ライフサイエンスコーパス: fusiform gyrus

1 ral prefrontal and parietal cortex and right fusiform gyrus).

2 tex at the junction of the right lingual and fusiform gyrus.

3 hesis in relation to face selectivity in the fusiform gyrus.

4 redict functional activation to faces in the fusiform gyrus.

5 tion following a lesion to the right lateral fusiform gyrus.

6 and FH effects were found bilaterally in the fusiform gyrus.

7 ct responses, especially in the amygdala and fusiform gyrus.

8 timuli, whereas the opposite was true in the fusiform gyrus.

9 pathway from the occipital visual cortex to fusiform gyrus.

10 ntal cortex and from orbitofrontal cortex to fusiform gyrus.

11 ortex, the inferior parietal lobule, and the fusiform gyrus.

12 ace-selective functional MRI response in the fusiform gyrus.

13 ositively with differential activity of left fusiform gyrus.

14 iation of activity in left amygdala and left fusiform gyrus.

15 reduced activation within the left anterior fusiform gyrus.

16 r temporal cortex, intraparietal sulcus, and fusiform gyrus.

17 eral temporal lobe (Brodmann area 20/21) and fusiform gyrus.

18 drites of neocortical pyramidal cells in the fusiform gyrus.

19 evoked by words in the posterior part of the fusiform gyrus.

20 teral aspect of the collateral sulcus on the fusiform gyrus.

21 n of inferior temporal regions including the fusiform gyrus.

22 rus, whereas concrete items adapted the left fusiform gyrus.

23 rated by either imagery or perception in the fusiform gyrus.

24 tween their neonate's amygdala and bilateral fusiform gyrus.

25 amily income and total SA and SA in the left fusiform gyrus.

26 in prefrontal cortex, occipital cortex, and fusiform gyrus.

27 l gyrus, left parahippocampal gyrus and left fusiform gyrus.

28 ween higher-level language areas and the mid fusiform gyrus.

29 onse profiles such as the lateral and medial fusiform gyrus.

30 for face-selectivity to arise in the lateral fusiform gyrus.

31 the downstream face-selective region in the fusiform gyrus.

32 9557 in the right occipital cortex and right fusiform gyrus.

33 t posterior hippocampus, parahippocampus and fusiform gyrus.

34 parahippocampus (0.032 vs 0.037; p<0.0001), fusiform gyrus (0.036 vs 0.041; p<0.0001), inferior temp

35 cortical thickness (maximum Cohen's d (left fusiform gyrus) = -0.33).

36 emporal gyrus (13% difference) and bilateral fusiform gyrus (10% difference in both hemispheres).

37 0.001), anterior vermis (40%, P < 0.001) and fusiform gyrus (20%, P < 0.001) compared with controls o

38 as well as the insula, cingulate cortex, and fusiform gyrus, a regional distribution that was nearly

39 cus functional connectivity localized to the fusiform gyrus, a visual processing region also identifi

40 l thickness in the right parahippocampal and fusiform gyrus across both time points was found in both

41 social impairments were linked to decreased fusiform gyrus activation during implicit emotion regula

42 was inversely correlated with the change in fusiform gyrus activation in the fasted state but not in

43 paired performance and reduced left anterior fusiform gyrus activation was observed when control subj

44 Amygdala, anterior cingulate, and fusiform gyrus activity increased linearly with the CS-U

45 ior hippocampus, parahippocampal cortex, and fusiform gyrus activity linearly increased across the 30

46 Amygdala, anterior cingulate, and fusiform gyrus activity paralleled the CS-UCS pairing ra

47 were associated with reduced CT in the right fusiform gyrus (adjusted beta = 0.54; 95% CI 0.17 to 0.9

48 n: beta [SE], 43.3 [13.4] mm3; P = .006) and fusiform gyrus (age interaction: beta [SE], 168.3 [51.4]

49 d connections to the occipital lobe from the fusiform gyrus along with longer association fibers that

50 ined semantic feature representations in the fusiform gyrus also predicted true recognition.

51 la, middle occipital, anterior cingulate and fusiform gyrus, amygdala, striatum, pulvinar, and substa

52 We found that activity in the fusiform gyrus, an area associated with the processing o

53 modulation of the afferent connections from fusiform gyrus and AMG to VPFC.

54 Activation in the fusiform gyrus and amygdala was strongly and positively

55 ault mode network, superior parietal lobule, fusiform gyrus and anterior insula.

56 as well as the left primary auditory cortex, fusiform gyrus and cerebellum.

57 sing the identified reference regions (i.e., fusiform gyrus and crus-cerebellum) were significantly a

58 matter loss in the left parahippocampal and fusiform gyrus and greater gray matter increases in the

59 s in the pars orbitalis, paracentral lobule, fusiform gyrus and inferior temporal gyrus was lowest in

60 Differences were prominent in the fusiform gyrus and lateral temporal lobe.

61 d with less perfusion in the right occipital/fusiform gyrus and left subgenual ACC.

62 sociated with decreased FC between the right fusiform gyrus and left superior occipital cortex.

63 The inferior temporal cortex, fusiform gyrus and middle temporal cortex had the larges

64 ion and the ankle DF/PF tasks, the bilateral fusiform gyrus and middle temporal gyrus, right inferior

65 effects within right amygdala, hippocampus, fusiform gyrus and orbitofrontal cortex.

66 mygdala and orbitofrontal cortex and between fusiform gyrus and orbitofrontal cortex.

67 orm; (2) body-selective regions in posterior fusiform gyrus and posterior inferior temporal sulcus ov

68 l sulcus encoded response complexity and the fusiform gyrus and precuneus organized its activity acco

69 in right lateral occipital cortex and right fusiform gyrus and sources in a control region (left V1)

70 in ReHo between the two bands were found in fusiform gyrus and superior frontal gyrus (slow-4> slow-

71 hippocampus, dorsolateral prefrontal cortex, fusiform gyrus and superior frontal gyrus-583 subjects)

72 ve expressions led to shared activity in the fusiform gyrus and superior temporal sulcus.

73 Fusiform gyrus and temporal pole cortical thickness was

74 more left-sided in autism), whereas adjacent fusiform gyrus and temporooccipital inferior temporal gy

75 ted by visual semantic loops within the left fusiform gyrus and that these neural processes may be me

76 osed to neutral body postures, activates the fusiform gyrus and the amygdala.

77 field being represented more medially on the fusiform gyrus and the inferior field more laterally, th

78 duced grey matter volume in the right middle fusiform gyrus and the inferior temporal gyrus.

79 uced and increased fMRI responses in the mid-fusiform gyrus and the lateral occipital cortex, respect

80 in the left inferior prefrontal cortex, the fusiform gyrus and the medial temporal lobe including bo

81 ups predicted activity in the right anterior fusiform gyrus and the temporal poles, where accuracy li

82 amage to the inferior temporal gyrus, to the fusiform gyrus and to a white matter network including t

83 y-related patterns of activation in ventral (fusiform gyrus) and lateral (superior and middle tempora

84 h brain regions with foveal tendencies (e.g. fusiform gyrus), and activations of layer-units with sel

85 dalar region) cingulate, parahippocampal and fusiform gyrus, and anterior insula were seen along with

86 r temporal cortex, lateral occipital cortex, fusiform gyrus, and banks of the superior temporal sulcu

87 between right superficial amygdala and right fusiform gyrus, and between left superficial amygdala an

88 ate cortex, superior temporal gyrus, insula, fusiform gyrus, and caudate nucleus.

89 emisphere in caudate, hippocampal formation, fusiform gyrus, and cerebellum, and in right temporal co

90 ht visual association cortex (area 18), left fusiform gyrus, and cerebellum.

91 ippocampus, parahippocampal gyrus, amygdala, fusiform gyrus, and choroid plexus but not in other brai

92 rome group was found in the cingulate gyrus, fusiform gyrus, and frontal cortex in response to all fa

93 ed decreased activity in the right amygdala, fusiform gyrus, and inferior occipital gyrus compared wi

94 eral temporal lobe, including temporal pole, fusiform gyrus, and insula, and extending into occipital

95 ctivation patterns within the visual cortex, fusiform gyrus, and lateral temporal lobe.

96 t anterior insula, left lingual gyrus, right fusiform gyrus, and left cerebellum.

97 cortex, cerebellum, parahippocampal cortex, fusiform gyrus, and occipital cortex.

98 as the lingual gyrus, middle temporal gyrus, fusiform gyrus, and precuneus all showed delayed hemodyn

99 lts showed that the visual cortex, bilateral fusiform gyrus, and right parahippocampal gyrus were act

100 ft lingual gyrus), anterior cingulate, right fusiform gyrus, and right sublobar insula were significa

101 including Brodmann's areas 18 and 19 and the fusiform gyrus, and several cortical regions associated

102 left hippocampus, parahippocampal gyrus, and fusiform gyrus, and significantly greater gray matter in

103 s, entorhinal cortex, parahippocampal gyrus, fusiform gyrus, and superior, middle, and inferior tempo

104 more consistent activation of the amygdala, fusiform gyrus, and thalamus than emerging adults, who s

105 cur in the anterior medial temporal lobe and fusiform gyrus, and that these changes occur at least 3

106 ith word-related potentials in the posterior fusiform gyrus, and was independent of stimulus colour.

107 s in schizophrenia and draw attention to the fusiform gyrus as a structure of particular interest in

108 l resolution imaging techniques identify the fusiform gyrus as subserving processing of invariant fac

109 of the salience network; and a subregion of fusiform gyrus associated with face perception.

110 nd anterior to face-selective regions on the fusiform gyrus at the group level and within individual

111 al orbitofrontal cortex), visual processing (fusiform gyrus), auditory processing (transverse tempora

112 cortex), BA 37 (posterior, inferior temporal/fusiform gyrus), BA 38 (anterior temporal cortex) and BA

113 l gyrus) and 37 (posterior-inferior temporal/fusiform gyrus) best predicted impairment in reading wor

114 tal depression was associated with a reduced fusiform gyrus (beta [SE], -480.5 [189.2] mm3; P = .002)

115 r areas are consistently activated: the left fusiform gyrus, bilateral middle and inferior frontal gy

116 was detected in the mesial temporal lobe and fusiform gyrus bilaterally among persons without a first

117 Faces primarily activated the fusiform gyrus bilaterally, and also activated the right

118 blood flow to left posterior middle temporal/fusiform gyrus, Broca's area, and/or Wernicke's area acc

119 ed face-responsive visual areas in the human fusiform gyrus, but their role in recognizing familiar i

120 olor, and place selectivity that tracked the fusiform gyrus/collateral sulcus.

121 tex, with some additional involvement of the fusiform gyrus, compared to controls.

122 ly increased in temporal regions, insula and fusiform gyrus, consistent with those areas known to be

123 iculum, and entorhinal cortex), and anterior fusiform gyrus (corrected P < .05; uncorrected P = .001)

124 that responded to viewing pictorial stimuli (fusiform gyrus) correlated with self-reported visualizer

125 significantly associated with reduced right fusiform gyrus CT (adjusted beta = 0.72; 95% CI 0.29 to

126 ssociations between EMD and right insula and fusiform gyrus CT were not significant.

127 s (Cohen's d=-0.293; P=1.71 x 10(-21)), left fusiform gyrus (d=-0.288; P=8.25 x 10(-21)) and left ros

128 cipants (both absolutely and relative to the fusiform gyrus), despite apparently normal levels of fac

129 age, the VWFA was instead found in the right fusiform gyrus, despite the fact that the left-hemispher

130 on in the dorsolateral prefrontal cortex and fusiform gyrus during emotional face processing (faces-s

131 temporal gyrus, superior temporal gyrus, and fusiform gyrus during memory encoding reduced odds of re

132 y in both posterior hippocampi and the right fusiform gyrus during smooth pursuit eye movements.

133 Clinically, the ability to recruit the fusiform gyrus during the task in noise was negatively c

134 in dorsomedial prefrontal cortex (DMPFC) and fusiform gyrus emphasized a human-nonhuman distinction.

135 The VTC, particularly the fusiform gyrus, exhibits robust axis-based feature codin

136 present evidence that expertise recruits the fusiform gyrus 'face area'.

137 ebles') recruits face-selective areas in the fusiform gyrus (FFA) and occipital lobe (OFA).

138 lts, particularly those anchored in the left fusiform gyrus (FFG) (the visual word form area).

139 ns involved in face processing including the fusiform gyrus (FFG) and posterior cingulate cortex (PCC

140 ther than to identity changes, whereas right fusiform gyrus (FFG) shows sensitivity to identity rathe

141 of the face processing network, such as the fusiform gyrus (FFG).

142 ition is linked to dopamine (DA) activity in fusiform gyrus (FFG).

143 ions for the size of activation in the right fusiform gyrus (FG) and right inferior temporal gyri (IT

144 own to respond to face and gaze stimuli, the fusiform gyrus (FG) and superior temporal sulcus (STS),

145 ction (IFJ), middle temporal gyrus (MTG) and fusiform gyrus (FG) are active during response inhibitio

146 hat spatially informative cues activated the fusiform gyrus (FG) as well as frontoparietal components

147 le of face-selective neural responses of the fusiform gyrus (FG) in face perception in a patient impl

148 ic representations in lingual gyrus (LG) and fusiform gyrus (FG) were associated with high memory viv

149 Four regions of interest (ROIs), the fusiform gyrus (FG), inferior temporal gyrus, middle tem

150 The fusiform gyrus (FG), or occipitotemporal gyrus, is thoug

151 Recent research indicates that the human fusiform gyrus (FG), which is a hominoid-specific struct

152 tients with lesions in the VTC including the fusiform gyrus (FG).

153 nterior cytoarchitectonic areas (e.g., areas fusiform gyrus [FG]1-FG4) and another that contains a se

154 most strongly associated with activation in fusiform gyrus (fMRI) as well as the N170 and visual awa

155 inputs in midline occipital cortex and right fusiform gyrus, followed by (3) nonlinear task-dependent

156 the extrastriate visual cortex (for example, fusiform gyrus for changing faces).

157 regions (temporal pole for word matching and fusiform gyrus for face matching).

158 ties in distinct but adjacent regions in the fusiform gyrus for only faces in one region (the FFA*) a

159 auditory spelling task and from calcarine to fusiform gyrus for the visual spelling task.

160 ese characteristics, with reports of altered fusiform gyrus function while viewing socioemotional sti

161 s (absolute volume/intracranial contents) of fusiform gyrus gray matter compared with controls (9%) a

162 is associated with a bilateral reduction in fusiform gyrus gray matter volume that is evident at the

163 For comparison, superior temporal gyrus and fusiform gyrus gray matter volumes were also measured.

164 had smaller bilateral anterior and posterior fusiform gyrus gray matter volumes, compared to the heal

165 Face-selective neural responses in the human fusiform gyrus have been widely examined.

166 l (parahippocampal gyrus, hazard ratio=3.73; fusiform gyrus, hazard ratio=4.14), insula (hazard ratio

167 nsisting of hippocampus, parahippocampus and fusiform gyrus (HPF) as defined by a published template.

168 ance imaging (fMRI), we found an area in the fusiform gyrus in 12 of the 15 subjects tested that was

169 sed to measure the gray matter volume of the fusiform gyrus in 22 patients with first-episode schizop

170 oked responses in the left amygdala and left fusiform gyrus in both runs and experiments.

171 with ASD had lower FC than TC in cerebellum, fusiform gyrus, inferior occipital gyrus and posterior i

172 /middle temporal gyrus plus the right middle fusiform gyrus/inferior temporal gyrus.

173 r temporal gyrus, transverse temporal gyrus, fusiform gyrus, insula) in patients with schizophrenia a

174 ed abnormal hyperactivation in the amygdala, fusiform gyrus, insula, anterior cingulate cortex, and d

175 with significantly higher activation of the fusiform gyrus, insula, temporoparietal junction, inferi

176 tivity model included the early visual area, fusiform gyrus, intraparietal sulcus, and inferior front

177 ability was evident in the temporal pole and fusiform gyrus ipsilateral to the seizure focus followin

178 y controls and patients-the thalamus and the fusiform gyrus ipsilateral to the side of surgery (PFWE

179 The fusiform gyrus is an important region implicated in such

180 ese findings indicate that the right lateral fusiform gyrus is critically involved in object recognit

181 ative to healthy subjects, suggests that the fusiform gyrus is the site of a defective anatomical sub

182 The fusiform gyrus is understood to be involved in the proce

183 show that the strength of rsFC between left fusiform gyrus (L-FG) and higher-order language systems

184 - left intraparietal sulcus (L.IPS) and left fusiform gyrus (L.FFG).

185 The large fusiform gyrus library (117 subjects) with high sequenci

186 ortical dysfunction in the temporal lobe and fusiform gyrus may be related to epileptic activity in I

187 suggests that an area in the lingual sulcus/fusiform gyrus may correspond to ventral V4 (V4v).

188 fMRI revealed that the left fusiform gyrus may facilitate the production of backward

189 as associated with responses to faces in the fusiform gyrus, measured with functional magnetic resona

190 d automatic semantic priming in the left mid-fusiform gyrus (mid-FFG) and strategic semantic priming

191 ces on post hoc analysis: posterior temporal fusiform gyrus (more left-sided in autism), whereas adja

192 In addition, the anterior region of the fusiform gyrus, most often cited as the location of the

193 ealthy participants showed activation in the fusiform gyrus, occipital lobe, and inferior frontal cor

194 ied a putative face-specific area within the fusiform gyrus of human visual cortex; the precise role

195 bust face-selective responses in the lateral fusiform gyrus of individual blind participants during h

196 flood in the Parahippocampal Gyrus, and Left Fusiform Gyrus, of those afflicted with AN.

197 s (p(uncorrected) < 0.05, SBC = -0.32), left fusiform gyrus (P(FDR) < 0.01, SBC = -0.51).

198 e area in specific cortical regions (cuneus, fusiform gyrus, pars triangularis) in both populations.

199 processing and structural alterations in the fusiform gyrus, part of the ventral visual stream.

200 For the left fusiform gyrus, patients with schizophrenia showed an 11

201 work and that a right anterior region of the fusiform gyrus plays a central role within the informati

202 creased rCBF to motor cortex, visual cortex, fusiform gyrus, posterolateral temporal lobe, and right

203 showed activations, not seen in normals, in fusiform gyrus, precentral gyrus, and intra-parietal sul

204 e object-specific feature representations in fusiform gyrus predicted accurate memory, coarse-grained

205 ctivity, was correlated with GMV in the left fusiform gyrus (r = -0.19, P(uncorrected) = 0.049) and r

206 the left parahippocampal gyrus and the left fusiform gyrus, recruited during facial expression proce

207 erior temporal gyrus reduction and bilateral fusiform gyrus reductions, these data suggest that schiz

208 Although prior research suggests that fusiform gyrus represents the sex and race of faces, it

209 gyrus and bilateral middle/inferior temporal/fusiform gyrus, respectively) that showed reversed effec

210 sults show that bilateral posterior areas in fusiform gyrus responded more strongly for faces with po

211 contact modulated BOLD activity in the right fusiform gyrus (rFG) and left inferior occipital gyrus (

212 tinct behaviors are constructed in the right fusiform gyrus (rFG).

213 zed beta coefficient (SBC) = -0.26) and left fusiform gyrus (SBC = -0.25) in sample 1 were replicated

214 e right anterior cingulate cortex), and left fusiform gyrus (SDM estimate = -0.146; P = .003).

215 The right fusiform gyrus showed adaptation to faces (not objects)

216 ons, the lateral section of the right middle fusiform gyrus showed the largest face-selective respons

217 The mid fusiform gyrus showed the strongest, earliest response a

218 s placed over high-order visual areas (e.g., fusiform gyrus) showed both effects of spatial and objec

219 ormality and anatomical abnormalities in the fusiform gyrus shown with magnetic resonance imaging (MR

220 ateral occipito-temporal sulcus and adjacent fusiform gyrus shows maximal selectivity for words and h

221 the visual word-form area (part of the left fusiform gyrus specialized for printed words); and persi

222 activity in left amygdala, bilateral insula, fusiform gyrus, STS, and reward-related areas.

223 esion also extended laterally to involve the fusiform gyrus substantially.

224 tentials recorded from nearby regions of the fusiform gyrus suggest that the attention effect is due

225 ted with decreased grey matter volume in the fusiform gyrus suggesting that LBD neurodegeneration-rel

226 uperior Temporal Gyrus (t=1.403, p=0.00780), Fusiform Gyrus (t=1.26), and Parahippocampal Gyrus (t=1.

227 rebellum, including putamen, insula, cuneus, fusiform gyrus, thalamus and caudate nucleus, and increa

228 wer spectra in the primary visual cortex and fusiform gyrus that are maximally discriminative of data

229 ther fusiform face area (FFA)-the portion of fusiform gyrus that is functionally-defined by its prefe

230 ate adults, an area along the left posterior fusiform gyrus that is often referred to as the "visual

231 eralized hyperactivation in the amygdala and fusiform gyrus that was subject to intersession habituat

232 ct patches of face-selective activity in the fusiform gyrus that were interspersed within a large exp

233 dala, middle and inferior temporal gyri, and fusiform gyrus the most severely damaged.

234 ies have described a localized region in the fusiform gyrus [the fusiform face area (FFA)] that respo

235 ted, in addition, more anterior parts of the fusiform gyrus, the hippocampus and the ventrolateral fr

236 Voxels in the right temporal pole, the right fusiform gyrus, the right caudate and right subcallosal

237 laims have been made, and within the lateral fusiform gyrus, they are restricted to a small area (200

238 Reduced right parahippocampal and fusiform gyrus thickness are familial trait markers for

239 ediated the association with inattention and fusiform gyrus thickness mediated the association with i

240 found positive correlations between the left fusiform gyrus to amygdala connectivity and different st

241 , and may serve in concert with amygdala and fusiform gyrus to modulate visual attention toward motiv

242 over time in activation of the amygdala and fusiform gyrus to neutral facial stimuli in adults with

243 es modulated unidirectional connections from fusiform gyrus to orbitofrontal cortex.

244 ced modulation of connectivity from the left fusiform gyrus to the left amygdala and from the right a

245 as the amygdala, hippocampus, temporal pole, fusiform gyrus, visual primary cortex, and motor areas (

246 olume (0.93 [0.91-0.96], P < .001), and left fusiform gyrus volume (0.97 [0.96-0.99], P < .001).

247 Right fusiform gyrus volume differed in patients with schizoph

248 e association of these deficits with smaller fusiform gyrus volume in patients with schizophrenia, re

249 In addition, right posterior fusiform gyrus volume was significantly correlated with

250 that the intensity of the activation in the fusiform gyrus was associated with significantly stronge

251 tent of dendritic trees in the subiculum and fusiform gyrus was examined by Sholl analysis.

252 In contrast, the fusiform gyrus was preferentially recruited in a viewpoi

253 s in orthographic processing circuits (i.e., fusiform gyrus) was predictive of smaller gains in fluen

254 wed that repetition suppression in bilateral fusiform gyrus, was selectively correlated with priming

255 ophy of the bilateral temporal poles and the fusiform gyrus were associated with prosopagnosia in rtv

256 oral gyrus, whereas larger resections of the fusiform gyrus were associated with worsening of visual

257 The inferior frontal gyrus (IFG) and fusiform gyrus were engaged by both tasks.

258 ing, whereas PrC, anterior HC, and posterior fusiform gyrus were recruited during discrimination lear

259 mygdala, parahippocampal gyrus. and anterior fusiform gyrus when participants were in a hungry state

260 ocampal gyrus, left orbitofrontal cortex and fusiform gyrus whereas patients with left hippocampal sc

261 s activated a discrete region of the lateral fusiform gyrus, whereas letterstrings activated a nearby

262 , but previous studies have not included the fusiform gyrus (which may have a role in facial recognit

263 cal area in the collateral sulcus and medial fusiform gyrus, which was place-selective according to b

264 , ventral IPS, lateral occipital region, and fusiform gyrus], which was accompanied by activation tha

265 ed fMRI to measure neural responses from the fusiform gyrus while subjects observed a rapid stream of

266 ties in the right temporal pole and anterior fusiform gyrus; while in the Alzheimer's disease group,

267 e temporal pole, inferior temporal gyrus and fusiform gyrus, with carry-over effects 6 months after t

268 us, left temporoparietal junction, and right fusiform gyrus, with patients showing relative hypoactiv

269 ivated inferior frontal gyrus, amygdala, and fusiform gyrus, with significantly stronger activation e