ライフサイエンスコーパス: cingulate

1 ial prefrontal cortex including the anterior cingulate.

2 more functionally connected to the subgenual cingulate.

3 c resonance spectroscopy to measure anterior cingulate (AC) glutamate (Glu) and glutamine (Gln) and a

4 tion of the orbitofrontal (OFC) and anterior cingulate (ACC) cortices has been linked with several ps

5 In the present study, we show that posterior cingulate activities responding to heartbeat signals cov

6 presupplementary motor area/dorsal anterior cingulate activity was a predictor of both language reco

7 a network of cortical (motor cortex, insula, cingulate, amygdala) and sub-cortical (putamen, thalamus

8 vation of reduced perfusion in the posterior cingulate and cuneal cortex, which are regions assumed t

9 s in the cognitive control network (anterior cingulate and dorsal and ventrolateral prefrontal cortic

10 peractivation in cognitive control (anterior cingulate and frontopolar cortex) brain regions followin

11 dorsal and ventral portions of the anterior cingulate and medial prefrontal cortices, along with pos

12 /or peri-insular projections to the anterior cingulate and medial prefrontal cortices.

13 n addition, baseline MOR availability in the cingulate and orbitofrontal cortices was associated with

14 solateral, ventrolateral, orbital), anterior cingulate and parietal cortical regions.

15 ted with increased glucose metabolism in the cingulate and prefrontal brain areas.

16 the wild." Our results showed less anterior cingulate and prefrontal cortex involvement for more nat

17 same variant was found to be associated with cingulate and prefrontal grey matter volumes.

18 This analysis showed that cingulate and superior rostral were the sulci most consi

19 ps in the occipital, sensory-motor, anterior cingulate and supplementary motor cortices.

20 In contrast, the cingulate and the secondary motor areas send denser proj

21 k consisting of bilateral frontal, parietal, cingulate, and insular regions.

22 s in the medial prefrontal cortex, posterior cingulate, and occipital cortices during evaluation of p

23 l regions such as occipitotemporal, anterior cingulate, and orbitofrontal cortices.

24 se functional activations in the prefrontal, cingulate, and parietal cortex measured during cocaine-c

25 within transitional cortical areas (insular, cingulate, and piriform cortices) and hippocampus proper

26 n in multiple regions (e.g., in the caudate, cingulate, and precentral gyrus) and decreased activatio

27 ain grey matter volumes in frontal, anterior cingulate, and precuneus cortex regions.

28 correlated with lower total brain, posterior cingulate, and precuneus volumes.

29 ior frontal cortex, lingual gyrus, posterior cingulate, and putamen.

30 Blunting in key frontal, cingulate, and striatal areas was evident in unaffected,

31 isorder is in the rostro-dorsomedial, fronto-cingulate, and ventral-striatal regions that mediate rew

32 The prefrontal cingulate area (Cg), visual, oculomotor, and auditory ar

33 were placed in subdivisions of the anterior cingulate area 24b/c and in medial prefrontal areas 32 a

34 nd bilateral connections with prefrontal and cingulate areas as well as strong reciprocal connections

35 , 2014, and underwent DBS of the subcallosal cingulate between November, 2011, and April, 2014.

36 he glyptodonts were clearly related to other cingulates, but their precise phylogenetic position as s

37 hemisphere); bilateral precuneus, posterior cingulate, calcarine, and occipital-parietal cortex; and

38 presupplementary motor area/dorsal anterior cingulate contributes to language recovery after stroke.

39 tials were calculated and ranked as follows: cingulate cortex > insula > caudate/putamen > frontal co

40 the retrosplenial cortex (RSC) and anterior cingulate cortex (ACA) are activated during PS.

41 the retrosplenial cortex (RSC) and anterior cingulate cortex (ACA) contain a large number of neurons

42 the medial prefrontal cortex (mPFC)/anterior cingulate cortex (ACC) and brainstem pons region.

43 ould be associated with overlapping anterior cingulate cortex (ACC) and insular volumetric reductions

44 he fronto-striatal circuit: midline anterior cingulate cortex (ACC) and left dorsal striatum.

45 regions including the right dorsal anterior cingulate cortex (ACC) and left rostral ACC.

46 Reduction in volume in the anterior cingulate cortex (ACC) and lower structural covariance b

47 In GF mice, the volumes of the anterior cingulate cortex (ACC) and periaqueductal grey, areas in

48 structural connectivity between the anterior cingulate cortex (ACC) and posterior cingulate cortex (P

49 a (4-8 Hz) oscillations in both the anterior cingulate cortex (ACC) and the DLPFC during REM sleep.

50 ignificantly lower in the bilateral anterior cingulate cortex (ACC) and the right superior frontal gy

51 e frontal eye fields (FEFs) and the anterior cingulate cortex (ACC) are commonly coactivated for cogn

52 These signals emerged first in anterior cingulate cortex (ACC) before dorsolateral prefrontal co

53 restingly, neural activities in the anterior cingulate cortex (ACC) correlated with noxious intensiti

54 The anterior cingulate cortex (ACC) has been shown to be crucial for

55 The anterior cingulate cortex (ACC) has shown decreased glutamate lev

56 erior cingulate cortex (PCC) to the anterior cingulate cortex (ACC) in the 10-Hz range.

57 gnificant increased activity of the Anterior Cingulate Cortex (ACC) in the low frequency band suggest

58 Anterior cingulate cortex (ACC) is thought to control a wide rang

59 Recent evidence suggests that anterior cingulate cortex (ACC) maturation during adolescence con

60 ateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) of the primate play distinctive r

61 ateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) play temporally distinct roles du

62 he prevailing view that dopamine in anterior cingulate cortex (ACC) plays a role in evaluating effort

63 Furthermore, activity in dorsal anterior cingulate cortex (ACC) reflected individual choice tende

64 The function of the anterior cingulate cortex (ACC) remains controversial, yet many t

65 disrupt the reward function of the anterior cingulate cortex (ACC), biasing the ACC to favor goal-di

66 that imposing rhythms in the mouse anterior cingulate cortex (ACC), by using optogenetics to induce

67 ntification, GPC+PC levels from the anterior cingulate cortex (ACC), caudate and putamen of 16 RC BD-

68 ippocampus, ventral hippocampus, or anterior cingulate cortex (ACC), during consolidation and retriev

69 to compare TSPO availability in the anterior cingulate cortex (ACC), prefrontal cortex, and insula be

70 Among cortical areas, the anterior cingulate cortex (ACC, areas 24a and 24b) appears to be

71 nt patterns of neural activations within the cingulate cortex (CC) play roles in representing opposit

72 ection of physical pain, the dorsal anterior cingulate cortex (dACC) and anterior insula (AI), have b

73 clusion was decreased in the dorsal anterior cingulate cortex (dACC) and the middle frontal gyrus, ke

74 odel proposed that the human dorsal anterior cingulate cortex (dACC) detects conflict and induces ada

75 function are associated with dorsal anterior cingulate cortex (dACC) excitotoxic lesions and pharmaco

76 The dorsal anterior cingulate cortex (dACC) has attracted great interest fro

77 Dorsal anterior cingulate cortex (dACC) mediates updating and maintenanc

78 d activity of neurons in the dorsal anterior cingulate cortex (dACC) of macaques choosing between gam

79 rtex (mPFC) suggest that the dorsal anterior cingulate cortex (dACC) region is responsive to a wide v

80 peared in the medial occipital and posterior cingulate cortex (each left and right).

81 ificantly lower in the bilateral ACC, median cingulate cortex (MCC) and right SFG.

82 s associated with expression of CADM2 in the cingulate cortex (P-value=4 x 10(-4)).

83 in a city with increased pregenual anterior cingulate cortex (pACC) activity.

84 ging (PEPSI) MRS scans of pregenual anterior cingulate cortex (pACC) and ventral posterior cingulate

85 hemical signatures in the pregenual anterior cingulate cortex (pACC), a structure known to be involve

86 ction in glucose metabolism in the posterior cingulate cortex (PCC) predicts conversion to Alzheimer'

87 nterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) regions of the default mode netwo

88 ging tasks that neurons in primate posterior cingulate cortex (PCC) signal decision salience during f

89 served directed influence from the posterior cingulate cortex (PCC) to the anterior cingulate cortex

90 ormation, basal ganglia, thalamus, posterior cingulate cortex (PCC), precuneus, and cerebellum.

91 e centromedial amygdala and rostral anterior cingulate cortex (rACC), anterior vmPFC, and subgenual c

92 rved for the three conditions, the subgenual cingulate cortex (SCC) exhibited increased functional co

93 ivity analyses using a bilateral subcallosal cingulate cortex (SCC) seed was applied to 122 patients

94 al cortex (LPFC), insula, subgenual anterior cingulate cortex (sgACC), and medial prefrontal cortex (

95 ingulate cortex (pACC) and ventral posterior cingulate cortex (vPCC)-regions possibly affected by OCD

96 stress disorder, or MDD (subgenual anterior cingulate cortex [sgACC], left dorsolateral prefrontal c

97 analyses highlighted higher dorsal anterior cingulate cortex activation in poker players, as compare

98 ed by a failure to maintain ventral anterior cingulate cortex activation in response to fearful stimu

99 oms, such that decreases in ventral anterior cingulate cortex activation over repeated presentations

100 a, superior temporal gyrus, and anterior/mid-cingulate cortex among non-lapsers; the opposite pattern

101 vity between the left amygdala and subgenual cingulate cortex and between the right amygdala and caud

102 al prefrontal cortex, including the anterior cingulate cortex and bilateral insula.

103 -parietal cortex; and right rostral anterior cingulate cortex and central sulcus/postcentral gyrus.

104 Main analyses were performed in blocks from cingulate cortex and confirmed in blocks from the striat

105 sponses than controls in the dorsal anterior cingulate cortex and in the superior frontal gyrus.

106 eated females showed decreased metabolism in cingulate cortex and increased metabolism in the globus

107 d short-range and long-range FC in posterior cingulate cortex and medial prefrontal cortex.

108 olfactory), and prefrontal regions (anterior cingulate cortex and orbitofrontal cortex) to the claust

109 d Gly levels were found in both the anterior cingulate cortex and posterior cingulate cortex of patie

110 levels were measured in vivo in the anterior cingulate cortex and posterior cingulate cortex of the s

111 , and glutamate (Glu) levels in the anterior cingulate cortex and right dorsolateral prefrontal corte

112 network of regions involving dorsal anterior cingulate cortex and supplementary motor area encoded th

113 led that PVHCrh fibers project abundantly to cingulate cortex and the nucleus accumbens shell, and mo

114 in the Ch4 terminal regions of the anterior cingulate cortex and the superior and inferior parietal

115 We show that dorsal anterior cingulate cortex and three other brain regions hold mult

116 king effect was found in the dorsal anterior cingulate cortex and ventral striatum, such that the nor

117 earch into the gyral surface of the anterior cingulate cortex and ventromedial prefrontal cortex coul

118 The medial prefrontal - anterior cingulate cortex appears most tightly related to the ado

119 llular adaptations may occur in the anterior cingulate cortex as a function of child abuse.

120 ee of structural impairment in the subgenual cingulate cortex before therapy seems to be associated w

121 e previously shown abnormally high posterior cingulate cortex connectivity in the chronic phase after

122 d between the left AI/FO and dorsal anterior cingulate cortex correlated positively with improvement

123 in cholinergic transmission in the anterior cingulate cortex could be closely associated with the de

124 ral responses to heartbeats in the posterior cingulate cortex covary with changes in bodily self-cons

125 functional and structural frontoinsular and cingulate cortex deficits and with reduced agreeableness

126 tion and the left angular gyrus and anterior cingulate cortex during motor intention.

127 ea and the caudal portion of dorsal anterior cingulate cortex encoded the difference in reward (posit

128 he right amygdala and the subgenual anterior cingulate cortex following errors was observed in patien

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

130 tistically significant only in the posterior cingulate cortex for the WBN data.

131 he medial prefrontal cortex on the posterior cingulate cortex in depression is a neural correlate of

132 ntral striatum, dorsal putamen, and anterior cingulate cortex in OCD.

133 a "hyperregulatory" effect on the posterior cingulate cortex in the depressed group, with self-appra

134 n rhesus monkeys, we found that the anterior cingulate cortex innervated mostly the basolateral and C

135 By contrast, the anterior cingulate cortex innervates other amygdalar parts, activ

136 ther addictions in which the anterior-/ mid- cingulate cortex is impaired and fails to support the ne

137 from healthy subjects that the anterior mid-cingulate cortex is part of a network associated with th

138 ationship was only present when anterior mid-cingulate cortex lesion volume was defined as the overla

139 , methadone-treated females showed increased cingulate cortex metabolism, whereas buprenorphine-treat

140 the anterior cingulate cortex and posterior cingulate cortex of patients with first-episode psychosi

141 region to the medial prefrontal and anterior cingulate cortex of the common marmoset (Callithrx jacch

142 the anterior cingulate cortex and posterior cingulate cortex of the subjects by using the echo time-

143 Subgenual anterior cingulate cortex postmortem samples from four MDD cohort

144 neighboring insular regions and the anterior cingulate cortex showed weaker functional connectivity i

145 While the gyral surface of the anterior cingulate cortex signalled social prediction errors in t

146 High activities of the anterior cingulate cortex significantly mediated relationships be

147 e medial prefrontal cortex and the posterior cingulate cortex than in the control group (odds ratio=0

148 verging evidence has linked the anterior mid-cingulate cortex to negative affect, pain and cognitive

149 Perigenual anterior cingulate cortex tracked one's own performance.

150 re acquired from the medial frontal/anterior cingulate cortex using a macromolecule-suppressed MEGA-P

151 e regions, but lower variability of anterior cingulate cortex volume.

152 tivity between amygdala and posterior middle cingulate cortex was found in female patients but negati

153 Habituation in the ventral anterior cingulate cortex was positively associated with the slop

154 nfluenced by aversive pruning, the subgenual cingulate cortex was robustly recruited.

155 claustrum, whereas neurons projecting to the cingulate cortex were densely packed and more evenly dis

156 P < .05) in the dorsal striatum and anterior cingulate cortex were not mitigated by nicotine or varen

157 incentive delay task and in dorsal anterior cingulate cortex when they performed the go/no-go task;

158 connecting orbitofrontal and dorsal anterior cingulate cortex with subcortical nuclei have been the t

159 dorsolateral prefrontal cortex and anterior cingulate cortex) correlated positively with hearing los

160 control (esp. IFG/AI and the dorsal anterior cingulate cortex) were strongly recruited during specifi

161 zed to the superior frontal gyrus and dorsal cingulate cortex), accompanied by attenuated top-down in

162 la), and conflict monitoring (e.g., anterior cingulate cortex).

163 itofrontal cortex, hippocampus, and anterior cingulate cortex).

164 s (mean, 32%; range, 31%-36% except anterior cingulate cortex, 24%; analysis of variance, effect of d

165 by focal degeneration in subgenual anterior cingulate cortex, amygdala, and medial pulvinar thalamus

166 ion brain regions (medial prefrontal cortex, cingulate cortex, and insula) and lower activation in se

167 ht inferior parietal lobule, right posterior cingulate cortex, and right ventral precuneus.

168 largest effects in frontal, anterior/middle cingulate cortex, and temporal regions; Biotype2, interm

169 ault mode network, particularly the anterior cingulate cortex, and the central executive network rela

170 are surprisingly heterogeneous in the mouse cingulate cortex, and the minority of GINs express only

171 inferior and middle frontal gyri, precuneus, cingulate cortex, caudate, and postcentral gyrus (all re

172 For the anterior cingulate cortex, compared with BPND values in healthy s

173 ncluding medial prefrontal cortex, posterior cingulate cortex, hippocampus, and supplemental motor ar

174 hippocampus, nucleus accumbens, and anterior cingulate cortex, in individuals with chronic pain.

175 l gains and losses in the subgenual anterior cingulate cortex, insula cortex, and left amygdala, brai

176 vely altered measures of GMV in the anterior cingulate cortex, orbital frontal cortex, temporal pole,

177 g in three regions of interest: the anterior cingulate cortex, orbitofrontal cortex, and striatum.

178 onsists of the dorsal and pregenual anterior cingulate cortex, parahippocampal area and precuneus.

179 through its interactions with the posterior cingulate cortex, precuneus, dorsomedial PFC, and amygda

180 ly and appeared in the medial insula, medial cingulate cortex, secondary somatosensory cortex, fronta

181 ent's outcome were frontal cortex, posterior cingulate cortex, thalamus, putamen, pallidum, caudate,

182 l prefrontal cortex, the anterior and middle cingulate cortex, the orbitofrontal cortex and the media

183 he caudal half of posterior parietal cortex, cingulate cortex, visual areas within the superior tempo

184 temporal gyrus, inferior temporal gyrus, and cingulate cortex, was associated with word comprehension

185 hances cellular activity within the anterior cingulate cortex, whereas chronic administration produce

186 eneration accompanied an overactive anterior cingulate cortex, which in turn resulted in a high level

187 ved in a more anterior cluster in the dorsal cingulate cortex, which overlapped with a network of str

188 ivity in ventral striatum/subgenual anterior cingulate cortex, while updates in self-esteem resulting

189 be associated with activity in the subgenual cingulate cortex, with neural signatures that were disti

190 ing to posttraining alterations in posterior cingulate cortex-dlPFC rsFC statistically mediated mindf

191 ral parietal lobules, and the left posterior cingulate cortex.

192 ntral striatum, dorsal putamen, and anterior cingulate cortex.

193 h stronger engagement of the dorsal anterior cingulate cortex.

194 ciated with tinnitus distress, including the cingulate cortex.

195 ompanied by oxidative stress in the anterior cingulate cortex.

196 uctal gray, hippocampus, and dorsal anterior cingulate cortex.

197 cluding ventromedial prefrontal and anterior cingulate cortex.

198 superior occipital gyrus/cuneus and anterior cingulate cortex.

199 xercise in an executive region, the anterior cingulate cortex.

200 the medial wall, and the rostral and caudal cingulate cortex.

201 and midline cerebellar vermis and subgenual cingulate cortex.

202 perior colliculus and anterior and posterior cingulate cortex.

203 sfunction of the GABAergic system within the cingulate cortex.

204 ippocampus, parahippocampus and parts of the cingulate cortex.

205 a region to which it projects, the anterior cingulate cortex.

206 g the parahippocampal gyrus to the posterior cingulate cortex.

207 ciated with reduced activity in the anterior cingulate cortex.

208 l prefrontal cortex, and the dorsal anterior cingulate cortex.

209 ism in the left pSTS and bilateral posterior cingulate cortex.

210 erve executive functions orchestrated by the cingulate cortex.

211 y ACC node in the CEN: right dorsal anterior cingulate cortex/medial frontal gyrus (R dACC/MFG).

212 d rs-fc between the PAG and rostral anterior cingulate cortex/medial prefrontal cortex (rACC/mPFC), k

213 nostic group x video interaction in anterior cingulate cortex/ventromedial prefrontal cortex (mPFC),

214 ral prefrontal cortex and subgenual anterior cingulate cortex; and 3) hyperconnectivity between the r

215 ft superior frontal gyrus (SFG) and anterior cingulate cortex; and 3) the Baduanjin group showed a si

216 orsolateral PFC (DLPFC), and dorsal anterior cingulated cortex (dACC) among the three groups.

217 In contrast, the cingulate cortical areas are important for emotional exp

218 and the left rostral and pregenual anterior cingulate cortices (rACC/pgACC), which control parasympa

219 central, prefrontal, fusiform, and posterior cingulate cortices before CBT-I.

220 ctivation in medial prefrontal and posterior cingulate cortices during goal-directed action selection

221 ve control, engaging prefrontal and anterior cingulate cortices similarly to many types of effortful

222 ecuneus, medial orbitofrontal, and posterior cingulate cortices, i.e., several of the core regions of

223 neration that includes the frontoinsular and cingulate cortices, provides a unique lesion model for e

224 bvFTD and semantic dementia but included the cingulate cortices, thalami, and cerebellum in patients

225 operculoinsular, primary somatosensory, and cingulate cortices, whereas hard task difficulty was rep

226 ger in R than NR between the right posterior cingulate (cue-alpha) and the left fusiform gyri (item-g

227 ed the safety and feasibility of subcallosal cingulate DBS as a treatment for treatment-resistant dep

228 llowed by 6 months of open-label subcallosal cingulate DBS.

229 -prefrontal activation and reduced posterior cingulate deactivation, whereas OCD patients showed temp

230 ective analysis of responders to subcallosal cingulate deep brain stimulation (SCC DBS) for depressio

231 e rostral and dorsal anterior cingulate, mid-cingulate, dorsomedial prefrontal cortex, and lateral or

232 connectivity, with increased dorsal anterior cingulate-driven connectivity paths.

233 presupplementary motor area/dorsal anterior cingulate during the decision-making task.

234 es of fMRI studies showed that medial fronto-cingulate dysfunction was driven by hot executive functi

235 presupplementary motor area/dorsal anterior cingulate forms part of the cingular-opercular network,

236 ndividual patients share atrophy in anterior cingulate, frontoinsula, striatum, and amygdala, indicat

237 ated with decreased FA in the genu, cingulum cingulate gyri, centrum semiovale, inferior longitudinal

238 ateral prefrontal cortex and the angular and cingulate gyri.

239 he right caudate nucleus and bilateral (para)cingulate gyrus increased in patients after real-rTMS wh

240 vity for gains was reduced in CD in the left cingulate gyrus post-cocaine and in the left putamen in

241 ular gyrus, mid-frontal cortex, and anterior cingulate gyrus).

242 frontal cortex and supplementary motor area, cingulate gyrus, cuneus and occipital gyrus, and insula

243 grey matter loss over time in the posterior cingulate gyrus, lateral and medial temporal lobe, and o

244 d temporal cortices as well as the posterior cingulate gyrus, precuneus, and mesial temporal cortex.

245 ule, the superior temporal gyrus, the middle cingulate gyrus, the putamen and the superior parietal l

246 roimaging outcomes of DBS of the subcallosal cingulate in a group of patients during 12 months of act

247 sula, lateral prefrontal cortex and anterior cingulate in response to negative affective cues, as wel

248 lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe, supramarginal gyrus,

249 lingual gyrus, cuneus, precuneus, posterior cingulate, inferior parietal lobe, supramarginal gyrus,

250 es in the inferior parietal lobule, anterior cingulate, inferior temporal lobule, the dentate nucleus

251 frontal cortex (OFC), anterior and posterior cingulate, insula and temporal lobes (Cohen's d effect s

252 ons of the salience network (dorsal anterior cingulate, insula, and thalamus) showed early learning t

253 results suggest that DBS of the subcallosal cingulate is safe and associated with improvements in mo

254 ne whether patterns of hypometabolism or the cingulate island sign differed between PCA and DLB.

255 The cingulate island sign was present in both DLB and PCA, a

256 e visually assessed to determine whether the cingulate island sign was present in each subject.

257 bolism compared with precuneus/cuneus (i.e., cingulate island sign) is a feature of DLB.

258 eus plus cuneus was calculated to assess the cingulate island sign.

259 cient, 197.4-275; P < .001) in the posterior cingulate, lateral parietal, hippocampal, and parahippoc

260 lateral (LPMCv), supplementary (M2), rostral cingulate (M3) and caudal cingulate (M4) motor regions t

261 tary (M2), rostral cingulate (M3) and caudal cingulate (M4) motor regions through the corona radiata

262 GABA+/creatine in the dorsal anterior cingulate may constitute an intermediate phenotype with

263 ronger inter-subject correlations in insula, cingulate, medial and lateral prefrontal, superior tempo

264 ly in the anterior insula, caudate, anterior cingulate, medial frontal gyrus, and dorsolateral prefro

265 G PET, whereas relative sparing of posterior cingulate metabolism compared with precuneus/cuneus (i.e

266 Posterior cingulate metabolism decreased when both amyloid and neo

267 on errors in the rostral and dorsal anterior cingulate, mid-cingulate, dorsomedial prefrontal cortex,

268 he rostral supplementary motor area, rostral cingulate motor area and cerebellum likely contributes t

269 es from the supplementary motor area and the cingulate motor areas on the medial wall of the hemisphe

270 ild spatial memory impairments and disrupted cingulate network connectivity measured by resting-state

271 decreased grey matter volume in the anterior cingulate, orbitofrontal cortex, left dorsolateral prefr

272 aled GM reductions in the bilateral anterior cingulate/paracingulate gyri (ACG/ApCG), left cerebellum

273 ell as expanded gray matter in the posterior cingulate (Pcorrected <0.05), and these changes were rel

274 ex (PFC) but increased GBCr in the posterior cingulate, precuneus, lingual gyrus, and cerebellum.

275 ress had reduced activation in the posterior cingulate/precuneus, middle temporal gyrus, and superior

276 ual's rTMS cortical target and the subgenual cingulate predicts antidepressant response.

277 responsiveness exhibited by dorsal anterior cingulate/presupplemental motor area or by anterior insu

278 excitatory neurotransmission, increases onto cingulate pyramidal neurons during peri-pubertal develop

279 ore negatively correlated with the subgenual cingulate (r = -.55, p < .005).

280 DB was uniquely associated with the cingulate (R>L), right subcallosal and right anterior fr

281 ysis; and reduced activation of the anterior cingulate region (t=-2.961, p=3.69 x 10(-3)) in the mone

282 nce of accelerated Glu aging in the anterior cingulate region in SZ compared with healthy controls.

283 ation of inhibitory neurotransmission in the cingulate region of the mouse medial frontal cortex, an

284 presupplementary motor area/dorsal anterior cingulate region with recovery of language was confirmed

285 larger surface areas in several frontal and cingulate regions and showed trends toward larger dentat

286 gions, as well as left inferior-parietal and cingulate regions, maximally around question offset, wit

287 ith a focus on the hippocampus and posterior cingulate regions.

288 ic stimulation to a subject-specific frontal-cingulate reward pathway, this pattern of results was re

289 al prefrontal cortices, along with posterior cingulate, sensory associative, and striatal regions.

290 cortex (rACC), anterior vmPFC, and subgenual cingulate significantly decreased from late childhood to

291 ould be supported by neurons in the anterior cingulate that represent expected value and uncertainty

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

293 A ratio of metabolism in the posterior cingulate to precuneus plus cuneus was calculated to ass

294 ng indicates greater homogeneity of anterior cingulate volume and, considered with the significantly

295 levels were associated with larger posterior cingulate volume, and higher triglyceride levels (standa

296 patient's stimulation site and the subgenual cingulate was assessed using resting-state functional co

297 of the T1/T2-weighted ratio in the posterior cingulate was related to performance in attention.

298 a DBS system targeting bilateral subcallosal cingulate white matter and randomised to 6 months of act

299 p brain stimulation (DBS) of the subcallosal cingulate white matter has shown promise as an intervent

300 carfentanil BPND was reduced in the anterior cingulate with no differences in [(18)F]fluorodopa Ki co