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

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

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

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

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

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

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

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

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

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

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

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

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

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

14 demonstrated increased activity of the left anterior cingulate cortex.

15 nectivity between anterior insula and dorsal anterior cingulate cortex.

16 tion of the corpus callosum derived from the anterior cingulate cortex.

17 ract between the amygdala and the perigenual anterior cingulate cortex.

18 Among these are the orbitofrontal and the anterior cingulate cortex.

19 pplementary and supplementary motor area and anterior cingulate cortex.

20 tal sulcus-and were integrated in the dorsal anterior cingulate cortex.

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

22 o detected a stimulus-evoked decrease in the anterior cingulate cortex.

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

24 vation among BD-youths than BD-adults in the anterior cingulate cortex.

25 cortex, dorsolateral prefrontal cortex, and anterior cingulate cortex.

26 area Spt, inferior parietal lobule, and the anterior cingulate cortex.

27 ula, precuneus, orbitofrontal, and pregenual anterior cingulate cortex.

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

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

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

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

32 gions, including ventromedial prefrontal and anterior cingulate cortex.

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

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

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

36 izophrenia samples from cohort 1 (OFC: +45%; anterior cingulate cortex: +44%) and cohort 2 (OFC: +40%

37 h increased brain activations in the rostral anterior cingulate cortex, a region that has been associ

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

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

40 decreases in the volume and thickness of the anterior cingulate cortex (ACC) after chronic APD treatm

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

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

43 Neurons within the anterior cingulate cortex (ACC) and its target region in

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

45 n several 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 cov

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

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

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

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

51 The anterior cingulate cortex (ACC) and prefrontal cortex (P

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

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

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

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

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

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

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

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

60 oscopy to examine myo-Inositol levels in the anterior cingulate cortex (ACC) in 59 schizophrenia spec

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

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

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

64 The anterior cingulate cortex (ACC) is one of several brain

65 ctions are ignored, and normal engagement of anterior cingulate cortex (ACC) is suppressed.

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

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

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

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

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

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

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

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

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

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

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

77 nonhuman primates have found neurons in the anterior cingulate cortex (ACC) that signal the net valu

78 ration was measured in the left thalamus and anterior cingulate cortex (ACC) using 3-Tesla proton mag

79 Within this network, anterior cingulate cortex (ACC) was dynamically coupled

80 ted the properties of neural networks in the anterior cingulate cortex (ACC), a brain region mediatin

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

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

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

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

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

86 al amygdala (BLA) complex with the pregenual anterior cingulate cortex (ACC), dorsomedial prefrontal

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

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

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

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

91 um and medial frontal cortex, especially the anterior cingulate cortex (ACC).

92 forms of long-term potentiation (LTP) in the anterior cingulate cortex (ACC); a presynaptic form (pre

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

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

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

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

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

98 gyrus activity and ADHD symptoms and between anterior cingulate cortex activity and novelty seeking.

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

100 both viscerosensory brain (anterior insula, anterior cingulate cortex, amygdala) and autonomic-cardi

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

102 striatum, substantia nigra), but also within anterior cingulate cortex, amygdala, entorhinal cortex,

103 the salience network, which includes dorsal anterior cingulate cortex and adjacent cortex in the sup

104 Group differences were most prominent in the anterior cingulate cortex and adjacent prefrontal areas.

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

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

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

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

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

110 n the Pittsburgh compound B retention in the anterior cingulate cortex and functional connectivities

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

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

113 urons of the dorsolateral prefrontal cortex, anterior cingulate cortex and orbitofrontal cortex in th

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

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

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

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

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

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

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

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

122 ting-state activities between the perigenual anterior cingulate cortex and the dorsolateral prefronta

123 nvolving the dorsolateral prefrontal cortex, anterior cingulate cortex and the orbitofrontal cortex.

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

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

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

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

128 detection and control implementation by the anterior cingulate cortex and ventrolateral prefrontal c

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

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

131 -0.163; P = .001) (extending into the right anterior cingulate cortex), and left fusiform gyrus (SDM

132 ion in the amygdala, fusiform gyrus, insula, anterior cingulate cortex, and dorsomedial prefrontal co

133 ight amygdala and bilateral IFG, OFC, vmPFC, anterior cingulate cortex, and frontopolar cortex was as

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

135 number of areas, including ventral striatum, anterior cingulate cortex, and medial prefrontal cortex

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

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

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

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

140 uding the dorsomedial prefrontal cortex, the anterior cingulate cortex, and the inferior frontal gyru

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

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

143 revealed a gray matter cluster in the right anterior cingulate cortex, anterior to the eventual lesi

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

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

146 nections between the auditory cortex and the anterior cingulate cortex as well as adjacent prefrontal

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

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

149 ctly associated with lower GM volumes in the anterior cingulate cortex (beta = -.18; P = .01) and hig

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

151 rinking is associated with activation in the anterior cingulate cortex (Brodmann area 32) and the orb

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

153 ng data in nine candidate regions (amygdala, anterior cingulate cortex, caudate, frontal cortex, hypo

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

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

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

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

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

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

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

161 Dorsal anterior cingulate cortex (dACC) activation is commonly

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

163 known to alter neural activity in the dorsal anterior cingulate cortex (dACC) and basal ganglia in as

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

165 owed reduced neural activation in the dorsal anterior cingulate cortex (dACC) and right insula in res

166 nd subcortical regions, including the dorsal anterior cingulate cortex (dACC) and thalamus.

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

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

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

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

171 We demonstrate that dorsal anterior cingulate cortex (dACC) carries signals indexin

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

173 By contrast, the dorsal anterior cingulate cortex (dACC) encoded stimulus value

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

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

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

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

178 Although the dorsal anterior cingulate cortex (dACC) is thought to be the co

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

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

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

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

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

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

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

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

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

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

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

190 he role of positive dorsal medial prefrontal/anterior cingulate cortex (dmPFC/ACC)-amygdala circuit c

191 ression and decreased brain responses in the anterior cingulate cortex/dorso-medial PFC (provoking<no

192 and four cortical regions-rostral and dorsal anterior cingulate cortex, dorsolateral prefrontal corte

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

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

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

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

197 ver, IL-6 mediated the association of dorsal anterior cingulate cortex engagement with preclinical at

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

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

200 ne expression, in postmortem tissue from the anterior cingulate cortex from 13 bipolar disorder case

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

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

203 ctional connectivity, and decreased amygdala-anterior cingulate cortex functional connectivity previo

204 d significantly more negative right amygdala-anterior cingulate cortex functional connectivity to emo

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

206 nction present in BD-youths, as well as that anterior cingulate cortex hypoactivation is relevant to

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

208 d connectivity specifically with the ventral anterior cingulate cortex in subjects with OCD.

209 mate studies suggest that a subregion of the anterior cingulate cortex in the gyrus (ACCg) is engaged

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

211 A region of the anterior cingulate cortex in the right hemisphere displa

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

213 Infusion of methylphenidate into the anterior cingulate cortex, infralimbic cortex, basolater

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

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

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

217 The dorsal anterior cingulate cortex is a key part of this network

218 The anterior cingulate cortex is implicated in the neurobiol

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

220 ogy and higher von Economo neuron density in anterior cingulate cortex may represent biological corre

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

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

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

224 60172 and ACEA into the infralimbic, but not anterior cingulate, cortex mitigated decision-making def

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

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

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

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

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

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

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

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

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

234 ecific effects: hyperactivation in subgenual anterior cingulate cortex (P < .05) and ventrolateral pr

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

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

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

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

239 ) levels, which occurs in the prefrontal and anterior cingulate cortex (PFC and ACC) during MDE; howe

240 e network was negatively correlated with the anterior cingulate cortex Pittsburgh compound B levels.

241 Anterior cingulate cortex Pittsburgh compound B retentio

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

243 d with losses in bilateral ventral striatum, anterior cingulate cortex, posterior cingulate cortex, a

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

245 Subgenual anterior cingulate cortex postmortem samples from four M

246 sed gray matter in this region of the dorsal anterior cingulate cortex predicted improved response (m

247 Projections from the anterior cingulate cortex preferentially targeted 6DC, w

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

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

250 ht CUD group had lower error-induced rostral anterior cingulate cortex (rACC) activity as associated

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

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

253 rsFC between the left pMPFC and the rostral anterior cingulate cortex (rACC), medial frontal pole (m

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

255 nificantly greater deactivation in subgenual anterior cingulate cortex (sACC) than either the TLE-onl

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

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

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

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

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

261 In contrast, the anterior cingulate cortex showed a major significant los

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

263 ch are normally tightly linked to the dorsal anterior cingulate cortex, showed increased activity fol

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

265 High activities of the anterior cingulate cortex significantly mediated relatio

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

267 The subgenual anterior cingulate cortex (subgenual ACC) plays an impor

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

269 nicotine exhibited a weaker response in the anterior cingulate cortex (t168 = 4.46; peak Montreal Ne

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

271 ula and increases in the lateral PFC, dorsal anterior cingulate cortex, thalamus, and cuneus.

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

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

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

275 eceipt of painful stimulation in the rostral anterior cingulate cortex, the dorsolateral prefrontal c

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

277 correlates of underestimation (right rostral anterior cingulate cortex, uncorrected significance leve

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

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

280 suggest that KOR availability in an amygdala-anterior cingulate cortex-ventral striatal neural circui

281 50 volume of distribution values in amygdala-anterior cingulate cortex-ventral striatal neural circui

282 volume of distribution values in an amygdala-anterior cingulate cortex-ventral striatal neural circui

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

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

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

286 reappraisal-related engagement of the dorsal anterior cingulate cortex was associated with greater pr

287 The anterior cingulate cortex was engaged by all tasks.

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

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

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

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

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

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

294 task-evoked functional connectivity with the anterior cingulate cortex, whereas the rIFC had stronger

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

296 denser and larger in pOFC compared with the anterior cingulate cortex, which is also strongly connec

297 Candidate areas included the dorsal anterior cingulate cortex, which is involved in associat

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

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

300 ctures, especially in the right amygdala and anterior cingulate cortex, with reductions in amygdala r