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1 la), and conflict monitoring (e.g., anterior cingulate cortex).
2 itofrontal cortex, hippocampus, and anterior cingulate cortex).
3 nd the salience network (insula and anterior cingulate cortex).
4 uctal gray, hippocampus, and dorsal anterior cingulate cortex.
5 cluding ventromedial prefrontal and anterior cingulate cortex.
6 superior occipital gyrus/cuneus and anterior cingulate cortex.
7 xercise in an executive region, the anterior cingulate cortex.
8 the medial wall, and the rostral and caudal cingulate cortex.
9 and midline cerebellar vermis and subgenual cingulate cortex.
10 perior colliculus and anterior and posterior cingulate cortex.
11 sfunction of the GABAergic system within the cingulate cortex.
12 ippocampus, parahippocampus and parts of the cingulate cortex.
13 a region to which it projects, the anterior cingulate cortex.
14 g the parahippocampal gyrus to the posterior cingulate cortex.
15 sula, supplementary motor area, and anterior cingulate cortex.
16 d for stimulation-avoiders, in the posterior cingulate cortex.
17 und 12% of all GABAergic interneurons in the cingulate cortex.
18 properties of GABAergic interneurons in the cingulate cortex.
19 wever, there were no changes in the anterior cingulate cortex.
20 m, restricted to the retrosplenial/posterior cingulate cortex.
21 pregenual and subgenual regions of anterior cingulate cortex.
22 ween the parahippocampal gyrus and posterior cingulate cortex.
23 gs predicted activation only in the anterior cingulate cortex.
24 sequencing data set (N=61) from the anterior cingulate cortex.
25 ear to be conflict-related signals in monkey cingulate cortex.
26 otion streams in the temporal, parietal, and cingulate cortex.
27 ulation of neurons within the mouse anterior cingulate cortex.
28 ciated with reduced activity in the anterior cingulate cortex.
29 l prefrontal cortex, and the dorsal anterior cingulate cortex.
30 ism in the left pSTS and bilateral posterior cingulate cortex.
31 erve executive functions orchestrated by the cingulate cortex.
32 ciated with tinnitus distress, including the cingulate cortex.
33 ral parietal lobules, and the left posterior cingulate cortex.
34 ntral striatum, dorsal putamen, and anterior cingulate cortex.
35 h stronger engagement of the dorsal anterior cingulate cortex.
36 ompanied by oxidative stress in the anterior cingulate cortex.
37 ompared to controls in regions including the cingulate cortex (1.6-fold increase) and the reticular f
38 ists of lesions made within the anterior mid-cingulate cortex, 20 patients with treatment-resistant d
39 s (mean, 32%; range, 31%-36% except anterior cingulate cortex, 24%; analysis of variance, effect of d
41 the retrosplenial cortex (RSC) and anterior cingulate cortex (ACA) contain a large number of neurons
43 ould be associated with overlapping anterior cingulate cortex (ACC) and insular volumetric reductions
47 en the EPN and projections from the anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC) to
48 density in the ventral (subgenual) anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC).
50 structural connectivity between the anterior cingulate cortex (ACC) and posterior cingulate cortex (P
51 a (4-8 Hz) oscillations in both the anterior cingulate cortex (ACC) and the DLPFC during REM sleep.
52 Here, we compared the role of the anterior cingulate cortex (ACC) and the posterior insular cortex
53 ignificantly lower in the bilateral anterior cingulate cortex (ACC) and the right superior frontal gy
54 e frontal eye fields (FEFs) and the anterior cingulate cortex (ACC) are commonly coactivated for cogn
56 restingly, neural activities in the anterior cingulate cortex (ACC) correlated with noxious intensiti
60 gnificant increased activity of the Anterior Cingulate Cortex (ACC) in the low frequency band suggest
64 vels in prefrontal cortex (PFC) and anterior cingulate cortex (ACC) occur in rodent models of depress
65 ateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) of the primate play distinctive r
66 nfralimbic (IL) cortex (but not the anterior cingulate cortex (ACC) or prelimbic cortex), reduced IL
67 ateral prefrontal cortex (LPFC) and anterior cingulate cortex (ACC) play temporally distinct roles du
68 he prevailing view that dopamine in anterior cingulate cortex (ACC) plays a role in evaluating effort
69 Furthermore, activity in dorsal anterior cingulate cortex (ACC) reflected individual choice tende
72 Endogenous opioid signaling in the anterior cingulate cortex (ACC), an area encoding pain aversivene
73 ral volumes (amygdala, hippocampus, anterior cingulate cortex (ACC), and ventral medial prefrontal co
74 disrupt the reward function of the anterior cingulate cortex (ACC), biasing the ACC to favor goal-di
75 that imposing rhythms in the mouse anterior cingulate cortex (ACC), by using optogenetics to induce
76 ntification, GPC+PC levels from the anterior cingulate cortex (ACC), caudate and putamen of 16 RC BD-
77 ippocampus, ventral hippocampus, or anterior cingulate cortex (ACC), during consolidation and retriev
78 reduced grey matter (GM) volumes in anterior cingulate cortex (ACC), left insula, left secondary soma
79 to compare TSPO availability in the anterior cingulate cortex (ACC), prefrontal cortex, and insula be
82 zed to the superior frontal gyrus and dorsal cingulate cortex), accompanied by attenuated top-down in
83 analyses highlighted higher dorsal anterior cingulate cortex activation in poker players, as compare
84 ed by a failure to maintain ventral anterior cingulate cortex activation in response to fearful stimu
85 oms, such that decreases in ventral anterior cingulate cortex activation over repeated presentations
87 ctivation of the left amygdala and posterior cingulate cortex, along with blunted responses of the bi
88 a, superior temporal gyrus, and anterior/mid-cingulate cortex among non-lapsers; the opposite pattern
89 by focal degeneration in subgenual anterior cingulate cortex, amygdala, and medial pulvinar thalamus
90 rior temporal lobe (RSATL) and the subgenual cingulate cortex and adjacent septal region (SCSR) when
91 vity between the left amygdala and subgenual cingulate cortex and between the right amygdala and caud
94 -parietal cortex; and right rostral anterior cingulate cortex and central sulcus/postcentral gyrus.
95 Main analyses were performed in blocks from cingulate cortex and confirmed in blocks from the striat
97 ate functional connectivity between anterior cingulate cortex and dorso-medial prefrontal cortex (rho
98 unctional connectivity between the posterior cingulate cortex and dorsolateral prefrontal cortex, com
100 eated females showed decreased metabolism in cingulate cortex and increased metabolism in the globus
103 ices involving motor costs is found in human cingulate cortex and not ventromedial prefrontal cortex
104 olfactory), and prefrontal regions (anterior cingulate cortex and orbitofrontal cortex) to the claust
105 d Gly levels were found in both the anterior cingulate cortex and posterior cingulate cortex of patie
106 levels were measured in vivo in the anterior cingulate cortex and posterior cingulate cortex of the s
107 , and glutamate (Glu) levels in the anterior cingulate cortex and right dorsolateral prefrontal corte
108 he ventromedial prefrontal cortex, posterior cingulate cortex and right superior frontal gyrus (SFG)
109 the balance between striatal-dorsal anterior cingulate cortex and striatal-anterior prefrontal/orbito
110 network of regions involving dorsal anterior cingulate cortex and supplementary motor area encoded th
111 on of central hubs in the subgenual anterior cingulate cortex and thalamus that lead to a cascade of
112 r depression pathology, such as the anterior cingulate cortex and the amygdala via the uncinate fasci
113 led that PVHCrh fibers project abundantly to cingulate cortex and the nucleus accumbens shell, and mo
114 in the Ch4 terminal regions of the anterior cingulate cortex and the superior and inferior parietal
116 o controls from right IFG to dorsal anterior cingulate cortex and to left IFG and dorsolateral prefro
117 king effect was found in the dorsal anterior cingulate cortex and ventral striatum, such that the nor
118 earch into the gyral surface of the anterior cingulate cortex and ventromedial prefrontal cortex coul
119 comprehension were observed in the anterior cingulate cortex and were not shared by category-switchi
120 P = .001) (extending into the right anterior cingulate cortex), and left fusiform gyrus (SDM estimate
122 tions in temporoparietal junction, posterior cingulate cortex, and dorsal medial prefrontal cortex.
123 in the orbital frontal cortex and posterior cingulate cortex, and exhibited increased resting-state
124 oroparietal junction, as well as the insula, cingulate cortex, and fusiform gyrus, a regional distrib
125 cortex, hippocampus and VTA, hippocampus and cingulate cortex, and hippocampus and hypothalamus.
126 t regions such as amygdala, insula, anterior cingulate cortex, and hippocampus play an important role
127 ion brain regions (medial prefrontal cortex, cingulate cortex, and insula) and lower activation in se
128 cagemate increases activity in the anterior cingulate cortex, and oxytocin receptor antagonist infus
129 frontal gyrus, right paracingulate/anterior cingulate cortex, and right supramarginal gyrus than con
131 ahippocampus, insula, anterior and posterior cingulate cortex, and several primary sensory areas (all
132 e observed in the secondary motor cortex and cingulate cortex, and sparse hrGFP-positive fibers were
133 largest effects in frontal, anterior/middle cingulate cortex, and temporal regions; Biotype2, interm
135 ault mode network, particularly the anterior cingulate cortex, and the central executive network rela
136 are surprisingly heterogeneous in the mouse cingulate cortex, and the minority of GINs express only
137 ral prefrontal cortex and subgenual anterior cingulate cortex; and 3) hyperconnectivity between the r
138 ft superior frontal gyrus (SFG) and anterior cingulate cortex; and 3) the Baduanjin group showed a si
142 posterior portion of the subgenual anterior cingulate cortex/basal forebrain (sgACC) drives learning
143 ee of structural impairment in the subgenual cingulate cortex before therapy seems to be associated w
144 expression in the secondary motor cortex and cingulate cortex, but decreased c-Fos expression in the
145 inferior and middle frontal gyri, precuneus, cingulate cortex, caudate, and postcentral gyrus (all re
146 , in right medial prefrontal cortex/anterior cingulate cortex, caudate, anterior insula, and thalamus
147 nt patterns of neural activations within the cingulate cortex (CC) play roles in representing opposit
148 ossible way by which prefrontal and anterior cingulate cortex circuits implement their control functi
150 ed amygdala activation and amygdala-anterior cingulate cortex connectivity (P corrected for familywis
151 e previously shown abnormally high posterior cingulate cortex connectivity in the chronic phase after
152 n reduced brain myo-inositol in the anterior cingulate cortex, consistent with CNS target engagement.
153 d between the left AI/FO and dorsal anterior cingulate cortex correlated positively with improvement
154 dorsolateral prefrontal cortex and anterior cingulate cortex) correlated positively with hearing los
155 in cholinergic transmission in the anterior cingulate cortex could be closely associated with the de
156 ral responses to heartbeats in the posterior cingulate cortex covary with changes in bodily self-cons
158 ection of physical pain, the dorsal anterior cingulate cortex (dACC) and anterior insula (AI), have b
159 ent patients showed a higher dorsal anterior cingulate cortex (dACC) and insula response to negative
160 clusion was decreased in the dorsal anterior cingulate cortex (dACC) and the middle frontal gyrus, ke
161 broadly, the insula and the dorsal anterior cingulate cortex (dACC) are key nodes of the salience ne
162 ate in the basal ganglia and dorsal anterior cingulate cortex (dACC) as measured by magnetic resonanc
164 odel proposed that the human dorsal anterior cingulate cortex (dACC) detects conflict and induces ada
165 function are associated with dorsal anterior cingulate cortex (dACC) excitotoxic lesions and pharmaco
167 ates over the function(s) of dorsal anterior cingulate cortex (dACC) have persisted for decades.
168 dies in humans implicate the dorsal anterior cingulate cortex (dACC) in regulating the conflict betwe
170 d activity of neurons in the dorsal anterior cingulate cortex (dACC) of macaques choosing between gam
171 rtex (mPFC) suggest that the dorsal anterior cingulate cortex (dACC) region is responsive to a wide v
174 precuneus, anterior insula, dorsal anterior cingulate cortex (dACC), and left dorsolateral prefronta
175 l prefrontal cortex (VLPFC), dorsal anterior cingulate cortex (dACC), left DLPFC, hippocampus, and le
179 functional and structural frontoinsular and cingulate cortex deficits and with reduced agreeableness
180 ing to posttraining alterations in posterior cingulate cortex-dlPFC rsFC statistically mediated mindf
182 c brain regions, such as the dorsal anterior cingulate cortex during trials on which participants mak
184 ea and the caudal portion of dorsal anterior cingulate cortex encoded the difference in reward (posit
185 mediated IGF2 overexpression in the anterior cingulate cortex enhanced remote fear memory formation a
186 he right amygdala and the subgenual anterior cingulate cortex following errors was observed in patien
189 tials were calculated and ranked as follows: cingulate cortex > insula > caudate/putamen > frontal co
190 zed anatomic differences between the VTA and cingulate cortex, hippocampus and VTA, hippocampus and c
191 ncluding medial prefrontal cortex, posterior cingulate cortex, hippocampus, and supplemental motor ar
192 in SCZs in the amygdala, caudate, posterior cingulate cortex, hippocampus, hypothalamus, and insula.
193 in the superior temporal gyrus and posterior cingulate cortex in 22q11DS relative to nondeleted group
194 he medial prefrontal cortex on the posterior cingulate cortex in depression is a neural correlate of
195 tmortem investigations were conducted in the cingulate cortex in five SuperAgers, five cognitively av
197 a "hyperregulatory" effect on the posterior cingulate cortex in the depressed group, with self-appra
198 re, we show that a subregion of the anterior cingulate cortex in the gyrus (ACCg) shows a degree of s
199 hippocampus, nucleus accumbens, and anterior cingulate cortex, in individuals with chronic pain.
200 n rhesus monkeys, we found that the anterior cingulate cortex innervated mostly the basolateral and C
202 l gains and losses in the subgenual anterior cingulate cortex, insula cortex, and left amygdala, brai
203 ther addictions in which the anterior-/ mid- cingulate cortex is impaired and fails to support the ne
205 from healthy subjects that the anterior mid-cingulate cortex is part of a network associated with th
206 ationship was only present when anterior mid-cingulate cortex lesion volume was defined as the overla
207 The anterior insula (AI) and mid-anterior cingulate cortex (mACC) have repeatedly been implicated
208 ssociation hubs, such as the dorsal anterior cingulate cortex, may be a neurobiological marker of the
210 y ACC node in the CEN: right dorsal anterior cingulate cortex/medial frontal gyrus (R dACC/MFG).
211 d rs-fc between the PAG and rostral anterior cingulate cortex/medial prefrontal cortex (rACC/mPFC), k
212 , methadone-treated females showed increased cingulate cortex metabolism, whereas buprenorphine-treat
213 ACEA into the infralimbic, but not anterior cingulate, cortex mitigated decision-making deficits and
215 rrelated negatively with local volume of the cingulate cortex, nucleus accumbens, thalamus, raphe nuc
216 d proton spectroscopy in the dorsal anterior cingulate cortex of 289 individuals: 184 healthy control
217 properties of GABAergic interneurons in the cingulate cortex of FVB-Tg(GadGFP)45704Swn/J mice expres
218 tivity to neural activity of dorsal anterior cingulate cortex of monkeys which revealed similar netwo
219 the anterior cingulate cortex and posterior cingulate cortex of patients with first-episode psychosi
220 nucleus, putamen, hippocampus, and anterior cingulate cortex of patients with SAD compared with heal
221 region to the medial prefrontal and anterior cingulate cortex of the common marmoset (Callithrx jacch
222 the anterior cingulate cortex and posterior cingulate cortex of the subjects by using the echo time-
223 vely altered measures of GMV in the anterior cingulate cortex, orbital frontal cortex, temporal pole,
224 default mode network and subgenual anterior cingulate cortex/orbital frontal cortex, and the magnitu
225 ic structures such as the anterior/posterior cingulate cortex, orbitofrontal cortex, and medial tempo
226 g in three regions of interest: the anterior cingulate cortex, orbitofrontal cortex, and striatum.
227 with voxelwise GM volume loss in the middle cingulate cortex (P < .001) and a cluster in the precent
230 ging (PEPSI) MRS scans of pregenual anterior cingulate cortex (pACC) and ventral posterior cingulate
231 hemical signatures in the pregenual anterior cingulate cortex (pACC), a structure known to be involve
232 onsists of the dorsal and pregenual anterior cingulate cortex, parahippocampal area and precuneus.
233 ction in glucose metabolism in the posterior cingulate cortex (PCC) predicts conversion to Alzheimer'
234 nterior cingulate cortex (ACC) and posterior cingulate cortex (PCC) regions of the default mode netwo
235 ging tasks that neurons in primate posterior cingulate cortex (PCC) signal decision salience during f
236 served directed influence from the posterior cingulate cortex (PCC) to the anterior cingulate cortex
237 acromolecular protein pools in the posterior cingulate cortex (PCC), a central DMN hub region, was se
240 , increased rsFC strength with the posterior cingulate cortex (PCC)/precuneus was seen in the relapse
241 the anterior insula and the dorsal anterior cingulate cortex, plays a crucial role in this process t
242 y' consists of dorsal and pregenual anterior cingulate cortex, posterior cingulate extending into the
244 d medial temporal lobe structures, posterior cingulate cortex, precuneus, and medial prefrontal corte
245 through its interactions with the posterior cingulate cortex, precuneus, dorsomedial PFC, and amygda
246 , or consistent processing, in the posterior cingulate cortex predicts associative memory formation a
247 card game, neurons in their rostral anterior cingulate cortex (rACC) encode both the expected value o
248 e centromedial amygdala and rostral anterior cingulate cortex (rACC), anterior vmPFC, and subgenual c
249 not relaxation training, increased posterior cingulate cortex rsFC with left dlPFC (p < .05, correcte
250 currently ongoing debate about the anterior cingulate cortex's role in sequential foraging decisions
251 rved for the three conditions, the subgenual cingulate cortex (SCC) exhibited increased functional co
252 ivity analyses using a bilateral subcallosal cingulate cortex (SCC) seed was applied to 122 patients
253 esting-state connectivity with the subgenual cingulate cortex (SCC), known to be of core pathophysiol
254 ly and appeared in the medial insula, medial cingulate cortex, secondary somatosensory cortex, fronta
255 ependent fMRI and a restrosplenial/posterior cingulate cortex seed, aged rats demonstrated a large-sc
256 or alterations in DMN rsFC using a posterior cingulate cortex seed-based analysis and found that mind
257 lves projections from the subgenual anterior cingulate cortex (sgACC) to the periaqueductal gray to t
258 al cortex (LPFC), insula, subgenual anterior cingulate cortex (sgACC), and medial prefrontal cortex (
260 stress disorder, or MDD (subgenual anterior cingulate cortex [sgACC], left dorsolateral prefrontal c
262 neighboring insular regions and the anterior cingulate cortex showed weaker functional connectivity i
263 While the gyral surface of the anterior cingulate cortex signalled social prediction errors in t
266 found in the amygdala and subgenual anterior cingulate cortex, suggesting a stronger affective respon
267 ent's outcome were frontal cortex, posterior cingulate cortex, thalamus, putamen, pallidum, caudate,
268 e medial prefrontal cortex and the posterior cingulate cortex than in the control group (odds ratio=0
269 o DMN-related iCAPs consisting the posterior cingulate cortex that differentially interact with the a
270 brain imaging revealed a region of anterior cingulate cortex that was thicker in SuperAgers compared
271 Gray matter reduction mainly in the anterior cingulate cortex, the basal ganglia, and the cerebellum
272 l prefrontal cortex, the anterior and middle cingulate cortex, the orbitofrontal cortex and the media
273 on-of-interest MRI structural analysis found cingulate cortex to be thinner in cognitively average 80
274 verging evidence has linked the anterior mid-cingulate cortex to negative affect, pain and cognitive
276 re acquired from the medial frontal/anterior cingulate cortex using a macromolecule-suppressed MEGA-P
277 nostic group x video interaction in anterior cingulate cortex/ventromedial prefrontal cortex (mPFC),
279 he caudal half of posterior parietal cortex, cingulate cortex, visual areas within the superior tempo
281 ingulate cortex (pACC) and ventral posterior cingulate cortex (vPCC)-regions possibly affected by OCD
282 tivity between amygdala and posterior middle cingulate cortex was found in female patients but negati
285 temporal gyrus, inferior temporal gyrus, and cingulate cortex, was associated with word comprehension
287 claustrum, whereas neurons projecting to the cingulate cortex were densely packed and more evenly dis
288 ate-glutamine concentrations in the anterior cingulate cortex were measured using MR spectroscopy.
289 P < .05) in the dorsal striatum and anterior cingulate cortex were not mitigated by nicotine or varen
290 control (esp. IFG/AI and the dorsal anterior cingulate cortex) were strongly recruited during specifi
291 incentive delay task and in dorsal anterior cingulate cortex when they performed the go/no-go task;
292 hances cellular activity within the anterior cingulate cortex, whereas chronic administration produce
293 on of value between choice options, in human cingulate cortex, whereas two distinct brain circuits dr
294 eneration accompanied an overactive anterior cingulate cortex, which in turn resulted in a high level
295 ved in a more anterior cluster in the dorsal cingulate cortex, which overlapped with a network of str
296 ivity in ventral striatum/subgenual anterior cingulate cortex, while updates in self-esteem resulting
298 connecting orbitofrontal and dorsal anterior cingulate cortex with subcortical nuclei have been the t
299 us/parahippocampal gyrus; and, (2) posterior cingulate cortex with supplementary motor area, precentr
300 be associated with activity in the subgenual cingulate cortex, with neural signatures that were disti
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