ライフサイエンスコーパス: cingulate

1 e anterior insula and anterior and posterior cingulate.

2 aversive interoceptive event in the anterior cingulate and bilateral anterior insula and right inferi

3 usion was found in APOE epsilon4+group (left cingulate and lateral frontal and parietal regions p<0.0

4 ets show differential activation in anterior cingulate and lateral prefrontal cortices while they vie

5 th greater attenuation in bilateral anterior cingulate and left insula.

6 ivation of MORs at inputs from both anterior cingulate and medial prefrontal cortices as well as at b

7 ndividual layer 2/3 pyramidal neurons in the cingulate and medial secondary motor subregions of the m

8 ions post-training (right cerebellum, middle cingulate and medial superior gyrus and left postcentral

9 Centrality of cingulate and orbito-frontal as well as other brain area

10 development and maturation, particularly in cingulate and orbitofrontal regions.

11 a continued research focus on the subgenual cingulate and other selected regions' role in depression

12 n white matter bundles innervating posterior cingulate and parietal cortex, basal ganglia, and tempor

13 Cingulate and prefrontal regions did not fully replicate

14 positively in the ventral striatum, anterior cingulate and somatosensory cortex, and negatively in th

15 regions whose cortical hubs are the anterior cingulate and ventral anterior insular (i.e., frontoinsu

16 l lobule [IPL], prefrontal cortex [PFC], and cingulate), and aimed to visualize this using diffusion

17 utamen, dorsal anterior cingulate, posterior cingulate, and amygdala.

18 h the goal of capturing prefrontal, anterior cingulate, and basal ganglia connections linked to the l

19 tivation in the amygdala, bilateral anterior cingulate, and bilateral insula during the emotion face-

20 sensory cortex, whereas activity in insular, cingulate, and motor regions is best explained in terms

21 cal thickness in medial prefrontal, anterior cingulate, and orbitofrontal areas.

22 adjustments in dorsomedial frontal, anterior cingulate, and orbitofrontal cortex.

23 teral dorsolateral-frontal cortex, posterior cingulate, and parietal metabolism; and rapid eye moveme

24 abolism (temporoparietal, frontal, posterior cingulate, and precuneus cortices) and relative increase

25 hree other brain regions (amygdala, anterior cingulate, and prefrontal cortex).

26 rief review of prefrontal cortical, anterior cingulate, and striatal connections and the different me

27 frontoparietal, medial prefrontal-posterior cingulate, and subcortical-posterior insular cortices, w

28 nd in children with ADHD, mainly in frontal, cingulate, and temporal regions; the largest significant

29 ition, while the most ventromedial subgenual cingulate area 25 (A25) is associated with emotion and e

30 reas may interact through pregenual anterior cingulate area 32 (A32), which is strongly connected wit

31 ait anxiety reveals dysregulation in primate cingulate areas 25 and 32 and the anterior hippocampus (

32 is revealed that sensorimotor, parietal, and cingulate brain areas all contributed to the reduced P30

33 ocampus, para hippocampus, amygdala, insula, cingulate, caudate, thalamus, and cerebellum) in T2DM pa

34 prefrontal, hippocampus, amygdala, insular, cingulate, cerebellum, caudate, basal-forebrain, and tha

35 cortex and elevated levels in the posterior cingulate, consistent with white matter and social-brain

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

110 stimulation, to reversibly disrupt anterior cingulate cortex activity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

140 The cingulate cortex contributes to complex, adaptive behavi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

158 al and functional organisation within rodent cingulate cortex itself.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

179 For cingulate cortex, a structure implicated in behavioural

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 fined areas that form the pregenual anterior cingulate cortex.

216 ut focal thickness reduction in temporal and cingulate cortex.

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

218 ly increased from parietal to prefrontal and cingulate cortex.

219 ll uncertainty in insula and dorsal anterior cingulate cortex.

220 tex and diminished responses within anterior cingulate cortex.

221 affective networks are located in regions of cingulate cortex.

222 he medial prefrontal cortex and the anterior cingulate cortex.

223 complementary roles of the amygdala and the cingulate cortex.

224 dorsolateral prefrontal cortex and anterior cingulate cortex.

225 dorsolateral prefrontal cortex and anterior cingulate cortex.

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

227 g glutamate levels in the bilateral anterior cingulate cortex.

228 on the nonhomologous partitioning of rodent cingulate cortex.

229 vity, suggesting the involvement of anterior cingulate cortex.

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

231 ortex, temporoparietal junction, and rostral cingulate cortex.

232 smaller structure in prefrontal and anterior cingulate cortex.

233 anterior cingulate cortex and left posterior cingulate cortex.

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

235 , -8; k=2,102 and k=1,305, respectively) and cingulate cortex/medial prefrontal cortex (-12, -8, 68;

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

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

238 ions known to project to frontal, motor, and cingulate cortical areas.

239 well as variation in prelimbic and anterior cingulate cortical thickness at postnatal Day 1 (P1) in

240 s, in anterior middle and pregenual anterior cingulate cortices (aMCC, pgACC).

241 was identified, which included the thalamus, cingulate cortices (anterior, mid- and posterior), cauda

242 control in the rostral and ventral anterior cingulate cortices and bilateral thalamus/caudate, as we

243 ere associated with higher GWC in insula and cingulate cortices and with lower GWC in pre- and postce

244 LGI in the precuneus and cingulate cortices correlated positively with IQ scores

245 nificantly lower in the frontal and anterior cingulate cortices in schizophrenia with large effect si

246 y between the rostral and posterior anterior cingulate cortices must be considered when examining cir

247 c inclusions in the prefrontal, temporal and cingulate cortices or the underlying white matter might

248 Regions of the prefrontal and cingulate cortices play important roles in the regulatio

249 sure revealed that activity of the thalamus, cingulate cortices, and angular gyri are fundamental for

250 only at baseline in the anterior and medial cingulate cortices, as well as in the prefrontal cortex

251 the thalamus, anterior, middle and posterior cingulate cortices, caudate nucleus and nucleus accumben

252 ral, entorhinal, retrosplenial, and anterior cingulate cortices, the subicular complex, and the dorsa

253 d aberrant GBC changes in the prefrontal and cingulate cortices, warranting further investigations of

254 ced activation in the posterior and anterior cingulate cortices.

255 ciated with pain processing, the insular and cingulate cortices.

256 gyrus (SFG), supramarginal gyrus (SMG), and cingulate gyrus (CG) from 4 parcellation protocols as im

257 gyrus and the bilateral middle and posterior cingulate gyrus (N = 187).

258 l behavior of primates and that the anterior cingulate gyrus and the mSTS support these computations.

259 asolateral amygdala and the rostral anterior cingulate gyrus of the medial prefrontal cortex while mo

260 th reduced fractional anisotropy in the left cingulate gyrus part of the cingulum, left posterior tha

261 brain regions, including the precuneus, the cingulate gyrus, and the hippocampus, regions commonly a

262 opulations from four brain regions (anterior cingulate gyrus, hippocampus, prefrontal cortex, and nuc

263 a bilateral lower activity in the posterior cingulate gyrus, insula and precuneus in the bed rest gr

264 Neurons in the anterior cingulate gyrus, previously implicated in vicarious rein

265 milar eigenvector centrality patterns in the cingulate had previously been associated to CSF biomarke

266 t brain regions (prefrontal cortex, anterior cingulate, hippocampus) and primary visual cortex for co

267 ex cognition are connected with the anterior cingulate in a pattern that allows them to indirectly co

268 ied here.SIGNIFICANCE STATEMENT The anterior cingulate is a critical hub in prefrontal networks throu

269 bilateral parietal, precuneus, and anterior cingulate metabolism; visual hallucinations (VH) with bi

270 nformation in the superior frontal, anterior cingulate, middle temporal gyrus, and precuneus regions.

271 ent (BP1, generated in the supplementary and cingulate motor area) was linked to motivational, intent

272 r (globus pallidus, thalamus), and cortices (cingulate, motor, somatosensory, entorhinal).

273 an macaque neurons in both regions, and that cingulate neurons are more efficient than amygdala neuro

274 Thus, certain cingulate neurons encode diverse, evaluative signals nee

275 ant variables that are encoded by individual cingulate neurons.

276 l cortex (p(adj) = 0.03) and right posterior cingulate (p(adj) = 0.04), brain areas associated with e

277 ral insulae/orbitofrontal cortices, anterior cingulate/paracingulate gyri, and inferior parietal cort

278 network, associations between left posterior cingulate (PCC) and right retrosplenial cortical activit

279 medial prefrontal cortex/pregenual anterior cingulate (pgACC).

280 for emotional regulation, with the anterior cingulate playing a balancing role for integration of co

281 rior frontal gyrus, putamen, dorsal anterior cingulate, posterior cingulate, and amygdala.

282 TA projections to 10 target nuclei: anterior cingulate, prelimbic, and infralimbic cortex; nucleus ac

283 itment of the medial prefrontal and anterior cingulate regions during failed inhibition accords with

284 ausal role of these different prefrontal and cingulate regions in threat-elicited behaviors from expe

285 including frontal, parietal, posterior, and cingulate regions with the results being remarkably cons

286 l tests dependent on prefrontal and anterior cingulate regions, showing that while performance on the

287 een functional connectivity in the posterior cingulate/retrosplenial cortex and precuneus and both ag

288 Deep brain stimulation of the subcallosal cingulate (SCC DBS) has been studied as a potential trea

289 ption of C(4) plants, whereas litopterns and cingulates show delta(13)C values that remain mostly wit

290 somesial activity and the latter with dorsal cingulate, striatal and anterior insular activity.

291 Furthermore, the relationship between cingulate-striatal brain circuits and nicotine dependenc

292 analysis with the striatum recapitulated the cingulate-striatum relationship observed in humans.

293 vania cases were cut from amygdala, anterior cingulate, superior/mid-temporal, and middle frontal gyr

294 ltimodal integration network (insula, dorsal cingulate, temporoparietal junction (TPJ)) is implicated

295 edial prefrontal cortex, the dorsal anterior cingulate, the dorsolateral prefrontal cortex, and the l

296 at specific locations on the right cingulum cingulate, the right cingulum hippocampus and anterior c

297 ontrol downstream activity from the anterior cingulate to the subgenual cingulate, which is associate

298 op-down neurons projecting from the anterior cingulate to visual cortex are highly functionally integ

299 d regions (e.g. putamen, perigenual anterior cingulate/ventromedial prefrontal cortex) could distingu

300 from the anterior cingulate to the subgenual cingulate, which is associated with heightened activity