gyrus, insula, and str

144 n, the authors studied two components of the superior temporal gyrus: Heschl's gyrus and the planum t

145 An anteromedial Heschl's gyrus/superior temporal gyrus (HG/STG) region, engaged by the

146 ditory cortex and surrounding regions of the superior temporal gyrus; however, the manner in which th

147 t inferior frontal gyrus and left middle and superior temporal gyrus in a pattern that is consistent

148 ased between left inferior frontal gyrus and superior temporal gyrus in autism, and large-scale conne

149 gnificant reduction in left asymmetry in the superior temporal gyrus in both patients and controls.

150 included the anterior, posterior, and total superior temporal gyrus in both the left and right hemis

151 tence of volumetric alterations in the right superior temporal gyrus in children and adolescents with

152 The authors studied the superior temporal gyrus in nonpsychotic children at risk

153 demonstrated greater activation in the left superior temporal gyrus in response to BSL than hearing

154 in post-mortem cortical gray matter from the superior temporal gyrus in SZ.

155 rior superior temporal gyrus toward anterior superior temporal gyrus in the human brain.

156 to greater understanding of the role of the superior temporal gyrus in the premorbid vulnerability t

157 input to area TH is from the rostral part of superior temporal gyrus, including the auditory associat

158 Projections to the superior temporal gyrus, including the dorsal bank of th

159 orbitofrontal cortex, and uncus, and in the superior temporal gyrus, insula, and anterior cingulate

160 l as primary motor cortex, the Broca's area, superior temporal gyrus, insula, and claustrum.

161 orphology of the posterior cingulate cortex, superior temporal gyrus, insula, fusiform gyrus, and cau

162 contrast, we found that increased posterior superior temporal gyrus interhemispheric functional conn

163 The superior temporal gyrus is associated with developmental

164 , the data suggest that the right hemisphere superior temporal gyrus is particularly involved during

165 tial processing, whereas the left hemisphere superior temporal gyrus is particularly involved during

166 he prefrontal cortex and inferiorly into the superior temporal gyrus), left medial superior frontal g

167 ompetition in left supramarginal gyrus, left superior temporal gyrus, left middle temporal gyrus (MTG

168 sal anterior cingulate cortex (ACC), insula, superior temporal gyrus; left frontal and parietal operc

169 pre-distractor alpha/beta power in the left superior temporal gyrus (lSTG).

170 ence of low gamma modulations in the ACC and Superior Temporal Gyrus may associate with increases of

171 ty in the dorsolateral prefrontal cortex and superior temporal gyrus may contribute to the taste perc

172 -sided volumetric abnormalities found in the superior temporal gyrus may reflect a particularly early

173 nounced in the posterior portion of the left superior temporal gyrus (mean=9.6%) than in the anterior

174 hree brain areas (i.e., hypothalamus, insula/superior temporal gyrus, medial prefrontal cortex).

175 ormative activity in the anterior portion of superior temporal gyrus, middle temporal gyrus, right oc

176 pecific tuning to individual vowels, whereas superior temporal gyrus neurons have nonspecific, sinuso

177 aging was used to measure the right and left superior temporal gyrus of 29 young nonpsychotic subject

178 tivation were significantly decreased in the superior temporal gyrus of patients with SZ.

179 Post-mortem tissue from the superior temporal gyrus of schizophrenia and control sub

180 found that the volumes of the right and left superior temporal gyrus of the subjects at risk for schi

181 as to investigate gray matter volumes in the superior temporal gyrus of the temporal lobe (left and r

182 ndicated the causal relationship between (i) superior-temporal gyrus of either hemisphere and auditor

183 impaired after removal of either the rostral superior temporal gyrus or the medial temporal lobe but

184 ic regions of the temporal lobe, such as the superior temporal gyrus or the right temporal lobe, did

185 ) and decreased activation in the insula and superior temporal gyrus (P < 0.01 for all).

186 A PS x ED interaction was shown in the superior temporal gyrus (P < 0.01).

187 r "where" (in planum temporale and posterior superior temporal gyrus) pathways as early as approximat

188 n areas hMT+/V5+ and implicate the posterior superior temporal gyrus/planum temporale in auditory mot

189 specifically, IA participants recruited left superior temporal gyrus/planum temporale, matching the p

190 e posterior cingulate, precuneus, insula and superior temporal gyrus preferentially differentiates to

191 tion preferentially engaged a portion of the superior temporal gyrus previously implicated in visual

192 the parainsula, and rostral portions of the superior temporal gyrus project both to the lateral, bas

193 ere localized primarily to lateral posterior superior temporal gyrus (pSTG) and modulated binaural-cu

194 auditory association cortex in the posterior superior temporal gyrus (pSTG) of epileptic patients.

195 ts (both male and female) over the posterior superior temporal gyrus (pSTG), a brain area known to be

196 highly predictive contexts in left posterior superior temporal gyrus (pSTG), an area previously assoc

197 In conjunction with findings of left superior temporal gyrus reduction and bilateral fusiform

198 g controls in the superior frontal gyrus and superior temporal gyrus, regions previously linked to sc

199 temporal sulcus and the lateral bank of the superior temporal gyrus, respectively.

200 chizophrenia (N=14) and comparison (N=14) of superior temporal gyrus revealed a smaller molecular mas

201 isions of the parabelt, and in cortex of the superior temporal gyrus rostral to the parabelt with par

202 activity at single electrodes over the human superior temporal gyrus selectively represented intonati

203 The superior temporal gyrus showed less activation in the sc

204 The superior temporal gyrus showed the most prevalent and co

205 Within the superior temporal gyrus, significantly greater metabolic

206 showed sustained delay-period activity, the superior temporal gyrus (STG) activated more vigorously

207 relationship was fully mediated by bilateral superior temporal gyrus (STG) activation.

208 ty between the left AI/FO and left posterior superior temporal gyrus (STG) and between the left AI/FO

209 re connected with the dorsal TG, the rostral superior temporal gyrus (STG) and dorsal bank of STS, an

210 ion during stress in hippocampus, precuneus, superior temporal gyrus (STG) and insula.

211 egions beyond HG and PT, specifically in the superior temporal gyrus (STG) and planum polare (PP).

212 involved in speech processing, including the superior temporal gyrus (STG) and the posterior inferior

213 entified as differentially expressed between superior temporal gyrus (STG) and the remaining cerebral

214 e sleep fMRI method show that defects in the superior temporal gyrus (STG) in response to language ar

215 nsiderable evidence has implicated the human superior temporal gyrus (STG) in speech processing.

216 musia [5-8] suggest that the right posterior superior temporal gyrus (STG) in the human brain is spec

217 The human superior temporal gyrus (STG) is critical for extracting

218 The human superior temporal gyrus (STG) is critical for speech per

219 The association cortex of the superior temporal gyrus (STG) is implicated in complex s

220 The superior temporal gyrus (STG) is on the inferior-lateral

221 gnetoencephalographic brain responses in the superior temporal gyrus (STG) is uniquely consistent wit

222 trypsin-, trypsin-, and caspase-like) in the superior temporal gyrus (STG) of 25 SZ and 25 comparison

223 We studied the superior temporal gyrus (STG) of subjects from the Mount

224 The superior temporal gyrus (STG) participates in high-order

225 Previous studies revealed that posterior superior temporal gyrus (STG) responds to acoustic scale

226 itory regions on the supratemporal plane and superior temporal gyrus (STG) were investigated using Gr

227 left inferior frontal gyrus (IFG), posterior superior temporal gyrus (STG), and inferior parietal lob

228 in humans, as in monkeys, is located on the superior temporal gyrus (STG), and is functionally and s

229 damage in neglect patients lies in the right superior temporal gyrus (STG), and not in the right post

230 iated with neglect is the mid portion of the superior temporal gyrus (STG), on the lateral surface of

231 etry of the inferior frontal gyrus (IFG) and superior temporal gyrus (STG), the sensory and visual co

232 nemes) is consistently localized to left mid-superior temporal gyrus (STG), whereas activation associ

233 tructure of the reward system, and the right superior temporal gyrus (STG).

234 ge: the primary auditory cortex (A1) and the superior temporal gyrus (STG).

235 racterized the distribution of PCM1 in human superior temporal gyrus (STG).

236 ssion during stimulation of sites within the superior temporal gyrus (STG).

237 ced gray matter volume of the left posterior superior temporal gyrus (STG).

238 d dorsolateral prefrontal cortex but not the superior temporal gyrus (STG).

239 training increased synaptic gain in the left superior temporal gyrus (STG).

240 al activity in a peri-auditory region of the superior temporal gyrus (STG).

241 erior frontal gyrus (IFG), and the bilateral superior temporal gyrus (STG).

242 ocal areas of non-primary auditory cortex on superior temporal gyrus (STG).

243 In contrast, the anterior superior temporal gyrus (STG)/superior temporal sulcus w

244 x [PCC], inferior parietal lobule [IPL], and superior temporal gyrus (STG]) were drawn on the MRI sca

245 voked potential at Cz, M50 at left and right superior temporal gyrus [STG]) and 100 msec (N100 at Cz,

246 n of iHGP with task performance in posterior superior temporal gyrus (STGp) that was observed in heal

247 jacent auditory-related areas of the rostral superior temporal gyrus (STGr) and temporal pole.

248 It is connected with the rostral superior temporal gyrus (STGr) and the dorsal bank of th

249 sk-specific activation increase in the right superior temporal gyrus/sulcus (STG/STS) during speaker

250 eas, including somatosensory cortex, insula, superior temporal gyrus, supramarginal gyrus, striatum,

251 n increase in neurotransmission in the right Superior Temporal Gyrus (t=1.403, p=0.00780), Fusiform G

252 fferent brain regions (medial frontal gyrus, superior temporal gyrus, thalamus, and subventricular zo

253 n associated with mentalizing (i.e. the left superior temporal gyrus) than joy.

254 l responses, most notably in right posterior superior temporal gyrus, than an identical shift that oc

255 ding that neurons in the rostral part of the superior temporal gyrus (the superior temporal polysenso

256 nts) in the middle and posterior part of the superior temporal gyrus, the adjacent part of the middle

257 ally significant gender interactions for the superior temporal gyrus, the amygdala/hippocampal comple

258 e of temporal lobe structures, including the superior temporal gyrus, the amygdala/hippocampal comple

259 For the superior temporal gyrus, the decrease exceeded that of w

260 stcentral gyrus, the paracentral lobule, the superior temporal gyrus, the middle cingulate gyrus, the

261 the right posterior superior temporal sulcus/superior temporal gyrus, the right medial anterior tempo

262 the left dorsolateral prefrontal cortex and superior temporal gyrus; the right ventrolateral prefron

263 mic regions (sensorimotor, Broca's area, and superior temporal gyrus), these behavior- and location-d

264 from nonprimary auditory cortex in the human superior temporal gyrus to determine what acoustic infor

265 performance and a feedback connection (right superior temporal gyrus to right primary auditory cortex

266 on and an inter-hemispheric connection (left superior temporal gyrus to right superior temporal gyrus

267 thors obtained bilateral measurements of the superior temporal gyrus (total, gray matter, and white m

268 l acoustic features of speech from posterior superior temporal gyrus toward anterior superior tempora

269 The left superior temporal gyrus tracked the approximately 0.5 Hz

270 rontal cortex, inferior frontal gyrus, right superior temporal gyrus, ventral posterior cingulate cor

271 rder and a negative correlation between left superior temporal gyrus volume and odd speech.

272 h schizotypal personality disorder showed no superior temporal gyrus volume differences, but prelimin

273 minently in schizophrenia research, and left superior temporal gyrus volume has been shown to be smal

274 onship between language-related symptoms and superior temporal gyrus volume is similar to that seen i

275 association between abnormal speech and left superior temporal gyrus volume, a finding similar to tha

276 an inverse correlation between age and left superior temporal gyrus volume.

277 significant group differences were found in superior temporal gyrus volume.

278 llucinations were inversely related to right superior temporal gyrus volume.

279 measured prefrontal, inferior parietal, and superior temporal gyrus volumes and examined the pattern

280 Bilateral superior temporal gyrus volumes were positively correlat

281 The superior temporal gyrus was drawn on coronal images acqu

282 The superior temporal gyrus was manually delineated on coron

283 Prolonged ATT in the left superior temporal gyrus was negatively correlated with t

284 ty in the medial prefrontal cortex and right superior temporal gyrus was observed in children with AS

285 he total and gray matter volume of the right superior temporal gyrus was significantly lower in patie

286 r the visual spelling task from calcarine to superior temporal gyrus was stronger than all other effe

287 ight middle temporal gyri and left posterior superior temporal gyrus were present in schizophrenia bu

288 Neurons in the lateral belt areas of the superior temporal gyrus were tuned to the best center fr

289 al processing occurred in the left posterior superior temporal gyrus (Wernicke's area) and motor prod

290 nts during the stories: (1) within the right superior temporal gyrus when a verb in the text implied

291 ly 50% in severe Alzheimer's hippocampus and superior temporal gyrus when normalized to expression of

292 increased coupling within the left posterior superior temporal gyrus, whereas perceptually equivalent

293 imotor interface areas (e.g., left posterior superior temporal gyrus), which was reliable only when t

294 The superior temporal gyrus, which contains the auditory cor

295 malities have been reported in the posterior superior temporal gyrus, which includes the Heschl gyrus

296 ual cortex, and the posterior portion of the superior temporal gyrus, which is known as a region invo

297 quire retrieval of learned associations, the superior temporal gyrus, which responds well to sounds,

298 s from the human nonprimary auditory cortex (superior temporal gyrus) while subjects listened to spee

299 tivity with the medial prefrontal cortex and superior temporal gyrus, while aberrant limbic connectiv

300 ing generators of the auditory MMN along the superior temporal gyrus with no evidence of a somatosens