ライフサイエンスコーパス: cingulate cortex

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

2 to deep limbic regions such as the subgenual cingulate cortex.

3 ly increased from parietal to prefrontal and cingulate cortex.

4 tex and diminished responses within anterior cingulate cortex.

5 affective networks are located in regions of cingulate cortex.

6 ll uncertainty in insula and dorsal anterior cingulate cortex.

7 he medial prefrontal cortex and the anterior cingulate cortex.

8 complementary roles of the amygdala and the cingulate cortex.

9 dorsolateral prefrontal cortex and anterior cingulate cortex.

10 dorsolateral prefrontal cortex and anterior cingulate cortex.

11 he superior temporal, precentral, and middle cingulate cortex.

12 on the nonhomologous partitioning of rodent cingulate cortex.

13 g glutamate levels in the bilateral anterior cingulate cortex.

14 vity, suggesting the involvement of anterior cingulate cortex.

15 ated both the rostral and posterior anterior cingulate cortex.

16 r lateral prefrontal cortex and the anterior cingulate cortex.

17 ciated with tinnitus distress, including the cingulate cortex.

18 and parietal lobes, precuneus, and posterior cingulate cortex.

19 ciated with reduced activity in the anterior cingulate cortex.

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

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

22 ortex, temporoparietal junction, and rostral cingulate cortex.

23 erve executive functions orchestrated by the cingulate cortex.

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

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

26 smaller structure in prefrontal and anterior cingulate cortex.

27 anterior cingulate cortex and left posterior cingulate cortex.

28 ic class), with an epicenter in the anterior cingulate cortex.

29 fined areas that form the pregenual anterior cingulate cortex.

30 ut focal thickness reduction in temporal and cingulate cortex.

31 hubs in medial prefrontal, but not posterior cingulate, cortex.

32 nd to a lesser extent in the mid-to-anterior cingulate cortex (11.1%, 5 of 45).

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

34 tivity between the amygdala and the anterior cingulate cortex, a network involved in regulating anxio

35 ividuals failed to use their dorsal anterior cingulate cortex, a region known to adjust learning rate

36 For cingulate cortex, a structure implicated in behavioural

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

38 Recent work has identified the anterior cingulate cortex (ACC) among other brain regions involve

39 heta power (7-9 Hz, ~120 ms) in mid-anterior cingulate cortex (ACC) and a later beta power suppressio

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

41 ne (Glx), and GABA levels in dorsal anterior cingulate cortex (ACC) and glutamate and Glx levels in l

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

43 vidual neurons in parts of both the anterior cingulate cortex (ACC) and posterior cingulate cortex (P

44 the prefrontal cortex, namely, the anterior cingulate cortex (ACC) and somatomotor cortex (SC).

45 The medial thalamus (MThal), anterior cingulate cortex (ACC) and striatum play important roles

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

47 revious research has focused on the anterior cingulate cortex (ACC) as a key brain region in the miti

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

49 rved early strong activation of the anterior cingulate cortex (ACC) corresponding to the noxious stim

50 rs showed an increase in NAc-dorsal anterior cingulate cortex (ACC) FC relative to non-responders (p

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

52 Research has implicated the anterior cingulate cortex (ACC) in attaching value to social outc

53 in the amygdala in both sexes, the anterior cingulate cortex (ACC) in females, and the hippocampus i

54 ses in the pyramidal neurons of the anterior cingulate cortex (ACC) in mice with a mutation in Shank3

55 ial prefrontal cortex including the anterior cingulate cortex (ACC) in social cognition in adolescenc

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

57 d glutamate metabolism in pregenual anterior cingulate cortex (ACC) in type 1 diabetes (T1D) without

58 The anterior cingulate cortex (ACC) is important for decision-making

59 of the frontal cortex known as the anterior cingulate cortex (ACC) is particularly well suited for t

60 Hyperexcitability of the anterior cingulate cortex (ACC) is thought to drive aversion asso

61 sed connectivity to pain areas like anterior cingulate cortex (ACC) might underlie maladaptive pain p

62 yer 5 (L5) pyramidal neurons in the anterior cingulate cortex (ACC) of adult male mice we found good

63 rsomedial frontal cortex (DMFC) and anterior cingulate cortex (ACC) of monkeys in a task in which neg

64 in the prefrontal cortex (PFC) and anterior cingulate cortex (ACC) predicts reduction of depressive

65 sion task for mice to show that the anterior cingulate cortex (ACC) predicts the state that actions w

66 colleagues show that removal of the anterior cingulate cortex (ACC) prevents monkeys from learning wh

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

68 The functional connectivity of the anterior cingulate cortex (ACC) was evaluated with: the precuneus

69 levels in the left thalamus and the anterior cingulate cortex (ACC) were measured using 1[H]-magnetic

70 examined effects on activity in the anterior cingulate cortex (ACC), a brain region important in mood

71 stration disrupts neural signals in anterior cingulate cortex (ACC), a brain region thought to contri

72 orrelates of this phenomenon in the anterior cingulate cortex (ACC), a brain structure implicated in

73 ty, and lower mPFC FC with adjacent anterior cingulate cortex (ACC), a crucial region of emotion modu

74 he sensory pain information, to the anterior cingulate cortex (ACC), a key area for processing pain a

75 ed positive FC between amygdala and anterior cingulate cortex (ACC), and had increased positive FC be

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

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

78 and glutamine concentrations in the anterior cingulate cortex (ACC), left insula, and visual cortex u

79 in regions, including the amygdala, anterior cingulate cortex (ACC), nucleus accumbens (NAcc), and or

80 the S1, primary visual cortex (V1), anterior cingulate cortex (ACC), posterior parietal cortex (PPC),

81 everal brain regions, including the anterior cingulate cortex (ACC), were sensitive to an interaction

82 cture of children's hippocampus and anterior cingulate cortex (ACC).

83 cortex modulates belief updating in anterior cingulate cortex (ACC).

84 s binding potential (BP(ND)) in the anterior cingulate cortex (ACC).

85 a subdivision of the mouse PFC, the anterior cingulate cortex (ACC).

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

87 1), and a deep cortical region, the anterior cingulate cortex (ACC, experiment 2), in macaques.

88 us accumbens) and cortical (insula, anterior cingulate cortex [ACC]) regions even in the absence of c

89 demonstrate frontal-insula-parietal-anterior cingulate cortex activation during the heartbeat detecti

90 Attenuation of anterior cingulate cortex activation for processing of panic-rela

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

92 Anterior cingulate cortex activity also reflected whether the int

93 men in smokers and decreased dorsal anterior cingulate cortex activity on nicotine across groups.

94 stimulation, to reversibly disrupt anterior cingulate cortex activity.

95 ed object category in the striatum, anterior cingulate cortex, amygdala, occipitotemporal cortex, and

96 e across lateral prefrontal cortex, anterior cingulate cortex and anterior striatum when outcomes wer

97 (i) FDG-PET uptake in the bilateral anterior cingulate cortex and anterior temporal pole was associat

98 hat activity in two brain areas-the anterior cingulate cortex and basal forebrain-tracks these contex

99 nterconnected subregions of primate anterior cingulate cortex and basal ganglia predict the moment of

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

101 clinical study, reduced precuneus/posterior cingulate cortex and hippocampal grey matter density wer

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

103 associated with cognitive control (anterior cingulate cortex and inferior frontal gyrus) helped dish

104 such as dorsal medial and lateral prefrontal/cingulate cortex and insula in maintaining anxiety respo

105 The dorsal anterior cingulate cortex and insula may play important roles in

106 obe, frontal lobe, supplementary motor area, cingulate cortex and insula were commonly activated both

107 r signals, b) arise earliest in the anterior cingulate cortex and later in dorsolateral prefrontal co

108 cted focusing on the left subgenual anterior cingulate cortex and left posterior cingulate cortex.

109 higher nodal centrality metrics in the left cingulate cortex and left thalamus.

110 ffspring had: (1) SST mRNA reductions in the cingulate cortex and nucleus accumbens shell, regardless

111 alities in connectivity between the anterior cingulate cortex and other prefrontal cortical regions m

112 nhanced pain responses in pregenual anterior cingulate cortex and periaqueductal gray.

113 ventral caudate and clusters within the mid-cingulate cortex and posterior cingulate cortex (n = 14,

114 ependent of age, dysfunction in the anterior cingulate cortex and posterior regions was more pronounc

115 d with schizotypy in the bilateral posterior cingulate cortex and precuneus (and for disorganized sch

116 with eigenvector centrality in the anterior cingulate cortex and primary motor cortex; and (iii) abn

117 the bilateral posterior insula, TPJ, middle cingulate cortex and putamen.

118 Simultaneous imaging of anterior cingulate cortex and SEF revealed a time delay in the di

119 c responses in anterior insula, anterior/mid-cingulate cortex and supplementary motor area, but showe

120 to the parasympathetic role of the anterior cingulate cortex and the AI.

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

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

123 Moreover, the anterior cingulate cortex and the temporoparietal junction update

124 tified a circuit between the dorsal anterior cingulate cortex and the ventral striatum that negativel

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

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

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

128 ventromedial prefrontal cortex, and anterior cingulate cortex) and decreased cortical thickness in ot

129 nsular cortex, bilateral precuneus/posterior cingulate cortex, and bilateral temporal, angular, and s

130 ateral orbitofrontal cortex, dorsal anterior cingulate cortex, and dorsolateral prefrontal cortex.

131 rus, prefrontal cortex, insula, and anterior cingulate cortex, and increases in activation in the par

132 n activation in the parietal lobe, posterior cingulate cortex, and inferior frontal gyrus in response

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

134 ntal cortex (orbital part of area 12 [12o]), cingulate cortex, and lateral prefrontal cortex.

135 e amygdala, hippocampus, pallidum, striatum, cingulate cortex, and prefrontal cortex using positron e

136 insula, somatosensory and premotor regions, cingulate cortex, and temporal cortex for control but no

137 areas: thalamus, ventral striatum, posterior cingulate cortex, and temporal cortex.

138 tegrated into a value signal in the anterior cingulate cortex, and the fidelity of this integration p

139 basolateral amygdala, hippocampus, anterior cingulate cortex, and ventral tegmental area.

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

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

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

143 The use of the anterior cingulate cortex as a target ROI resulted in larger effe

144 r medial prefrontal cortex and the posterior cingulate cortex, as reflected by higher correlation wit

145 ers in the bilateral insula, prefrontal, and cingulate cortex associated with the reduction in drinki

146 ily the ventral anterior insula and anterior cingulate cortex, based on functional connectivity patte

147 T-proBNP and GMD in the medial and posterior cingulate cortex but also in precuneus and hippocampus,

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

149 Here, we show that the mouse cingulate cortex (Cg) regulates visual processing not on

150 distress associated with weaker hippocampal-cingulate cortex connectivity and stronger hippocampal-t

151 trimester-associated with weaker hippocampal-cingulate cortex connectivity and stronger hippocampal-t

152 tress inversely correlated while hippocampal-cingulate cortex connectivity positively correlated with

153 The cingulate cortex contributes to complex, adaptive behavi

154 social anxiety group, their dorsal anterior cingulate cortex (dACC) activity did not covary with the

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

156 trolled decision-making, the dorsal anterior cingulate cortex (dACC) and dorsolateral prefrontal cort

157 errors and error history in dorsal anterior cingulate cortex (dACC) and pre-supplementary motor area

158 anges in pharmacoBOLD in the dorsal anterior cingulate cortex (dACC) and symptoms reflected on the Br

159 The dorsal anterior cingulate cortex (dACC) and the anterior insula (AI) con

160 uctured hierarchically, with dorsal anterior cingulate cortex (dACC) at the highest level, recruiting

161 Activity in the dorsal anterior cingulate cortex (dACC) is observed across a variety of

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

163 earch has suggested that the dorsal anterior cingulate cortex (dACC) plays a key role in nicotine dep

164 GSH in dorsal anterior cingulate cortex (dACC) was acquired as a secondary 3T (

165 of brain areas consisting of dorsal anterior cingulate cortex (dACC), anterior insula, and intraparie

166 efrontal cortex (DLPFC), the dorsal anterior cingulate cortex (dACC), the ventro-medial prefrontal co

167 f multivoxel activity in the dorsal anterior cingulate cortex (dACC), ventromedial prefrontal cortex

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

169 of the salience network (the dorsal anterior cingulate cortex [dACC] and the anterior insula) of 20 p

170 In one of the two, the anterior cingulate cortex did as well, but neither striatal regio

171 nted into the orbitofrontal cortex, anterior cingulate cortex, dorsal anterior striatum, and ventral

172 from three different brain regions (anterior cingulate cortex, dorsolateral prefrontal cortex, and pr

173 the vmPFC, hippocampus, and dorsal anterior cingulate cortex during this extinction retention test.

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

175 and macaques, and although the amygdala and cingulate cortex evolved to enable emotion and cognition

176 and highlight the critical role of anterior cingulate cortex for future-oriented cognition.

177 nuation of neural activation in the anterior cingulate cortex for processing of panic-trigger/panic-s

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

179 ablish the causal importance of the anterior cingulate cortex for this translation process, we used a

180 altered functional connectivity of anterior cingulate cortex, frontal association cortex, parasubicu

181 s within the default mode network (posterior cingulate cortex), frontoparietal network (left dorsolat

182 erved in humans: hippocampal-dorsal anterior cingulate cortex functional connectivity-but not hippoca

183 t superior temporal gyrus, ventral posterior cingulate cortex, globus pallidus, and calcarine cortex

184 es were 1.74, 1.79, 1.46, 0.80, and 0.77 for cingulate cortex, globus pallidus, insula, striatum, and

185 lling for CD symptoms while rostral anterior cingulate cortex GMV was negatively associated to CD sym

186 The anterior and posterior cingulate cortex have been implicated in adaptive decisi

187 nalyses identified portions of the subgenual cingulate cortex, hippocampus, amygdala, and putamen as

188 ntal cortex, ventral cingulate gyrus, dorsal cingulate cortex, hypothalamus, amygdala, right striatum

189 n progenitor cells into the rostral anterior cingulate cortex in a chemotherapy-induced neuropathic p

190 nectivity from the thalamus to the posterior cingulate cortex in a way that depended on serotonin 2A

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

192 ween the right precuneus and right posterior cingulate cortex in DMN, among CD patients compared to H

193 bic cortex in rodents or the dorsal anterior cingulate cortex in humans.

194 entromedial sectors, along with the anterior cingulate cortex in patients with clinical anxiety.

195 ith CB(1)R binding in prefrontal regions and cingulate cortex in pre-HD (range: r = -0.64 to -0.72; P

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

197 of the medial prefrontal cortex and anterior cingulate cortex in the developers compared with healthy

198 tween nucleus accumbens and rostral anterior cingulate cortex in the patients with persistent pain.

199 g lasting inhibition of the rostral anterior cingulate cortex, in the mouse, has a profound pain reli

200 ice, we show that orbitofrontal and anterior cingulate cortex inactivation impacts task performance,

201 e activity of the MMN from the left anterior cingulate cortex, inferior frontal gyrus, and middle fro

202 ively correlated with bout length (posterior cingulate cortex, inferior occipital cortex, middle temp

203 oral lobe, as well as in the mid-to-anterior cingulate cortex, influence heart rate.

204 The relative deactivation in anterior cingulate cortex, informed by our behavioral study, may

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

206 th cortical thickness of the dorsal anterior cingulate cortex, insula and medial orbitofrontal cortex

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

208 king, and emotional regulation, the anterior cingulate cortex is considered to have a key role in the

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

210 The standard partitioning of rodent cingulate cortex is inconsistent with that in any other

211 al and functional organisation within rodent cingulate cortex itself.

212 for inter-areal connections between anterior cingulate cortex, lateral prefrontal cortex and anterior

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

214 olinium retention in the neocortex (anterior cingulate cortex: mean gadolinium concentration, 0.28 ug

215 frontal and posterior regions (the anterior cingulate cortex, medial frontal gyrus, cuneus, precuneu

216 , -8; k=2,102 and k=1,305, respectively) and cingulate cortex/medial prefrontal cortex (-12, -8, 68;

217 ithin the mid-cingulate cortex and posterior cingulate cortex (n = 14, voxel-wise p < 0.005).

218 egions and patients except for the posterior cingulate cortex of 1 patient.

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

220 l activity in the orbitofrontal and anterior cingulate cortex of two monkeys performing a valuation t

221 with cortical regions including the anterior cingulate cortex, orbitofrontal cortex, and insula.

222 triatum (p = .005), pallidum (p = .023), and cingulate cortex (p = .018).

223 (P = .01), occipital cortex (P = .004), and cingulate cortex (P = .02), and was associated with smal

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

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

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

227 ere positively correlated with the posterior cingulate cortex (PCC) activation during action inhibiti

228 nsmokers indicates that MT reduces posterior cingulate cortex (PCC) activity.

229 uated with: the precuneus (P), the posterior cingulate cortex (PCC) and the dorsomedial prefrontal co

230 nterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) in 2 male rhesus monkeys performi

231 oimaging experiments implicate the posterior cingulate cortex (PCC) in episodic memory processing, ma

232 ht on the lesser-known role of the posterior cingulate cortex (PCC) in memory encoding.

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

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

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

236 ion was mediated indirectly by the posterior cingulate cortex (PCC) via the right inferior parietal l

237 Moreover, activation of the posterior cingulate cortex (PCC) was observed during the noxious s

238 functional differences in the left posterior cingulate cortex (PCC), right amygdala, left hippocampus

239 that partake in DMN function, the posterior cingulate cortex (PCC), temporal parietal junction (TPJ)

240 (PPC), and the medial parietal and posterior cingulate cortex (PCC).

241 hese activations overlapped in the posterior cingulate cortex (PCC).

242 )/inferior frontal gyrus (IFG) and posterior cingulate cortex (PCC)/precuneus, ranked as the second '

243 ciated with tachycardia, perigenual anterior cingulate cortex (pgACC) activity and pgACC-amygdala con

244 uch as p32 and p24 of the pregenual anterior cingulate cortex (pgACC).

245 Activity in anterior cingulate cortex predicted pupil diameter.

246 tathione synthesis (gclm(-/-)), the anterior cingulate cortex presented early in the development incr

247 the amygdala (r = -0.69, p < 0.01), anterior cingulate cortex (r = -0.56, p = 0.02), caudate (r = -0.

248 Baseline rostral anterior cingulate cortex (rACC) activity is a well-replicated no

249 ndent (BOLD) signals in the rostral anterior cingulate cortex (rACC) tracked the level of imbalance a

250 or insular cortex (aIC) and rostral anterior cingulate cortex (rACC), may play a pivotal role in expe

251 connecting the amygdala and rostral anterior cingulate cortex (rACC), which receive rich dopaminergic

252 different subregions in the rostral anterior cingulate cortex (rACC).

253 n the right anterior insula, dorsal anterior cingulate cortex (rdACC), and ventrolateral prefrontal c

254 ness and glial density in subgenual anterior cingulate cortex, reduced neuronal density in some amygd

255 rompt in anterior insula and anterior/middle cingulate cortex, respectively, suggesting heightened em

256 ted increased functional connectivity in the cingulate cortex, retrosplenial cortex, and thalamus con

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

258 frontal cortex (DLPFC) to subgenual anterior cingulate cortex (sgACC) circuit.

259 Subgenual anterior cingulate cortex (sgACC) hyper-activity during rest has

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

261 learning was observed in subgenual anterior cingulate cortex (sgACC), and switching after harming ot

262 ver-activation of primate subgenual anterior cingulate cortex (sgACC, area 25) blunts appetitive anti

263 ity within area 25 of the subgenual anterior cingulate cortex (sgACC/25) has been implicated in these

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

265 anterior medial prefrontal/rostral anterior cingulate cortex showed an interaction between group (PD

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

267 supplementary motor area (or dorsal anterior cingulate cortex) showed a shared neural pattern respons

268 er the medial prefrontal cortex and anterior cingulate cortex significantly improved OCD symptoms and

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

270 stead found deactivation in insula, anterior cingulate cortex, superior temporal gyrus, amygdala, par

271 ractivation in the bilateral dorsal anterior cingulate cortex, supplementary motor area, and pre-supp

272 lot, while a network consisting of posterior cingulate cortex, temporoparietal junction, and medial p

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

274 ly interconnected circuits with the anterior cingulate cortex that anchors the salience network, a sy

275 o layer 5 of human frontoinsula and anterior cingulate cortex that appear to be selectively vulnerabl

276 ncoding, within multiple regions in mPFC and cingulate cortex that are critical for value-based decis

277 elates to a change in the pregenual anterior cingulate cortex that corresponds to increased activity

278 elated to a change in the pregenual anterior cingulate cortex that corresponds to increased activity

279 assessments in a sub-region of the anterior cingulate cortex (the prelimbic [PL] area) and striatum.

280 cluding dorsolateral prefrontal and anterior cingulate cortex, the phenomenon was most consistent wit

281 inhibitory circuits in the rostral anterior cingulate cortex underlies the affective (aversive), but

282 reward-processing areas such as the anterior cingulate cortex, ventral striatum, and insula.

283 cortical thickness in some areas (posterior cingulate cortex, ventromedial prefrontal cortex, and an

284 eporting STBs, and there is reduced anterior cingulate cortex volume related to STBs and NSSI.

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

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

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

288 CT in the middle cingulate cortex was inversely related to ELT in both ag

289 prefrontal cortex, orbitofrontal cortex, and cingulate cortex was positively correlated with improvem

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

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

292 teral nucleus accumbens and rostral anterior cingulate cortex were associated with positive response

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

294 medial prefrontal cortex and caudal anterior cingulate cortex were negatively associated to ADHD symp

295 cluding superior temporal gyrus and anterior cingulate cortex, were most abnormal in terms of modular

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

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

298 We identified neurons in the dorsal anterior cingulate cortex whose responses track these three varia

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

300 d MRI scanning, that in addition to anterior cingulate cortex within medial frontal cortex, a group o