ライフサイエンスコーパス: anterior cingulate

1 dorsomedial prefrontal cortex including the anterior cingulate.

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

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

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

5 on of an aversive interoceptive event in the anterior cingulate and bilateral anterior insula and rig

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

7 regions, including insula, middle occipital, anterior cingulate and fusiform gyrus, amygdala, striatu

8 increased N-acetyl-l-aspartate (NAA) in the anterior cingulate and insular cortices, and decreased N

9 s, marmosets show differential activation in anterior cingulate and lateral prefrontal cortices while

10 ciated with greater attenuation in bilateral anterior cingulate and left insula.

11 ed by activation of MORs at inputs from both anterior cingulate and medial prefrontal cortices as wel

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

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

14 ntrality positively in the ventral striatum, anterior cingulate and somatosensory cortex, and negativ

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

16 of brain regions whose cortical hubs are the anterior cingulate and ventral anterior insular (i.e., f

17 areas with the goal of capturing prefrontal, anterior cingulate, and basal ganglia connections linked

18 nuated activation in the amygdala, bilateral anterior cingulate, and bilateral insula during the emot

19 her cortical thickness in medial prefrontal, anterior cingulate, and orbitofrontal areas.

20 havioral adjustments in dorsomedial frontal, anterior cingulate, and orbitofrontal cortex.

21 than in three other brain regions (amygdala, anterior cingulate, and prefrontal cortex).

22 owing a brief review of prefrontal cortical, anterior cingulate, and striatal connections and the dif

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

24 istinct areas may interact through pregenual anterior cingulate area 32 (A32), which is strongly conn

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

124 Attenuation of anterior cingulate cortex activation for processing of p

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 Anterior cingulate cortex activity also reflected whethe

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

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

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

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

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

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

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

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

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

138 The dorsal anterior cingulate cortex and insula may play important

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

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

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

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

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

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

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

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

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

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

149 Moreover, the anterior cingulate cortex and the temporoparietal juncti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 Activity in anterior cingulate cortex predicted pupil diameter.

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

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

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

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

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

182 High activities of the anterior cingulate cortex significantly mediated relatio

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

233 poral cortex and diminished responses within anterior cingulate cortex.

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

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

236 regions: dorsolateral prefrontal cortex and anterior cingulate cortex.

237 including dorsolateral prefrontal cortex and anterior cingulate cortex.

238 measuring glutamate levels in the bilateral anterior cingulate cortex.

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

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

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

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

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

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

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

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

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

248 gions, including ventromedial prefrontal and anterior cingulate cortex.

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

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

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

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

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

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

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

256 genes, as well as variation in prelimbic and anterior cingulate cortical thickness at postnatal Day 1

257 h controls, in anterior middle and pregenual anterior cingulate cortices (aMCC, pgACC).

258 nhibitory control in the rostral and ventral anterior cingulate cortices and bilateral thalamus/cauda

259 ) was significantly lower in the frontal and anterior cingulate cortices in schizophrenia with large

260 interplay between the rostral and posterior anterior cingulate cortices must be considered when exam

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

262 ferotemporal, entorhinal, retrosplenial, and anterior cingulate cortices, the subicular complex, and

263 and enhanced activation in the posterior and anterior cingulate cortices.

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

265 tly lower right ventral striatum-left caudal anterior cingulate FC to loss (OBP versus OCP: p = 0.028

266 hat lower right ventral striatum-left caudal anterior cingulate FC to loss and greater right pars orb

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

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

269 gic social behavior of primates and that the anterior cingulate gyrus and the mSTS support these comp

270 een the basolateral amygdala and the rostral anterior cingulate gyrus of the medial prefrontal cortex

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

272 euronal populations from four brain regions (anterior cingulate gyrus, hippocampus, prefrontal cortex

273 Neurons in the anterior cingulate gyrus, previously implicated in vicar

274 y relevant brain regions (prefrontal cortex, anterior cingulate, hippocampus) and primary visual cort

275 ith complex cognition are connected with the anterior cingulate in a pattern that allows them to indi

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

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

278 y identified here.SIGNIFICANCE STATEMENT The anterior cingulate is a critical hub in prefrontal netwo

279 with areal expansion of lateral prefrontal, anterior cingulate, lateral temporal, and superior parie

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

281 ried with bilateral parietal, precuneus, and anterior cingulate metabolism; visual hallucinations (VH

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

283 global information in the superior frontal, anterior cingulate, middle temporal gyrus, and precuneus

284 rrelated with central potentials, evoking an anterior cingulate origin.

285 he bilateral insulae/orbitofrontal cortices, anterior cingulate/paracingulate gyri, and inferior pari

286 nce spectroscopy ((1)H MRS) in the pregenual anterior cingulate (pgACC) and occipital cortices (OCC)

287 recruited medial prefrontal cortex/pregenual anterior cingulate (pgACC).

288 mechanism for emotional regulation, with the anterior cingulate playing a balancing role for integrat

289 ula, superior frontal gyrus, putamen, dorsal anterior cingulate, posterior cingulate, and amygdala.

290 BAergic VTA projections to 10 target nuclei: anterior cingulate, prelimbic, and infralimbic cortex; n

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

292 ter recruitment of the medial prefrontal and anterior cingulate regions during failed inhibition acco

293 chological tests dependent on prefrontal and anterior cingulate regions, showing that while performan

294 f Pennsylvania cases were cut from amygdala, anterior cingulate, superior/mid-temporal, and middle fr

295 e ventromedial prefrontal cortex, the dorsal anterior cingulate, the dorsolateral prefrontal cortex,

296 irectly control downstream activity from the anterior cingulate to the subgenual cingulate, which is

297 frontal top-down neurons projecting from the anterior cingulate to visual cortex are highly functiona

298 rd-related regions (e.g. putamen, perigenual anterior cingulate/ventromedial prefrontal cortex) could

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

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