ライフサイエンスコーパス: anterior cingulate

1 sed resting functional connectivity with the anterior cingulate.

2 onnectivity from the right IFG to the dorsal anterior cingulate.

3 on and conflict, including in the insula and anterior cingulate.

4 dorsomedial prefrontal cortex including the anterior cingulate.

5 d magnetic resonance spectroscopy to measure anterior cingulate (AC) glutamate (Glu) and glutamine (G

6 pical EPSC responses in all mPFC subregions, anterior cingulate (AC), prelimbic (PL), and infralimbic

7 Dysfunction of the orbitofrontal (OFC) and anterior cingulate (ACC) cortices has been linked with s

8 Some of the most robust changes were seen in anterior cingulate (ACC).

9 1.66) associated with differences in rostral anterior cingulate activity (P < .001).

10 thermore, presupplementary motor area/dorsal anterior cingulate activity was a predictor of both lang

11 they demonstrated significantly less rostral anterior cingulate activity while regulating happy compa

12 parts of the emotional network (for example, anterior cingulate, amygdala and thalamus) were increase

13 ng bilateral dorsolateral prefrontal cortex, anterior cingulate and anterior insula.

14 the medial prefrontal, middle frontal gyrus, anterior cingulate and caudate parcellations and with wh

15 cluded positive predictive weights in dorsal anterior cingulate and cerebellum and negative weights i

16 or regions in the cognitive control network (anterior cingulate and dorsal and ventrolateral prefront

17 eal spike-train correlations between primate anterior cingulate and dorsal prefrontal cortex during a

18 terior insula, lateral orbitofrontal cortex, anterior cingulate and dorsal striatum.

19 e and reactive attentional control in dorsal anterior cingulate and dorsolateral prefrontal cortices.

20 osterior, anterior temporal, orbito-frontal, anterior cingulate and fronto-insula) were applied to 25

21 on and hyperactivation in cognitive control (anterior cingulate and frontopolar cortex) brain regions

22 netization transfer ratio (MTR) in bilateral anterior cingulate and hCaud.

23 nt underactivation in the rostral and dorsal anterior cingulate and in the medial prefrontal cortex a

24 Anterior cingulate and medial frontal cortical activatio

25 uded both dorsal and ventral portions of the anterior cingulate and medial prefrontal cortices, along

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

27 s implicated in cognitive control, including anterior cingulate and middle frontal gyrus (n = 1015).

28 s implicated in cognitive control, including anterior cingulate and middle frontal gyrus.

29 rt learning dependent upon engagement of the anterior cingulate and orbito-frontal cortices.

30 ntal (dorsolateral, ventrolateral, orbital), anterior cingulate and parietal cortical regions.

31 orded "in the wild." Our results showed less anterior cingulate and prefrontal cortex involvement for

32 spatial resolution from individual regions (anterior cingulate and primary motor, somatosensory, and

33 ther groups in the occipital, sensory-motor, anterior cingulate and supplementary motor cortices.

34 ation in reward regions (striatum and dorsal anterior cingulate) and decision-making regions (dorsola

35 pain, including the orbitofrontal, subgenual anterior cingulate, and anterior insular cortex.

36 additional regions such as occipitotemporal, anterior cingulate, and orbitofrontal cortices.

37 ologic assessment of the frontal, occipital, anterior cingulate, and posterior cingulate cerebral cor

38 maller brain grey matter volumes in frontal, anterior cingulate, and precuneus cortex regions.

39 displayed an increased activation of insula, anterior cingulate, and prefrontal cortex in response to

40 key nodes in the frontoinsula and pregenual anterior cingulate, and the semantic appraisal network (

41 mbic inactivation had no effect, whereas the anterior cingulate appeared to play a permissive role in

42 an amine, were placed in subdivisions of the anterior cingulate area 24b/c and in medial prefrontal a

43 sual cortex is reciprocally connected to the anterior cingulate area, whereas the somatosensory and a

44 ms of integrity of an anterior insula/dorsal anterior cingulate-based network, which may relate to ex

45 /orbitofrontal and decreased striatal-dorsal anterior cingulate connectivity; trait impulsivity, both

46 ty of the presupplementary motor area/dorsal anterior cingulate contributes to language recovery afte

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

48 including the retrosplenial cortex (RSC) and anterior cingulate cortex (ACA) contain a large number o

49 found in the medial prefrontal cortex (mPFC)/anterior cingulate cortex (ACC) and brainstem pons regio

50 d abuse would be associated with overlapping anterior cingulate cortex (ACC) and insular volumetric r

51 ions of the fronto-striatal circuit: midline anterior cingulate cortex (ACC) and left dorsal striatum

52 n several regions including the right dorsal anterior cingulate cortex (ACC) and left rostral ACC.

53 Reduction in volume in the anterior cingulate cortex (ACC) and lower structural cov

54 ) current density in the ventral (subgenual) anterior cingulate cortex (ACC) and orbitofrontal cortex

55 hip between the EPN and projections from the anterior cingulate cortex (ACC) and orbitofrontal cortex

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

57 hy based structural connectivity between the anterior cingulate cortex (ACC) and posterior cingulate

58 and theta (4-8 Hz) oscillations in both the anterior cingulate cortex (ACC) and the DLPFC during REM

59 Here, we compared the role of the anterior cingulate cortex (ACC) and the posterior insula

60 GMV was significantly lower in the bilateral anterior cingulate cortex (ACC) and the right superior f

61 The frontal eye fields (FEFs) and the anterior cingulate cortex (ACC) are commonly coactivated

62 These signals emerged first in anterior cingulate cortex (ACC) before dorsolateral pref

63 Interestingly, neural activities in the anterior cingulate cortex (ACC) correlated with noxious

64 The anterior cingulate cortex (ACC) has been shown to be cru

65 The anterior cingulate cortex (ACC) has shown decreased glut

66 the posterior cingulate cortex (PCC) to the anterior cingulate cortex (ACC) in the 10-Hz range.

67 served significant increased activity of the Anterior Cingulate Cortex (ACC) in the low frequency ban

68 The anterior cingulate cortex (ACC) is implicated in a broad

69 Anterior cingulate cortex (ACC) is thought to control a

70 Recent evidence suggests that anterior cingulate cortex (ACC) maturation during adoles

71 MAO-A levels in prefrontal cortex (PFC) and anterior cingulate cortex (ACC) occur in rodent models o

72 rsolateral prefrontal cortex (dlPFC) and the anterior cingulate cortex (ACC) of macaque monkeys as th

73 The lateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) of the primate play dist

74 of the infralimbic (IL) cortex (but not the anterior cingulate cortex (ACC) or prelimbic cortex), re

75 ENT The lateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) play temporally distinct

76 ne with the prevailing view that dopamine in anterior cingulate cortex (ACC) plays a role in evaluati

77 Furthermore, activity in dorsal anterior cingulate cortex (ACC) reflected individual cho

78 The function of the anterior cingulate cortex (ACC) remains controversial, y

79 Neurons in the anterior cingulate cortex (ACC) signal PEs when learning

80 Endogenous opioid signaling in the anterior cingulate cortex (ACC), an area encoding pain a

81 d structural volumes (amygdala, hippocampus, anterior cingulate cortex (ACC), and ventral medial pref

82 e use can disrupt the reward function of the anterior cingulate cortex (ACC), biasing the ACC to favo

83 ypothesis that imposing rhythms in the mouse anterior cingulate cortex (ACC), by using optogenetics t

84 olute quantification, GPC+PC levels from the anterior cingulate cortex (ACC), caudate and putamen of

85 dorsal hippocampus, ventral hippocampus, or anterior cingulate cortex (ACC), during consolidation an

86 rd area, reduced grey matter (GM) volumes in anterior cingulate cortex (ACC), left insula, left secon

87 mography to compare TSPO availability in the anterior cingulate cortex (ACC), prefrontal cortex, and

88 gly dependent on cortical areas, such as the anterior cingulate cortex (ACC).

89 Among cortical areas, the anterior cingulate cortex (ACC, areas 24a and 24b) appea

90 Dorsal anterior cingulate cortex (dACC) activation is commonly

91 o the detection of physical pain, the dorsal anterior cingulate cortex (dACC) and anterior insula (AI

92 , persistent patients showed a higher dorsal anterior cingulate cortex (dACC) and insula response to

93 social exclusion was decreased in the dorsal anterior cingulate cortex (dACC) and the middle frontal

94 More broadly, the insula and the dorsal anterior cingulate cortex (dACC) are key nodes of the sa

95 ed glutamate in the basal ganglia and dorsal anterior cingulate cortex (dACC) as measured by magnetic

96 Dorsal anterior cingulate cortex (dACC) carries a wealth of val

97 uential model proposed that the human dorsal anterior cingulate cortex (dACC) detects conflict and in

98 in this function are associated with dorsal anterior cingulate cortex (dACC) excitotoxic lesions and

99 The dorsal anterior cingulate cortex (dACC) has attracted great int

100 Debates over the function(s) of dorsal anterior cingulate cortex (dACC) have persisted for deca

101 aging studies in humans implicate the dorsal anterior cingulate cortex (dACC) in regulating the confl

102 Dorsal anterior cingulate cortex (dACC) mediates updating and m

103 e recorded activity of neurons in the dorsal anterior cingulate cortex (dACC) of macaques choosing be

104 rontal cortex (mPFC) suggest that the dorsal anterior cingulate cortex (dACC) region is responsive to

105 In the PTSD group, dorsal anterior cingulate cortex (dACC) resting metabolism posi

106 ynaptic feedforward inhibition in the dorsal anterior cingulate cortex (dACC) subregion of the mPFC.

107 D youth showed hyperactivation of the dorsal anterior cingulate cortex (dACC) to threat images.

108 ions with precuneus, anterior insula, dorsal anterior cingulate cortex (dACC), and left dorsolateral

109 trolateral prefrontal cortex (VLPFC), dorsal anterior cingulate cortex (dACC), left DLPFC, hippocampu

110 Recording from the dorsal anterior cingulate cortex (dACC), they find neurons whos

111 re able to hold simultaneously in the dorsal anterior cingulate cortex (dACC).

112 The anterior insula (AI) and mid-anterior cingulate cortex (mACC) have repeatedly been im

113 rought up in a city with increased pregenual anterior cingulate cortex (pACC) activity.

114 copic imaging (PEPSI) MRS scans of pregenual anterior cingulate cortex (pACC) and ventral posterior c

115 nd neurochemical signatures in the pregenual anterior cingulate cortex (pACC), a structure known to b

116 (R = 0.53, P < .05) and the bilateral dorsal anterior cingulate cortex (R = 0.47, P < .05), 2 structu

117 ers in a card game, neurons in their rostral anterior cingulate cortex (rACC) encode both the expecte

118 etween the centromedial amygdala and rostral anterior cingulate cortex (rACC), anterior vmPFC, and su

119 tion involves projections from the subgenual anterior cingulate cortex (sgACC) to the periaqueductal

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

121 eptor availability in the aINS and subgenual anterior cingulate cortex (sgACC).

122 symptoms inversely correlated with subgenual anterior cingulate cortex (sgACC, Z=3.7) and right anter

123 in the salience network (insular cortex and anterior cingulate cortex [ACC] and the right parahippoc

124 traumatic stress disorder, or MDD (subgenual anterior cingulate cortex [sgACC], left dorsolateral pre

125 n imaging analyses highlighted higher dorsal anterior cingulate cortex activation in poker players, a

126 s predicted by a failure to maintain ventral anterior cingulate cortex activation in response to fear

127 TSD symptoms, such that decreases in ventral anterior cingulate cortex activation over repeated prese

128 erlapping network activity, but different in anterior cingulate cortex activity.

129 entromedial prefrontal cortex, including the anterior cingulate cortex and bilateral insula.

130 sulcus, bilateral precuneus as well as left anterior cingulate cortex and caudate.

131 occipital-parietal cortex; and right rostral anterior cingulate cortex and central sulcus/postcentral

132 eater age-related decreases of DLPFC NAA and anterior cingulate cortex and DLPFC Glu levels.

133 esting-state functional connectivity between anterior cingulate cortex and dorso-medial prefrontal co

134 bility responses than controls in the dorsal anterior cingulate cortex and in the superior frontal gy

135 eraction with individual risk preferences in anterior cingulate cortex and insula.

136 tor, and olfactory), and prefrontal regions (anterior cingulate cortex and orbitofrontal cortex) to t

137 er Glu and Gly levels were found in both the anterior cingulate cortex and posterior cingulate cortex

138 and Gly levels were measured in vivo in the anterior cingulate cortex and posterior cingulate cortex

139 itol (mI), and glutamate (Glu) levels in the anterior cingulate cortex and right dorsolateral prefron

140 flecting the balance between striatal-dorsal anterior cingulate cortex and striatal-anterior prefront

141 the same network of regions involving dorsal anterior cingulate cortex and supplementary motor area e

142 ractivation of central hubs in the subgenual anterior cingulate cortex and thalamus that lead to a ca

143 s in major depression pathology, such as the anterior cingulate cortex and the amygdala via the uncin

144 tly lower in the Ch4 terminal regions of the anterior cingulate cortex and the superior and inferior

145 We show that dorsal anterior cingulate cortex and three other brain regions

146 elative to controls from right IFG to dorsal anterior cingulate cortex and to left IFG and dorsolater

147 ype x smoking effect was found in the dorsal anterior cingulate cortex and ventral striatum, such tha

148 rther research into the gyral surface of the anterior cingulate cortex and ventromedial prefrontal co

149 tching in comprehension were observed in the anterior cingulate cortex and were not shared by categor

150 The medial prefrontal - anterior cingulate cortex appears most tightly related t

151 c, and cellular adaptations may occur in the anterior cingulate cortex as a function of child abuse.

152 entral positions as network hubs, and dorsal anterior cingulate cortex becoming more tightly coupled

153 erize a possible way by which prefrontal and anterior cingulate cortex circuits implement their contr

154 ace-related amygdala activation and amygdala-anterior cingulate cortex connectivity (P corrected for

155 (STG) and between the left AI/FO and dorsal anterior cingulate cortex correlated positively with imp

156 terations in cholinergic transmission in the anterior cingulate cortex could be closely associated wi

157 ial attention and the left angular gyrus and anterior cingulate cortex during motor intention.

158 f specific brain regions, such as the dorsal anterior cingulate cortex during trials on which partici

159 motor area and the caudal portion of dorsal anterior cingulate cortex encoded the difference in rewa

160 s type 2-mediated IGF2 overexpression in the anterior cingulate cortex enhanced remote fear memory fo

161 tion of the right amygdala and the subgenual anterior cingulate cortex following errors was observed

162 ained from orbitofrontal cortex (OFC) and/or anterior cingulate cortex from two separate cohorts (n =

163 Research on human anterior cingulate cortex has long indicated a role in d

164 lamus, ventral striatum, dorsal putamen, and anterior cingulate cortex in OCD.

165 Here, we show that a subregion of the anterior cingulate cortex in the gyrus (ACCg) shows a de

166 mygdala in rhesus monkeys, we found that the anterior cingulate cortex innervated mostly the basolate

167 By contrast, the anterior cingulate cortex innervates other amygdalar par

168 The anterior cingulate cortex is implicated in the neurobiol

169 h J-edited proton spectroscopy in the dorsal anterior cingulate cortex of 289 individuals: 184 health

170 ervoir activity to neural activity of dorsal anterior cingulate cortex of monkeys which revealed simi

171 , caudate nucleus, putamen, hippocampus, and anterior cingulate cortex of patients with SAD compared

172 -insular region to the medial prefrontal and anterior cingulate cortex of the common marmoset (Callit

173 Subgenual anterior cingulate cortex postmortem samples from four M

174 porating neighboring insular regions and the anterior cingulate cortex showed weaker functional conne

175 While the gyral surface of the anterior cingulate cortex signalled social prediction er

176 High activities of the anterior cingulate cortex significantly mediated relatio

177 We identified features of anterior cingulate cortex structure and connectivity tha

178 tructural brain imaging revealed a region of anterior cingulate cortex that was thicker in SuperAgers

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

180 e dorsolateral prefrontal cortex (DLPFC) and anterior cingulate cortex under three conditions (the N-

181 pectra were acquired from the medial frontal/anterior cingulate cortex using a macromolecule-suppress

182 y in these regions, but lower variability of anterior cingulate cortex volume.

183 Habituation in the ventral anterior cingulate cortex was positively associated with

184 r, glutamate-glutamine concentrations in the anterior cingulate cortex were measured using MR spectro

185 orrected P < .05) in the dorsal striatum and anterior cingulate cortex were not mitigated by nicotine

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

187 r tracts connecting orbitofrontal and dorsal anterior cingulate cortex with subcortical nuclei have b

188 bute to a currently ongoing debate about the anterior cingulate cortex's role in sequential foraging

189 ns (i.e., dorsolateral prefrontal cortex and anterior cingulate cortex) correlated positively with he

190 circuitry (ventral striatum, dorsal caudate, anterior cingulate cortex) during processing of immediat

191 ntal cortex, dorsolateral prefrontal cortex, anterior cingulate cortex) that was not present when the

192 ognitive control (esp. IFG/AI and the dorsal anterior cingulate cortex) were strongly recruited durin

193 -0.163; P = .001) (extending into the right anterior cingulate cortex), and left fusiform gyrus (SDM

194 errant salience network activity (insula and anterior cingulate cortex), prefrontal hypoactivation, s

195 cortex and the salience network (insula and anterior cingulate cortex).

196 sula, orbitofrontal cortex, hippocampus, and anterior cingulate cortex).

197 rior insula), and conflict monitoring (e.g., anterior cingulate cortex).

198 in regions (mean, 32%; range, 31%-36% except anterior cingulate cortex, 24%; analysis of variance, ef

199 companied by focal degeneration in subgenual anterior cingulate cortex, amygdala, and medial pulvinar

200 ggest that regions such as amygdala, insula, anterior cingulate cortex, and hippocampus play an impor

201 stressed cagemate increases activity in the anterior cingulate cortex, and oxytocin receptor antagon

202 superior frontal gyrus, right paracingulate/anterior cingulate cortex, and right supramarginal gyrus

203 n of pain-processing regions such as insula, anterior cingulate cortex, and thalamus.

204 n the default mode network, particularly the anterior cingulate cortex, and the central executive net

205 dala connectivity with middle frontal gyrus, anterior cingulate cortex, bilateral precuneus, and left

206 ven trial, in right medial prefrontal cortex/anterior cingulate cortex, caudate, anterior insula, and

207 For the anterior cingulate cortex, compared with BPND values in

208 al ebselen reduced brain myo-inositol in the anterior cingulate cortex, consistent with CNS target en

209 By contrast, activity in dorsal anterior cingulate cortex, frontal operculum/anterior in

210 ding the hippocampus, nucleus accumbens, and anterior cingulate cortex, in individuals with chronic p

211 potential gains and losses in the subgenual anterior cingulate cortex, insula cortex, and left amygd

212 ortical association hubs, such as the dorsal anterior cingulate cortex, may be a neurobiological mark

213 ut the representation of pleasantness in the anterior cingulate cortex, not S1.

214 athophysiology of MDD, namely, the subgenual anterior cingulate cortex, nucleus accumbens, midline th

215 interactively altered measures of GMV in the anterior cingulate cortex, orbital frontal cortex, tempo

216 BR binding in three regions of interest: the anterior cingulate cortex, orbitofrontal cortex, and str

217 tivity' consists of the dorsal and pregenual anterior cingulate cortex, parahippocampal area and prec

218 chored in the anterior insula and the dorsal anterior cingulate cortex, plays a crucial role in this

219 n activity' consists of dorsal and pregenual anterior cingulate cortex, posterior cingulate extending

220 vity was found in the amygdala and subgenual anterior cingulate cortex, suggesting a stronger affecti

221 rved in lateral frontoparietal cortices, the anterior cingulate cortex, thalamus, and cuneus.

222 Gray matter reduction mainly in the anterior cingulate cortex, the basal ganglia, and the ce

223 in and enhances cellular activity within the anterior cingulate cortex, whereas chronic administratio

224 neurodegeneration accompanied an overactive anterior cingulate cortex, which in turn resulted in a h

225 with activity in ventral striatum/subgenual anterior cingulate cortex, while updates in self-esteem

226 nd right superior occipital gyrus/cuneus and anterior cingulate cortex.

227 llowing exercise in an executive region, the anterior cingulate cortex.

228 ortex and a region to which it projects, the anterior cingulate cortex.

229 dorsal insula, supplementary motor area, and anterior cingulate cortex.

230 jects, however, there were no changes in the anterior cingulate cortex.

231 tion from pregenual and subgenual regions of anterior cingulate cortex.

232 ess ratings predicted activation only in the anterior cingulate cortex.

233 dent RNA sequencing data set (N=61) from the anterior cingulate cortex.

234 a subpopulation of neurons within the mouse anterior cingulate cortex.

235 y between lateral parietal cortex and dorsal anterior cingulate cortex.

236 temporal gyrus, as well as left caudate and anterior cingulate cortex.

237 sely connected prefrontal region, the dorsal anterior cingulate cortex.

238 was associated with reduced activity in the anterior cingulate cortex.

239 the medial prefrontal cortex, and the dorsal anterior cingulate cortex.

240 lamus, ventral striatum, dorsal putamen, and anterior cingulate cortex.

241 iated with stronger engagement of the dorsal anterior cingulate cortex.

242 e all accompanied by oxidative stress in the anterior cingulate cortex.

243 periaqueductal gray, hippocampus, and dorsal anterior cingulate cortex.

244 gions, including ventromedial prefrontal and anterior cingulate cortex.

245 vity in a posterior portion of the subgenual anterior cingulate cortex/basal forebrain (sgACC) drives

246 y of a key ACC node in the CEN: right dorsal anterior cingulate cortex/medial frontal gyrus (R dACC/M

247 ed reduced rs-fc between the PAG and rostral anterior cingulate cortex/medial prefrontal cortex (rACC

248 tween the default mode network and subgenual anterior cingulate cortex/orbital frontal cortex, and th

249 ed a diagnostic group x video interaction in anterior cingulate cortex/ventromedial prefrontal cortex

250 Hypoactivation of the rostral anterior cingulate cortex/ventromedial prefrontal cortex

251 dorsolateral prefrontal cortex and subgenual anterior cingulate cortex; and 3) hyperconnectivity betw

252 nd the left superior frontal gyrus (SFG) and anterior cingulate cortex; and 3) the Baduanjin group sh

253 (VPFC), dorsolateral PFC (DLPFC), and dorsal anterior cingulated cortex (dACC) among the three groups

254 60172 and ACEA into the infralimbic, but not anterior cingulate, cortex mitigated decision-making def

255 ft insula and the left rostral and pregenual anterior cingulate cortices (rACC/pgACC), which control

256 l executive control, engaging prefrontal and anterior cingulate cortices similarly to many types of e

257 activation (left ventral pallidum, bilateral anterior cingulate cortices, right hypothalamus and bila

258 GABA+ levels in the dorsal anterior cingulate did not differ between untreated pati

259 icipants, while they demonstrated no rostral anterior cingulate difference between happy and sad emot

260 king DMN connectivity, with increased dorsal anterior cingulate-driven connectivity paths.

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

262 p of other-predictive neurons in the primate anterior cingulate essential for enacting cooperative in

263 The presupplementary motor area/dorsal anterior cingulate forms part of the cingular-opercular

264 vity in PS youths, implicating the bilateral anterior cingulate, frontal pole, medial temporal lobe,

265 nd even individual patients share atrophy in anterior cingulate, frontoinsula, striatum, and amygdala

266 r participants with schizophrenia have lower anterior cingulate GABA levels compared with older contr

267 ions (angular gyrus, mid-frontal cortex, and anterior cingulate gyrus).

268 ted obese people by opposite activity in the anterior cingulate gyrus.

269 work involving the motor/premotor cortex and anterior cingulate gyrus.

270 y gray matter volume in the frontal pole and anterior cingulate gyrus.

271 iatum, insula, lateral prefrontal cortex and anterior cingulate in response to negative affective cue

272 olic values in the inferior parietal lobule, anterior cingulate, inferior temporal lobule, the dentat

273 ions from higher limbic regions and from the anterior cingulate, insula, and orbitofrontal cortical a

274 We found that anterior cingulate, insula, and superior temporal gyrus

275 Regions of the salience network (dorsal anterior cingulate, insula, and thalamus) showed early l

276 GABA+/creatine in the dorsal anterior cingulate may constitute an intermediate phenot

277 articularly in the anterior insula, caudate, anterior cingulate, medial frontal gyrus, and dorsolater

278 can 1 of 21.3% +/- 21.4%, on average, in the anterior cingulate, medial prefrontal cortex, orbital pr

279 function and structure in rostral and dorsal anterior cingulate/medial prefrontal cortex (fMRI z = 2.

280 Commission errors in the rostral and dorsal anterior cingulate, mid-cingulate, dorsomedial prefronta

281 ormal neural activity in striatum and dorsal anterior cingulate; normalization of behavior was associ

282 and medial PFC (prelimbic, infralimbic, and anterior cingulate) on probabilistic reversal learning w

283 ted with decreased grey matter volume in the anterior cingulate, orbitofrontal cortex, left dorsolate

284 ults revealed GM reductions in the bilateral anterior cingulate/paracingulate gyri (ACG/ApCG), left c

285 activation in the medial prefrontal cortex, anterior cingulate, precuneus region of the parietal cor

286 mposed of the anterior insula and the dorsal anterior cingulate, predicted reliable improvement in ad

287 ree of MD responsiveness exhibited by dorsal anterior cingulate/presupplemental motor area or by ante

288 ions analysis; and reduced activation of the anterior cingulate region (t=-2.961, p=3.69 x 10(-3)) in

289 how evidence of accelerated Glu aging in the anterior cingulate region in SZ compared with healthy co

290 ip of the presupplementary motor area/dorsal anterior cingulate region with recovery of language was

291 us and cortex in the prefrontal, insular and anterior cingulate regions.

292 ed across diagnoses in 3 regions: the dorsal anterior cingulate, right insula, and left insula.

293 potential of the insula (t = 2.41; P = .04), anterior cingulate (t = 2.27; P = .04), and dorsolateral

294 versity could be supported by neurons in the anterior cingulate that represent expected value and unc

295 cover specific neurons in the primate dorsal anterior cingulate that selectively predict an opponent'

296 ight inferior parietal, right thalamus, left anterior cingulate) that exhibited multiple aberrant con

297 onosynaptic prefrontal cortex (predominantly anterior cingulate) to hippocampus (CA3 to CA1 region) p

298 his finding indicates greater homogeneity of anterior cingulate volume and, considered with the signi

299 tabolism than HC in frontal cortex including anterior cingulate, which was associated with negative e

300 , [(11)C]carfentanil BPND was reduced in the anterior cingulate with no differences in [(18)F]fluorod