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 r cingulate cortex, parahippocampal area and precuneus.

4 osterior cingulate cortex, and right ventral precuneus.

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

6 ing additional repetition suppression in the precuneus.

7 vividness judgments tracked activity in the precuneus.

8 ticularly in the inferior temporal gyrus and precuneus.

9 x and the right superior parietal cortex and precuneus.

10 and egocentric direction information in the precuneus.

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

12 tional connectivity in one brain region: the precuneus.

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

14 rontal cortex, temporoparietal junction, and precuneus.

15 ased connectivity between the sgACC and left precuneus.

16 d metabolism in the intraparietal sulcus and precuneus.

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

18 efficiency was correlated with volume of the precuneus.

19 both regions and in local efficiency for the precuneus.

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

21 arietal lobes, temporoparietal junction, and precuneus.

22 activation than control participants was the precuneus.

23 had abnormal recruitment of the cingulum or precuneus.

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

25 ontomedian cortex as well as hippocampus and precuneus.

26 gulate, ventrolateral prefrontal cortex, and precuneus.

27 vity in the right inferior frontal gyrus and precuneus.

28 imilar gaze effects in left anterior STS and precuneus.

29 d and the dorsolateral PFC, hippocampus, and precuneus.

30 ate the possible body part topography of the precuneus.

31 sentation of the body should be found in the precuneus.

32 cluster localized primarily to the bilateral precuneus.

33 bilaterally in the middle temporal gyrus 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 The precuneus, a structure of central importance to cerebral

39 al sulcus/temporoparietal junction (TPJ) and precuneus across males and females, but males recruited

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

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

42 activity and directly correlated with right precuneus activity.

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

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

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

46 l analysis, we found a new homunculus in the precuneus: an anterior-to-posterior, dorsal-to-ventral,

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

48 and gray matter, which was most prominent in precuneus and associated white matter tracts.

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

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

51 posterior cingulate/retrosplenial cortex and precuneus and both ageing and AD.

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

53 LGI in the precuneus and cingulate cortices correlated positively w

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

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

56 nhanced the coupling between the cmA and the precuneus and dorsomedial prefrontal cortex.

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

58 l and posterior cingulate cortex but also in precuneus and hippocampus, which are key regions implica

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

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

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

62 at a whole-body gradient can be found in the precuneus and is connected to multiple brain areas in a

63 at a whole-body gradient can be found in the precuneus and is connected to multiple brain areas with

64 most prominent loci of pathology were in the precuneus and lateral parietal regions.

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

66 nt life stress was associated with less left precuneus and left postcentral cortical thickness and sm

67 GNA was associated with increased precuneus and middle frontal gyrus activity, whereas PNA

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

69 ssociation between reduced efficiency in the precuneus and nonverbal abstract reasoning deficits (cal

70 somatosensory cortex, and negatively in the precuneus and orbitofrontal cortex.

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

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

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

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

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

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

77 ickness (increase in left paracentral, right precuneus and right but not left superior frontal thickn

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

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

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

81 as well as increased RSFC between the right precuneus and right posterior cingulate cortex in DMN, a

82 d increased negative FC between amygdala and precuneus and superior occipital gyrus (SOG).

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

84 y cortical surface area and thickness of the precuneus and temporoparietal junction, classically invo

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

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

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

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

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

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

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

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

93 the bilateral posterior cingulate cortex and precuneus (and for disorganized schizotypy, also in medi

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

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

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

97 ratitude activated mentalizing-related (e.g. precuneus) and reward-related regions (e.g. putamen) mor

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

99 negatively covaried with bilateral parietal, precuneus, and anterior cingulate metabolism; visual hal

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

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

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

103 en this structure and the prefrontal cortex, precuneus, and hippocampus.

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

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

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

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

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

109 l gyrus, bilateral-parietal cortex, and left precuneus, and negatively with metabolism in the insula,

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

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

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

113 was evident in temporal and parietal lobes, precuneus, and posterior cingulate cortex.

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

115 10, involving anterior cingulate BA32), left precuneus, and right parahippocampal gyrus.

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

117 gulate cortex, medial frontal gyrus, cuneus, precuneus, and superior parietal lobule [F=19.04-28.51,

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

119 ntal cortex, prefrontal and temporal cortex, precuneus, and supramarginal gyrus.

120 BD) with bilateral parieto-occipital cortex, precuneus, and ventrolateral-frontal metabolism.

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

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

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

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

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

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

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

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

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

130 = -.18; P = .01) and higher GM volume in the precuneus (beta = .18; P = .009).

131 Within precuneus, bilateral middle temporal gyrus and the left

132 ral parieto-occipital association cortex and precuneus bilaterally.

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

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

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

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

137 8F-florbetapir standard uptake value ratios, precuneus cerebral metabolic rates for glucose, hippocam

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

139 Reduction of precuneus choline acetyltransferase activity co-occurs w

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

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

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

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

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

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

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

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

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

149 ration was associated with frontal polar and precuneus connectivity.

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

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

152 e brain regions in the mesial temporal lobe, precuneus cortex, and angular gyrus.

153 Precuneus cortex, distributed parietal lobe activity, an

154 Left precuneus cortical thickness accounted for 17.0% of the

155 Stress-linked precuneus cortical thickness represents a candidate pros

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

157 oparietal, frontal, posterior cingulate, and precuneus cortices) and relative increases in metabolism

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

159 Precuneus cTBS altered MTL-neocortical communication by

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

175 In contrast, the precuneus in ASD children demonstrated hypoconnectivity

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

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

178 The results revealed lower GMV in the left precuneus in ketamine users, with a larger decrease in t

179 in the posterior cingulate gyrus, insula and precuneus in the bed rest group in both ERP time frames

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

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

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

183 how that activity in the hippocampus and the precuneus increases during the quiet rest periods and pr

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

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

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

187 tical communication and demonstrate that the precuneus is a critical cortical node of oscillatory act

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 d the salience network with the thalamus and precuneus networks.

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

207 Data indicate that precuneus neurotrophin pathways are resilient to amyloid

208 Precuneus NGF upstream and downstream signaling levels r

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

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

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

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

213 sponse complexity and the fusiform gyrus and precuneus organized its activity according to the releva

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

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

216 ngulate cortex (ACC) was evaluated with: the precuneus (P), the posterior cingulate cortex (PCC) and

217 51 for temporal lobe [P = 0.002] to 0.82 for precuneus [P < 0.0001]) in all tested regions.

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

219 iddle/inferior temporal gyrus (pMTG/ITG) and precuneus (PC) and additionally observed general semanti

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

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

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

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

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

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

234 In the clinical study, reduced precuneus/posterior cingulate cortex and hippocampal gre

235 ding the bilateral insular cortex, bilateral precuneus/posterior cingulate cortex, and bilateral temp

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

237 The precuneus (PreC; Brodmann area 7), a key hub within the

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

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

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

241 ed with visual attention and salience (e.g., precuneus, r = -0.35) to unhealthy relative to healthier

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

243 s (IFG) and posterior cingulate cortex (PCC)/precuneus, ranked as the second 'most important' FC base

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

245 were obtained in the posterior cingulate and precuneus region.

246 connections, including lateral parietal and precuneus regions of the Default Mode Network.

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 terior cingulate, middle temporal gyrus, and precuneus regions.

251 redictable sequences reduced activity in the precuneus relative to unpredictable sequences.

252 ly less gray matter thickness and density in precuneus, relative to controls.

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

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

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

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

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

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

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 higher functional connectivity between left precuneus (seed) and right precuneus than the control gr

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

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

265 and graded liability effects of cannabis on precuneus structure.

266 elations to the other known functions of the precuneus such as self-processing, motor imagery, reachi

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

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

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

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

271 d benefit-value in mentalizing-related (e.g. precuneus, temporo-parietal junction) and reward-related

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 vity between left precuneus (seed) and right precuneus than the control group.

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

276 in clusters of brain regions, including the precuneus, the cingulate gyrus, and the hippocampus, reg

277 Left precuneus thickness in the stress-associated cluster sig

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

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

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

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

282 0.06; P = .004) were associated with larger precuneus volume.

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

284 ty within ventromedial prefrontal cortex and precuneus was additionally modulated by global SPEs.

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

286 51 uptake in the inferior temporal gyrus and precuneus was associated with increased cognitive impair

287 The precuneus was found to be involved in numerous motor, co

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

289 Precuneus was negatively correlated with the DLPFC activ

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

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

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

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

294 1 binding in the inferior temporal gyrus and precuneus were also evident in PD-impaired patients.

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

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

297 y in left dorsolateral prefrontal cortex and precuneus while making hard decisions.

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