ライフサイエンスコーパス: posterior cingulate

1 as the frontal cortex, temporal cortex, and posterior cingulate.

2 ortical regions, including the precuneus and posterior cingulate.

3 ontal cortex, and decreased MI levels in the posterior cingulate.

4 al cortex, right frontal eye-fields, and the posterior cingulate.

5 uding the striatum, insula, and anterior and posterior cingulate.

6 ng the posterior superior temporal lobes and posterior cingulate.

7 fically the anterior insula and anterior and posterior cingulate.

8 hin-subject change in the thalamus (-11.4%), posterior cingulate (-9%), occipital (-7%), parietal (-7

9 In the present study, we show that posterior cingulate activities responding to heartbeat s

10 ortex preferentially targeted 6DC, while the posterior cingulate and adjacent medial wall areas prefe

11 ional connectivity than patients between the posterior cingulate and both left fusiform and medial fr

12 The observation of reduced perfusion in the posterior cingulate and cuneal cortex, which are regions

13 The measurements of posterior cingulate and hippocampal glucose metabolism w

14 was significantly higher overall and in the posterior cingulate and lateral temporal regions in the

15 in functional connectivity in the bilateral posterior cingulate and left parietal DMN nodes in DM1 p

16 ted with functional connectivity between the posterior cingulate and medial frontal gyrus for combine

17 A positive functional correlation between posterior cingulate and medial prefrontal cortices, majo

18 ibutable to age or structural atrophy in the posterior cingulate and medial temporal areas.

19 ween particular nodes of the DMN, namely the posterior cingulate and medial temporal cortex.

20 functional connectivity observed between the posterior cingulate and medial temporal regions.

21 controls in white matter bundles innervating posterior cingulate and parietal cortex, basal ganglia,

22 e and insular cortices, and decreased NAA in posterior cingulate and parietal cortices.

23 f the connections between a medioprefrontal, posterior cingulate and parietal seed regions.

24 of (1)H-MRS metabolites were obtained in the posterior cingulate and precuneus region.

25 phy were detected in the hippocampus and the posterior cingulate and precuneus regions, and with dise

26 temporal sulcus, parahippocampal cortex, and posterior cingulate and retrosplenial cortex.

27 th ASD demonstrated hyperconnectivity of the posterior cingulate and retrosplenial cortices with pred

28 limited areas of abnormality centred on the posterior cingulate and rostral temporal lobes, respecti

29 significant slope changes confirmed for the posterior cingulate and ventral striatum.

30 s T2DM patients in the DMN between the seed (posterior cingulate) and bilateral middle temporal gyrus

31 including several core hubs of the default (posterior cingulate) and executive (dorsolateral prefron

32 l gyrus, putamen, dorsal anterior cingulate, posterior cingulate, and amygdala.

33 la, posterior parietal regions, anterior and posterior cingulate, and dorsolateral prefrontal cortex

34 s of the default mode network (angular gyri, posterior cingulate, and medial prefrontal cortex) encod

35 ortical connectivity among middle cingulate, posterior cingulate, and medial prefrontal cortices than

36 involving the posterior parietal cortex, the posterior cingulate, and medial temporal lobe structures

37 activities in the medial prefrontal cortex, posterior cingulate, and occipital cortices during evalu

38 with bilateral dorsolateral-frontal cortex, posterior cingulate, and parietal metabolism; and rapid

39 t-sided brain regions (dorsolateral frontal, posterior cingulate, and posterior parietal).

40 ses in metabolism (temporoparietal, frontal, posterior cingulate, and precuneus cortices) and relativ

41 k factors correlated with lower total brain, posterior cingulate, and precuneus volumes.

42 the superior frontal cortex, lingual gyrus, posterior cingulate, and putamen.

43 e caudate nucleus, hippocampus, anterior and posterior cingulate, and regions associated with attenti

44 ng lateral frontoparietal, medial prefrontal-posterior cingulate, and subcortical-posterior insular c

45 tex (right hemisphere); bilateral precuneus, posterior cingulate, calcarine, and occipital-parietal c

46 frontal, occipital, anterior cingulate, and posterior cingulate cerebral cortices and the cerebellar

47 relative hypometabolism in the thalamus and posterior cingulate compared with those with C9orf72-neg

48 erisylvian cortex and elevated levels in the posterior cingulate, consistent with white matter and so

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 The posterior cingulate cortex and frontal eye field represe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 Aberrant posterior cingulate cortex hyperconnectivity was linked

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

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

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

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

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

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

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

125 The posterior cingulate cortex is a highly connected and met

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

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

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

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

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

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

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

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

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

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

136 The posterior cingulate cortex showed increased pattern simi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

181 connecting the parahippocampal gyrus to the posterior cingulate cortex.

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

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

184 tivity between the parahippocampal gyrus and posterior cingulate cortex.

185 ntromedial prefrontal cortex, interacts with posterior cingulate cortex.

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

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

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

189 isruption in the ventromedial prefrontal and posterior cingulate cortex.

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

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

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

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

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

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

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

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

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

199 subgenual anterior cingulate cortex and left posterior cingulate cortex.

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

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

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

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

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

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

206 tal gyri (IFG), left posterior IFG, SMG, and posterior cingulate cortices (PCC).

207 y lower in the parietotemporal, frontal, and posterior cingulate cortices and hippocampus of mild AD

208 in the precentral, prefrontal, fusiform, and posterior cingulate cortices before CBT-I.

209 enhanced activation in medial prefrontal and posterior cingulate cortices during goal-directed action

210 rbitofrontal, lateral temporal and precuneus/posterior cingulate cortices in Alzheimer's disease.

211 default-mode network (medial prefrontal and posterior cingulate cortices) were relatively deactivate

212 plicating the thalamus, anterior, middle and posterior cingulate cortices, caudate nucleus and nucleu

213 ral responses in ventromedial prefrontal and posterior cingulate cortices, core nodes of the "default

214 in the precuneus, medial orbitofrontal, and posterior cingulate cortices, i.e., several of the core

215 bolism in the visual association (BA 18) and posterior cingulate cortices, with mild involvement also

216 signals source-localized to the anterior and posterior cingulate cortices.

217 was stronger in R than NR between the right posterior cingulate (cue-alpha) and the left fusiform gy

218 or multiple comparisons), less precuneus and posterior cingulate deactivation (all p<0.010 after corr

219 rsolateral-prefrontal activation and reduced posterior cingulate deactivation, whereas OCD patients s

220 parahippocampal activations and precuneus or posterior cingulate deactivations, regional grey matter

221 lationships in bilateral posterior parietal, posterior cingulate, dorsal anterior cingulate (ACC), an

222 upling in experienced meditators between the posterior cingulate, dorsal anterior cingulate, and dors

223 Posterior cingulate epilepsy (PCE) is misleading because

224 sal and pregenual anterior cingulate cortex, posterior cingulate extending into the precuneus/cuneus

225 A reduction in posterior cingulate functional connectivity mediated by

226 gene dose was significantly associated with posterior cingulate glucose metabolism (r = 0.29, P = .0

227 were significant group differences in their posterior cingulate glucose metabolism measurements (P =

228 ithms used, they suggest that a reduction in posterior cingulate glucose metabolism precedes a reduct

229 allows neuropathologic quantification in the posterior cingulate gray matter.

230 In the posterior cingulate group, all 4 patients had electrocli

231 n the angular (1.40 vs. 1.48, P < 0.001) and posterior cingulate gyri ROIs (1.63 vs. 1.72, P < 0.001)

232 recentral gyrus and the bilateral middle and posterior cingulate gyrus (N = 187).

233 anterior ventral precuneus (BA7), along with posterior cingulate gyrus (PCC, BA23, sad condition) and

234 his study revealed that the network from the posterior cingulate gyrus and the semiology of PCE (moto

235 es) who underwent antemortem (1)H-MRS of the posterior cingulate gyrus at 3 tesla were included in th

236 Posterior cingulate gyrus epilepsy may present with elec

237 es in semantic dementia, and hippocampus and posterior cingulate gyrus in Alzheimer's disease.

238 /myoinositol (mI), and mI/Cr measured in the posterior cingulate gyrus reveal evidence of disease pro

239 ng electrophysiological connections from the posterior cingulate gyrus to parietal, temporal, mesial

240 istochemical evaluation was performed on the posterior cingulate gyrus using antibodies to synaptic v

241 s, entorhinal cortex, parahippocampal gyrus, posterior cingulate gyrus, cortex of the temporal lobes

242 relative to control participants, within the posterior cingulate gyrus, hippocampus, and other region

243 or cingulate gyrus) and parietal (precuneus, posterior cingulate gyrus, inferior parietal lobule (IPL

244 n revealed a bilateral lower activity in the posterior cingulate gyrus, insula and precuneus in the b

245 nd greater grey matter loss over time in the posterior cingulate gyrus, lateral and medial temporal l

246 ex, left posteroinferior temporal lobe, left posterior cingulate gyrus, left frontal lobe expressive

247 rietal, and temporal cortices as well as the posterior cingulate gyrus, precuneus, and mesial tempora

248 r temporal gyri; superior parietal lobe; and posterior cingulate gyrus, resulted in a fitted accuracy

249 later accumulation of cNFT pathology in the posterior cingulate gyrus.

250 reactivity and both NAA/Cr and NAA/mI in the posterior cingulate gyrus.

251 evoked responses in the hippocampus and the posterior cingulate gyrus.

252 We found greater connectivity with the posterior cingulate in dementia with Lewy bodies and wit

253 ital lobe, lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe, supramargin

254 ital lobe, lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe, supramargin

255 the orbitofrontal cortex (OFC), anterior and posterior cingulate, insula and temporal lobes (Cohen's

256 ion coefficient, 197.4-275; P < .001) in the posterior cingulate, lateral parietal, hippocampal, and

257 dial temporal lobes as well as the bilateral posterior cingulate, lingual gyri, and cerebellum that s

258 n in bilateral vlPFC, bilateral anterior and posterior cingulate, medial frontal gyrus, and bilateral

259 f body-ownership and self-location, with the posterior cingulate mediating between them.

260 n (18)F-FDG PET, whereas relative sparing of posterior cingulate metabolism compared with precuneus/c

261 Posterior cingulate metabolism decreased when both amylo

262 right striatum, the parietal cortex, and the posterior cingulate on negative feedback trials, relativ

263 cortex, and MI levels were decreased in the posterior cingulate (P = .002).

264 bitofrontal cortex (p(adj) = 0.03) and right posterior cingulate (p(adj) = 0.04), brain areas associa

265 ppocampus (p=0.0051), anterior (p=0.022) and posterior cingulate (p=0.036), insula (p=0.0051), fronta

266 e spatial network, associations between left posterior cingulate (PCC) and right retrosplenial cortic

267 th hypometabolism in orbitofrontal (OFC) and posterior cingulate (PCC) cortices.

268 anterior cingulate (ACC) and medial parietal/posterior cingulate (PCC) cortices.

269 0.05) as well as expanded gray matter in the posterior cingulate (Pcorrected <0.05), and these change

270 re were significant hypometabolic effects in posterior cingulate, precuneus, and parietal regions but

271 betapir binding was seen in the anterior and posterior cingulate, precuneus, and parietotemporal and

272 obe, temporal-parietal association cortices, posterior cingulate, precuneus, hippocampus, amygdala, c

273 l (premotor and supplementary motor cortex), posterior cingulate, precuneus, lateral occipital, tempo

274 ontal cortex (PFC) but increased GBCr in the posterior cingulate, precuneus, lingual gyrus, and cereb

275 TG), angular gyrus, ventral temporal cortex, posterior cingulate/precuneus (PC), and lateral and dors

276 Whereas angular gyrus and posterior cingulate/precuneus were significantly activat

277 fMRI response (deactivation) of DMN regions (posterior cingulate/precuneus, medial prefrontal cortex)

278 ildhood stress had reduced activation in the posterior cingulate/precuneus, middle temporal gyrus, an

279 ver, the strength of this correlation in the posterior cingulate predicted the amount of information

280 firmed epilepsy arising from the anterior or posterior cingulate region.

281 ess reductions, particularly in parietal and posterior cingulate regions extending into the precuneus

282 e brain, with a focus on the hippocampus and posterior cingulate regions.

283 The posteromedial cortex (PMC) including the posterior cingulate, retrosplenial cortex, and medial pa

284 ation between functional connectivity in the posterior cingulate/retrosplenial cortex and precuneus a

285 e and medial prefrontal cortices, along with posterior cingulate, sensory associative, and striatal r

286 eement across the species, with nodes of the posterior cingulate showing high degree and betweenness

287 ase of microglial activation in anterior and posterior cingulate, striatum, frontal, temporal, pariet

288 ions are integrated in medial prefrontal and posterior cingulate structures, with the amygdala acting

289 ts correlated with increased activity in the posterior cingulate (t = 4.11).

290 anterior temporal, dorsolateral prefrontal, posterior cingulate, temporal fusiform and occipitotempo

291 temporal, precuneus, lateral orbitofrontal, posterior cingulate, thalamus and ventral diencephalon w

292 better with SUVRWM (Pearson r: from 0.63 for posterior cingulate to 0.89 for precuneus, P < 0.0001) t

293 e bilateral occipitotemporal activation from posterior cingulate to anteromedial temporal cortex.

294 A ratio of metabolism in the posterior cingulate to precuneus plus cuneus was calcula

295 In the posterior cingulate, treatment-related changes in serum

296 SV-tracking activity emerged in the posterior cingulate, ventral striatum, anterior cingulat

297 Total MoCA score was associated with posterior cingulate volume (standardized estimate, 0.13;

298 olesterol levels were associated with larger posterior cingulate volume, and higher triglyceride leve

299 decrease of the T1/T2-weighted ratio in the posterior cingulate was related to performance in attent

300 Functional coupling of posterior cingulate with striatum and amygdala was also