ライフサイエンスコーパス: orbitofrontal

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

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

3 Using optogenetics in mice, we show that orbitofrontal and anterior cingulate cortex inactivation

4 theses, we recorded neuronal activity in the orbitofrontal and anterior cingulate cortex of two monke

5 Fiber tracts connecting orbitofrontal and dorsal anterior cingulate cortex with

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

7 oral and orbitofrontal cortices, and between orbitofrontal and nucleus accumbens, predict individual

8 llum, brainstem, basal ganglia, thalami, and orbitofrontal and sensorimotor cortex.

9 work and decreased cortical thickness in the orbitofrontal and temporal cortex.

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

11 Both orbitofrontal and ventrolateral prefrontal areas contrib

12 ociated with significant hypoconnectivity in orbitofrontal and ventromedial prefrontal cortical-stria

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

14 n medial prefrontal, anterior cingulate, and orbitofrontal areas.

15 Disinhibition is related to right ATL and orbitofrontal atrophy, and face recognition to right ATL

16 found to relate positively to the degree of orbitofrontal atrophy.

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

18 hickness asymmetry in mostly medial frontal, orbitofrontal, cingulate and inferior temporal areas, an

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

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

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

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

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

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

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

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

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

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

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

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

31 Orbitofrontal cortex (OFC) administration of nicotine or

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

48 The orbitofrontal cortex (OFC) contributes to such learning

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 Orbitofrontal cortex (OFC) predicts the consequences of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 These processes involve the orbitofrontal cortex (OFC).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 Left anterior hippocampal and orbitofrontal cortex activations correlated with improve

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

169 The orbitofrontal cortex is critical for goal-directed behav

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 The posterior orbitofrontal cortex sends a powerful pathway that targe

185 Posterior lateral orbitofrontal cortex specifically detected rare reward e

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

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

188 Orbitofrontal cortex thus represents decision confidence

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

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

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

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

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

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

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

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

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

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

199 The orbitofrontal cortex, a structure generally overlooked i

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

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

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

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

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

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

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

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

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

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

210 0.25) in the left superior temporal cortex, orbitofrontal cortex, and left superior frontal cortex.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

241 Within orbitofrontal cortex, these neurons also sustain coding

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

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

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

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

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

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

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

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

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

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

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

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

254 , the striatum consistently outperformed the orbitofrontal cortex.

255 necting ventromedial subthalamic nucleus and orbitofrontal cortex.

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

257 egration in the superior temporal sulcus and orbitofrontal cortex.

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

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

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

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

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

263 dorsomedial frontal, anterior cingulate, and orbitofrontal cortex.

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

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

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

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

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

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

270 mposite score was negatively associated with orbitofrontal cortical thickness (p < 0.05, corrected).

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

272 mygdala, hippocampus, and lateral and medial orbitofrontal cortices (OFCs), were examined.

273 reduced volume in the ventral prefrontal and orbitofrontal cortices among youth reporting STBs, and t

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

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

276 onstrate a critical role of the piriform and orbitofrontal cortices in relapse to opioid seeking afte

277 s on top-down control from the prelimbic and orbitofrontal cortices over striatal activity through di

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

279 tural connectivity between supratemporal and orbitofrontal cortices, and between orbitofrontal and nu

280 Regions included the bilateral insulae/orbitofrontal cortices, anterior cingulate/paracingulate

281 as occipitotemporal, anterior cingulate, and orbitofrontal cortices.

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

283 Volumes of left and right lateral orbitofrontal gyri (LOFG), left superior temporal gyrus,

284 ion in the dorsomedial prefrontal cortex and orbitofrontal gyrus, and higher relative HDAC expression

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

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

287 ctivation impacts task performance, but only orbitofrontal inactivation reverts mice from an inferenc

288 licated in emotion regulation, including the orbitofrontal, lateral temporal, and medial temporal cor

289 trate that a connectivity-defined cell type, orbitofrontal neurons projecting to the striatum, carrie

290 prefrontal "reward" network, and the lateral orbitofrontal "nonreward" network.

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

292 onses of neurons in two core reward regions, orbitofrontal (OFC) and ventromedial prefrontal cortex (

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

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

295 iminished CMA connectivity with ventromedial/orbitofrontal regions.

296 nd maturation, particularly in cingulate and orbitofrontal regions.

297 r temporal areas, and also with asymmetry of orbitofrontal surface area.

298 An orbitofrontal variability encoding emerged around the sa

299 ivisions of the prefrontal cortex, including orbitofrontal, ventrolateral, dorsolateral, and ventrome

300 We found functional connectivity changes in orbitofrontal, ventromedial prefrontal, inferotemporal,