ライフサイエンスコーパス: orbitofrontal cortex

1 subjects (in insula, amygdala, putamen, and orbitofrontal cortex).

2 s; decreased brain activity in right lateral orbitofrontal cortex).

3 frontal cortex and decreased activity in the orbitofrontal cortex.

4 ces decoding of reward signals in the medial orbitofrontal cortex.

5 essary for the representation of outcomes in orbitofrontal cortex.

6 iously conceived as largely dependent on the orbitofrontal cortex.

7 er gray matter volumes in caudate and medial orbitofrontal cortex.

8 ight pulvinar thalamic nucleus and the right orbitofrontal cortex.

9 al temporal lobe, opercular cortex and right orbitofrontal cortex.

10 ked by visual cues between the VMPFC and the orbitofrontal cortex.

11 manipulations of dopamine and lesions of the orbitofrontal cortex.

12 in regions but not in the infant amygdala or orbitofrontal cortex.

13 d regions of the caudate, thalamus and right orbitofrontal cortex.

14 -dependent signal change in the amygdala and orbitofrontal cortex.

15 nnectivity and cortical thickness within the orbitofrontal cortex.

16 nd a small, circumscribed lesion in the left orbitofrontal cortex.

17 e amygdala, subgenual prefrontal cortex, and orbitofrontal cortex.

18 cingulate cortex (Brodmann area 32) and the orbitofrontal cortex.

19 al cortex, anterior cingulate cortex and the orbitofrontal cortex.

20 fic) satiation effects in both the vmPFC and orbitofrontal cortex.

21 cale for appetite and aversive values in the orbitofrontal cortex.

22 he amygdala/hippocampal complex, insula, and orbitofrontal cortex.

23 amygdala, the anterior hippocampus, and the orbitofrontal cortex.

24 mplitude coupling in LFP recordings from rat orbitofrontal cortex.

25 eductions were found in the bilateral medial orbitofrontal cortex.

26 ht amygdala, hippocampus, fusiform gyrus and orbitofrontal cortex.

27 l correlates in striatum, insula, and medial orbitofrontal cortex.

28 a in the mPFC and hippocampus but not in the orbitofrontal cortex.

29 , the striatum consistently outperformed the orbitofrontal cortex.

30 pairments can be linked to lateral or medial orbitofrontal cortex.

31 egration in the superior temporal sulcus and orbitofrontal cortex.

32 ng in addiction, here showing a role for the orbitofrontal cortex.

33 ations were seen in the ventral striatum and orbitofrontal cortex.

34 anges in hippocampus, insula, subgenual, and orbitofrontal cortex, a circuit implicated in the contro

35 e, but the striatal network outperformed the orbitofrontal cortex, a finding replicated both in simul

36 displayed decreased activation of the medial orbitofrontal cortex, a key region of reward processing.

37 We find that anticipatory signals in the orbitofrontal cortex about upcoming choice increase over

38 e appeal of high-energy foods and associated orbitofrontal cortex activation.

39 Left anterior hippocampal and orbitofrontal cortex activations correlated with improve

40 study provides evidence for the key role of orbitofrontal cortex activity in choice behavior and sho

41 associated with nucleus accumbens and medial orbitofrontal cortex activity, whereas distress was pref

42 vity of the striatum after gratification and orbitofrontal cortex after regret, respectively.

43 he OFC, the agranular insula and the lateral orbitofrontal cortex (AI-OPNs and LO-OPNs, respectively)

44 ted hyperconnectivity in a network involving orbitofrontal cortex along with a less resilient global

45 correlated with externalizing behaviors, an orbitofrontal cortex-amygdala network predicted rates of

46 ntral medial prefrontal cortex-amygdala, and orbitofrontal cortex-amygdala-hippocampus.

47 the DMS CINs also depended completely on the orbitofrontal cortex, an area that has been proposed to

48 encoded in patterns of brain activity in the orbitofrontal cortex, an area that has been separately i

49 lower was their D2-type BPND in the lateral orbitofrontal cortex, an important region in value-based

50 taste, olfactory, and flavor stimuli in the orbitofrontal cortex and a region to which it projects,

51 iors exhibited positive correlations between orbitofrontal cortex and amygdala structure, while these

52 in key parental brain regions, including the orbitofrontal cortex and amygdala.

53 correlated inversely with activations in the orbitofrontal cortex and brainstem during the stress con

54 idoethylpiperazine [(18)F]MPPF uptake in the orbitofrontal cortex and dorsal ACC.

55 esearch showing some rule selectivity in the orbitofrontal cortex and dorsal striatum.

56 y, we examined activity of single neurons in orbitofrontal cortex and in ventral and dorsal striatum

57 and RSFC between the midbrain and striatum, orbitofrontal cortex and insula in methamphetamine-depen

58 ation revealed that the two regions studied, orbitofrontal cortex and nucleus accumbens, are not sequ

59 and similar effects were found in the right orbitofrontal cortex and right inferior frontal gyrus.

60 and functional abnormalities in left lateral orbitofrontal cortex and right supplementary motor area,

61 in connectivity of subgenual cingulate with orbitofrontal cortex and thalamus.

62 g of distant connectivity alterations of the orbitofrontal cortex and the basal ganglia represents in

63 he anterior and middle cingulate cortex, the orbitofrontal cortex and the medial and ventromedial sup

64 In rats and nonhuman primates, both the orbitofrontal cortex and the ventral striatum have been

65 We recorded neural ensembles from orbitofrontal cortex and ventral striatum in rats encoun

66 ckwards toward the lost option, cells within orbitofrontal cortex and ventral striatum represented th

67 ous, including the medial prefrontal cortex, orbitofrontal cortex, and different locations within the

68 attern separation between odor categories in orbitofrontal cortex, and impeded within-category genera

69 nucleus accumbens, striatum, insular cortex, orbitofrontal cortex, and medial forebrain bundle.

70 as the anterior/posterior cingulate cortex, orbitofrontal cortex, and medial temporal areas in diffe

71 al tegmental area, medial prefrontal cortex, orbitofrontal cortex, and nucleus accumbens).

72 ctivity among regions such as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus (PHG) du

73 of interest: the anterior cingulate cortex, orbitofrontal cortex, and striatum.

74 ially the left hippocampus, the left lateral orbitofrontal cortex, and the bilateral isthmus cingulat

75 d nucleus accumbens, left-hemisphere insula, orbitofrontal cortex, and ventromedial prefrontal cortex

76 grey matter in the anterior insula, lateral orbitofrontal cortex, anterior cingulate and dorsal stri

77 empathy depends on coordinated functions of orbitofrontal cortex, anterior insula, anterior cingulat

78 hypometabolism in the medial occipital lobe, orbitofrontal cortex, anterior temporal lobe, and caudat

79 ronto-striatal circuit that differs from the orbitofrontal cortex-anterior cingulate cortex-caudate c

80 y excitotoxic lesions of either the anterior orbitofrontal cortex (antOFC) or ventrolateral prefronta

81 TEMENT The lateral and medial regions of the orbitofrontal cortex are cytoarchitectonically distinct

82 We recorded single-units from macaque orbitofrontal cortex (Area 13) in a riskless choice task

83 dentified the ventromedial prefrontal cortex/orbitofrontal cortex as the main structure in this circu

84 We found that activation of medial orbitofrontal cortex biased intense bivalent motivation

85 functional connectivity involved the medial orbitofrontal cortex Brodmann area 13, which is implicat

86 akened functional connectivity of the medial orbitofrontal cortex Brodmann area 13.

87 Second, the lateral orbitofrontal cortex Brodmann area 47/12 had increased f

88 eased functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 is related to d

89 t the functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 with these thre

90 The lateral orbitofrontal cortex Brodmann area 47/12, involved in no

91 xpression and smaller hippocampal and medial orbitofrontal cortex, but not amygdala, volumes relative

92 late cortex and striatal-anterior prefrontal/orbitofrontal cortex circuits was significantly associat

93 c pathway, and increased 5-HT2cR mRNA in the orbitofrontal cortex compared with LI rats.

94 e ensemble in the nucleus accumbens, but not orbitofrontal cortex, compared with their surrounding ne

95 es, as well as between the right amygdala to orbitofrontal cortex connectivity and levels of craving.

96 Here we asked how the orbitofrontal cortex contributes to memory where context

97 ver, we find that multivoxel patterns in the orbitofrontal cortex correlate with value.

98 teral prefrontal cortex and amygdala-lateral orbitofrontal cortex coupling were shown in male BPD pat

99 ted Fos neurons in central amygdala, but not orbitofrontal cortex, decreased "incubated" nicotine see

100 these regions, but with the exception of the orbitofrontal cortex, densities normalized with a recove

101 ons of regret, and humans with damage to the orbitofrontal cortex do not express regret.

102 isted of voxels with unique projections from orbitofrontal cortex, dorsolateral prefrontal cortex, an

103 hibit convergent anatomical connections from orbitofrontal cortex, dorsolateral prefrontal cortex, an

104 ce has generally treated prefrontal regions (orbitofrontal cortex, dorsolateral prefrontal cortex, in

105 ined the role of parvalbumin interneurons in orbitofrontal cortex during reversal learning by recordi

106 he degree of both affective processes in the orbitofrontal cortex during self-reflection and cognitiv

107 whole, showed hyperactivation in the medial orbitofrontal cortex during the acquisition of avoidance

108 ual areas, and later in frontal regions with orbitofrontal cortex emerging last.

109 ts of the ARs in the caudate nucleus and the orbitofrontal cortex for all of the subjects, and a non-

110 e performed with (123)I-PIP using postmortem orbitofrontal cortex from cognitively normal and AD huma

111 hometry analyses demonstrated greater medial orbitofrontal cortex gray matter intensity in controls t

112 d increased gray matter volume of the medial orbitofrontal cortex (gyrus rectus).

113 and emotional processing (thalamus, insula, orbitofrontal cortex, hippocampus, and anterior cingulat

114 cant reductions in gray matter volume in the orbitofrontal cortex, hippocampus, and cerebellum; white

115 ala and from the right amygdala to the right orbitofrontal cortex in dependent patients.

116 g of the functions of different parts of the orbitofrontal cortex in emotion helps to provide new ins

117 teral and ventromedial prefrontal cortex and orbitofrontal cortex in healthy volunteers.

118 ess by recording single-unit activity in the orbitofrontal cortex in rats performing a choice task in

119 pecifically, BOLD was higher in the inferior orbitofrontal cortex in response to savory food cues.

120 rontal cortex, anterior cingulate cortex and orbitofrontal cortex in the frontal lobe from a total of

121 ce has implicated the posterior parietal and orbitofrontal cortex in the processing of value.

122 We found that orbitofrontal cortex inactivation disrupts waiting-based

123 nt avoidance were seen immediately, those of orbitofrontal cortex inactivation were delayed and their

124 ns were observed in the putamen, insula, and orbitofrontal cortex (indicating relative preservation o

125 r show that this property of CINs depends on orbitofrontal cortex input and is correlated with choice

126 vealed hypoactivation in additional hedonic (orbitofrontal cortex, insula, globus pallidus, putamen,

127 Cortical thickness in lateral orbitofrontal cortex, insula, inferior parietal cortex,

128 and dorsal anterior cingulate cortex (ACC), orbitofrontal cortex, insula, nucleus accumbens, amygdal

129 task as well as from other sources, that the orbitofrontal cortex is a critical node in the neural ci

130 In humans, the orbitofrontal cortex is active during expressions of reg

131 The orbitofrontal cortex is critical for goal-directed behav

132 rey matter volume in the anterior cingulate, orbitofrontal cortex, left dorsolateral prefrontal corte

133 in schizophrenia patients and patients with orbitofrontal cortex lesions.

134 bstantial number of studies showing that the orbitofrontal cortex links events to reward values, wher

135 The lateral orbitofrontal cortex (lOFC) and basolateral amygdala (BL

136 ionally distinct learning signals in lateral orbitofrontal cortex (lOFC) and the dopaminergic ventral

137 The lateral orbitofrontal cortex (lOFC) has been described as signal

138 t work in macaques has suggested the lateral orbitofrontal cortex (lOFC) is relatively more concerned

139 sed if pharmacologic inactivation of lateral orbitofrontal cortex (lOFC) or DBS of the ventral striat

140 credit assignment, whereas damage to medial orbitofrontal cortex meant that patients were more likel

141 dies, MAM (vs. SHAM) rats displayed abnormal orbitofrontal cortex-mediated decision-making processes,

142 ial/ventral orbitofrontal, and ventrolateral orbitofrontal cortex, mediodorsal thalamus, or nucleus a

143 reward values are represented in the medial orbitofrontal cortex (mOFC) at the time of choice [7-9].

144 s or chemogenetic inactivation of the medial orbitofrontal cortex (mOFC) in rats induces failures in

145 Contrary to IL and AI, we found that medial orbitofrontal cortex (mOFC) projects densely through dor

146 overlapping valuation signals in the medial orbitofrontal cortex (mOFC) were observed for the three

147 a given reward, or "reinforcer." The medial orbitofrontal cortex (mOFC), a subregion of the ventrome

148 us accumbens, amygdala, anterior insula, and orbitofrontal cortex (n = 18 had analyzable fMRI data).

149 the ventromedial prefrontal cortex (vmPFC), orbitofrontal cortex, nucleus accumbens, hypothalamus, a

150 Using microarray data from orbitofrontal cortex of control subjects (n=209; 16-96 y

151 The orbitofrontal cortex of MAM rats showed lower resting-st

152 extracellular recordings in the striatum and orbitofrontal cortex of mice that learned the temporal r

153 d large-scale recordings in the striatum and orbitofrontal cortex of mice trained on a stimulus-rewar

154 (primarily glial) nuclei separated from the orbitofrontal cortex of postmortem human brain.

155 processing of affect; nucleus accumbens and orbitofrontal cortex of the reward circuit; anterior ins

156 46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirm

157 critical for odor memory and perception- and orbitofrontal cortex (OFC) - a region involved in revers

158 Orbitofrontal cortex (OFC) administration of nicotine or

159 The orbitofrontal cortex (OFC) and amygdala are both necessa

160 Recent studies have challenged the view that orbitofrontal cortex (OFC) and amygdala mediate flexible

161 pERK expression in medial prefrontal (mPFC), orbitofrontal cortex (OFC) and areas in striatum and amy

162 The orbitofrontal cortex (OFC) and basolateral amygdala (BLA

163 bregions of the frontal cortex including the orbitofrontal cortex (OFC) and dorsomedial prefrontal co

164 prefrontal cortex activation and suppressed orbitofrontal cortex (OFC) and hippocampus activation af

165 presentations of identity-specific reward in orbitofrontal cortex (OFC) and identity-general reward i

166 multaneously decrease neural activity in the orbitofrontal cortex (OFC) and increase activity in NAC

167 ned the activation patterns of cue-activated orbitofrontal cortex (OFC) and nucleus accumbens (NAc) s

168 omic and functional connectivity between the orbitofrontal cortex (OFC) and the amygdala in mice.

169 STATEMENT Dysfunctional interactions between orbitofrontal cortex (OFC) and the amygdala underlie sev

170 Reciprocal connections between the orbitofrontal cortex (OFC) and the basolateral nucleus o

171 parallel, fMRI cross-adaptation in the right orbitofrontal cortex (OFC) and the left anterior tempora

172 Postmortem samples were obtained from orbitofrontal cortex (OFC) and/or anterior cingulate cor

173 ateral nucleus of the amygdala (BLA) and the orbitofrontal cortex (OFC) are involved in behavior that

174 h studied, the role of prominent inputs from orbitofrontal cortex (OFC) are less well understood.

175 enced value representations within the human orbitofrontal cortex (OFC) are thought to be organized t

176 The basolateral amygdala (BLA) and orbitofrontal cortex (OFC) are two reciprocally connecte

177 The hippocampus and orbitofrontal cortex (OFC) both make important contribut

178 including the basolateral amygdala (BLA) and orbitofrontal cortex (OFC) can accompany these same diso

179 lations of neurons and HGA recorded from the orbitofrontal cortex (OFC) encode similar information, a

180 ing economic decisions, offer value cells in orbitofrontal cortex (OFC) encode the values of offered

181 adigm, we identified reward-based changes in orbitofrontal cortex (OFC) for the whole odor and for a

182 urface expression assays using both mPFC and orbitofrontal cortex (OFC) from individual EC or IC rats

183 specific rewards, which have been linked to orbitofrontal cortex (OFC) function.

184 The orbitofrontal cortex (OFC) has been broadly implicated i

185 The orbitofrontal cortex (OFC) has been described as signali

186 The orbitofrontal cortex (OFC) has been implicated in both t

187 Although the orbitofrontal cortex (OFC) has been studied intensely fo

188 In prefrontal areas, the orbitofrontal cortex (OFC) has been suggested to have an

189 The number of papers about the orbitofrontal cortex (OFC) has grown from 1 per month in

190 The orbitofrontal cortex (OFC) has long been associated with

191 Orbitofrontal cortex (OFC) has long been known to play a

192 to either medial prefrontal cortex (mPFC) or orbitofrontal cortex (OFC) immediately prior to performa

193 Dysfunction of the orbitofrontal cortex (OFC) impairs the ability of indivi

194 tly recorded local field potentials from the OrbitoFrontal Cortex (OFC) in five human subjects perfor

195 utions of the basolateral amygdala (BLA) and orbitofrontal cortex (OFC) in rats to learning under exp

196 ored the role of basal IL-6 signaling in the orbitofrontal cortex (OFC) in reversal learning, a form

197 reased stress-induced activity in the medial orbitofrontal cortex (OFC) in the high CA group (p<0.01,

198 parate lines of research have implicated the orbitofrontal cortex (OFC) in the judgment of social tra

199 The role of the orbitofrontal cortex (OFC) in value processing is a focu

200 directed behavior.SIGNIFICANCE STATEMENT The orbitofrontal cortex (OFC) is critical for goal-directed

201 The orbitofrontal cortex (OFC) is critically involved in thi

202 The macaque orbitofrontal cortex (OFC) is essential for selecting go

203 The orbitofrontal cortex (OFC) is known to play a crucial ro

204 Rat orbitofrontal cortex (OFC) is located in the dorsal bank

205 The orbitofrontal cortex (OFC) is thought to link stimuli an

206 Orbitofrontal cortex (OFC) lesions produce deficits in r

207 The orbitofrontal cortex (OFC) may guide value-based respons

208 olume, higher functional connectivity in the orbitofrontal cortex (OFC) network, and higher structura

209 nd recorded from dorsomedial PFC (dmPFC) and orbitofrontal cortex (OFC) neurons while they were freel

210 the activity of neurons in the amygdala and orbitofrontal cortex (OFC) of monkeys during a Pavlovian

211 rk identified three groups of neurons in the orbitofrontal cortex (OFC) of monkeys engaged in economi

212 monkeys with bilateral lesions of either the orbitofrontal cortex (OFC) or the amygdala could learn a

213 Neurons in the orbitofrontal cortex (OFC) predominantly encoded rewards

214 The primate orbitofrontal cortex (OFC) receives dopaminergic input f

215 al techniques in mice, we found that pairing orbitofrontal cortex (OFC) stimulation with sound stimul

216 reward contingencies, with the medial versus orbitofrontal cortex (OFC) subregions contributing diffe

217 The lateral orbitofrontal cortex (OFC) supports model-based behavior

218 orm of cognitive flexibility mediated by the orbitofrontal cortex (OFC) that we have used previously

219 from the anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC) to assess network similaritie

220 graphic organization of projections from the orbitofrontal cortex (OFC) to the parahippocampal region

221 ed repetitive element loci (RE) in the human orbitofrontal cortex (OFC) using directional RNA sequenc

222 The caudate has dense connections with the orbitofrontal cortex (OFC) via the frontostriatal loops,

223 PFC, dorsomedial PFC, ventromedial PFC, and orbitofrontal cortex (OFC) were delineated.

224 Dysfunction of the orbitofrontal cortex (OFC), a critical cortical subregio

225 One hedonic hotspot was found in anterior orbitofrontal cortex (OFC), and another was found in pos

226 and ventral striatum, left insula and middle orbitofrontal cortex (OFC), and right insula projecting

227 The inferior frontal gyrus (IFG), orbitofrontal cortex (OFC), and ventromedial PFC (vmPFC)

228 er cortical gray matter than controls in the orbitofrontal cortex (OFC), anterior and posterior cingu

229 Other frontal regions, in particular the orbitofrontal cortex (OFC), are critical in directing be

230 entral medial prefrontal cortex (vmPFC), and orbitofrontal cortex (OFC), brain regions implicated in

231 restingly, we found that inactivation of the orbitofrontal cortex (OFC), but not the dorsal or ventra

232 Previous studies have implicated orbitofrontal cortex (OFC), dorsolateral prefrontal cort

233 Orbitofrontal cortex (OFC), medial frontal cortex (MFC),

234 vity in both medial and lateral parts of the orbitofrontal cortex (OFC), only the lateral OFC represe

235 vironmental context exposure is dependent on orbitofrontal cortex (OFC)-basolateral amygdala (BLA) in

236 LA-driven intra-amygdaloid paths and concise orbitofrontal cortex (OFC)-CeA-driven extra-amygdaloid c

237 are generated in a neural circuit within the orbitofrontal cortex (OFC).

238 eural dynamics, we conduct recordings in the orbitofrontal cortex (OFC).

239 d by medial frontal cortex (mFC) and then by orbitofrontal cortex (OFC).

240 ree viewing while we recorded neurons in the orbitofrontal cortex (OFC).

241 ortex and having reciprocal connections with orbitofrontal cortex (OFC).

242 bgenual) anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC).

243 eories of value representation in area 13 of orbitofrontal cortex (OFC).

244 d the efferent pathway from mouse PCX to the orbitofrontal cortex (OFC).

245 her the primary gustatory cortex (GC) or the orbitofrontal cortex (OFC).

246 m (VS), medial prefrontal cortex (mPFC), and orbitofrontal cortex (OFC).

247 ntingencies and making decisions engages the orbitofrontal cortex (OFC).

248 cognitive tasks that are dependent upon the orbitofrontal cortex (OFC).

249 to be due to altered functioning within the orbitofrontal cortex (OFC).

250 tion of frontal cortical areas including the orbitofrontal cortex (OFC).

251 e organization of functional networks in the orbitofrontal cortex (OFC).

252 ut by how that response (specifically in the orbitofrontal cortex; OFC) is mirrored at a later time w

253 ng value-guided learning, whereas the medial orbitofrontal cortex (often referred to as ventromedial

254 removal of serotonin or dopamine within the orbitofrontal cortex or dorsal striatum, respectively, i

255 ulated the food-related signal in the medial orbitofrontal cortex (P=0.01) and nucleus accumbens (P=0

256 The orbitofrontal cortex plays a central role in good-based

257 once the stimulus is presented suggest that orbitofrontal cortex plays a role in transforming immedi

258 The primate amygdala projects to posterior orbitofrontal cortex (pOFC) directly and possibly indire

259 mygdala sends dense projections to posterior orbitofrontal cortex (pOFC) in pathways that are critica

260 nterior cingulate cortex (ACC) and posterior orbitofrontal cortex (pOFC) in rhesus monkeys to compare

261 irectional dialogue of the primate posterior orbitofrontal cortex (pOFC) with the amygdala is essenti

262 Here we show that basolateral amygdala to orbitofrontal cortex projections are required for expect

263 ts in the ventromedial prefrontal cortex and orbitofrontal cortex regardless of stimulus type and dis

264 bjects were presented, neuronal ensembles in orbitofrontal cortex represented distinct value-based sc

265 Elevated orbitofrontal cortex response to cues signaling impendin

266 into occipital cortex (left hemisphere) and orbitofrontal cortex (right hemisphere); bilateral precu

267 The posterior orbitofrontal cortex sends a powerful pathway that targe

268 Consistent with the proposal that orbitofrontal cortex signals inferred information, firin

269 response was higher in reward-related areas (orbitofrontal cortex, striatum) in a low-protein state t

270 es spread to frontal (lateral premotor area, orbitofrontal cortex, supplementary motor area, anteior

271 Lateral orbitofrontal cortex supported contingent learning and r

272 (P < .01) distant connectivity in the medial orbitofrontal cortex, temporal cortex, posterior cingula

273 poral pole), and c) emotion-related regions (orbitofrontal cortex, temporal pole, and amygdala).

274 TSPO VT was measured in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal

275 r TSPO VT is elevated in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal

276 n had greater activation in the left lateral orbitofrontal cortex than did low-risk children (t43 = -

277 lteration involving the ventral striatum and orbitofrontal cortex that predicted overall illness seve

278 al deficits and reduced synaptic efficacy in orbitofrontal cortex, the reversal of which by optogenet

279 Within orbitofrontal cortex, these neurons also sustain coding

280 One synapse on, in the orbitofrontal cortex, these sensory inputs are combined

281 In conclusion, orbitofrontal cortex theta-gamma PAC strength differenti

282 gative connectivity between the amygdala and orbitofrontal cortex (thresholded at z > 1.70, P < .05).

283 facilitate adaptive behavior by enabling the orbitofrontal cortex to use environmental stimuli to gen

284 ontal regions (anterior cingulate cortex and orbitofrontal cortex) to the claustrum in mice.

285 significantly correlated with TSPO VT in the orbitofrontal cortex (uncorrected Pearson correlation r

286 neurons in central and basolateral amygdala, orbitofrontal cortex, ventral and dorsal medial prefront

287 There was reduced activation in the orbitofrontal cortex, ventral striatum, inferior tempora

288 hippocampus, amygdala, ventral striatum, and orbitofrontal cortex volumes were related to lifetime ca

289 m, ventral pallidum, amygdala, midbrain, and orbitofrontal cortex (voxel threshold p < 0.005; cluster

290 to MA use, smaller cortical thickness in the orbitofrontal cortex was associated with family history

291 The craving-related signal in the medial orbitofrontal cortex was attenuated by inactivation of t

292 tional connectivity between the amygdala and orbitofrontal cortex was compared between ASDs subgroups

293 Moreover, blunted activation of the medial orbitofrontal cortex was significantly correlated with a

294 Remarkably, pyramidal neurons within the orbitofrontal cortex were also found to be smaller in si

295 st (the caudate, the putamen, and the medial orbitofrontal cortex) were tested at a statistical thres

296 dorsolateral prefrontal cortex, and lateral orbitofrontal cortex-were examined.

297 increases in striatum, amygdala, and medial orbitofrontal cortex, whereas it decreased metabolism in

298 the same time, through its modulation of the orbitofrontal cortex, which processes salience attributi

299 ogical activity of individual neurons of the orbitofrontal cortex while rats performed a risk task th

300 diagnosis-by-age-by-distance interaction in orbitofrontal cortex with short-range FC being lower in