ライフサイエンスコーパス: precuneus

1 nd the left frontoparietal network (ie, left precuneus).

2 reductions in several structures (e.g., the precuneus).

3 and egocentric direction information in the precuneus.

4 cluster localized primarily to the bilateral precuneus.

5 BD-adults in the inferior frontal gyrus and precuneus.

6 tional connectivity in one brain region: the precuneus.

7 nterior IPS, and a foot bias in the anterior precuneus.

8 ased connectivity between the sgACC and left precuneus.

9 d metabolism in the intraparietal sulcus and precuneus.

10 ral gyrus, cerebellum, cingulate cortex, and precuneus.

11 efficiency was correlated with volume of the precuneus.

12 both regions and in local efficiency for the precuneus.

13 some common to both ADHD and ASD, such as in precuneus.

14 arietal lobes, temporoparietal junction, and precuneus.

15 activation than control participants was the precuneus.

16 had abnormal recruitment of the cingulum or precuneus.

17 frontal gyrus, right mid-cingulate and right precuneus.

18 gulate, ventrolateral prefrontal cortex, and precuneus.

19 vity in the right inferior frontal gyrus and precuneus.

20 imilar gaze effects in left anterior STS and precuneus.

21 rontal cortex, anterior cingulate cortex and precuneus.

22 cortex (MPFC) and posterior cingulate cortex/precuneus.

23 tal gyrus, anterior cingulate cortex and the precuneus.

24 roparietal junction, and posterior cingulate/precuneus.

25 middle and inferior frontal gyri, and right precuneus.

26 ontal cortex, posterior cingulate cortex and precuneus.

27 r cingulate cortex, parahippocampal area and precuneus.

28 osterior cingulate cortex, and right ventral precuneus.

29 idence of an HD signal in RSC, thalamus, and precuneus.

30 ing additional repetition suppression in the precuneus.

31 vividness judgments tracked activity in the precuneus.

32 ticularly in the inferior temporal gyrus and precuneus.

33 x and the right superior parietal cortex and precuneus.

34 f the left dorsal anterior INS with the left precuneus; (3) disease-related differences in the connec

35 the parietal cortex (-37.6%; P < .0001) and precuneus (-31.8%; P = .0006).

36 tion between APOE genotype and gender in the precuneus, a major default mode hub.

37 uals who are at increased risk for AD in the precuneus, a salient region for early AD changes.

38 Region of interest analysis of the precuneus across stroke participants revealed a positive

39 By means of a critical analysis of precuneus activation patterns in response to different m

40 roups also displayed significantly increased precuneus activation relative to controls.

41 activity and directly correlated with right precuneus activity.

42 d with left inferior frontal gyrus and right precuneus activity.

43 tary motor cortex and left postcentral gyrus/precuneus after ECT.

44 , inferior and superior parietal lobules and precuneus, all of which were unilaterally activated in t

45 ior frontal gyrus, gyrus rectus, cuneus, and precuneus along the mesial wall of the right hemisphere.

46 etworks: the default-mode network, including precuneus and angular gyrus, and the salience network, i

47 , showing the largest CBF differences in the precuneus and bilateral parietal cortex.

48 ed in left middle frontal gyrus of CEN, left precuneus and bilateral superior frontal gyrus of DMN, a

49 e rest-task-rest CBF pattern in the anterior precuneus and CBF level in the insula, a hub of the sali

50 n in the fronto-parietal association cortex, precuneus and cingulate gyrus during and following seizu

51 vity of the posterior cingulate cortex (PCC)/precuneus and dorsolateral prefrontal cortex (PFC) durin

52 Analyses of network statistics for the precuneus and dorsolateral prefrontal cortex revealed si

53 and transient less selective modulations in precuneus and FEF.

54 pected to be high in Abeta deposition (e.g., precuneus and frontal and temporal cortices) in AD patie

55 icant reduction in cortical thickness in the precuneus and hippocampus associated with episodic memor

56 Core regions at the precuneus and inferior parietal lobe were activated for

57 istent order of cortical activity inside the precuneus and inferior parietal lobes, with space orient

58 t posterior cingulate and parietal cortices (precuneus and inferior parietal lobule), as expected.

59 ty between medial aPFC and the right central precuneus and intraparietal sulcus/inferior parietal lob

60 ARTICLE: Although some brain regions such as precuneus and lateral temporo-parietal cortex have been

61 Greater activation in the precuneus and middle temporal gyrus predicted lower weig

62 d compared with non-depressed AD patients in precuneus and parahippocampal cortex.

63 he default mode network (DMN), including the precuneus and posterior cingulate cortex.

64 r correction for multiple comparisons), less precuneus and posterior cingulate deactivation (all p<0.

65 teromedial cortices (PMCs), primarily in the precuneus and posterior cingulate gyrus.

66 onents of the default network, including the precuneus and posterior cingulate, are particularly vuln

67 ied for some cortical regions, including the precuneus and posterior cingulate.

68 us building, and vice versa) BOLD signals in precuneus and posterior parahippocampal cortex were atte

69 the hippocampus, posterior cingulate cortex, precuneus and primary visual cortex and correlated with

70 Conversely, right precuneus and right anterior insula ranked first and 15t

71 tients, hypoactivation was seen in the right precuneus and right inferior frontal gyrus (P = .013 and

72 nitial hyperactivation was seen in the right precuneus and right inferior parietal gyrus (P = .047 an

73 s revealed that the fALFF values of the left precuneus and right ITG/IOG were positively correlated w

74 regions demonstrated thinner angular gyrus, precuneus and superior parietal lobule in carriers compa

75 Furthermore, precuneus and surrounding posteromedial areas are amongs

76 nstruction of updated representations in the precuneus and the context-dependent planning of motor ac

77 reas rest increased connectivity between the precuneus and the default-mode network (DMN).

78 Only activation profiles in the precuneus and the dorsal premotor cortex (PMd) were indi

79 , and cerebellum as well as increases in the precuneus and the fusiform and lingual gyrus.

80 s showed increased connectivity in the right precuneus and the global connectivity indexed with goodn

81 consisting of the posterior cingulate cortex/precuneus and the medial frontal cortex yielded optimal

82 patients with MCI, CBF was decreased in the precuneus and the parietal and occipital lobes compared

83 tional synchronicity of activity between the precuneus and the rest of the default mode network at re

84 onnectivity (compared with rest) between the precuneus and the right frontoparietal network, whereas

85 tbeats in two regions of the DN, the ventral precuneus and the ventromedial prefrontal cortex, covari

86 ce-localized to the visual cortex-cuneus and precuneus) and bottom-up inhibition deficits (reduced po

87 right inferior frontal and inferior parietal/precuneus) and cerebellar regions.

88 ion and increase the functional local (right precuneus) and global connectivity within the DMN, which

89 Decreased fALFF in the bilateral insular, precuneus, and anterior cingulate cortices also was foun

90 n group had an increased FC in the cingulum, precuneus, and bilateral parietal cortex and a lower FC

91 thalamus, posterior cingulate cortex (PCC), precuneus, and cerebellum.

92 network comprising the intraparietal sulcus, precuneus, and dorsolateral prefrontal cortex is involve

93 V3/V3A/V7; within the default mode network, precuneus, and inferior parietal lobule; and, within the

94 gyrus, anterior cingulate cortex, bilateral precuneus, and left supramarginal gyrus for fearful (rel

95 al cortex, lateral inferior parietal cortex, precuneus, and medial and lateral temporal cortices, wer

96 lobe structures, posterior cingulate cortex, precuneus, and medial prefrontal cortex possibly reflect

97 es as well as the posterior cingulate gyrus, precuneus, and mesial temporal cortex.

98 insular cortex, posterior cingulate cortex, precuneus, and occipital cortex in patients with TLE as

99 ypometabolic effects in posterior cingulate, precuneus, and parietal regions but also significant pos

100 een in the anterior and posterior cingulate, precuneus, and parietotemporal and frontal grey matter,

101 ting from sensorimotor areas including dmFC, precuneus, and posterior parietal cortex.

102 etal lobe, right intraparietal sulcus, right precuneus, and right cuneus.

103 10, involving anterior cingulate BA32), left precuneus, and right parahippocampal gyrus.

104 ior insulae, medial superior frontal cortex, precuneus, and subcortical regions such as bilateral hip

105 DHD, including the inferior parietal cortex, precuneus, and superior temporal cortex.

106 r frontal gyrus, the anterior cingulate, the precuneus, and the posterior cingulate.

107 network, the hippocampus, prefrontal cortex, precuneus, and visual cortex served as "hubs" of high co

108 tices, the anterior cingulate gyrus, and the precuneus; and induced a more "youth-like" connectivity

109 l, inferior parietal, and fusiform gyri; the precuneus; and the dorsomedial prefrontal cortex (dMPFC)

110 nterior insula, thalamus, pulvinar, caudate, precuneus, anterior cingulate cortex, and medial prefron

111 e hyperconnectivity of multiple regions with precuneus, anterior insula, dorsal anterior cingulate co

112 that a reach-dominant region in the anterior precuneus (aPCu), extending into medial intraparietal su

113 durations (approximately 36 s) than STS and precuneus (approximately 12 s).

114 al gyrus/superior temporal sulcus, bilateral precuneus as well as left anterior cingulate cortex and

115 vation in left dorsal frontal areas and left precuneus associated with better task performance.

116 ivity in the left middle temporal cortex and precuneus at 3-month follow-up.

117 n located in the posterior cingulate/ventral precuneus (BA 23/31) was the area with the highest lFCD,

118 rebellar vermis, as well as increases in the precuneus (BA 7).

119 y and sad conditions of the anterior ventral precuneus (BA7), along with posterior cingulate gyrus (P

120 ticularly in the posterior cingulate (BA31), precuneus (BA7m) and angular gyrus (BA39).

121 tivity between the right anterior insula and precuneus being lower in autism, activation in each regi

122 = -.18; P = .01) and higher GM volume in the precuneus (beta = .18; P = .009).

123 Within precuneus, bilateral middle temporal gyrus and the left

124 ral parieto-occipital association cortex and precuneus bilaterally.

125 omography scans, in the parieto-temporal and precuneus brain regions was associated with greater 18F-

126 nonsmokers in prefrontal cortex, insula, and precuneus, but the BEN sex difference in smokers was les

127 the connectivity hubs was higher for ventral precuneus, cerebellum, and subcortical hubs than for cor

128 atio, age 15 years (95% CI, 10-24 years) for precuneus cerebral metabolic rate for glucose, age 15 ye

129 8F-florbetapir standard uptake value ratios, precuneus cerebral metabolic rates for glucose, hippocam

130 ed mutation carriers had significantly lower precuneus cerebral metabolic rates for glucose, smaller

131 Reduction of precuneus choline acetyltransferase activity co-occurs w

132 the cerebellum and a network comprising the precuneus, cingulate & middle frontal lobe was significa

133 ity in the inferior and middle frontal gyri, precuneus, cingulate cortex, caudate, and postcentral gy

134 otion-dependent functional connectivity with precuneus, cingulate gyrus, and striatum/subcallosal cin

135 r frontal cluster and 83.6% (p = .02) in the precuneus cluster.

136 GMVs in the superior frontal and precuneus clusters were associated with initiation of su

137 gyrus (P = .01) with extension to the medial precuneus compared with that in control subjects.

138 oral cortex, posterior cingulate cortex, and precuneus, compared with that in healthy subjects.

139 (F = 11.11; P < .001) as well as lower left precuneus connectivity (F = 7.48; P = .001) compared wit

140 onnectivity analyses suggested that amygdala-precuneus connectivity is associated with hyperactivity/

141 n subjective craving and dorsal striatum and precuneus connectivity with frontal regions.

142 ration was associated with frontal polar and precuneus connectivity.

143 FW decreases in the post-central gyrus and precuneus correlated negatively with balance changes.

144 volumes in frontal, anterior cingulate, and precuneus cortex regions.

145 Precuneus cortex, distributed parietal lobe activity, an

146 ding, whereas the inferior parietal lobe and precuneus cortical sources were identified during retrie

147 migraineurs had thicker posterior insula and precuneus cortices compared with male migraineurs and he

148 Metabolism in parietal and precuneus cortices of AD patients was negatively correla

149 ulnerable brain regions such as parietal and precuneus cortices.

150 HER amplitude in the ventral precuneus covaried with the "I" self-dimension, whereas

151 posterior cingulate metabolism compared with precuneus/cuneus (i.e., cingulate island sign) is a feat

152 i) increased amyloid-beta burden in the left precuneus/cuneus and medial-temporal regions was associa

153 , increased amyloid-beta burden in bilateral precuneus/cuneus and parietal regions was associated wit

154 rtex, posterior cingulate extending into the precuneus/cuneus as well as the parahippocampal and infe

155 actions with the posterior cingulate cortex, precuneus, dorsomedial PFC, and amygdala.

156 ciated with greater Abeta burden measured by precuneus DVR (B = 0.08 [0.01-0.15]; P = .03).

157 (B = 0.08 [95% CI, 0.03-0.14]; P = .005) and precuneus DVR (B = 0.11 [0.03-0.18]; P = .007).

158 the supplementary motor area (BA 6), and the precuneus, encoded intentions during task-free delays.

159 w in several diagnostic groups, including in precuneus, entorhinal cortex and hippocampus (dementia),

160 and thalamus in NM, but in HD, increases in precuneus FCD were associated with improved cognitive pe

161 Metabolic activity in the contralateral precuneus fell to subnormal levels by the final time poi

162 d in visual cortex but increased activity in precuneus, frontopolar, and premotor cortex, compared to

163 associations between subjective craving and precuneus functional connectivity with sensorimotor regi

164 rontal (right anterior insula) to posterior (precuneus) functional connectivity during deictic shifti

165 rior cortical regions, including the cuneus, precuneus, fusiform, and posterior parietal cortical reg

166 l association cortices, posterior cingulate, precuneus, hippocampus, amygdala, caudate, and fornix/st

167 verity of social impairments in ASD, whereas precuneus hypoconnectivity was unrelated to social defic

168 In contrast, the precuneus in ASD children demonstrated hypoconnectivity

169 medial PFC in male IBS subjects and with the precuneus in female IBS subjects.

170 hese results highlight the importance of the precuneus in higher-order memory processing and suggest

171 of the right hemisphere, and the cuneus and precuneus in the left hemisphere, independent of familia

172 otemporal cortex, parahippocampal gyrus, and precuneus) in highly educated prodromal AD patients but

173 lower activation in self-reference regions (precuneus) in response to milkshake receipt predict weig

174 sterior cingulate regions extending into the precuneus, in a pattern similar to that observed in mild

175 precisely localized set of structures in the precuneus, inferior parietal, and medial frontal cortex.

176 Self-esteem had an impact on precuneus, insula and STG activation during stress acros

177 The posterior cingulate, precuneus, insula and superior temporal gyrus preferenti

178 shment system (Brodmann area 47/12) with the precuneus (involved in the sense of self and agency), an

179 osplenial cortex, and medial parietal cortex/precuneus is an epicenter of cortical interactions in a

180 herefore, it has recently been proposed that precuneus is involved in the interwoven network of the n

181 noted in the medial frontal cortex, then the precuneus, lateral frontal and parietal lobes, and final

182 ementary motor cortex), posterior cingulate, precuneus, lateral occipital, temporal and dorsolateral

183 s, amygdala, superior and inferior temporal, precuneus, lateral orbitofrontal, posterior cingulate, t

184 elated positively with glucose metabolism in precuneus, lateral parietal and occipital regions of int

185 bution volume ratio (P=0.075) and within the precuneus (left, P=0.061; right, P=0.079).

186 ctivity of the anterior cingulum, PCC and/or precuneus, left dorsolateral PFC, and right inferior par

187 sed functional connectivity in the salience, precuneus, left executive control, language, and visuosp

188 left medial and inferior frontal gyri, right precuneus, left inferior parietal lobule, and left postc

189 cant differences in the posterior cingulate, precuneus, left insula and superior temporal gyrus.

190 ty in the bilateral dorsolateral prefrontal, precuneus, left postcentral, and inferior parietal regio

191 temporal gyrus (ITG), left postcentral gyrus/precuneus, left supplementary motor area, and left lingu

192 t increased GBCr in the posterior cingulate, precuneus, lingual gyrus, and cerebellum.

193 n visual and memory metacognition (i.e., the precuneus may contain common mechanisms for both types o

194 wo critical nodes, right anterior insula and precuneus, may play a critical role for deictic shifting

195 the dorsal frontoparietal regions (anterior precuneus, medial intraparietal sulcus, frontal eye fiel

196 ta accumulation preferentially starts in the precuneus, medial orbitofrontal, and posterior cingulate

197 ivation) of DMN regions (posterior cingulate/precuneus, medial prefrontal cortex).

198 results importantly clarify the roles of the precuneus, medial prefrontal cortex, and lateral parieta

199 In addition to the precuneus, medial, anterior intraparietal, and superior

200 educed activation in the posterior cingulate/precuneus, middle temporal gyrus, and superior occipital

201 findings indicate that the posterior DMN and precuneus network are commonly affected in AD variants,

202 egions of interest support posterior DMN and precuneus network involvement across AD variants, wherea

203 (superior parietal cortex) and default-mode (precuneus) networks and in cerebellum and higher connect

204 Data indicate that precuneus neurotrophin pathways are resilient to amyloid

205 Precuneus NGF upstream and downstream signaling levels r

206 orsolateral prefrontal cortex of the FPN and precuneus of the DMN.

207 ppocampal or parahippocampal activations and precuneus or posterior cingulate deactivations, regional

208 o significant differences between groups for precuneus or primary visual cortex connectivity.

209 , and associated neural responses in insula, precuneus, orbitofrontal, and pregenual anterior cingula

210 ophy of the left temporoparietal regions and precuneus (P < .05, family-wise error corrected).

211 phy extended into temporoparietal cortex and precuneus (p < 0.001 uncorrected).

212 frontal gyrus (p = .001, FWE corrected), and precuneus (p = .019, FWE corrected) cluster.

213 51 for temporal lobe [P = 0.002] to 0.82 for precuneus [P < 0.0001]) in all tested regions.

214 rom 0.63 for posterior cingulate to 0.89 for precuneus, P < 0.0001) than with SUVRCB (Pearson r: from

215 ical, frontal, temporal, posterior cingulate-precuneus, parietal, and basal ganglia ROIs, and was hig

216 terior and posterior cingulate cortex (PCC), precuneus, parietal, temporal, occipital, and frontal co

217 ention were positively correlated locally in precuneus/parietal cortex.

218 ts, involving the posterior cingulate cortex/precuneus, parietotemporal and frontal cortices, and med

219 tion (TPJ), medial prefrontal cortex (MPFC), precuneus (PC), and anterior temporal sulci (aSTS).

220 ventral temporal cortex, posterior cingulate/precuneus (PC), and lateral and dorsomedial prefrontal c

221 entrations in the posterior cingulate cortex/precuneus (PCC/PCu), a key component of the DMN, and fun

222 ft inferior parietal lobule (IPL), bilateral precuneus (PCN), bilateral premotor cortex, and left inf

223 cluding the posterior cingulate cortex (PCC)/precuneus (PCu) and retrosplenial cortex.

224 ward activity in the midbrain, thalamus, and precuneus (pFWE<0.05).

225 Our results indicate that the precuneus plays a core role not only in DMN, but also mo

226 of metabolism in the posterior cingulate to precuneus plus cuneus was calculated to assess the cingu

227 ly involving lateral temporoparietal cortex, precuneus, posterior cingulate cortex and middle frontal

228 the posteromedial cortices (the ensemble of precuneus, posterior cingulate cortex, and retrosplenial

229 area, anteior cingulate gyrus) and parietal (precuneus, posterior cingulate gyrus, inferior parietal

230 frontal cortex (right hemisphere); bilateral precuneus, posterior cingulate, calcarine, and occipital

231 teral occipital lobe, lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe,

232 teral occipital lobe, lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe,

233 ncluding the superior temporal sulcus (STS), precuneus, posterior lateral sulcus (LS), temporal parie

234 MWF and GMV measurements than noncarriers in precuneus, posterior/middle cingulate, lateral temporal,

235 glucose metabolism in the bilateral MTL and precuneus-posterior cingulate cortex and right lingual g

236 such as orbitofrontal, lateral temporal and precuneus/posterior cingulate cortices in Alzheimer's di

237 ucose metabolism than late-onset patients in precuneus/posterior cingulate, lateral temporo-parietal

238 r, whereas FFA connectivity with IFJ and the precuneus predicted enhanced expectation-related WM perf

239 temporal gyrus extending to the hippocampus, precuneus, putamen, thalamus, and middle occipital gyrus

240 = .019) and poor WM performance in the right precuneus (r = -0.55; P = .027) in younger patients at i

241 nal local interconnectivity decreases in the precuneus (r = -0.64), medial orbitofrontal cortex (r =

242 creased postconcussion symptoms in the right precuneus (r = 0.57; P = .026) and right inferior fronta

243 etamol retention (eg, posterior cingulum and precuneus, r = -0.72).

244 edial prefrontal cortex, anterior cingulate, precuneus region of the parietal cortex, and striatum-fi

245 In addition, the posterior cingulate/precuneus region, medial prefrontal cortex, and right ce

246 were obtained in the posterior cingulate and precuneus region.

247 gray matter volumes of the frontal polar and precuneus regions themselves correlated across individua

248 hippocampus and the posterior cingulate and precuneus regions, and with disease progression, atrophy

249 r involving the left hemisphere temporal and precuneus regions.

250 < 0.001) in parts of bilateral parietal and precuneus regions.

251 ngulate gyrus, temporoparietal junction, and precuneus-represented or updated expertise beliefs about

252 nation in right inferior parietal cortex and precuneus, respectively.

253 Daily beverage consumption also increased precuneus response to both juice logos compared with a t

254 ahippocampal area, left geniculum body, left precuneus, right anterior cingulate cortex, right claust

255 ment alone increased metabolism in the right precuneus, right inferior parietal lobule and right midd

256 ed significantly decreased fALFF in the left precuneus, right inferior temporal and occipital gyrus(I

257 Gray matter regions (left precuneus, right temporal, frontal, and parietal lobes a

258 ., within left lateral premotor cortex; left precuneus; right posterior cerebellum) was more active w

259 lso demonstrated greater (positive) amygdala-precuneus RSFC (z >2.3, corrected P < .05) in contrast t

260 amygdala-hippocampal/brainstem and amygdala-precuneus RSFC have not previously been highlighted in d

261 ed P < .05) in contrast to negative amygdala-precuneus RSFC in the adolescents serving as controls.

262 n targets are defined visually, the anterior precuneus selectively encodes the motor goal in gaze-cen

263 ially the prominent regions of the bilateral precuneus showed reduced nodal efficiency, and the reduc

264 terior intraparietal sulcus (pIPS) and right precuneus] significantly predicted individual acuity thr

265 superior parietal lobule (SPL) and the right precuneus-SPL, which were all more activated during loca

266 l (standardized estimate, 0.06; P < .05) and precuneus (standardized estimate, 0.08; P < .023) volume

267 al cortical hubs (posterior cingulate cortex/precuneus), strongly overlapping with regional hypometab

268 al cortex, insula, inferior parietal cortex, precuneus, superior temporal cortex, and lingual gyrus m

269 her activation during stress in hippocampus, precuneus, superior temporal gyrus (STG) and insula.

270 ntified in autism a second key system in the precuneus/superior parietal lobule region with reduced f

271 ows at the top of the hierarchy, such as the precuneus, temporal parietal junction, and medial fronta

272 al cognition (dorsomedial prefrontal cortex, precuneus, temporoparietal junction), respectively.

273 um, insula) and in the default-mode network (precuneus, temporoparietal junction, medial prefrontal c

274 d increased functional connectivity with the precuneus, the angular gyrus, and the temporal visual co

275 putamen, mid-insula, Rolandic operculum, and precuneus to a cue signaling impending milkshake receipt

276 y from E4- in functional connectivity of the precuneus to several regions previously defined as havin

277 analysis, the higher In+Out degrees of upper precuneus (UPCU) during right-hand MR or higher In+Out d

278 CC), posterior cingulate cortex (PCC), upper precuneus (UPCU), caudate nucleus (CN), cingulate motor

279 between visual metacognitive efficiency and precuneus volume, which may account for the behavioral c

280 0.06; P = .004) were associated with larger precuneus volume.

281 lower total brain, posterior cingulate, and precuneus volumes.

282 eased connectivity between the sgACC and the precuneus was also found in the MDD group relative to th

283 51 uptake in the inferior temporal gyrus and precuneus was associated with increased cognitive impair

284 sample of subjects that PiB retention in the precuneus was inversely related to NP performance, espec

285 tivity between the right anterior insula and precuneus was lower in autism while answering a question

286 ed with age, while glucose metabolism in the precuneus was maintained across the lifespan (right hemi

287 Precuneus was negatively correlated with the DLPFC activ

288 elated with HbA1c; and the rsFC in the right precuneus was positively associated with cognitive perfo

289 ermore, the changed connectivity in the left precuneus was positively correlated to the improvement o

290 th with the posterior cingulate cortex (PCC)/precuneus was seen in the relapsed versus early remissio

291 mean [SD] parameter estimates for the right precuneus were -0.590 [0.50] for noncarriers and -0.087

292 1 binding in the inferior temporal gyrus and precuneus were also evident in PD-impaired patients.

293 ventro-medial prefrontal cortex (vmPFC) and precuneus were recruited by both cultural/linguistic gro

294 hereas angular gyrus and posterior cingulate/precuneus were significantly activated during memory ret

295 e left dorsal posterior cingulate cortex and precuneus, where decreased risk resulted in greater acti

296 ion, medial prefrontal cortex, amygdala, and precuneus, whereas for unpleasant pictures significant L

297 wed similar increased thickness of the right precuneus, which receives rich input from the thalamic p

298 dorsal striatum, ventral tegmental area, and precuneus with frontal, visual, sensory, and motor-relat

299 Additionally, connectivity of the precuneus with the left middle temporal gyrus and connec

300 ay connecting the posterior cingulate cortex/precuneus with the thalamus, relative to the healthy vol