ライフサイエンスコーパス: posterior cingulate cortex

1 l area, orbitofrontal cortex, brainstem, and posterior cingulate cortex).

2 temporal and parietal lobes, precuneus, and posterior cingulate cortex.

3 ntromedial prefrontal cortex, interacts with posterior cingulate cortex.

4 DCS enhanced connectivity of the left dorsal posterior cingulate cortex.

5 associated with motor control in the dorsal posterior cingulate cortex.

6 ted greater activation within the insula and posterior cingulate cortex.

7 isruption in the ventromedial prefrontal and posterior cingulate cortex.

8 he temporal pole and the caudal anterior and posterior cingulate cortex.

9 ventrolateral prefrontal cortex, insula, and posterior cingulate cortex.

10 rved with the middle temporal cortex and the posterior cingulate cortex.

11 late/supplementary motor area, and bilateral posterior cingulate cortex.

12 e network (DMN), including the precuneus and posterior cingulate cortex.

13 htly greater gray matter volumes in the left posterior cingulate cortex.

14 d by key regions, including the anterior and posterior cingulate cortex.

15 or parahippocampal cortex, and retrosplenial/posterior cingulate cortex.

16 rs in the dorsal hippocampus, but not in the posterior cingulate cortex.

17 ive compared with neutral conditions was the posterior cingulate cortex.

18 s dementia; the largest reduction was in the posterior cingulate cortex.

19 cortex, and reached maximal densities in the posterior cingulate cortex.

20 ode network, including the angular gyrus and posterior cingulate cortex.

21 derlying cortical source of this activity in posterior cingulate cortex.

22 sentation of the traumatic narratives in the posterior cingulate cortex.

23 mpanzee and rhesus macaque brain tissue from posterior cingulate cortex.

24 uding the amygdala, insula, hippocampus, and posterior cingulate cortex.

25 pital cortex, anterior cingulate cortex, and posterior cingulate cortex.

26 work, including medial prefrontal cortex and posterior cingulate cortex.

27 ross pedalism in the left pSTS and bilateral posterior cingulate cortex.

28 right lateral parietal lobules, and the left posterior cingulate cortex.

29 subgenual anterior cingulate cortex and left posterior cingulate cortex.

30 ior and superior colliculus and anterior and posterior cingulate cortex.

31 connecting the parahippocampal gyrus to the posterior cingulate cortex.

32 vely signed for stimulation-avoiders, in the posterior cingulate cortex.

33 ometabolism, restricted to the retrosplenial/posterior cingulate cortex.

34 tivity between the parahippocampal gyrus and posterior cingulate cortex.

35 ces, with hubs in medial prefrontal, but not posterior cingulate, cortex.

36 he mitochondrial electron transport chain in posterior cingulate cortex, 65% of those in the middle t

37 ice have age-related metabolic reductions in posterior cingulate cortex, a finding that does not appe

38 (2) = 15.87), located within the SN, and the posterior cingulate cortex, a focal hub of the DMN.

39 hole-brain analyses initiated by seeding the posterior cingulate cortex, a region of high amyloid bur

40 er, prestimulus connectivity between FFA and posterior cingulate cortex, a region of the default netw

41 gions, such as the thalamus and anterior and posterior cingulate cortex (ACC and PCC).

42 Kisspeptin's enhancement of posterior cingulate cortex activity in response to attra

43 er uncertainty is negatively correlated with posterior cingulate cortex activity.

44 ed the onset of seizures in the right dorsal posterior cingulate cortex, adjacent to the marginal sul

45 nced the connectivity in the right DLPFC and posterior cingulate cortex, all of which were related to

46 ncreased activation of the left amygdala and posterior cingulate cortex, along with blunted responses

47 We recorded from the posterior cingulate cortex, an area implicated in the co

48 inked to the default mode network, including posterior cingulate cortex and angular gyrus.

49 crete regions of increased activation in the posterior cingulate cortex and anterior insula in respon

50 tion reduced functional connectivity between posterior cingulate cortex and bilateral anterior cingul

51 antia nigra, left periaqueductal grey, right posterior cingulate cortex and bilateral cerebellum.

52 d marked metabolic reduction (21-22%) in the posterior cingulate cortex and cinguloparietal transitio

53 mporal lobe degeneration-there is also early posterior cingulate cortex and diencephalic damage.

54 ng-state functional connectivity between the posterior cingulate cortex and dorsolateral prefrontal c

55 The posterior cingulate cortex and frontal eye field represe

56 In the clinical study, reduced precuneus/posterior cingulate cortex and hippocampal grey matter d

57 In the clinical study, reduced precuneus/posterior cingulate cortex and hippocampal grey matter d

58 MCI patients showed primarily posterior cingulate cortex and hippocampal hypometabolis

59 ge in Bnip3 levels did not occur in the male posterior cingulate cortex and hippocampus.

60 ated in this network, several, including the posterior cingulate cortex and inferior parietal lobes,

61 ith reduced short-range and long-range FC in posterior cingulate cortex and medial prefrontal cortex.

62 g lateral temporoparietal cortex, precuneus, posterior cingulate cortex and middle frontal gyrus.

63 p had greater connectivity between the right posterior cingulate cortex and other brain areas.

64 correlated with schizotypy in the bilateral posterior cingulate cortex and precuneus (and for disorg

65 Furthermore, features associated with the posterior cingulate cortex and precuneus nodes of the de

66 aled that brain features associated with the posterior cingulate cortex and precuneus, dorsolateral a

67 cant APOE4 and FH effects in the left dorsal posterior cingulate cortex and precuneus, where decrease

68 ponses in anterior medial prefrontal cortex, posterior cingulate cortex and precuneus.

69 s in (1) functional connectivity between the posterior cingulate cortex and regions across the brain,

70 etabolism in the bilateral MTL and precuneus-posterior cingulate cortex and right lingual gyrus (r(2)

71 ation of the ventromedial prefrontal cortex, posterior cingulate cortex and right superior frontal gy

72 as well as a neural system encompassing the posterior cingulate cortex and superior frontal gyrus.

73 ons and (b) a product of interactions of the posterior cingulate cortex and the hippocampus.

74 lving delay evoked greater activation in the posterior cingulate cortex and the striatum.

75 tive in the absence of a task, including the posterior cingulate cortex and the superior frontal gyru

76 campus, posterior parahippocampal gyrus, and posterior cingulate cortex and with elevated connectivit

77 ction in ASDs (mid- and posterior insula and posterior cingulate cortex), and highlighted less common

78 ulate cortex, isthmus cingulate cortex [IC], posterior cingulate cortex, and amygdala).

79 ilateral insular cortex, bilateral precuneus/posterior cingulate cortex, and bilateral temporal, angu

80 ain activations in temporoparietal junction, posterior cingulate cortex, and dorsal medial prefrontal

81 luctuation in the orbital frontal cortex and posterior cingulate cortex, and exhibited increased rest

82 the ventromedial prefrontal cortex, insula, posterior cingulate cortex, and hippocampus in the impro

83 ncreases in activation in the parietal lobe, posterior cingulate cortex, and inferior frontal gyrus i

84 edial orbitofrontal cortex, temporal cortex, posterior cingulate cortex, and precuneus, compared with

85 conditioning, as well as in the cerebellum, posterior cingulate cortex, and putamen during extinctio

86 omedial cortices (the ensemble of precuneus, posterior cingulate cortex, and retrosplenial region), a

87 ventral striatum, anterior cingulate cortex, posterior cingulate cortex, and right anterior insula.

88 ampus, right inferior parietal lobule, right posterior cingulate cortex, and right ventral precuneus.

89 gdala, parahippocampus, insula, anterior and posterior cingulate cortex, and several primary sensory

90 cortex, anterior PFC, orbitofrontal cortex, posterior cingulate cortex, and somatosensory associatio

91 following areas: thalamus, ventral striatum, posterior cingulate cortex, and temporal cortex.

92 ithin PM network areas, including precuneus, posterior cingulate cortex, angular gyrus, and parahippo

93 nction with connected regions, including the posterior cingulate cortex, anterior cingulate cortex, a

94 orsolateral prefrontal cortex, frontal pole, posterior cingulate cortex, anterior cingulate cortex, t

95 , and suggest that the medial prefrontal and posterior cingulate cortex are part of a neural system s

96 of the retrosplenial cortex and the adjacent posterior cingulate cortex (area 23) in the macaque monk

97 he anterior medial prefrontal cortex and the posterior cingulate cortex, as reflected by higher corre

98 plementary motor cortex, premotor cortex and posterior cingulate cortex, as well as the left primary

99 /middle frontal gyrus and the left precuneus/posterior cingulate cortex, because this connection has

100 unction, dorsal premotor cortex, insula, and posterior cingulate cortex bilaterally.

101 between NT-proBNP and GMD in the medial and posterior cingulate cortex but also in precuneus and hip

102 ional T1w/T2w values compared to PWoH in the posterior cingulate cortex, caudal anterior cingulate co

103 The posterior cingulate cortex (CGp) is a major hub of the d

104 Neuronal activity in posterior cingulate cortex (CGp) is modulated by visual

105 Posterior cingulate cortex (CGp) is strongly connected w

106 To investigate the contribution of posterior cingulate cortex (CGp) to these processes, we

107 Neuronal activity in posterior cingulate cortex (CGp), a brain area linked to

108 We investigated the hypothesis that the posterior cingulate cortex (CGp), a region linked to def

109 We hypothesized that posterior cingulate cortex (CGp), an area linking reward

110 network hubs than boys, predominantly in the posterior cingulate cortex (Cohen d = -0.36), and lower

111 ated neuronal discrimination in anterior and posterior cingulate cortex confirmed the previously hypo

112 We have previously shown abnormally high posterior cingulate cortex connectivity in the chronic p

113 Relative to control participants, decreased posterior cingulate cortex connectivity to MTL and incre

114 ons of neural responses to heartbeats in the posterior cingulate cortex covary with changes in bodily

115 ctivation, and CTL, but not ALC, deactivated posterior cingulate cortex/cuneus.

116 connectivity between the dorsal and ventral posterior cingulate cortex (d/vPCC) and the dorsal anter

117 Dynamic causal modeling revealed that posterior cingulate cortex desynchronization can be expl

118 confirmed the importance of medial parietal/posterior cingulate cortex differences in aging and DAT.

119 e pretraining to posttraining alterations in posterior cingulate cortex-dlPFC rsFC statistically medi

120 reased negative correlation in the precuneus/posterior cingulate cortex (DMN).

121 al inferior parietal cortex (angular gyrus), posterior cingulate cortex, dorsomedial and ventral pref

122 that this component emanated from the dorsal posterior cingulate cortex (dPCC).

123 D showed functional differences in the right posterior cingulate cortex during resting-state experime

124 lusters appeared in the medial occipital and posterior cingulate cortex (each left and right).

125 nectivity of the hypothalamus, amygdala, and posterior cingulate cortex, each probing a distinct netw

126 vmPFC, mid-cingulate, and posterior cingulate cortex encoded the relative value be

127 tal cortex during response selection and the posterior cingulate cortex for cognitive processes.

128 to be statistically significant only in the posterior cingulate cortex for the WBN data.

129 key regions within the default mode network (posterior cingulate cortex), frontoparietal network (lef

130 Our own work has consistently shown abnormal posterior cingulate cortex function following traumatic

131 Understanding posterior cingulate cortex function is likely to be of c

132 d regional CBF in the thalamus, hippocampus, posterior cingulate cortex, fusiform, and visual cortex

133 yrus, right superior temporal gyrus, ventral posterior cingulate cortex, globus pallidus, and calcari

134 One influential hypothesis is that the posterior cingulate cortex has a central role in support

135 The anterior and posterior cingulate cortex have been implicated in adapt

136 ional characteristics of amyloid-beta in the posterior cingulate cortex, hippocampus and cerebellum o

137 regions, including medial prefrontal cortex, posterior cingulate cortex, hippocampus, and supplementa

138 .05) lower in SCZs in the amygdala, caudate, posterior cingulate cortex, hippocampus, hypothalamus, a

139 Aberrant posterior cingulate cortex hyperconnectivity was linked

140 network linking medial prefrontal cortex and posterior cingulate cortex (i.e., the default mode netwo

141 ic tasks, activity was greater mainly in the posterior cingulate cortex, implying selective contribut

142 was seen in the superior temporal gyrus and posterior cingulate cortex in 22q11DS relative to nondel

143 ective connectivity from the thalamus to the posterior cingulate cortex in a way that depended on ser

144 ctional uncoupling from the deeper layers of posterior cingulate cortex in AD, whereas no such effect

145 ior and ventral parts of the medial parietal/posterior cingulate cortex in association with hearing u

146 tering mood, and increased activation in the posterior cingulate cortex in BD (vs.

147 and lateral frontal association cortices and posterior cingulate cortex in comparison to normal contr

148 uence of the medial prefrontal cortex on the posterior cingulate cortex in depression is a neural cor

149 d RSFC between the right precuneus and right posterior cingulate cortex in DMN, among CD patients com

150 d the anterior and posterior portions of the posterior cingulate cortex in geriatric depression.

151 ult suggests a functional importance for the posterior cingulate cortex in impairment of learning and

152 mined glucose metabolism in the anterior and posterior cingulate cortex in schizophrenia.

153 cortex had a "hyperregulatory" effect on the posterior cingulate cortex in the depressed group, with

154 The posterior cingulate cortex, in contrast, may be more hig

155 in the right inferior frontal cortex and the posterior cingulate cortex increased with age.

156 found in DMN, including in angular gyrus and posterior cingulate cortex, indicating that DMN and mult

157 were positively correlated with bout length (posterior cingulate cortex, inferior occipital cortex, m

158 stems theory, and we propose that the dorsal posterior cingulate cortex influences attentional focus

159 The posterior cingulate cortex is a highly connected and met

160 ld a narrative, the anterior medial parietal/posterior cingulate cortex is concerned with linking thi

161 thmicity of field potentials recorded in the posterior cingulate cortex is thought to have a septo-hi

162 dorsolateral prefrontal cortex (DLPFC), left posterior cingulate cortex, left inferior parietal lobul

163 rior and middle temporal gyri, insula, right posterior cingulate cortex, lingual gyrus, striate corte

164 mainly represented the SV for food, and the posterior cingulate cortex mainly represented the SV for

165 In particular, the right posterior cingulate cortex may act as a critical informa

166 insula) and several regions of DMN including posterior cingulate cortex, medial frontal cortex, poste

167 rain regions linked to emotional processing: posterior cingulate cortex, medial prefrontal cortex, ri

168 clusters within the mid-cingulate cortex and posterior cingulate cortex (n = 14, voxel-wise p < 0.005

169 superior temporal gyrus, dorsal anterior and posterior cingulate cortex, nucleus accumbens area, and

170 n in all regions and patients except for the posterior cingulate cortex of 1 patient.

171 nd in both the anterior cingulate cortex and posterior cingulate cortex of patients with first-episod

172 in vivo in the anterior cingulate cortex and posterior cingulate cortex of the subjects by using the

173 the human "default-mode network," including posterior cingulate cortex, orbital prefrontal cortex, a

174 cting limbic structures such as the anterior/posterior cingulate cortex, orbitofrontal cortex, and me

175 revealed a set of brain regions, such as the posterior cingulate cortex, parahippocampal gyri, and fr

176 ntal cortex, ventromedial prefrontal cortex, posterior cingulate cortex, parahippocampal gyrus, amygd

177 dle frontal gyrus, angular gyrus, precuneus, posterior cingulate cortex, parahippocampal gyrus, hippo

178 gnificantly associated with PD in precuneus, posterior cingulate cortex (pC/pCC) and medial prefronta

179 severity were positively correlated with the posterior cingulate cortex (PCC) activation during actio

180 to bias attention predictively is related to posterior cingulate cortex (PCC) activation.

181 rk with nonsmokers indicates that MT reduces posterior cingulate cortex (PCC) activity.

182 in functional imaging studies, including the posterior cingulate cortex (PCC) and a medial frontal re

183 s) were measured between hippocampus and the posterior cingulate cortex (PCC) and between the amygdal

184 stronger or weaker connectivity between the posterior cingulate cortex (PCC) and DMN regions, depend

185 ved significantly increased rsFC between the posterior cingulate cortex (PCC) and dorsal attention ne

186 omprehensive template from core seeds in the posterior cingulate cortex (PCC) and medial prefrontal c

187 ) was evaluated with: the precuneus (P), the posterior cingulate cortex (PCC) and the dorsomedial pre

188 shown that certain brain regions, including posterior cingulate cortex (PCC) and ventral anterior ci

189 her FC within the cerebellum and between the posterior cingulate cortex (PCC) and vision-related regi

190 ut degrees of cingulate motor area (CMA) and posterior cingulate cortex (PCC) during left-hand MR imp

191 e recorded the activity of single neurons in posterior cingulate cortex (PCC) in 2 male monkeys searc

192 both the anterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) in 2 male rhesus monkey

193 Neuroimaging experiments implicate the posterior cingulate cortex (PCC) in episodic memory proc

194 sheds light on the lesser-known role of the posterior cingulate cortex (PCC) in memory encoding.

195 The posterior cingulate cortex (PCC) is a central part of th

196 Posterior cingulate cortex (PCC) is an enigmatic region

197 A reduction in glucose metabolism in the posterior cingulate cortex (PCC) predicts conversion to

198 ween the anterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) regions of the default

199 trols most complex motor behaviours, and the posterior cingulate cortex (PCC) regulates visual, among

200 erent foraging tasks that neurons in primate posterior cingulate cortex (PCC) signal decision salienc

201 revealed a set of overlapping regions within posterior cingulate cortex (PCC) that contained decodabl

202 We observed directed influence from the posterior cingulate cortex (PCC) to the anterior cingula

203 s association was mediated indirectly by the posterior cingulate cortex (PCC) via the right inferior

204 Moreover, activation of the posterior cingulate cortex (PCC) was observed during the

205 ealed that responses in the amygdala and the posterior cingulate cortex (PCC) were stronger while enc

206 grity of macromolecular protein pools in the posterior cingulate cortex (PCC), a central DMN hub regi

207 e, we show that morphological differences in posterior cingulate cortex (PCC), a hub of functional br

208 tex (DLPFC), medial frontal/cingulate gyrus, posterior cingulate cortex (PCC), and ventromedial prefr

209 g characteristic (ROC) curve analysis of the posterior cingulate cortex (PCC), and voxel-based morpho

210 tified in nonclinical samples, including the posterior cingulate cortex (PCC), as well as the parahip

211 the ventromedial prefrontal cortex (vmPFC), posterior cingulate cortex (PCC), parahippocampus, insul

212 eticular formation, basal ganglia, thalamus, posterior cingulate cortex (PCC), precuneus, and cerebel

213 er PiB retention in AD-affected anterior and posterior cingulate cortex (PCC), precuneus, parietal, t

214 lled the default network, which includes the posterior cingulate cortex (PCC), retrosplenial cortex,

215 nsidered, functional differences in the left posterior cingulate cortex (PCC), right amygdala, left h

216 patterns were obtained in anterior (ACC) and posterior cingulate cortex (PCC), superior frontal gyrus

217 ious sites that partake in DMN function, the posterior cingulate cortex (PCC), temporal parietal junc

218 ving in the anterior cingulate cortex (ACC), posterior cingulate cortex (PCC), upper precuneus (UPCU)

219 g conflict, control subjects deactivated the posterior cingulate cortex (PCC), whereas alcoholic subj

220 erable uncertainty about the function of the posterior cingulate cortex (PCC).

221 ncephalography data localized the ERN to the posterior cingulate cortex (PCC).

222 ssing including the fusiform gyrus (FFG) and posterior cingulate cortex (PCC).

223 directional anatomical connectivity with the posterior cingulate cortex (PCC).

224 al cortex (PPC), and the medial parietal and posterior cingulate cortex (PCC).

225 ted in topographically adjacent areas within posterior cingulate cortex (PCC).

226 , ventromedial prefrontal cortex (vmPFC) and posterior cingulate cortex (pCC).

227 ion, and these activations overlapped in the posterior cingulate cortex (PCC).

228 des of the DMN: medial prefrontal cortex and posterior cingulate cortex (PCC).

229 PFC FC with other DMN regions, including the posterior cingulate cortex (PCC)/precuneus (PCu) and ret

230 strated modifications of the activity of the posterior cingulate cortex (PCC)/precuneus and dorsolate

231 as a seed, increased rsFC strength with the posterior cingulate cortex (PCC)/precuneus was seen in t

232 tex (DLPFC)/inferior frontal gyrus (IFG) and posterior cingulate cortex (PCC)/precuneus, ranked as th

233 , hippocampus [Hip], entorhinal cortex [EC], posterior cingulate cortex [PCC], inferior parietal lobu

234 mode network (DMN), including the precuneus/posterior cingulate cortex (Pcu/PCC) and the medial pref

235 en associated with activity in the precuneus/posterior cingulate cortex (PPCC), we examined this regi

236 tration of D-betaHB (N = 16), and (2) in the posterior cingulate cortex pre- and post-administration

237 arful faces, but increased activation in the posterior cingulate cortex / precuneus to happy faces.

238 rior medial temporal lobe, subcallosal area, posterior cingulate cortex, precuneus and possibly the s

239 racted from seed regions in the hippocampus, posterior cingulate cortex, precuneus and primary visual

240 lateral and medial temporal lobe structures, posterior cingulate cortex, precuneus, and medial prefro

241 nd lateral frontal cortices, insular cortex, posterior cingulate cortex, precuneus, and occipital cor

242 formation, through its interactions with the posterior cingulate cortex, precuneus, dorsomedial PFC,

243 asure neurotransmitter concentrations in the posterior cingulate cortex/precuneus (PCC/PCu), a key co

244 ty with posterior DMN regions, including the posterior cingulate cortex/precuneus (PCC/Precun) and le

245 We found that an ROI consisting of the posterior cingulate cortex/precuneus and the medial fron

246 cific suppression of high-gamma power in the posterior cingulate cortex/precuneus node of the DMN dur

247 twork, as well as the pathway connecting the posterior cingulate cortex/precuneus with the thalamus,

248 gnitive impairment in typical cortical hubs (posterior cingulate cortex/precuneus), strongly overlapp

249 inically affected AD patients, involving the posterior cingulate cortex/precuneus, parietotemporal an

250 ncluding medial prefrontal cortex (MPFC) and posterior cingulate cortex/precuneus.

251 processing (amygdala, medial prefrontal and posterior cingulate cortex) predicted punishment magnitu

252 similarity, or consistent processing, in the posterior cingulate cortex predicts associative memory f

253 thickness in the left rACC, caudal ACC, and posterior cingulate cortex (ps < = 0.01).

254 dial prefrontal cortex, r = -0.66, P = .003; posterior cingulate cortex, r = -0.65, P = .001).

255 matter adjacent to the hippocampus, multiple posterior cingulate cortex regions, and insular white ma

256 reased activation in the medial parietal and posterior cingulate cortex, regions that have previously

257 , including medial prefrontal cortex (MPFC), posterior cingulate cortex/retrosplenial (PCC/Rsp), infe

258 physiological co-activation of retrosplenial/posterior cingulate cortex (RSC/PCC) and angular gyrus (

259 ning, and not relaxation training, increased posterior cingulate cortex rsFC with left dlPFC (p < .05

260 tum, medial prefrontal cortex, amygdala, and posterior cingulate cortex satisfy necessary and suffici

261 on level-dependent fMRI and a restrosplenial/posterior cingulate cortex seed, aged rats demonstrated

262 topology of the default network, based on a posterior cingulate cortex seed, consistent with prior r

263 e tested for alterations in DMN rsFC using a posterior cingulate cortex seed-based analysis and found

264 The posterior cingulate cortex showed increased pattern simi

265 fect correlated with brain morphology of the posterior cingulate cortex, superior temporal gyrus, ins

266 o cheat a lot, while a network consisting of posterior cingulate cortex, temporoparietal junction, an

267 ed to patient's outcome were frontal cortex, posterior cingulate cortex, thalamus, putamen, pallidum,

268 es showed significantly higher uptake in the posterior cingulate cortex than all other males.

269 between the medial prefrontal cortex and the posterior cingulate cortex than in the control group (od

270 nce for two DMN-related iCAPs consisting the posterior cingulate cortex that differentially interact

271 chronically implanted into the anterior and posterior cingulate cortex, the anterior-ventral and med

272 , projections to the PAG also arise from the posterior cingulate cortex, the dorsal dysgranular, and

273 In monkeys with lesions in the posterior cingulate cortex, the RT variability significa

274 ory 5-HT(1A) binding inversely modulated the posterior cingulate cortex, the strongest hub in the res

275 ial prefrontal cortex (vmPFC), striatum, and posterior cingulate cortex] track the SV of uncertain ch

276 ntral striatum, medial prefrontal cortex and posterior cingulate cortex--tracks the revealed subjecti

277 during subsequent rest, rostral anterior and posterior cingulate cortex, ventral striatum, and insula

278 increased cortical thickness in some areas (posterior cingulate cortex, ventromedial prefrontal cort

279 uents of the canonical default-mode network (posterior cingulate cortex, ventromedial/dorsomedial pre

280 anterior cingulate cortex (pACC) and ventral posterior cingulate cortex (vPCC)-regions possibly affec

281 Mean metabolic reduction in the posterior cingulate cortex was significantly greater tha

282 In both hippocampus and posterior cingulate cortex we identified an extensive ar

283 sy brains of AD cases and normal controls in posterior cingulate cortex, which is metabolically affec

284 ted in the left insula/frontal operculum and posterior cingulate cortex, which were assigned to ventr

285 sed activation in the ventral medial PFC and posterior cingulate cortex with age.

286 ted increased functional connectivity of the posterior cingulate cortex with medial temporal lobe reg

287 hippocampus/parahippocampal gyrus; and, (2) posterior cingulate cortex with supplementary motor area

288 suggest a decrement of cytochrome oxidase in posterior cingulate cortex, with progressive reduction w

289 reduced ChAT activity in the hippocampus and posterior cingulate cortex, without affecting ChAT activ