ライフサイエンスコーパス: orbitofrontal

1 , but no differences in nucleus accumbens or orbitofrontal activation, compared with inexperienced tr

2 elf-esteem was associated with the bilateral orbitofrontal activity during evaluation of one's own po

3 ficantly decreased mid-insula, amygdala, and orbitofrontal activity while attending to interoceptive

4 ing behaviors in children; and indicate that orbitofrontal-amygdala network properties may influence

5 nce, with significant underactivation in the orbitofrontal and anterior cingulate cortices compared w

6 ed higher-order brain regions, including the orbitofrontal and cingulate cortices.

7 ce of increased striatal-anterior prefrontal/orbitofrontal and decreased striatal-dorsal anterior cin

8 Fiber tracts connecting orbitofrontal and dorsal anterior cingulate cortex with

9 BPD exhibited higher activity in the lateral orbitofrontal and dorsolateral prefrontal cortices compa

10 Here we show that different regions of the orbitofrontal and medial prefrontal cortex make distinct

11 lly, the learning-induced pattern effects in orbitofrontal and perirhinal cortex predicted the magnit

12 f inferior frontal gyrus, alongside insular, orbitofrontal and temporal cortex in our patient cohort.

13 In the commonly injured orbitofrontal and temporal pole regions CoV was <3.5% fo

14 Among these are the orbitofrontal and the anterior cingulate cortex.

15 Both orbitofrontal and ventrolateral prefrontal areas contrib

16 Dysregulation of the orbitofrontal and ventrolateral prefrontal cortices is i

17 egory codes within the perirhinal, piriform, orbitofrontal, and insular cortices suggests that these

18 eferentially starts in the precuneus, medial orbitofrontal, and posterior cingulate cortices, i.e., s

19 istration into the prelimbic, medial/ventral orbitofrontal, and ventrolateral orbitofrontal cortex, m

20 al circuits-the caudate, thalamic, striatal, orbitofrontal, anterior cingulate and dorsolateral regio

21 ntal areas and the caudal portion of lateral orbitofrontal area (LO).

22 (MO), ventral (VO), and ventrolateral (VLO) orbitofrontal areas and the caudal portion of lateral or

23 The reduced functional connectivity in left orbitofrontal-both thalamic regions with suicidal ideati

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 46, n = 2), the vLPFC (A46v, n = 2), and the orbitofrontal cortex (OF; n = 2) were placed for confirm

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

40 Orbitofrontal cortex (OFC) administration of nicotine or

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 Orbitofrontal cortex (OFC) lesions produce deficits in r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

127 Left anterior hippocampal and orbitofrontal cortex activations correlated with improve

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 We found that orbitofrontal cortex inactivation disrupts waiting-based

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

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

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

173 The orbitofrontal cortex is critical for goal-directed behav

174 in schizophrenia patients and patients with orbitofrontal cortex lesions.

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

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

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

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

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

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

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

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

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

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

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

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

187 Elevated orbitofrontal cortex response to cues signaling impendin

188 The posterior orbitofrontal cortex sends a powerful pathway that targe

189 Lateral orbitofrontal cortex supported contingent learning and r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 Within orbitofrontal cortex, these neurons also sustain coding

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

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

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

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

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

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

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

235 frontal cortex and decreased activity in the orbitofrontal cortex.

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

237 essary for the representation of outcomes in orbitofrontal cortex.

238 iously conceived as largely dependent on the orbitofrontal cortex.

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

240 ight pulvinar thalamic nucleus and the right orbitofrontal cortex.

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

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

243 manipulations of dopamine and lesions of the orbitofrontal cortex.

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

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

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

247 nnectivity and cortical thickness within the orbitofrontal cortex.

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

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

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

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

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

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

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

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

256 , the striatum consistently outperformed the orbitofrontal cortex.

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

258 egration in the superior temporal sulcus and orbitofrontal cortex.

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

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

261 and from the anterior cingulate, insula, and orbitofrontal cortical areas.

262 significant asymmetry in both olfactory and orbitofrontal cortical odor-evoked activity, which is ex

263 superior frontal, middle frontal, and medial orbitofrontal cortical regions as well as a greater rate

264 hylphenidate was infused into prefrontal and orbitofrontal cortical regions as well as into several s

265 eft-sided ventral striatal-ventrolateral and orbitofrontal cortical reward-processing circuitry, resu

266 in the cerebellum, pons, left amygdala, and orbitofrontal cortices (cluster level, family-wise error

267 ision and taste, both the medial and lateral orbitofrontal cortices (OFC) maintained a valence code i

268 perisylvian, posterior temporo-parietal, and orbitofrontal cortices (P < 0.01, t-test).

269 atients with bvFTD, with the addition of the orbitofrontal cortices and nucleus accumbens in patients

270 he development of dorsal frontal and lateral orbitofrontal cortices as well as the effects of family

271 seline MOR availability in the cingulate and orbitofrontal cortices was associated with the rate of s

272 , and emotion categories in the fusiform and orbitofrontal cortices were stereotypically biased and c

273 volumes in either the anterior cingulate or orbitofrontal cortices.

274 he anterior cingulate and the prefrontal and orbitofrontal cortices.

275 as occipitotemporal, anterior cingulate, and orbitofrontal cortices.

276 When the opponent looked angry, BLA-orbitofrontal coupling was reduced, and BLA reactivity w

277 Patients with lateral orbitofrontal damage had impaired credit assignment, whe

278 Orbitofrontal ensembles also represent the different spa

279 iously conceived as essentially dependent on orbitofrontal functions.

280 and middle frontal gyri, lateral and medial orbitofrontal gyri, right anterior insula, putamen, thal

281 the right hippocampus/parahippocampus, right orbitofrontal gyrus, right inferior temporal gyrus (ITG)

282 gh-gamma activity was attenuated in the left orbitofrontal gyrus.

283 Responses of orbitofrontal neurons are strongly modulated by the dist

284 These results show that orbitofrontal neurons provide a behaviourally relevant s

285 Dysfunction of the orbitofrontal (OFC) and anterior cingulate (ACC) cortice

286 D patients correlated with hypometabolism in orbitofrontal (OFC) and posterior cingulate (PCC) cortic

287 To study how the interaction between orbitofrontal (OFC) and rhinal (Rh) cortices influences

288 entity and value are coded in piriform (PC), orbitofrontal (OFC) and ventromedial prefrontal (vmPFC)

289 ry-specific ensemble patterns in perirhinal, orbitofrontal, piriform, and insular cortices.

290 ene silencing, we knocked down Gabra1 in the orbitofrontal prefrontal cortex (oPFC) in mice, decreasi

291 es on the principal pyramidal neurons of the orbitofrontal prefrontal cortex (oPFC) were also imaged

292 lapping hypofunction in ventral striatal and orbitofrontal regions in depression and schizophrenia du

293 as such as the thalamus, globus pallidus and orbitofrontal regions of the right hemisphere (with the

294 iminished CMA connectivity with ventromedial/orbitofrontal regions.

295 Left orbitofrontal, right retrosplenial cingulate, and medial

296 n over time in a region including insula and orbitofrontal, rostral, and dorsolateral prefrontal cort

297 cognitive modulation of pain, including the orbitofrontal, subgenual anterior cingulate, and anterio

298 predicted from the organization of the human orbitofrontal sulci.

299 Deficits in the right orbitofrontal-temporal-limbic and left inferior frontal

300 An orbitofrontal variability encoding emerged around the sa