ライフサイエンスコーパス: orbitofrontal cortex

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

2 d by the evolution of a neural schema in the orbitofrontal cortex.

3 r temporal sulcus, the posterior insula, and orbitofrontal cortex.

4 ic symptoms with the local efficiency of the orbitofrontal cortex.

5 rtex/superior frontal gyrus, and left medial orbitofrontal cortex.

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

7 , the striatum consistently outperformed the orbitofrontal cortex.

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

9 egration in the superior temporal sulcus and orbitofrontal cortex.

10 n the right superior temporal cortex and the orbitofrontal cortex.

11 t project to the MDmc, which projects to the orbitofrontal cortex.

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

13 necting ventromedial subthalamic nucleus and orbitofrontal cortex.

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

15 s indicates that this behavior relies on the orbitofrontal cortex.

16 frontal cortex and decreased activity in the orbitofrontal cortex.

17 efrontal cortex, temporal cortex, and medial orbitofrontal cortex.

18 dorsomedial frontal, anterior cingulate, and orbitofrontal cortex.

19 ty in reversal tasks lies beyond the central orbitofrontal cortex.

20 cortex, and negatively in the precuneus and orbitofrontal cortex.

21 ubstance, included the insula and the medial orbitofrontal cortex.

22 ampus/parahippocampus, striatum, insula, and orbitofrontal cortex.

23 l, motor, and prefrontal (i.e., ventromedial orbitofrontal) cortex.

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

25 erience-specific neuronal populations in the orbitofrontal cortex, a major reward-processing hub that

26 , participants had increased activity in the orbitofrontal cortex, a region often implicated in valua

27 gaging connectivity between rACC and lateral orbitofrontal cortex, a region reflecting outcome value

28 The orbitofrontal cortex, a structure generally overlooked i

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

30 Left anterior hippocampal and orbitofrontal cortex activations correlated with improve

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

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

33 l operculum, supramarginal gyrus, and medial orbitofrontal cortex (all seed-based d mapping z value >

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

35 connectivity between hypothalamus and right orbitofrontal cortex, amygdala, and hippocampus.

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

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

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

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

40 fiber bundle connecting the amygdala to the orbitofrontal cortex and a key component of the medial t

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

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

43 ve control and emotion regulation (e.g., the orbitofrontal cortex and anterior insula), expressed as

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

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

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

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

48 a positive functional connectivity with the orbitofrontal cortex and insula to implicit happiness, b

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

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

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

52 ine, enhancement of connectivity between the orbitofrontal cortex and subcortical regions correlated

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

54 VC DBS connected primarily to the medial orbitofrontal cortex, and amSTN DBS to the lateral orbit

55 in affect and reward, such as the striatum, orbitofrontal cortex, and amygdala.

56 ilateral mid-insula as well as the striatum, orbitofrontal cortex, and bilateral amygdala.

57 that connectivity to the prefrontal cortex, orbitofrontal cortex, and cingulate cortex was positivel

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

59 bic regions such as the amygdala, insula and orbitofrontal cortex, and functional abnormalities in ov

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

61 ons including the anterior cingulate cortex, orbitofrontal cortex, and insula.

62 0.25) in the left superior temporal cortex, orbitofrontal cortex, and left superior frontal cortex.

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

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

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

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

67 nit activity were acutely implanted into the orbitofrontal cortex, anterior cingulate cortex, dorsal

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

69 y matter changes were prominent in posterior orbitofrontal cortex/anterior insula but were also found

70 econd analysis, neural activity in posterior orbitofrontal cortex/anterior insula was measured at res

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

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

73 ting that cortical mechanisms, especially in orbitofrontal cortex, are likely involved in attentional

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

75 anterior cingulate cortex, insula and medial orbitofrontal cortex as well as amygdala volume in fear

76 a neural state model encoded in human medial orbitofrontal cortex, as measured using multivariate fun

77 , FDR-corrected p (p(FDR))=<0.001-0.002) and orbitofrontal cortex (beta=0.51-0.57, t=3.53-4.30, p(FDR

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

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

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

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

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

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

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

85 of a downstream premotor area (ALM), but not orbitofrontal cortex, confined to the epoch preceding th

86 vo dopamine tone in the ventral striatum and orbitofrontal cortex correlate with model-based, but not

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

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

89 d, across an unbiased sample of neurons, the orbitofrontal cortex differentiated distractor condition

90 frontal cortex, and amSTN DBS to the lateral orbitofrontal cortex, dorsal anterior cingulate cortex,

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

92 lity of task representations recorded in the orbitofrontal cortex during decision-making, which were

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

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

95 eus accumbens, medial prefrontal cortex, and orbitofrontal cortex, during information expectation ver

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

97 With learning, orbitofrontal cortex ensembles converged onto a low-dime

98 FC to loss and greater right pars orbitalis-orbitofrontal cortex FC to reward may be trait-level neu

99 s OCP: p = 0.001, OBP versus OHP: p = 0.038) orbitofrontal cortex FC to reward versus OCP and OHP, re

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

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

102 subcortical networks, notably affecting the orbitofrontal cortex, frontal gyrus, amygdala, hippocamp

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

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

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

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

107 Our results not only reveal a role for the orbitofrontal cortex in learning but also have implicati

108 ctivation in the anterior insula and lateral orbitofrontal cortex in response to a high-fat/high-suga

109 lateral dorsolateral prefrontal cortex, left orbitofrontal cortex, inferior frontal gyrus, right supe

110 right-sided network of regions involving the orbitofrontal cortex, inferomedial temporal lobe and cer

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

112 ptogenetic stimulation revealed that lateral orbitofrontal cortex input to SPNs was reduced in KOs (~

113 These included decreases in orbitofrontal cortex, insula, amygdala, and temporal cor

114 hanges in GMD in some regions, including the orbitofrontal cortex, insula, and amygdala, were persist

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

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

117 Conversely, the orbitofrontal cortex is argued to track a subject's posi

118 The orbitofrontal cortex is critical for goal-directed behav

119 new optogenetic lesion study shows that the orbitofrontal cortex is essential for integrating inform

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

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

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

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

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

125 Recordings from lateral orbitofrontal cortex (lOFC) revealed encoding of reward

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

127 Activity in the orbitofrontal cortex, medial prefrontal cortex, and puta

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

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

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

131 entromedial prefrontal cortex (vmPFC)/medial orbitofrontal cortex (mOFC) organize abstract and discre

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

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

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

135 monitor and manipulate the activity of many orbitofrontal cortex neurons at the single-cell level in

136 Here, we show that single orbitofrontal cortex neurons in rats encode statistical

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

138 ession was also significantly reduced in the orbitofrontal cortex of high cocaine-escalating rats.

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

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

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

142 or vectorial, multi-component bundles in the orbitofrontal cortex of monkeys.

143 , with a blunted response to the drug in the orbitofrontal cortex of PWSICdel mice, but no difference

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

145 emonstrate that aspiration lesion of central orbitofrontal cortex, of the type known to affect discri

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

147 Orbitofrontal cortex (OFC) administration of nicotine or

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

149 ically between drug-activated neurons in the orbitofrontal cortex (OFC) and coactive DS neurons.

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

151 This process is thought to involve the orbitofrontal cortex (OFC) and hippocampus (HPC), but th

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

153 we used this model to study the role of the orbitofrontal cortex (OFC) and its afferent projections

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

155 ed consequences, a process that involves the orbitofrontal cortex (OFC) and potentially, the plastici

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

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

158 in piriform and in two downstream areas, the orbitofrontal cortex (OFC) and the medial prefrontal cor

159 IFICANCE STATEMENT Considering that both the orbitofrontal cortex (OFC) and the opioid system regulat

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

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

162 the function of several anatomically defined orbitofrontal cortex (OFC) circuits during adaptive, fle

163 In rodents, the orbitofrontal cortex (OFC) contains neural signatures of

164 The orbitofrontal cortex (OFC) contributes to such learning

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

166 is, when agents make choices, neurons in the orbitofrontal cortex (OFC) encode the subjective value o

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

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

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

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

171 The orbitofrontal cortex (OFC) has been implicated in regula

172 nsequences of choices.SIGNIFICANCE STATEMENT Orbitofrontal cortex (OFC) has been implicated in repres

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

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

175 The orbitofrontal cortex (OFC) has long been implicated in s

176 Both hippocampus (HPC) and orbitofrontal cortex (OFC) have been shown to be critica

177 Both basal ganglia (BG) and orbitofrontal cortex (OFC) have been widely implicated i

178 ructure connecting these two regions via the orbitofrontal cortex (OFC) in 38 healthy human participa

179 MD from its other main cortical target, the orbitofrontal cortex (OFC) in a task assessing outcome d

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

181 sampled, we found greatest pathology in left orbitofrontal cortex (OFC) in FTLD-TDP, which was greate

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

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

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

185 Neural correlates implicate the orbitofrontal cortex (OFC) in value-based or economic de

186 nt cocaine-induced strengthening of upstream orbitofrontal cortex (OFC) inputs to the dorsomedial str

187 The orbitofrontal cortex (OFC) is a key brain region involve

188 ion later in life.SIGNIFICANCE STATEMENT The orbitofrontal cortex (OFC) is a subregion of the frontal

189 nd retrieving associations, while the medial orbitofrontal cortex (OFC) is an important region for re

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

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

192 Orbitofrontal cortex (OFC) is implicated in value-based

193 NCE STATEMENT It is widely accepted that the orbitofrontal cortex (OFC) is important for decision-mak

194 Here we show that neural activity in rat orbitofrontal cortex (OFC) is instead highly structured:

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

196 The orbitofrontal cortex (OFC) is necessary for inferring va

197 Animal lesion studies demonstrate that orbitofrontal cortex (OFC) is necessary for normal behav

198 The orbitofrontal cortex (OFC) is proposed to be critical to

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

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

201 and that low-frequency theta activity in the orbitofrontal cortex (OFC) negatively correlates with ph

202 Classically, specific orbitofrontal cortex (OFC) neurons are thought to repres

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

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

205 at heavy alcohol use activates mTORC1 in the orbitofrontal cortex (OFC) of rodents (Laguesse et al.,

206 quantitative real-time PCR (qRT-PCR) in the orbitofrontal cortex (OFC) of SCZ (N = 29; 20 male and 9

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

208 The orbitofrontal cortex (OFC) plays a critical role in eval

209 Orbitofrontal cortex (OFC) predicts the consequences of

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

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

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

213 optogenetic manipulations revealed that the orbitofrontal cortex (OFC) supports the BLA in these pro

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

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

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

217 f, as well as other RL related variables, in orbitofrontal cortex (OFC) while three male monkeys perf

218 ions of gray matter volume (GMV) in the left orbitofrontal cortex (OFC) with CpG 5,6 methylation.

219 lies on the frontal cortex, specifically the orbitofrontal cortex (OFC)(1-9).

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

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

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

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

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

225 CANCE STATEMENT Economic choices rely on the orbitofrontal cortex (OFC), but other brain regions may

226 nes of evidence link economic choices to the orbitofrontal cortex (OFC), but other brain regions may

227 ces between goods are thought to rely on the orbitofrontal cortex (OFC), but the decision mechanisms

228 Several brain areas, including the orbitofrontal cortex (OFC), have been associated with th

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

230 In orbitofrontal cortex (OFC), neurons encode the subjectiv

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

232 ry taste cortices, located in the insula and orbitofrontal cortex (OFC), respectively.

233 Within the orbitofrontal cortex (OFC), there is a prominent oscilla

234 in 3 regions linked to decision-making, the orbitofrontal cortex (OFC), ventral striatum (VS), and d

235 c signals in the nucleus accumbens (NAc) and orbitofrontal cortex (OFC), while freely moving rats per

236 representation of decision variables in the orbitofrontal cortex (OFC)-an area implicated in economi

237 ortion of mature spines in the ventrolateral orbitofrontal cortex (OFC).

238 conomic decisions are thought to rely on the orbitofrontal cortex (OFC).

239 These processes involve the orbitofrontal cortex (OFC).

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

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

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

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

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

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

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

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

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

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

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

251 e dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex (OFC).

252 alues in the striatum, amygdala, insula, and orbitofrontal cortex (OFC).

253 ous and complex in frontal areas such as the orbitofrontal cortex (OFC).

254 cortex (ACC), nucleus accumbens (NAcc), and orbitofrontal cortex (OFC).

255 n brain regions involved in decision-making (orbitofrontal cortex [OFC]) and action selection (striat

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

257 hree other frontal cortical regions: lateral orbitofrontal cortex (orbital part of area 12 [12o]), ci

258 d with cortical atrophy in the right lateral orbitofrontal cortex (p(adj) = 0.03) and right posterior

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

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

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

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

263 ated with longer sleep duration included the orbitofrontal cortex, prefrontal and temporal cortex, pr

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

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

266 tes of task representations that suggest the orbitofrontal cortex represents 'task states', deploying

267 ect and dorsal lateral prefrontal and medial orbitofrontal cortex responses to emotionally-conflictin

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

269 tern of functional connectivity to the right orbitofrontal cortex, right inferior temporal gyrus, and

270 of the stimulation site with right and left orbitofrontal cortex, right ventromedial prefrontal cort

271 The posterior orbitofrontal cortex sends a powerful pathway that targe

272 the activity of the cortex, particularly the orbitofrontal cortex, severely impairs higher order cogn

273 solateral prefrontal cortex, and the lateral orbitofrontal cortex, significantly moderated the effect

274 Posterior lateral orbitofrontal cortex specifically detected rare reward e

275 Contrary to predictions, lateral orbitofrontal cortex-striatal synapses were not responsi

276 ntravenous) administration in brain regions (orbitofrontal cortex, striatum, brainstem, and thalamus)

277 Lateral orbitofrontal cortex supported contingent learning and r

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

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

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

281 potent cellular-level subnetworks within the orbitofrontal cortex that can be precisely engaged to bi

282 e identified distinct populations within the orbitofrontal cortex that selectively responded to eithe

283 of the most influential accounts of central orbitofrontal cortex-that it mediates behavioral flexibi

284 , in a selective subset of regions including orbitofrontal cortex, the phenomenon was best explained

285 However, in a few other regions, including orbitofrontal cortex, the phenomenon was best explained

286 Within orbitofrontal cortex, these neurons also sustain coding

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

288 Orbitofrontal cortex thus represents decision confidence

289 the MDmc may convey signals forwarded to the orbitofrontal cortex to monitor and update the status of

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

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

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

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

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

295 havioral data suggest that the ventrolateral orbitofrontal cortex (VLO), which exhibits extensive con

296 the ventromedial prefrontal cortex / medial orbitofrontal cortex (vmPFC/mOFC) and nineteen age- and

297 Activity patterns in the orbitofrontal cortex were also found to be related to st

298 Here, we recorded from orbitofrontal cortex while monkeys chose between differe

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