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

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

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

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

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

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

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

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

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

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

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

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

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

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

14 connecting the parahippocampal gyrus to the posterior cingulate cortex.

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

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

17 tivity between the parahippocampal gyrus and posterior cingulate cortex.

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

19 ntromedial prefrontal cortex, interacts with posterior cingulate cortex.

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

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

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

23 isruption in the ventromedial prefrontal and posterior cingulate cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 The posterior cingulate cortex and frontal eye field represe

40 MCI patients showed primarily posterior cingulate cortex and hippocampal hypometabolis

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 Posterior cingulate cortex (CGp) is strongly connected w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 Aberrant posterior cingulate cortex hyperconnectivity was linked

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 The posterior cingulate cortex is a highly connected and met

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

178 The posterior cingulate cortex showed increased pattern simi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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