ライフサイエンスコーパス: occipital cortex

1 eye movements, but not in a control region (occipital cortex).

2 ps, LO1 and LO2, in object-selective lateral occipital cortex.

3 pagation from the V1 to the V2 region of the occipital cortex.

4 nd lower in sulcal, perirolandic, and medial occipital cortex.

5 stimulus size was reflected by activation in occipital cortex.

6 on compared with healthy control subjects in occipital cortex.

7 n the right fusiform gyrus and left superior occipital cortex.

8 uded areas V1, V3a, hV4, hMT(+), and lateral occipital cortex.

9 the healthy comparison group in the superior occipital cortex.

10 increased during 20S(-), most notably in the occipital cortex.

11 h as other regions in the insular and medial occipital cortex.

12 electrodes, suggesting an origin in parieto-occipital cortex.

13 al lobe and with other areas of parietal and occipital cortex.

14 s of the inhibitory neurotransmitter GABA in occipital cortex.

15 c lamina of frontal, parietal, temporal, and occipital cortex.

16 same effect in an adjacent area, the lateral occipital cortex.

17 was correlated with rCBF in the amygdala and occipital cortex.

18 tive N1 enhancement was localized to lateral occipital cortex.

19 sses that generate the hallucinations in the occipital cortex.

20 rrupting connections between the eye and the occipital cortex.

21 which the figure region is routed to lateral occipital cortex.

22 nd intact implicit encoding in earlier-stage occipital cortex.

23 parahippocampal cortex, fusiform gyrus, and occipital cortex.

24 ivity to color, objects and faces in ventral occipital cortex.

25 ed performance nor diminished BOLD signal in occipital cortex.

26 in relative brain GABA concentration in the occipital cortex.

27 r brain areas, including the pre-frontal and occipital cortex.

28 to large-scale cross-modal plasticity within occipital cortex.

29 raine attack have been shown to occur in the occipital cortex.

30 brainstem structures preceded activation of occipital cortex.

31 iver's brain via magnetic stimulation of the occipital cortex.

32 for myo-inositol or other metabolites in the occipital cortex.

33 erent times using an input function from the occipital cortex.

34 l ranged from 22 in the caudate to 90 in the occipital cortex.

35 r medial prefrontal cortex, hippocampus, and occipital cortex.

36 nged from -33% in the caudate to -20% in the occipital cortex.

37 regions and with expression of NR(1) in the occipital cortex.

38 well as relative metabolic increases in the occipital cortex.

39 ed to be very common throughout parietal and occipital cortex.

40 ive noise and of stimulus-specific biases in occipital cortex.

41 ion, and dysplastic in-folding of the mesial occipital cortex.

42 ha-band over ipsilateral centro-parietal and occipital cortex.

43 d at increasing GABA in the anterior lateral occipital cortex.

44 reases in alpha (8-13 Hz) frequency power in occipital cortex.

45 subcortically in bilateral basal ganglia and occipital cortex.

46 rper tuned profile in more posterior ventral occipital cortex.

47 and middle frontal gyri, the insula, and the occipital cortex.

48 n cooperation with perceptual systems of the occipital cortex.

49 the anterior and posterior superior-parieto-occipital cortex.

50 bust multivariate decoding being reported in occipital cortex.

51 variance in delay-period activity in lateral occipital cortex.

52 n no longer convey visual information to the occipital cortex.

53 pramarginal gyri as well as the left lateral occipital cortex.

54 MRS data were acquired from occipital cortex.

55 be, the right anterior insula, and bilateral occipital cortex.

56 a network of cognitive control, and with the occipital cortex.

57 ty, especially in the cerebellum and parieto-occipital cortex.

58 res correlated with metabolic changes in the occipital cortex.

59 V3a (50% reduction) and was least in lateral occipital cortex (20% reduction).

60 We measured putamen, caudate, and occipital cortex 6-(18)F-fluorodopa-derived radioactivit

61 In the occipital cortex, a region corresponding to the cytoarch

62 tions of the ipsilateral LGN by 5 days after occipital cortex ablation.

63 t OFC, right dorsolateral prefrontal cortex, occipital cortex, ACC, ventral striatum/nucleus accumben

64 rimary visual cortex, increased extrastriate occipital cortex activation selectively during maintaine

65 aphy (MEG) that tactile stimulation produces occipital cortex activations, starting as early as 35 ms

66 e nicotine induced a generalized increase in occipital cortex activity.

67 tain their connectivity with the reorganized occipital cortex and as a result influence processing of

68 dose DHA groups had greater decreases in the occipital cortex and cerebellar cortex, respectively.

69 ined the effects of inhibitory rTMS over the occipital cortex and found that the visual-vestibular po

70 ices in the frontal, parietal, temporal, and occipital cortex and in the subcortical region were obta

71 extraversion was correlated with rCBF in the occipital cortex and inferior temporal gyrus.

72 a different functional role than that in the occipital cortex and may be part of the neuronal mechani

73 Structural studies of occipital cortex and particularly optic radiations provi

74 set, face-selective sources in right lateral occipital cortex and right fusiform gyrus and sources in

75 ion were present for rs56039557 in the right occipital cortex and right fusiform gyrus.

76 al information flow between the left lateral occipital cortex and right intraparietal sulcus, as indi

77 roscopy data were acquired from the parietal-occipital cortex and supplementary motor area in all sub

78 iorally irrelevant information occurs in the occipital cortex and that representations of the informa

79 rmalities involve a circuit encompassing the occipital cortex and the cortical/subcortical systems ph

80 MTR reductions in bilateral parieto-occipital cortex and the genu of the corpus callosum wer

81 tree approach revealed the centrality of the occipital cortex and the peculiar aggregation of cerebel

82 omponent, which include the superior parieto-occipital cortex and the rostral superior parietal lobul

83 less gray matter in OCD were confined to the occipital cortex and were not predicted a priori.

84 Glucose concentrations in gray matter-rich occipital cortex and white matter-rich periventricular t

85 Occipital cortex and whole brain analysis comparing all

86 ining 5HT projections (frontal, temporal and occipital cortex) and cell bodies (midbrain).

87 data of two other regions: Brodmann area 19 (occipital cortex) and cerebellar cortex.

88 s between the anterior temporal lobe and the occipital cortex, and between bilateral occipital poles.

89 lts suggest that FEF and IPS modulate visual occipital cortex, and FEF modulates IPS, in relation to

90 temporal gyrus, middle temporal gyrus, right occipital cortex, and inferior frontal cortex was found

91 posterior than anterior HC, in frontal than occipital cortex, and ipsilaterally than contralaterally

92 ecovered, especially in the temporal cortex, occipital cortex, and medulla.

93 gdala and the prefrontal cortices, striatum, occipital cortex, and thalamus (all q values <0.1).

94 and the largest changes were in cerebellum, occipital cortex, and thalamus.

95 tween the right caudate and superior lateral occipital cortex, and the right caudate and anterior sup

96 ing the pseudo reference regions cerebellum, occipital cortex, and whole brain (WB) without ventricle

97 Furthermore, responses in left occipital cortex are abnormal and not modulated by pract

98 nial magnetic stimulation (TMS) to the human occipital cortex are immune to saccadic suppression, whe

99 Early visual areas in occipital cortex are known to be retinotopic.

100 ared to ATs, in the object sensitive lateral occipital cortex as well as in the face-sensitive occipi

101 ntal lobe, whereas microstate 4 involved the occipital cortex, as well as thalamic and brainstem stru

102 c TMS pulses were delivered over lateralized occipital cortex at 100, 200, or 400 ms into the retenti

103 a (rOFA), a face-selective region in lateral occipital cortex, at different latencies up to 210 ms af

104 d reduced cerebral metabolism in the primary occipital cortex (BA 17) that was revealed only by 3D-SS

105 This suggests that areas of occipital cortex become selective for language, relative

106 as 1 (LO1) and 2 (LO2), in the human lateral occipital cortex between the dorsal part of visual area

107 ving words, these subjects activated lateral occipital cortex bilaterally in addition to the language

108 h significant posterior flow deficits in the occipital cortex (Brodmann's areas 18 and 19), usually s

109 ch was observed in the frontal, parietal and occipital cortex but not in other brain areas.

110 ast re-routing of tactile information to the occipital cortex, but this has not been shown in humans.

111 onal partitioning of visual processes in the occipital cortex by Riddoch), but there were also other

112 his animal model, unilateral ablation of the occipital cortex causes unequivocal apoptosis of cortico

113 refrontal cortex, amygdala, temporal cortex, occipital cortex, cerebellum and thalamus (P<0.05 correc

114 The occipital cortex, cerebellum and whole brain were first

115 rom candidate pseudoreference regions (i.e., occipital cortex, cerebellum, and whole brain) to obtain

116 e that underpins size knowledge: the lateral occipital cortex codes perceptually based aspects (stati

117 uptake in the posterior temporoparietal and occipital cortex compared to clinically normal controls,

118 ophy additionally showing elevated uptake in occipital cortex compared with early-onset Alzheimer's d

119 which in humans, is more highly expressed in occipital cortex compared with the remainder of cortex t

120 guously and slowly (3.5 +/- 1.1 mm/min) over occipital cortex, congruent with the retinotopy of the v

121 observed in temporal, posterior parietal, or occipital cortex connectivity with the thalamus.

122 cortical activity in portions of the ventral occipital cortex, corresponding to known object areas wi

123 visual regions, only signals in the midline occipital cortex could be used to distinguish targets fr

124 formula (specific volumes-of-interest counts/occipital cortex counts) - 1.

125 roups, and the subgenual anterior cingulate, occipital cortex (cuneus), and posterior cerebellum were

126 tested an early blind patient with bilateral occipital cortex damage.

127 ulate; bilateral parahippocampal gyrus; left occipital cortex) demonstrated indistinguishable activit

128 ol, the normal alpha rhythm (8-13 Hz) in the occipital cortex disappears and a frontal alpha rhythm e

129 affecting distance judgments, while rTMS to occipital cortex disrupted distance but not roughness ju

130 PCr) and inorganic phosphate (Pi) within the occipital cortex during (activation) and after (recovery

131 st a complex interaction between frontal and occipital cortex during cocaine conditioning.

132 ion of compensatory increases in rCBF of the occipital cortex during incremental learning and the lef

133 ecuneus, middle temporal gyrus, and superior occipital cortex during the anticipation of potential re

134 dorsal occipital cortex or the right ventral occipital cortex, during the brief presentation of a tra

135 magnetic stimulation pulse delivered to the occipital cortex evoked a visual percept.

136 ranscranial magnetic stimulation of the left occipital cortex evoked contraction of right hand muscle

137 hese independently recorded variables, i.e., occipital cortex excitability and reactivity and EEG pha

138 Occipital cortex expression of PSD-95 was higher in the

139 tion of the changes in thickness across DF's occipital cortex, finding the most substantial loss in t

140 Hypoactivation in the occipital cortex for low spatial frequency faces may ind

141 hey showed relative hypoactivity in the left occipital cortex for the low spatial frequency faces.

142 s are distributed widely across the inferior occipital cortex, fusiform areas, and the cingulate gyru

143 ients also appeared to have persistently low occipital cortex GABA after chronic benzodiazepine treat

144 panic disorder had a 22% reduction in total occipital cortex GABA concentration (GABA plus homocarno

145 of this study was to determine whether these occipital cortex GABA concentrations are altered after a

146 report, using this technique, suggested that occipital cortex GABA concentrations are reduced in pati

147 Depressed subjects had significantly lower occipital cortex GABA concentrations compared with healt

148 Occipital cortex GABA concentrations in eight depressed

149 Occipital cortex GABA concentrations increase two-fold f

150 A significant increase in occipital cortex GABA concentrations was seen after SSRI

151 A significant increase in occipital cortex GABA concentrations was seen following

152 s of proton magnetic resonance spectroscopy, occipital cortex GABA concentrations were measured in 11

153 ajor depression is associated with increased occipital cortex GABA concentrations.

154 GABA neuronal response (blunted reduction of occipital cortex GABA level) to acute benzodiazepine adm

155 etic resonance spectroscopic measurements of occipital cortex GABA levels across the menstrual cycle

156 cts, who exhibited a significant decrease in occipital cortex GABA levels after this intervention.

157 a parallel-group, repeated-measures design, occipital cortex GABA responses to acute oral, open-labe

158 The levels of occipital cortex GABA, glutamate, N-acetylaspartate, asp

159 results indicate that superior IPS, but not occipital cortex, has a central role in VSTM storage.

160 We show that rTMS over the left occipital cortex impaired the facilitation of semantic r

161 t a silent zone at the posterior pole of the occipital cortex, implying a lack of complete cortical r

162 ntral striatum, inferior temporal gyrus, and occipital cortex in both depression and schizophrenia in

163 pathway in the cross-modal activation of the occipital cortex in congenitally blind humans.

164 alpha band range from posterior thalamus to occipital cortex in congenitally blind participants.

165 e EEG recordings from frontal, parietal, and occipital cortex in freely moving rats (n = 11) during a

166 y alpha-band activity (8-15 Hz) over parieto-occipital cortex in humans plays an important role in su

167 d potential responses were recorded over the occipital cortex in patients with schizophrenia and in a

168 , posterior cingulate cortex, precuneus, and occipital cortex in patients with TLE as compared with h

169 r cingulate cortices and deactivation in the occipital cortex in response to the drug-related stimulu

170 ted in visual attention continue to modulate occipital cortex in the early blind.

171 t in the perirhinal cortex compared with the occipital cortex in the perinatal period.

172 ontal and parietal control regions to visual occipital cortex in visuospatial attention, the goal mot

173 uperior parietal lobule and the left lateral occipital cortex) included the default mode network seed

174 .P.) requiring removal of the right inferior occipital cortex, including IOG-faces/OFA.

175 parietal cortices without any change in the occipital cortex, indicating that Fgf2 is necessary to r

176 Stimulation over the occipital cortex induced perception of continuously flic

177 Ablation of mouse occipital cortex induces precisely timed and uniform p53

178 to those with persistent ADHD in the medial occipital cortex, insula, parahippocampus, and prefronta

179 daptation for small shape changes in lateral occipital cortex irrespective of category membership, co

180 While occipital cortex is also critical for picture naming, it

181 emianopic patients and suggest that when the occipital cortex is damaged or inhibited, and the visual

182 corroborative clinical evidence suggest that occipital cortex is engaged in tactile tasks requiring f

183 The macaque dorsal occipital cortex is generally thought to contain an elon

184 The uniqueness of a memory role for occipital cortex is in its cross-modal responses to codi

185 at the spatial pattern of propagation in the occipital cortex is non-concentric with a variable exten

186 siform gyrus, and insula, and extending into occipital cortex (left hemisphere) and orbitofrontal cor

187 to localize object-specific ROIs in lateral occipital cortex (LO) and scene-specific ROIs in the par

188 probe whether dorsal regions of the lateral occipital cortex (LO) are activated in tactile recogniti

189 ent fMRI studies have identified the lateral occipital cortex (LO) as a potential neural origin of th

190 with scrambled line drawings in the lateral occipital cortex (LO) of the ventral stream, an area tha

191 (2) a decrease in activation of the lateral occipital cortex (LO), and (3) a decrease in the dorsal

192 region, such as the shape-selective lateral occipital cortex (LO), must still base its activation on

193 Meanwhile, the lateral occipital cortex (LOC) has been suggested to be critical

194 pattern in both the retinotopic and lateral occipital cortex (LOC) in humans contains category infor

195 l FFA and bilateral object-selective lateral occipital cortex (LOC) predicted the participants' abili

196 Neurostimulation was targeted at the lateral occipital cortex (LOC), a key region for object percepti

197 C) and the higher-level visual area, lateral occipital cortex (LOC), known to be critically involved

198 geting hippocampal interactions with lateral occipital cortex (LOC).

199 ing the most substantial loss in the lateral occipital cortex (LOC).

200 eural activity that was localized to lateral occipital cortex (LOC).

201 colocalized with BOLD activations in lateral occipital cortex (LOC).

202 nal development of mid-level vision [lateral occipital cortex (LOC)] early in infancy.

203 on of a mid-level visual region [the lateral occipital cortex (LOC)] in a population much younger tha

204 , mainly in areas 46, 9, 10, and 11, and the occipital cortex, mainly area V2.

205 The occipital cortex may be a suitable pseudoreference regio

206 rch suggests an enhanced excitability in the occipital cortex may underlie this reaction during IPS,

207 ), parietal cortex (mean increase: 25%), and occipital cortex (mean increase: 19%).

208 Occipital cortex metabolite levels were measured using p

209 pital face area, fusiform face area, lateral occipital cortex, mid fusiform, parahippocampal place ar

210 length (posterior cingulate cortex, inferior occipital cortex, middle temporal cortex, hippocampus, a

211 scranial magnetic stimulation (TMS) over the occipital cortex modulated the impact of memory on searc

212 ions between the left temporal lobe and left occipital cortex not showing evidence of development unt

213 The occipital cortex (OC) of early-blind humans is activated

214 relative to total creatine (GABA/Cr) in the occipital cortex (OC), anterior cingulate cortex (ACC),

215 We show that the occipital cortex of 6-month-old infants exhibits the sig

216 e report motor cortical function in the left occipital cortex of a subject who suffered a left middle

217 ing of auditory frequency information in the occipital cortex of anophthalmic people.

218 A concentrations have also been found in the occipital cortex of depressed subjects.

219 tamena, thalami, brain stem, cerebellum, and occipital cortex of each subject.

220 m the dorsolateral prefrontal cortex and the occipital cortex of elderly patients with schizophrenia

221 es varied from 22% in temporal pole to 6% in occipital cortex of neostriatal values.

222 ay matter volume that were restricted to the occipital cortex of patients.

223 ings of decreased GABA concentrations in the occipital cortex of subjects with MDD.

224 The significant findings in occipital cortex of the blind indicated that perceptual

225 It was hypothesized that the changes in occipital cortex of the blind reflected life-long skill

226 the right supraorbital area], but not of the occipital cortex or sham stimulation, increased the prop

227 or parietal cortex, the right or left dorsal occipital cortex or the right ventral occipital cortex,

228 me trials by (1) pretrial phase synchrony of occipital cortex oscillations in the 8-9 Hz (low alpha)

229 ups were detected in the posterior insula or occipital cortex (P > 0.05 for all comparisons).

230 halamus (P = .04), frontal cortex (P = .01), occipital cortex (P = .004), and cingulate cortex (P = .

231 anterior cingulate cortex (P =.003) and the occipital cortex (P =.01) in the depressed subjects.

232 cerebellum, with intermediate values in the occipital cortex, parietal cortex, and caudate putamen.

233 specific emotional stimuli were found in the occipital cortex, parietal cortex, and cerebellum.

234 ge of pERK1/2 levels in the temporal cortex, occipital cortex, parietal cortex, midbrain, and medulla

235 owed significant metabolic reductions in the occipital cortex, particularly in the primary visual cor

236 Furthermore, these findings suggest the occipital cortex plays a key role in supporting mental r

237 erior cingulate cortex (ACC) and the parieto-occipital cortex (POC) in adolescents (n=30) and emergin

238 anterior cingulate cortex (ACC) and parieto-occipital cortex (POC) in healthy individuals.

239 metic problem complexity in ventral temporal-occipital cortex, posterior parietal cortex, and medial

240 havior disorder (RBD) with bilateral parieto-occipital cortex, precuneus, and ventrolateral-frontal m

241 al cerebellum and in a region in the lateral occipital cortex presumably corresponding to the area KO

242 nd myelin integrity increased in insular and occipital cortex projections with maturity.

243 We calculate these parameters in mouse occipital cortex, rat CA1, monkey V1, and human temporal

244 Hz pattern also for EEG-derived measures of occipital cortex reactivity to the TMS pulses.

245 In anophthalmic animals, the occipital cortex receives direct subcortical auditory in

246 showed DOC changes in all regions except the occipital cortex, relative to controls.

247 osterior lateral occipitotemporal cortex and occipital cortex, respectively.

248 in the superior temporal sulcus and inferior occipital cortex, respectively.

249 are primarily processed in somatosensory and occipital cortex, respectively.

250 es in the mid-fusiform gyrus and the lateral occipital cortex, respectively.

251 In contrast, lateral occipital cortex responded more strongly to object chang

252 cortex was unresponsive to Braille words and occipital cortex responded to spoken words but not diffe

253 In congenitally blind individuals, the occipital cortex responds to various nonvisual inputs.

254 Larger occipital cortex responses to "new" Braille words sugges

255 Intracranial recordings from human occipital cortex revealed that spontaneous and stimulus-

256 seline BOLD response in the bilateral middle occipital cortex, selectively during the stimulus-proces

257 Immunofluorescence analysis of the occipital cortex showed an increase of fibrin(ogen)/Abet

258 ntrast, superior parietal lobule and parieto-occipital cortex showed greater activation to the apart

259 recruited by patients only: the left dorsal occipital cortex showed systematic activation in all con

260 Electroencephalogram recorded over the left occipital cortex showed: 1) coherence with electromyogra

261 trastriate occipital cortex, whereas primary occipital cortex shows consistent activity across all sc

262 ttsburgh Compound B retention selectively in occipital cortex, sparing regions typically labeled in A

263 sponse decrements in right frontal and right occipital cortex, strongly supporting the compensatory r

264 ntrol (medulla and pons), and vision (dorsal occipital cortex, superior colliculi and lateral genicul

265 nificantly higher mean SUVR in PMT overlying occipital cortex than both other groups, although not in

266 mplex interactions within the fronto-parieto-occipital cortex than previously anticipated.

267 aura changes depending on the region of the occipital cortex that is involved.

268 tion of the ipsilateral field within lateral occipital cortex that is normally associated with visual

269 A region in human lateral occipital cortex (the 'extrastriate body area' or EBA) h

270 , after suppressing the activity in the left occipital cortex, the congruency-dependent response faci

271 ical areas, including portions of the medial occipital cortex, the lateral parietal cortex, and the s

272 In occipital cortex, these patterns sometimes reflected the

273 information being encoded (fusiform/lateral occipital cortex), they each exerted opposite effects on

274 simplified reference tissue method with the occipital cortex time activity curve as an input functio

275 oops that are dominated by flow from parieto-occipital cortex to integrative frontal areas in the hig

276 scranial magnetic stimulation (TMS) over the occipital cortex to interfere with attentional reorienti

277 s in excitability affect the function of the occipital cortex to other, less provocative visual stimu

278 Occipital cortex total GABA levels were measured before

279 ed negative BOLD response (NBR) in the human occipital cortex, triggered by stimulating part of the v

280 voked potentials (SSVEPs) were measured over occipital cortex using electroencephalography (EEG).

281 Tissue from the occipital cortex (visual) was sectioned parallel to cort

282 te a cluster of visual field maps in ventral occipital cortex (VO cluster) anterior to hV4.

283 In ventral occipital cortex (VO), all colors elicit strong response

284 brain regions, including the ventrotemporal occipital cortex (VTOC), the posterior parietal cortex,

285 The lateral occipital cortex was also recruited into a left-laterali

286 Grey matter volume in the lateral occipital cortex was associated with component scores re

287 In contrast, neural similarity in occipital cortex was best predicted by shape similarity

288 unctional activation (measured with fMRI) in occipital cortex was more extensive when participants vi

289 By contrast, pattern similarity in lateral occipital cortex was related to memory only when context

290 tal, left superior parietal, and left middle occipital cortex) was evaluated using fMRI datasets acqu

291 ht posterior insula, anterior cingulate, and occipital cortex were examined in subjects at rest.

292 Granger causality from FEF and IPS to visual occipital cortex were significantly greater than both bo

293 scenes approximately 1 s before extrastriate occipital cortex, whereas primary occipital cortex shows

294 In particular, the inferior lateral occipital cortex, which is involved in visual-object per

295 ry and cognitive tasks evoke activity in the occipital cortex, which is normally visual.

296 istration in overlapping areas in the middle occipital cortex while performing the same task conditio

297 ctive cathodal-inhibitory tDCS over the left occipital cortex, while, in control Experiment 2, partic

298 We delivered an oscillatory current over the occipital cortex with tACS.

299 date nucleus to 14.5 +/- 5.3 mL/cm(3) in the occipital cortex, with intermediate values in the amygda

300 task involving the prefrontal, parietal, and occipital cortex (Z = 2.9-4.2, P = .03-.0003).