ライフサイエンスコーパス: lateral orbitofrontal cortex

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

2 ower GM in bilateral temporal poles and left lateral orbitofrontal cortex.

3 correlates directly with BOLD signal in the lateral orbitofrontal cortex.

4 tional, particularly sad, distractors in the lateral orbitofrontal cortex.

5 tions engaging connectivity between rACC and lateral orbitofrontal cortex, a region reflecting outcom

6 e perception (rostral ACC), decision making (lateral orbitofrontal cortex), action selection (caudal

7 reas, the BPM group exhibited decreased left lateral orbitofrontal cortex activation compared with bo

8 ons of the OFC, the agranular insula and the lateral orbitofrontal cortex (AI-OPNs and LO-OPNs, respe

9 ts), the lower was their D2-type BPND in the lateral orbitofrontal cortex, an important region in val

10 ed the anterior cingulate cortex, medial and lateral orbitofrontal cortex and amygdala, parahippocamp

11 irrored by opposite aversion-like signals in lateral orbitofrontal cortex and anterior cingulate cort

12 long-range white matter tract that connects lateral orbitofrontal cortex and Brodmann area 10 with t

13 ns to aversive stimuli were increased in the lateral orbitofrontal cortex and insula.

14 Focused optogenetic stimulation of the lateral orbitofrontal cortex and its terminals in the st

15 ticipants, including reduced GMV in the left lateral orbitofrontal cortex and lower cortical thicknes

16 f attention from dorsolateral prefrontal and lateral orbitofrontal cortex and may represent an organi

17 bsequent analysis localized these signals to lateral orbitofrontal cortex and posterior insula respec

18 uctural and functional abnormalities in left lateral orbitofrontal cortex and right supplementary mot

19 , basolateral and other), amygdala nuclei to lateral orbitofrontal cortex and stronger connections of

20 the ventromedial prefrontal cortex (VMPFC), lateral orbitofrontal cortex, and amygdala] while it sim

21 al connectivity among regions such as vmPFC, lateral orbitofrontal cortex, and parahippocampal gyrus

22 perior and inferior frontal gyri, medial and lateral orbitofrontal cortex, and parahippocampal gyrus,

23 ation in the ventromedial prefrontal cortex, lateral orbitofrontal cortex, and periaqueductal gray re

24 m, especially the left hippocampus, the left lateral orbitofrontal cortex, and the bilateral isthmus

25 ecreased grey matter in the anterior insula, lateral orbitofrontal cortex, anterior cingulate and dor

26 nd evaluation of wrong choices activated the lateral orbitofrontal cortex, anterior insula, superior

27 Second, the lateral orbitofrontal cortex Brodmann area 47/12 had inc

28 the increased functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 is rela

29 owed that the functional connectivity of the lateral orbitofrontal cortex Brodmann area 47/12 with th

30 The lateral orbitofrontal cortex Brodmann area 47/12, involv

31 ns (in particular angry expressions); namely lateral orbitofrontal cortex (Brodmann area 47) and medi

32 -dorsolateral prefrontal cortex and amygdala-lateral orbitofrontal cortex coupling were shown in male

33 l orbitofrontal cortex, and amSTN DBS to the lateral orbitofrontal cortex, dorsal anterior cingulate

34 n of several cortical regions, including the lateral orbitofrontal cortex, during reversal learning i

35 In the lateral orbitofrontal cortex, greater sleep fragmentatio

36 significantly lower bilateral volume in the lateral orbitofrontal cortex, hippocampus, accumbens are

37 owever, we find evidence for the role of the lateral orbitofrontal cortex in action sequencing.

38 brain stem regions and less deactivation in lateral orbitofrontal cortex in hypoglycemia unawareness

39 ses in activation in the anterior insula and lateral orbitofrontal cortex in response to a high-fat/h

40 d receipt of food but less activation in the lateral orbitofrontal cortex in response to receipt of f

41 Varenicline-induced activation of lateral orbitofrontal cortex in the brain at rest (t = 5

42 drive; optogenetic stimulation revealed that lateral orbitofrontal cortex input to SPNs was reduced i

43 cit was dependent on a circuit involving the lateral orbitofrontal cortex, insula, amygdala and tempo

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

45 ) display disrupted performance and abnormal lateral orbitofrontal cortex (LOFC) activity during reve

46 The lateral orbitofrontal cortex (lOFC) and basolateral amyg

47 We find that the lateral orbitofrontal cortex (lOFC) and hippocampus (HC)

48 computationally distinct learning signals in lateral orbitofrontal cortex (lOFC) and the dopaminergic

49 The lateral orbitofrontal cortex (lOFC) has been described a

50 Studies of neural dynamics in lateral orbitofrontal cortex (lOFC) have shown that subs

51 amygdala (BLA) and its interaction with the lateral orbitofrontal cortex (lOFC) in the ability to le

52 Recent work in macaques has suggested the lateral orbitofrontal cortex (lOFC) is relatively more c

53 The lateral orbitofrontal cortex (lOFC) is typically thought

54 en assessed if pharmacologic inactivation of lateral orbitofrontal cortex (lOFC) or DBS of the ventra

55 Recordings from lateral orbitofrontal cortex (lOFC) revealed encoding of

56 (HFD) exposure on GABAergic function in the lateral orbitofrontal cortex (lOFC), a region known to g

57 ctivity in three frontal cortical areas, the lateral orbitofrontal cortex (lOFC), medial orbitofronta

58 the prelimbic medial frontal cortex (PL) and lateral orbitofrontal cortex (lOFC), which have been imp

59 aptic electrophysiological properties in the lateral orbitofrontal cortex (lOFC).

60 regions (medial orbitofrontal cortex [mOFC], lateral orbitofrontal cortex, middle frontal cortex [MFC

61 Left lateral orbitofrontal cortex modulation serves as a warn

62 from the dorsolateral prefrontal cortex and lateral orbitofrontal cortex (n = 495) to quantify expre

63 t NE, a positive association between 3-month lateral orbitofrontal cortex ODI and prospective NE, and

64 ed MRI-based segmentations of the medial and lateral orbitofrontal cortex (OFC) and hippocampal volum

65 studies have demonstrated activations in the lateral orbitofrontal cortex (OFC) and the inferior fron

66 ence for dissociable roles of the medial and lateral orbitofrontal cortex (OFC) in major depressive d

67 The lateral orbitofrontal cortex (OFC) is critical for flexi

68 is question by recording both signals in the lateral orbitofrontal cortex (OFC) of rats during olfact

69 ons in expected reward identity and that the lateral orbitofrontal cortex (OFC) represents reward ide

70 Here, we show that the human lateral orbitofrontal cortex (OFC) represents the conten

71 The lateral orbitofrontal cortex (OFC) supports model-based

72 ral signatures of outcome integration in the lateral orbitofrontal cortex (OFC), where concurrently p

73 und in three other frontal cortical regions: lateral orbitofrontal cortex (orbital part of area 12 [1

74 ssociated with cortical atrophy in the right lateral orbitofrontal cortex (p(adj) = 0.03) and right p

75 05, partial r = -0.260; DRRI-aftermath right lateral orbitofrontal cortex: P = .03, partial r = -0.19

76 le/parietal operculum (PT/PO), and posterior lateral orbitofrontal cortex (plOFC) had local gray matt

77 l abnormality compared with controls for the lateral orbitofrontal cortex reward value signal and the

78 l percentage of high bets (P = 0.0015) and a lateral orbitofrontal cortex risky decision signal was a

79 the dorsolateral prefrontal cortex, and the lateral orbitofrontal cortex, significantly moderated th

80 Posterior lateral orbitofrontal cortex specifically detected rare

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

82 Lateral orbitofrontal cortex supported contingent learni

83 children had greater activation in the left lateral orbitofrontal cortex than did low-risk children

84 lphenidate induced greater increases in left lateral orbitofrontal cortex than when it was expected.

85 roach restricting analysis to the medial and lateral orbitofrontal cortex, the amygdala, the anterior

86 ard-guided learning and decision-making: the lateral orbitofrontal cortex, the ventromedial prefronta

87 ofrontal cortex and in the reward-evaluating lateral orbitofrontal cortex underlie a diminished smoki

88 ing (middle frontal gyrus), decision-making (lateral orbitofrontal cortex), visual processing (fusifo

89 dly, the mPFC was not involved; however, the lateral orbitofrontal cortex was critical.

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

91 dify behaviour through interactions with the lateral orbitofrontal cortex, which provides valence-bas