ライフサイエンスコーパス: temporal cortex

1 erior cingulate gyrus, precuneus, and mesial temporal cortex.

2 in delayed reconciliation of predictions in temporal cortex.

3 d from the prefrontal cortex and the ventral temporal cortex.

4 ble representations in higher-level, ventral-temporal cortex.

5 between different subregions of the ventral temporal cortex.

6 role of distinct subregions of the anterior temporal cortex.

7 00 cis-regulatory elements in prefrontal and temporal cortex.

8 ctivity (at approximately 90 Hz) in inferior temporal cortex.

9 y in the entorhinal cortex, hippocampus, and temporal cortex.

10 ed senile plaques, mainly in the frontal and temporal cortex.

11 ophrenia and comparison subjects in superior temporal cortex.

12 cortical thickness in the orbitofrontal and temporal cortex.

13 thalamic pulvinar nuclei and the left medial temporal cortex.

14 volume loss in the right posterior inferior temporal cortex.

15 t medial frontal cortex and the right middle temporal cortex.

16 F recovery in the right insular and superior temporal cortex.

17 l correct rewarded responses in the superior temporal cortex.

18 regions of the default mode network and the temporal cortex.

19 ntration ranged from 2.6-113 mg kg(-1) dw in temporal cortex.

20 rtex, lateral parietal cortex, and posterior temporal cortex.

21 ior parietal cortex, precuneus, and superior temporal cortex.

22 with predominately medial and anterolateral temporal cortex.

23 spike rate in the amygdala, hippocampus, and temporal cortex.

24 ion from posterior cingulate to anteromedial temporal cortex.

25 rimates, although other species also present temporal cortex.

26 system (X-system), specifically the lateral temporal cortex.

27 y the repetition probability in the inferior temporal cortex.

28 pment, and is abundant in both NCM and human temporal cortex.

29 n deposition in the GP, SN, red nucleus, and temporal cortex.

30 rful neuronal representation in the inferior temporal cortex.

31 and orbital prefrontal cortices and anterior temporal cortex.

32 BA receptor subunits normally present in the temporal cortex.

33 ortex and at 300 ms in the ventral occipital temporal cortex.

34 N, namely the posterior cingulate and medial temporal cortex.

35 late and parietal cortex, basal ganglia, and temporal cortex.

36 unctional connectivity, especially in fronto-temporal cortex.

37 fected brain regions, particularly in fronto-temporal cortex.

38 -order visual regions spanning occipital and temporal cortex.

39 ctivity and tau accumulation in the inferior temporal cortex.

40 al striatum, posterior cingulate cortex, and temporal cortex.

41 modal association cortex in both frontal and temporal cortex.

42 and activity of certain neurons in the human temporal cortex.

43 related circuitry, including the dorsocaudal temporal cortex.

44 orbitofrontal cortex, insula, amygdala, and temporal cortex.

45 orbitofrontal, lateral temporal, and medial temporal cortex.

46 hinning, particularly within the frontal and temporal cortex.

47 d been implanted with electrodes in superior temporal cortex.

48 uding the hippocampus, frontal, and inferior temporal cortex.

49 and are co-expressed with aromatase in human temporal cortex.

50 dorsomedial prefrontal cortex and posterior temporal cortex.

51 amygdala connectivity to the prefrontal and temporal cortex.

52 /- 0.15 vs. 1.49 +/- 0.10; P = 0.028), right temporal cortex (1.30 +/- 0.17 vs. 1.45 +/- 0.09; P = 0.

53 0.17 vs. 1.45 +/- 0.09; P = 0.046), and left temporal cortex (1.41 +/- 0.20 vs. 1.52 +/- 0.20; P = 0.

54 organization of object size in the occipito-temporal cortex(2).

55 f: (1) early theta oscillations in the right temporal cortex, (2) increased HFA in the left hemispher

56 with right premotor cortex and left insular-temporal cortex a network that might support active infe

57 was not different between both groups in the temporal cortex, a less vulnerable structure compared to

58 the left temporal pole and adjacent anterior temporal cortex, a pattern of atrophy that left sentence

59 were reflected by activity in left inferior temporal cortex, a region known to represent objects and

60 oro-parietal cortex, peaking in the anterior temporal cortex; a negative HbT response to emotional sp

61 deration of the sulcal patterning in ventral temporal cortex across hominoids, as well as revise the

62 ssociation of fiber bundles linking anterior temporal cortex/amygdala and prefrontal cortex in humans

63 se to novel and familiar stimuli in inferior temporal cortex, an area underlying visual object recogn

64 ) in the putamen, with a BPND of 0.25 in the temporal cortex and 1.92 in the putamen.

65 from three brain regions [prefrontal cortex, temporal cortex and cerebellum (CB)] dissected from 43 A

66 ns including dorsolateral prefrontal cortex, temporal cortex and cerebellum.

67 ter neural responses within ventral occipito-temporal cortex and diminished responses within anterior

68 rain, we immunostained surgical specimens of temporal cortex and hippocampus and autopsy brains for C

69 word-specific semantic processing in ventral temporal cortex and more anterior MTG, respectively.

70 gy that slowly spreads throughout the medial temporal cortex and neocortices independently of Abeta,

71 ygen-level dependent signals of the superior temporal cortex and other cortical regions acquired with

72 ons were also significant in frontal cortex, temporal cortex and pons: P ranging from 4.8 x 10(-12) t

73 A fusion between temporal cortex and posterior insula was present in 22 s

74 h functional connectivity in the left middle temporal cortex and precuneus at 3-month follow-up.

75 acute brain slices of adult human and mouse temporal cortex and probed the dynamical properties of u

76 The findings in right posterior inferior temporal cortex and right premotor cortex are consistent

77 e 7R+ and 7R- groups in cerebellum, inferior temporal cortex and striatum.

78 y matter) were quantified in the frontal and temporal cortex and thalamus in the nontumoral hemispher

79 d with functional connectivity in the middle temporal cortex and the anterior midcingulate cortex, wh

80 al frequency-specific networks involving the temporal cortex and the cerebellum.

81 ources were identified in the right superior temporal cortex and the orbitofrontal cortex.

82 , a correlation was observed with the middle temporal cortex and the posterior cingulate cortex.

83 n neural response patterns in human superior temporal cortex and the structural properties of ASR-der

84 o support form perception (including ventral temporal cortex and the superior temporal sulcus).

85 d by theta-gamma phase-amplitude coupling in temporal cortex and theta phase synchronization across f

86 clinical disorders of autism (e.g., superior temporal cortex) and antisociality (e.g., anterior prefr

87 ite matter, midbrain peduncles, red nucleus, temporal cortex) and correlated with changes in white ma

88 frontal gyrus, as well as the ventrolateral temporal cortex, and (3) motor/language activation durin

89 anges in activity in the amygdala, posterior temporal cortex, and cerebellum.

90 l connections to inferior frontal and medial temporal cortex, and cingulate gyri.

91 within this time window to the left anterior temporal cortex, and fMRI localized the effect more prec

92 y motor area, supramarginal gyrus, posterior temporal cortex, and inferior and middle frontal gyri.

93 nferior parietal cortex, precuneus, superior temporal cortex, and lingual gyrus mediated the associat

94 with higher volume of the prefrontal cortex, temporal cortex, and medial orbitofrontal cortex.

95 l prefrontal cortex, orbital frontal cortex, temporal cortex, and medial temporal lobe.

96 rior inferior frontal region or left ventral temporal cortex, and orthographic working memory deficit

97 ely in layer 6 of V1, V2, V3, MT, regions of temporal cortex, and other visual areas.

98 umulate amyloid, such as the frontal cortex, temporal cortex, and posterior cingulate.

99 detect Abeta plaques in the atrophic mesial temporal cortex, and potentially to evaluate changes in

100 tric modulation of medial prefrontal cortex, temporal cortex, and striatum.

101 ervations mirror results in macaque inferior temporal cortex, and taken together, these results sugge

102 x, insula, caudate, putamen, frontal cortex, temporal cortex, and thalamus.

103 eft posterior frontal cortex, left posterior temporal cortex, and the left intraparietal sulcus and a

104 ce from anterolateral HG throughout superior temporal cortex, and was more pronounced for clear compa

105 We recorded from the rostral superior temporal cortex as monkeys performed serial auditory del

106 tical recordings from human lateral superior temporal cortex as subjects listened to words and nonwor

107 ightly more anteriorly in posterior inferior temporal cortex as well as in ventral premotor cortex.

108 s I, III, and V of the prefrontal and middle temporal cortex, as well as in hippocampal fields CA1 an

109 ey cortical nodes in frontal, cingulate, and temporal cortex associated with externalizing behaviors

110 ust specific response over the left occipito-temporal cortex at the predefined frequency of 1.2 Hz (i

111 s disease and exhibited greater longitudinal temporal cortex atrophy on MRI.

112 61 to -0.0047) and area of the right lateral temporal cortex (beta = 0.024; CI: 0.0034-0.054).

113 d activity within the left anterior superior temporal cortex between 300 and 500 ms after a word is p

114 thy subjects with increasing age) and in the temporal cortex bilaterally (indicating a relative loss

115 time, GluCer isoform levels were analyzed in temporal cortex brain tissue samples from 26 PD patients

116 .SIGNIFICANCE STATEMENT The bimodal superior temporal cortex (bSTC) is a brain region that plays a cr

117 hysiology revealed that the bimodal superior temporal cortex (bSTC) is topographically organized acco

118 nguished according to lesion location in the temporal cortex, but in each group, some individuals had

119 namic face stimulus over bilateral posterior temporal cortex, but no activation in response to a movi

120 ndary, and association areas of the superior temporal cortex, but not motor cortex.

121 g, we found increased connectivity in medial temporal cortex, but reduction in precentral and sensory

122 iated with dysfunction in the prefrontal and temporal cortex, but such dysfunctional behaviors are ty

123 g homology to a putative ET cluster in human temporal cortex, but with a strikingly specific regional

124 hippocampus and immediately adjacent medial-temporal cortex by delivering theta-burst transcranial m

125 ions can be differentiated along the ventral temporal cortex by their real-world size.

126 left perisylvian language areas (frontal and temporal cortex) by way of the arcuate fasciculus (AF).

127 ining was that the basal ganglia and ventral temporal cortex came to represent attentional states mor

128 ponents, measured from sensors over auditory temporal cortex, came to distinguish between CS(+) and C

129 precentral and supramarginal gyri, superior temporal cortex, central operculum/posterior insula, and

130 phase synchronization between prefrontal and temporal cortex co-occurred with local cross-frequency p

131 nt to visual processing regions and inferior temporal cortex (Cohen's d=1.54).

132 d higher levels of processing in the ventral temporal cortex compared with those followed by a rememb

133 Human inferior temporal cortex contains category-selective visual regio

134 face- and place-selective regions of ventral temporal cortex correlate with behavioral performance fo

135 for task stimuli, activation in the inferior temporal cortex differed between the anxiety and healthy

136 by the cross-modal recruitment of the right temporal cortex during and after deafness.

137 ent that explored neural activity in ventral temporal cortex during object recognition and demonstrat

138 ting) predicted lower competition in ventral temporal cortex during subsequent retrieval.

139 dala and areas in the occipital and inferior temporal cortex during the viewing of fearful and aggres

140 er categorization and in the right posterior temporal cortex during vowel categorization.

141 itive impairment and dementia), and inferior temporal cortex (early and late mild cognitive impairmen

142 ndividuals, and (2) in deafness, is superior temporal cortex encompassing primary and secondary audit

143 often simultaneously reactivated in ventral temporal cortex--even when target memories were successf

144 xcitatory and inhibitory neurons in inferior temporal cortex exhibit distinct influences long-term vi

145 in human ventral cortex and monkey inferior temporal cortex ("face patches") raises the question of

146 demonstrated in the human posterior ventral temporal cortex for a variety of object categories.

147 and premotor regions, cingulate cortex, and temporal cortex for control but not body-focused videos.

148 Non-normalized results showed thinner temporal cortex for EPT, while ICV-normalized results sh

149 d neurons from archived tissue blocks of the temporal cortex from patients with Alzheimer's disease.

150 insula > caudate/putamen > frontal cortex > temporal cortex > thalamus, consistent with the reported

151 d an attention-related region in the macaque temporal cortex, here called the floor of the superior t

152 The interactive nature of the ventral temporal cortex highlights how top-down modulation const

153 l revealed a temporal atrophy factor (medial temporal cortex, hippocampus, and amygdala), a subcortic

154 te cortex, inferior occipital cortex, middle temporal cortex, hippocampus, and the precentral sulcus)

155 cted brain structures including the inferior temporal cortex, hippocampus, fornix, and mammillary bod

156 al in early visual cortex and human inferior temporal cortex (hIT).

157 that layer 2/3 pyramidal neurons from human temporal cortex (HL2/3 PCs) have a specific membrane cap

158 of the functional organization of the middle-temporal cortex (hMT+/V5) for vision.

159 s typically observed in the occipital middle-temporal cortex (hMT+/V5) region for computing visual mo

160 er transcriptomic analyses using frontal and temporal cortex, however, our proteomic analysis did not

161 that is most prominent in the left anterior temporal cortex; however, there is little consensus rega

162 95% CI, 1.71-6.38; Lewy bodies in frontal or temporal cortex in ACT: RR for TBI with LOC >1 hour, 5.7

163 e retinotopic organization of medial ventral temporal cortex in four monkeys (2 male and 2 female).

164 , prefrontal cortex, insula, hippocampus and temporal cortex in methamphetamine users, but not in con

165 gyrus, alongside insular, orbitofrontal and temporal cortex in our patient cohort.

166 tact functional organization of the occipito-temporal cortex in people born blind, supporting an orga

167 t of regions in the hippocampus and superior temporal cortex in skilled exploration of complex sound

168 luding frontal, parahippocampal, and lateral temporal cortex) in which Val homozygotes showed higher

169 ealed post-treatment decreases in CBF in the temporal cortex, including the amygdala.

170 ivity between the ventral caudate and medial temporal cortex increased as a function of caudate D2DR

171 correlated with atrophy involving the mesial temporal cortex, insula, and amygdala, regions previousl

172 e noxious stimulation, increased activity in temporal cortex, insula, pulvinar, caudate, and pons.

173 ily modeled, but the absence of evidence for temporal cortex involvement has suggested a fundamental

174 lesions to the dlPFC and inferior posterior temporal cortex (ipTC).

175 erential gene expression between frontal and temporal cortex is attenuated in autistic brains.

176 The visual occipito-temporal cortex is composed of several distinct regions

177 Occipito-temporal cortex is known to house visual object represen

178 s regarding which region within the anterior temporal cortex is most prominently damaged, which may i

179 ealed multiple subregions in monkey inferior temporal cortex (IT) that are selective for images of fa

180 ded activity from single neurons in inferior temporal cortex (IT) while monkeys performed a task that

181 f hundreds of neurons in V4 and the inferior temporal cortex (IT) while naive macaque monkeys passive

182 oscillations was found in the left inferior temporal cortex (IT), an area known to be involved in vi

183 othesis have been born out in human inferior temporal cortex (IT), an area of the brain crucial for t

184 ions for object vision culminate in inferior temporal cortex (IT), but the functional organization fo

185 of neural recordings across monkey inferior temporal cortex (IT), construct large-scale maps of neur

186 l area (MT), visual area four (V4), inferior temporal cortex (IT), lateral intraparietal area (LIP),

187 ual-object processing culminates in inferior temporal cortex (IT).

188 p of primate ventral visual stream [inferior temporal cortex (IT)] have selectivity for objects that

189 the prefrontal cortex (PFC) and the inferior temporal cortex (ITC) are involved in visual shape categ

190 site of tau deposition, and in the inferior temporal cortex (ITC), an early site of neocortical tau

191 te for this adult plasticity is the inferior temporal cortex (ITC).

192 uitry within a small region in human ventral temporal cortex known as the visual word form area (VWFA

193 r ratio was higher in the bilateral superior temporal cortex (left: +10.0%; P = .03 and right: +10.8%

194 ), we identify a region of left mid-superior temporal cortex (lmSTC) that flexibly encodes "who did w

195 By contrast, only left lateral posterior temporal cortex (LPTC) encodes action representations th

196 and small object preferences in the ventral temporal cortex, mirrored along the lateral surface.

197 ly influenced large areas of the frontal and temporal cortex, mirroring regions that are the most evo

198 l cortex (DLPFC) (MR, 0.26 mm; P = .001) and temporal cortex (MR, 0.33 mm; P = .047).

199 m, we investigated how neurons in the middle temporal cortex (MT) of macaque monkeys represent overla

200 ues to investigate how neurons in the middle temporal cortex (MT) represent multiple stimuli that com

201 sula and caudate; semantic variant, anterior temporal cortex; non-fluent variant, frontal operculum).

202 c kinetics were recovered, especially in the temporal cortex, occipital cortex, and medulla.

203 in the insula, prefrontal cortex, amygdala, temporal cortex, occipital cortex, cerebellum and thalam

204 by unbiased stereology-based quantitation in temporal cortex of 40 AD patients and 32 age-matched non

205 TDP-43 and is strikingly reduced in level in temporal cortex of human patient tissue.

206 sponse properties of neurons in the inferior temporal cortex of non-human primates.

207 ificant difference in beta2*-nAChR number in temporal cortex of the bipolar depressed and control gro

208 hat areas in the middle part of the superior temporal cortex, often associated with the processing of

209 9.7 [2.6]; P = 3.0 x 10(-4)) in the inferior temporal cortex only in subjects who were diagnosed with

210 -band ASSR (ITC > 0.25) in the left superior temporal cortex, orbitofrontal cortex, and left superior

211 gests that acetylcholine within the inferior temporal cortex ordinarily facilitates functional recove

212 How dependent is occipito-temporal cortex organization on object manipulation and

213 ASD) is characterized by marked DMN-occipito-temporal cortex (OTC) hypoconnectivity.

214 al prefrontal cortex (P < .001) and superior temporal cortex (P < .003) during negative valence tasks

215 anatomical region of interest) and anterior temporal cortex (P < 0.001 uncorrected over whole brain)

216 xon 3 in frontal cortex (P=9.2 x 10(-6)) and temporal cortex (P=2.6 x 10(-6)).

217 10(-8)), frontal cortex (P 1.3 x 10(-9)) and temporal cortex (P1.2 x 10(-11)).

218 s in the lateral occipital complex, inferior temporal cortex, parahippocampal cortex, and prefrontal

219 increased from posterior to anterior ventral temporal cortex, peaking in the temporal pole.

220 ectivity in the medial orbitofrontal cortex, temporal cortex, posterior cingulate cortex, and precune

221 ral gyrus (pMTG/ITG), angular gyrus, ventral temporal cortex, posterior cingulate/precuneus (PC), and

222 ded the orbitofrontal cortex, prefrontal and temporal cortex, precuneus, and supramarginal gyrus.

223 edial segregation of activation in posterior temporal cortex previously observed in response to image

224 ow demonstrated lateralized abnormalities of temporal cortex processing of language in autism across

225 tivariate pattern, in the posterior superior temporal cortex (pSTS) - a face-selective region that is

226 scence, predominantly in the temporal lobes (temporal cortex: random field theory corrected; left amy

227 volumes predicted degeneration in the medial temporal cortex, recapitulating a prior influential stag

228 at during visual working memory maintenance, temporal cortex regions, which exhibit enhanced PAC, int

229 dy category-selective regions of the primate temporal cortex respond to images of bodies, but it is u

230 amygdala, hippocampus) and anterior inferior temporal cortex responded abruptly when sufficient infor

231 Spatially coherent patches in human temporal cortex responded selectively to individual phon

232 'visual word-form area' in ventral occipito-temporal cortex (responding more to words than consonant

233 sounds and have abnormally right-lateralized temporal cortex response to language; this defect worsen

234 ental trends with a tendency towards greater temporal cortex response with increasing age and mainten

235 creased 30-Hz activity in the right superior temporal cortex, resulting in reinstating a left dominan

236 a number of regions, including the anterior temporal cortex, rostral medial prefrontal cortex, and a

237 Post-mortem temporal cortex samples from Alzheimer's disease patient

238 110,000 neuronal transcriptomes derived from temporal cortex samples of multiple temporal lobe epilep

239 001) and increased GMV in the right inferior temporal cortex (SDM estimate = 0.755; P < .001).

240 The transverse temporal cortex showed a trend (P = .02, but did not sur

241 ion in the dysplasics suggests that occipito-temporal cortex specialization is driven largely by inhe

242 by AW result in greater activity in the left temporal cortex starting at ~230 ms and persisting throu

243 ight CCL checkpoint proteins in the superior temporal cortex (STC) of persons with varying severities

244 ticity, in particular in regions of superior temporal cortex (STC) that primarily respond to auditory

245 sults identify a putative macaque homolog to temporal cortex structures known to play a central role

246 nd altered PPPP4R3A transcript expression in temporal cortex, suggesting a role at the molecular leve

247 ateral prefrontal cortices (DLPFC), the left temporal cortex, superior medial prefrontal gyrus (MPFC)

248 d the correlation coefficient between mesial temporal cortex SUVR and histopathology score for Abeta

249 The PVEC-related increase in mesial temporal cortex SUVR correlated with the Scheltens score

250 osite SUVRs and from 0.04 to 1.04 for mesial temporal cortex SUVRs.

251 levels as a function of LB pathology in the temporal cortex (TC) from autopsy-confirmed LBV/AD cases

252 e processing simultaneously across the human temporal cortex (TC) using intracranial recordings in ei

253 ed with significantly greater variability of temporal cortex, thalamus, putamen, and third ventricle

254 Recently, a ventral region in the macaque temporal cortex, the posterior infero-temporal dorsal ar

255 In left inferior frontal gyrus and posterior temporal cortex, the repetition of novel syntactic struc

256 hether a visual region in the human occipito-temporal cortex-the extrastriate body area-compensates f

257 l, right retrosplenial cingulate, and medial temporal cortex thickness were negatively correlated wit

258 tal cortex thickness, lower right transverse temporal cortex thickness, greater self-reported depress

259 ight hippocampal volume deficit and inferior temporal cortex thinning demonstrated a significant effe

260 itive impairment converters showed bilateral temporal cortex thinning relative to the Parkinson's dis

261 Even within inferior temporal cortex, this proto-organization was already pre

262 stimulus translation found in monkey visual temporal cortex, thus revealing a homology between shape

263 V(T) values (mL.cm(-3)) ranged from 10.1 in temporal cortex to 5.6 in cerebellum.

264 tory processing and associative areas in the temporal cortex to a greater extent than the hearing par

265 al white matter volume connecting the middle temporal cortex to the angular and supramarginal gyri.

266 pha-synuclein seeds are transported from the temporal cortex to the facial nuclei.

267 eds from sensory representations of words in temporal cortex to their corresponding articulatory gest

268 ng fNIRS, we examined activation of superior temporal cortex to visual speech in the same profoundly

269 of speech spreading from posterior superior temporal cortex toward inferior frontal gyrus were assoc

270 object representations in the human ventral temporal cortex using angular dispersion, a powerful, mu

271 contrast to Heschl's gyrus, in the superior-temporal cortex visual signal was comparable to somatose

272 ce-selective regions in the ventral occipito-temporal cortex (VOTC), with a right hemispheric dominan

273 gorical organization of the Ventral Occipito-Temporal Cortex (VOTC)?

274 eral face-selective responses in the ventral temporal cortex (VTC) and prosopagnosia is reported in p

275 es occur to gray and white matter in ventral temporal cortex (VTC) from childhood to adulthood, and h

276 he lateral parietal cortex (LPC) and ventral temporal cortex (VTC) have been shown to code for abstra

277 Human ventral temporal cortex (VTC) is critical for visual recognition

278 Ventral temporal cortex (VTC) is the latest stage of the ventral

279 ying the animacy organization of the ventral temporal cortex (VTC) remain hotly debated, with recent

280 ve to haptic perception and the left ventral temporal cortex (VTC) to size.

281 enultimate visual-processing region, ventral-temporal cortex (VTC), visual experience is not the orig

282 ndamental ability supported by human ventral temporal cortex (VTC).

283 y with medial and lateral regions of ventral temporal cortex (VTC).

284 category-selective visual regions in ventral temporal cortex (VTC).

285 high-level perceptual regions (e.g., ventral temporal cortex, VTC).

286 both lateral occipital complex and inferior temporal cortex was altered.

287 Activity in the superior temporal cortex was significantly reduced in anophthalmi

288 d the functional connections of the superior temporal cortex, we successfully identified the first-ep

289 ll as in face-selective areas in the ventral temporal cortex were highly correlated with the patterns

290 ons in a face-selective region of the monkey temporal cortex were reported to be selective for mirror

291 etal, cingulate, supramarginal, and superior temporal cortex were sensitive to combined memory load a

292 wed enhanced responses in the right superior temporal cortex when observing own-race pupil dilation.

293 with altered theta activity in the inferior temporal cortex when the control process (retrieval or s

294 or-to-anterior processing stream in occipito-temporal cortex, whereby successive areas code increasin

295 for the thickness asymmetry of the superior temporal cortex, which was not significant after adjustm

296 entral pathway areas such as V4 and inferior temporal cortex, while motion is preferentially processe

297 icant inter-brain coherence within the right temporal cortex, while significant coherence in male/mal

298 involvement of the hippocampus and parietal-temporal cortex with cognitive impairment and long-term

299 t inferior frontal cortex and left posterior temporal cortex, with dorsal foci for syntactic processi

300 t stimulus familiarity can be represented in temporal cortex without input from prefrontal cortex.