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

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

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

3 of overall uncertainty in insula and dorsal anterior cingulate cortex.

4 rgeting the medial prefrontal cortex and the anterior cingulate cortex.

5 regions: dorsolateral prefrontal cortex and anterior cingulate cortex.

6 including dorsolateral prefrontal cortex and anterior cingulate cortex.

7 measuring glutamate levels in the bilateral anterior cingulate cortex.

8 ch negativity, suggesting the involvement of anterior cingulate cortex.

9 nts populated both the rostral and posterior anterior cingulate cortex.

10 e anterior lateral prefrontal cortex and the anterior cingulate cortex.

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

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

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

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

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

16 ngs of a smaller structure in prefrontal and anterior cingulate cortex.

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

18 gions, including ventromedial prefrontal and anterior cingulate cortex.

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

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

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

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

23 ses (limbic class), with an epicenter in the anterior cingulate cortex.

24 onally defined areas that form the pregenual anterior cingulate cortex.

25 poral cortex and diminished responses within anterior cingulate cortex.

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

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

28 ed connectivity between the amygdala and the anterior cingulate cortex, a network involved in regulat

29 xious individuals failed to use their dorsal anterior cingulate cortex, a region known to adjust lear

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

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

32 Recent work has identified the anterior cingulate cortex (ACC) among other brain region

33 frontal theta power (7-9 Hz, ~120 ms) in mid-anterior cingulate cortex (ACC) and a later beta power s

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

35 e+glutamine (Glx), and GABA levels in dorsal anterior cingulate cortex (ACC) and glutamate and Glx le

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

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

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

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

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

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

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

43 from individual neurons in parts of both the anterior cingulate cortex (ACC) and posterior cingulate

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

45 egions of the prefrontal cortex, namely, the anterior cingulate cortex (ACC) and somatomotor cortex (

46 The medial thalamus (MThal), anterior cingulate cortex (ACC) and striatum play import

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

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

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

50 Previous research has focused on the anterior cingulate cortex (ACC) as a key brain region in

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

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

53 and observed early strong activation of the anterior cingulate cortex (ACC) corresponding to the nox

54 responders showed an increase in NAc-dorsal anterior cingulate cortex (ACC) FC relative to non-respo

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

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

57 Research has implicated the anterior cingulate cortex (ACC) in attaching value to so

58 responses in the amygdala in both sexes, the anterior cingulate cortex (ACC) in females, and the hipp

59 gic synapses in the pyramidal neurons of the anterior cingulate cortex (ACC) in mice with a mutation

60 f the medial prefrontal cortex including the anterior cingulate cortex (ACC) in social cognition in a

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 disrupted glutamate metabolism in pregenual anterior cingulate cortex (ACC) in type 1 diabetes (T1D)

64 The anterior cingulate cortex (ACC) is important for decisio

65 at a part of the frontal cortex known as the anterior cingulate cortex (ACC) is particularly well sui

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

67 Hyperexcitability of the anterior cingulate cortex (ACC) is thought to drive aver

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

69 le increased connectivity to pain areas like anterior cingulate cortex (ACC) might underlie maladapti

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

71 oma of layer 5 (L5) pyramidal neurons in the anterior cingulate cortex (ACC) of adult male mice we fo

72 d from dorsomedial frontal cortex (DMFC) and anterior cingulate cortex (ACC) of monkeys in a task in

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

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

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

76 TSPO V(T) in the prefrontal cortex (PFC) and anterior cingulate cortex (ACC) predicts reduction of de

77 tial decision task for mice to show that the anterior cingulate cortex (ACC) predicts the state that

78 sile and colleagues show that removal of the anterior cingulate cortex (ACC) prevents monkeys from le

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

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

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

82 lutamate levels in the left thalamus and the anterior cingulate cortex (ACC) were measured using 1[H]

83 substudy examined effects on activity in the anterior cingulate cortex (ACC), a brain region importan

84 lf-administration disrupts neural signals in anterior cingulate cortex (ACC), a brain region thought

85 neural correlates of this phenomenon in the anterior cingulate cortex (ACC), a brain structure impli

86 om severity, and lower mPFC FC with adjacent anterior cingulate cortex (ACC), a crucial region of emo

87 encodes the sensory pain information, to the anterior cingulate cortex (ACC), a key area for processi

88 d decreased positive FC between amygdala and anterior cingulate cortex (ACC), and had increased posit

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

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

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

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

93 lutamate and glutamine concentrations in the anterior cingulate cortex (ACC), left insula, and visual

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

95 ss 16 brain regions, including the amygdala, anterior cingulate cortex (ACC), nucleus accumbens (NAcc

96 amics in the S1, primary visual cortex (V1), anterior cingulate cortex (ACC), posterior parietal cort

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

98 Several brain regions, including the anterior cingulate cortex (ACC), were sensitive to an in

99 the structure of children's hippocampus and anterior cingulate cortex (ACC).

100 om LC to cortex modulates belief updating in anterior cingulate cortex (ACC).

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

102 utcome was binding potential (BP(ND)) in the anterior cingulate cortex (ACC).

103 uts from a subdivision of the mouse PFC, the anterior cingulate cortex (ACC).

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

105 periment 1), and a deep cortical region, the anterior cingulate cortex (ACC, experiment 2), in macaqu

106 en, nucleus accumbens) and cortical (insula, anterior cingulate cortex [ACC]) regions even in the abs

107 Adults demonstrate frontal-insula-parietal-anterior cingulate cortex activation during the heartbea

108 Attenuation of anterior cingulate cortex activation for processing of p

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

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

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

112 Anterior cingulate cortex activity also reflected whethe

113 ight putamen in smokers and decreased dorsal anterior cingulate cortex activity on nicotine across gr

114 ltrasound stimulation, to reversibly disrupt anterior cingulate cortex activity.

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

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

117 reinforced object category in the striatum, anterior cingulate cortex, amygdala, occipitotemporal co

118 ynchronize across lateral prefrontal cortex, anterior cingulate cortex and anterior striatum when out

119 gs were: (i) FDG-PET uptake in the bilateral anterior cingulate cortex and anterior temporal pole was

120 We show that activity in two brain areas-the anterior cingulate cortex and basal forebrain-tracks the

121 work of interconnected subregions of primate anterior cingulate cortex and basal ganglia predict the

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

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

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

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

126 in areas associated with cognitive control (anterior cingulate cortex and inferior frontal gyrus) he

127 The dorsal anterior cingulate cortex and insula may play important

128 tion error signals, b) arise earliest in the anterior cingulate cortex and later in dorsolateral pref

129 was conducted focusing on the left subgenual anterior cingulate cortex and left posterior cingulate c

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

131 al abnormalities in connectivity between the anterior cingulate cortex and other prefrontal cortical

132 ngs and enhanced pain responses in pregenual anterior cingulate cortex and periaqueductal gray.

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

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

135 were independent of age, dysfunction in the anterior cingulate cortex and posterior regions was more

136 egatively with eigenvector centrality in the anterior cingulate cortex and primary motor cortex; and

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

138 Simultaneous imaging of anterior cingulate cortex and SEF revealed a time delay

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

140 correlate to the parasympathetic role of the anterior cingulate cortex and the AI.

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

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

143 Moreover, the anterior cingulate cortex and the temporoparietal juncti

144 mans identified a circuit between the dorsal anterior cingulate cortex and the ventral striatum that

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 cortex, ventromedial prefrontal cortex, and anterior cingulate cortex) and decreased cortical thickn

150 -0.163; P = .001) (extending into the right anterior cingulate cortex), and left fusiform gyrus (SDM

151 to the lateral orbitofrontal cortex, dorsal anterior cingulate cortex, and dorsolateral prefrontal c

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

153 entral gyrus, prefrontal cortex, insula, and anterior cingulate cortex, and increases in activation i

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

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

156 two is integrated into a value signal in the anterior cingulate cortex, and the fidelity of this inte

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

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

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

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

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

162 The use of the anterior cingulate cortex as a target ROI resulted in la

163 of primarily the ventral anterior insula and anterior cingulate cortex, based on functional connectiv

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

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

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

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

168 e the low social anxiety group, their dorsal anterior cingulate cortex (dACC) activity did not covary

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

170 al to controlled decision-making, the dorsal anterior cingulate cortex (dACC) and dorsolateral prefro

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

172 monitored errors and error history in dorsal anterior cingulate cortex (dACC) and pre-supplementary m

173 nduced changes in pharmacoBOLD in the dorsal anterior cingulate cortex (dACC) and symptoms reflected

174 The dorsal anterior cingulate cortex (dACC) and the anterior insula

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

176 to be structured hierarchically, with dorsal anterior cingulate cortex (dACC) at the highest level, r

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

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

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

180 Activity in the dorsal anterior cingulate cortex (dACC) is observed across a va

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

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

183 rable research has suggested that the dorsal anterior cingulate cortex (dACC) plays a key role in nic

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

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

186 GSH in dorsal anterior cingulate cortex (dACC) was acquired as a secon

187 network of brain areas consisting of dorsal anterior cingulate cortex (dACC), anterior insula, and i

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

189 ateral prefrontal cortex (DLPFC), the dorsal anterior cingulate cortex (dACC), the ventro-medial pref

190 atterns of multivoxel activity in the dorsal anterior cingulate cortex (dACC), ventromedial prefronta

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

192 re nodes of the salience network (the dorsal anterior cingulate cortex [dACC] and the anterior insula

193 In one of the two, the anterior cingulate cortex did as well, but neither stria

194 ely implanted into the orbitofrontal cortex, anterior cingulate cortex, dorsal anterior striatum, and

195 rocytes) from three different brain regions (anterior cingulate cortex, dorsolateral prefrontal corte

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

197 g between the vmPFC, hippocampus, and dorsal anterior cingulate cortex during this extinction retenti

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

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

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

201 and attenuation of neural activation in the anterior cingulate cortex for processing of panic-trigge

202 To establish the causal importance of the anterior cingulate cortex for this translation process,

203 ation and altered functional connectivity of anterior cingulate cortex, frontal association cortex, p

204 n was observed in humans: hippocampal-dorsal anterior cingulate cortex functional connectivity-but no

205 en controlling for CD symptoms while rostral anterior cingulate cortex GMV was negatively associated

206 nterneuron progenitor cells into the rostral anterior cingulate cortex in a chemotherapy-induced neur

207 he prelimbic cortex in rodents or the dorsal anterior cingulate cortex in humans.

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

209 al, and ventromedial sectors, along with the anterior cingulate cortex in patients with clinical anxi

210 ruitment of the medial prefrontal cortex and anterior cingulate cortex in the developers compared wit

211 served between nucleus accumbens and rostral anterior cingulate cortex in the patients with persisten

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

213 e and long lasting inhibition of the rostral anterior cingulate cortex, in the mouse, has a profound

214 tics in mice, we show that orbitofrontal and anterior cingulate cortex inactivation impacts task perf

215 The source activity of the MMN from the left anterior cingulate cortex, inferior frontal gyrus, and m

216 dial temporal lobe, as well as in the mid-to-anterior cingulate cortex, influence heart rate.

217 The relative deactivation in anterior cingulate cortex, informed by our behavioral st

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

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

220 ations with cortical thickness of the dorsal anterior cingulate cortex, insula and medial orbitofront

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

222 cision-making, and emotional regulation, the anterior cingulate cortex is considered to have a key ro

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

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

225 cific gadolinium retention in the neocortex (anterior cingulate cortex: mean gadolinium concentration

226 n in some frontal and posterior regions (the anterior cingulate cortex, medial frontal gyrus, cuneus,

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

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

229 60172 and ACEA into the infralimbic, but not anterior cingulate, cortex mitigated decision-making def

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

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

232 d neuronal activity in the orbitofrontal and anterior cingulate cortex of two monkeys performing a va

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

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

235 ectivity with cortical regions including the anterior cingulate cortex, orbitofrontal cortex, and ins

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

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

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

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

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

241 was associated with tachycardia, perigenual anterior cingulate cortex (pgACC) activity and pgACC-amy

242 areas, such as p32 and p24 of the pregenual anterior cingulate cortex (pgACC).

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

244 Subgenual anterior cingulate cortex postmortem samples from four M

245 Activity in anterior cingulate cortex predicted pupil diameter.

246 it of glutathione synthesis (gclm(-/-)), the anterior cingulate cortex presented early in the develop

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

248 Baseline rostral anterior cingulate cortex (rACC) activity is a well-repl

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

250 evel-dependent (BOLD) signals in the rostral anterior cingulate cortex (rACC) tracked the level of im

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

252 he anterior insular cortex (aIC) and rostral anterior cingulate cortex (rACC), may play a pivotal rol

253 pathways connecting the amygdala and rostral anterior cingulate cortex (rACC), which receive rich dop

254 (FC) to different subregions in the rostral anterior cingulate cortex (rACC).

255 nchored in the right anterior insula, dorsal anterior cingulate cortex (rdACC), and ventrolateral pre

256 cal thickness and glial density in subgenual anterior cingulate cortex, reduced neuronal density in s

257 teral prefrontal cortex (DLPFC) to subgenual anterior cingulate cortex (sgACC) circuit.

258 Subgenual anterior cingulate cortex (sgACC) hyper-activity during

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

260 ree moral learning was observed in subgenual anterior cingulate cortex (sgACC), and switching after h

261 ow that over-activation of primate subgenual anterior cingulate cortex (sgACC, area 25) blunts appeti

262 ted activity within area 25 of the subgenual anterior cingulate cortex (sgACC/25) has been implicated

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

264 come, the anterior medial prefrontal/rostral anterior cingulate cortex showed an interaction between

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

266 tral pre-supplementary motor area (or dorsal anterior cingulate cortex) showed a shared neural patter

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

268 y dTMS over the medial prefrontal cortex and anterior cingulate cortex significantly improved OCD sym

269 High activities of the anterior cingulate cortex significantly mediated relatio

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

271 ch, we instead found deactivation in insula, anterior cingulate cortex, superior temporal gyrus, amyg

272 owed hyperactivation in the bilateral dorsal anterior cingulate cortex, supplementary motor area, and

273 unctionally interconnected circuits with the anterior cingulate cortex that anchors the salience netw

274 tricted to layer 5 of human frontoinsula and anterior cingulate cortex that appear to be selectively

275 innitus relates to a change in the pregenual anterior cingulate cortex that corresponds to increased

276 itus is related to a change in the pregenual anterior cingulate cortex that corresponds to increased

277 tological assessments in a sub-region of the anterior cingulate cortex (the prelimbic [PL] area) and

278 gions, including dorsolateral prefrontal and anterior cingulate cortex, the phenomenon was most consi

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

280 nction of inhibitory circuits in the rostral anterior cingulate cortex underlies the affective (avers

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

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

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

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

285 g youth reporting STBs, and there is reduced anterior cingulate cortex volume related to STBs and NSS

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

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

288 ween bilateral nucleus accumbens and rostral anterior cingulate cortex were associated with positive

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

290 ral/dorsomedial prefrontal cortex and caudal anterior cingulate cortex were negatively associated to

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

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

293 renia, including superior temporal gyrus and anterior cingulate cortex, were most abnormal in terms o

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

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

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

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

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

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

300 high-field MRI scanning, that in addition to anterior cingulate cortex within medial frontal cortex,