ライフサイエンスコーパス: temporal cortex

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

2 l correct rewarded responses in the superior temporal cortex.

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

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

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

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

7 with predominately medial and anterolateral temporal cortex.

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

9 ion from posterior cingulate to anteromedial temporal cortex.

10 rimates, although other species also present temporal cortex.

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

12 y the repetition probability in the inferior temporal cortex.

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

14 rful neuronal representation in the inferior temporal cortex.

15 and orbital prefrontal cortices and anterior temporal cortex.

16 BA receptor subunits normally present in the temporal cortex.

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

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

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

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

21 ncreased coupling of activity in frontal and temporal cortex.

22 in delayed reconciliation of predictions in temporal cortex.

23 l pallidum, left amygdala, and left inferior temporal cortex.

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

25 cal activation in the anterolateral superior temporal cortex.

26 p, most pronouncedly in the frontal lobe and temporal cortex.

27 essing region in left anterolateral superior temporal cortex.

28 iquely exhibited old > new activity in right temporal cortex.

29 topic cortex in right anterolateral superior temporal cortex.

30 rior frontal gyrus, middle frontal gyrus and temporal cortex.

31 also show face-selective activity in ventral temporal cortex.

32 etween selectivity and perception in ventral temporal cortex.

33 ipital cortex, rat CA1, monkey V1, and human temporal cortex.

34 eural responses in the prefrontal cortex and temporal cortex.

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

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

37 between different subregions of the ventral temporal cortex.

38 role of distinct subregions of the anterior temporal cortex.

39 00 cis-regulatory elements in prefrontal and temporal cortex.

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

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

42 dorsomedial prefrontal cortex and posterior temporal cortex.

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

44 ophrenia and comparison subjects in superior temporal cortex.

45 amygdala connectivity to the prefrontal and temporal cortex.

46 thalamic pulvinar nuclei and the left medial temporal cortex.

47 volume loss in the right posterior inferior temporal cortex.

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

49 /- 0.15 vs. 1.49 +/- 0.10; P = 0.028), right temporal cortex (1.30 +/- 0.17 vs. 1.45 +/- 0.09; P = 0.

50 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.

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

52 al cortices (-7%) and mild reductions in the temporal cortex (-5%) and hippocampus (-3%), compared wi

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

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

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

56 n than function words in middle and anterior temporal cortex, a sub-region of orbital frontal cortex,

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

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

59 reas have almost entirely layer III origins (temporal cortex and area AII), whereas others have a pre

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

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

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

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

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

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

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

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

68 connectivity between anterolateral superior temporal cortex and right anterior superior temporal cor

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

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

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

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

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

74 orbitofrontal, dorsolateral prefrontal, and temporal cortex and the hippocampus compared with contro

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

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

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

78 We studied the distribution of KLK6 in the temporal cortex and white matter by immunohistochemistry

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

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

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

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

83 (PCC/Rsp), inferior parietal lobule, lateral temporal cortex, and hippocampus regions.

84 e significantly increased in the frontal and temporal cortex, and in the locus coeruleus, of drug use

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

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

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

88 mined in the dorsolateral prefrontal cortex, temporal cortex, and motor cortex in 15 postmortem schiz

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

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

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

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

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

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

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

96 ssion that typically distinguish frontal and temporal cortex are significantly attenuated in the ASD

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

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

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

100 lyses also show that LM strongly projects to temporal cortex as well as the lateral entorhinal cortex

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

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

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

104 lateral parietal cortex (BA 39), and lateral temporal cortex (BA 21)], depressed, but not control sub

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

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

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

108 lthy control subjects activated the superior temporal cortex (Brodmann area [BA] 22) bilaterally, the

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

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

111 ory specific visual agnosia follows inferior temporal cortex but not LPFC damage.

112 to bilateral lesions of the ventral occipito-temporal cortex but spared dorsal LO.

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

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

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

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

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

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

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

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

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

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

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

124 Recordings from single cells in human medial temporal cortex confirm that sensory processing forms ex

125 al subjects with left anterolateral superior temporal cortex connectivity in a group of chronic aphas

126 ted with altered left anterolateral superior temporal cortex connectivity in aphasic stroke.

127 Human inferior temporal cortex contains category-selective visual regio

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

129 h comprehension, left anterolateral superior temporal cortex displayed positive functional connection

130 nance (fMRI) studies suggest that the infant temporal cortex does not differentiate speech from music

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

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

133 Visual selectivity from temporal cortex during the initial approximately 200 ms

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

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

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

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

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

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

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

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

142 6 mRNA and protein levels in the frontal and temporal cortex from 15 AD, 15 VaD and 15 control brains

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

144 tivity in 2-mm samples across human inferior temporal cortex from the fusiform face area (FFA) (appar

145 organization of left anterolateral superior temporal cortex functional connections during narrative

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

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

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

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

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

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

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

153 onnection of prefrontal cortex from inferior temporal cortex impairs a variety of complex visual lear

154 95% CI, 1.71-6.38; Lewy bodies in frontal or temporal cortex in ACT: RR for TBI with LOC >1 hour, 5.7

155 icantly decreased in the frontal but not the temporal cortex in AD.

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

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

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

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

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

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

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

163 ignificant structural asymmetries in lateral temporal cortex, including the planum temporale and supe

164 misphere dominance in frontal, parietal, and temporal cortex, including the TPJ region asymmetrically

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

166 emporal-parietal cortex, middle and anterior temporal cortex, inferior frontal gyrus, parahippocampal

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

168 ype in the raphe nuclei, medial and inferior temporal cortex, insula, medial prefrontal cortex, and a

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

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

171 temporal cortex and right anterior superior temporal cortex is a marker of receptive language outcom

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

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

174 an domain by demonstrating that anteromedial temporal cortex is critically involved in crossmodal int

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

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

177 The human occipito-temporal cortex is preferentially activated by images of

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

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

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

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

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

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

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

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

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

187 stage of the ventral visual stream [inferior temporal cortex (IT)] that signal object identity while

188 l cortical areas V1, V2, and V4 and inferior temporal cortex (IT)].

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

190 posterior visual areas, such as the inferior temporal cortex (ITC), and the prefrontal cortex.

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 lumes in the parahippocampal gyrus, superior temporal cortex, lateral orbital frontal cortex, and par

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

195 ctional connections with left anterior basal temporal cortex, left inferior frontal gyrus and homotop

196 neuronal projections from the ventrorostral temporal cortex lesion by studying the full extent of wh

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

198 sk-dependent, suggesting that posteroventral temporal cortex may encode visual categories, while more

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

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

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

202 colliculus (SC) to the motion area in middle temporal cortex (MT).

203 Temporal cortex neurons under normal conditions represen

204 the sources of action selectivity in monkey temporal cortex neurons.

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

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

207 We have examined ECE-2 expression in the temporal cortex of brain tissue from patients with AD, v

208 imilar object form topography in the ventral temporal cortex of chimpanzees and humans, in which face

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

210 r binding was significantly increased in the temporal cortex of patients with either multi-infarct va

211 at the architectonically distinct regions of temporal cortex of squirrels are also functionally disti

212 vels of MET protein expression in the mature temporal cortex of subjects with ASD.

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

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

215 uman primate ventral visual stream (inferior temporal cortex, or IT), we here test if this is a gener

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

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

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

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

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

221 10(-8)), frontal cortex (P 1.3 x 10(-9)) and temporal cortex (P1.2 x 10(-11)).

222 tion was found in the left fusiform/inferior temporal cortex: participants with autism spectrum disor

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

224 scattered throughout the posterior inferior temporal cortex (PIT), a swath of brain anterior to area

225 Several regions of the posterior-lateral-temporal cortex (PLTC) are reliably recruited when parti

226 oughout the human genome, in frontal cortex, temporal cortex, pons and cerebellum from 387 human dono

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

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

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

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

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

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

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

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

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

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

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

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

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

240 lesions in pSTS/MTG but spared anteromedial temporal cortex revealed equivalent unimodal and crossmo

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

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

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

244 al activation in the anterior portion of the temporal cortex, similarly to adults.

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

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

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

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

249 iddle frontal cortex, P = .01; left superior temporal cortex [STC], P = .007; right STC, P = .01).

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

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

252 that white-matter fibers in ventral occipito-temporal cortex support the integrated function of a dis

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

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

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

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

257 he medial temporal lobe (AH) or the inferior temporal cortex (TE) were paired with unoperated peers a

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

259 th-olds, in a more posterior location of the temporal cortex than in adults.

260 volved brain regions in the left frontal and temporal cortex that are uniquely capable of language pr

261 g the anterior insula and posterior superior temporal cortex, that are thought to be involved in soci

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

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

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

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

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

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

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

269 l responses in macaque areas V4 and inferior temporal cortex to preferred stimuli are typically suppr

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

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

272 creased responses in left and right superior temporal cortex to the human voice when compared to nonv

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

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

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

276 approximately 200 neurons from the inferior temporal cortex using a pattern classifier.

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

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

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

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

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

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

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

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

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

286 5-HT(1A) receptor maximal binding in the temporal cortex was also positively correlated with cogn

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

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

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

290 al lesions of prefrontal cortex and inferior temporal cortex were impaired compared with unoperated c

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

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

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

294 biological motion is mediated by the lateral temporal cortex, whether and when neural activity in thi

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

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

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

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

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

300 ge of feed-forward processing, presumably in temporal cortex, without top-down information from LPFC.