ライフサイエンスコーパス: angular gyrus

1 d connectivity between frontal areas and the angular gyrus.

2 ory retrieval, including the hippocampus and angular gyrus.

3 d to the left lateral parietal cortex in the angular gyrus.

4 nterior and posterior midline structures and angular gyrus.

5 pocampus, medial prefrontal cortex, and left angular gyrus.

6 rk, including posterior cingulate cortex and angular gyrus.

7 middle and inferior frontal gyri, and right angular gyrus.

8 eased, particularly with respect to the left angular gyrus.

9 In the posterior angular gyrus, a neural priming effect was observed for

10 or parietal lobule that was localized to the angular gyrus, a structure belonging to the heteromodal

11 The angular gyrus accounted for this difference in asymmetry

12 We suggest angular gyrus activation reflects the experiences of age

13 o structures in left temporoparietal cortex, angular gyrus (AG) and posterior middle temporal gyrus (

14 a novel functional dissociation between the angular gyrus (AG) and posterior middle temporal gyrus (

15 ial/posterior cingulate cortex (RSC/PCC) and angular gyrus (AG) in the high-frequency broadband (HFB,

16 Here, we test the hypothesis that the angular gyrus (AG) is critical for integrating semantic

17 The left angular gyrus (AG) is reliably activated across a wide r

18 tion (cTBS)-induced disruption of M1 and the angular gyrus (AG) of the IPL on learning a probabilisti

19 associated with a buildup of activity in the angular gyrus (AG) that predicted memory 24 h later.

20 such as the anterior temporal lobe (ATL) or angular gyrus (AG).

21 The angular gyrus also is thought to have functional links w

22 pocampus, medial prefrontal cortex, and left angular gyrus, among other regions.

23 volved during spatial attention and the left angular gyrus and anterior cingulate cortex during motor

24 tive and positively modulated FC was between angular gyrus and hippocampus, while the greatest overal

25 arge left-right asymmetry was present in the angular gyrus and inferior occipital gyrus.

26 ontrast, classifier performance for both the angular gyrus and insular cortex was reliably enhanced b

27 ts, only target-specific semantic effects in angular gyrus and MTG.

28 Instead, our results implicate the angular gyrus and parahippocampal region in this role.

29 Whereas angular gyrus and posterior cingulate/precuneus were sig

30 o long events in high-order areas (including angular gyrus and posterior medial cortex), which repres

31 eft-hemisphere language regions, such as the angular gyrus and the banks of the intraparietal sulcus.

32 l cortex, the intraparietal sulcus, the left angular gyrus and the inferior temporal gyrus.

33 in the left anterior temporal lobe, the left angular gyrus and the posterior bank of the left postcen

34 pontaneous neuronal excitability in both the angular gyrus and the primary motor cortex caused the re

35 FG) and of semantic competition in MTG, left angular gyrus, and IFG.

36 osterior middle temporal gyrus (LpMTG), left angular gyrus, and left intraparietal sulcus (LIPS), in

37 Rolandic operculum, superior parietal gyrus, angular gyrus, and middle temporal pole.

38 of agency, no priming-related activation of angular gyrus, and no priming-related changes in fronto-

39 n in posterior regions (Wernicke's area, the angular gyrus, and striate cortex) and relative overacti

40 efault-mode network, including precuneus and angular gyrus, and the salience network, including insul

41 ctional connectivity with the precuneus, the angular gyrus, and the temporal visual cortex Brodmann a

42 rieval precision scaled with activity in the angular gyrus, and vividness judgments tracked activity

43 nce that functionally distinct subregions of angular gyrus (AnG) contribute to the retrieval of episo

44 f investigation indicates the involvement of angular gyrus (AnG) in the retrieval of both episodic an

45 coding and retrieval can be decoded from the angular gyrus (ANG), a subregion of posterior lateral pa

46 Therefore, the angular gyrus appears to recombine consolidated schema c

47 BA 38 (anterior temporal cortex) and BA 39 (angular gyrus)--as discriminant variables, classified pa

48 A further test of angular gyrus asymmetry showed a reversal of the normal

49 The angular gyrus (BA39) was functionally correlated with BA

50 erior cingulate (BA31), precuneus (BA7m) and angular gyrus (BA39).

51 this difference in asymmetry, with the left angular gyrus being significantly larger (18.7%) than th

52 tion level-dependent signal in the posterior angular gyrus bilaterally, left occipitotemporal cortex,

53 n area 10, 32), right hippocampus, bilateral angular gyrus (Brodmann area 39), left posterior cingula

54 posterior nodes of the DMN, particularly the angular gyrus, but also more anterior and dorsal parieta

55 chema components, which converged within the angular gyrus during retrieval.

56 hat the anatomical disconnection of the left angular gyrus from other brain regions that are part of

57 are consistent with a critical role for the angular gyrus in conceptual combination.

58 temporal cortex in males and with the right angular gyrus in females.

59 elated in intensity with deactivation of the angular gyrus in females; no such relationships were obs

60 dividual differences in the structure of the angular gyrus in healthy adults are related to variabili

61 ndings demonstrate a causal role of the left angular gyrus in lexical-semantic integration and provid

62 hypothesizes functional linkages between the angular gyrus in the left hemisphere and visual associat

63 articularly evident in areas of LPC (namely, angular gyrus) in which activity scaled with subjective

64 ed in the sense of self and agency), and the angular gyrus (involved in language) is thus related to

65 We demonstrate that the RH angular gyrus is active during ASL processing only in na

66 s are the first to demonstrate that the left angular gyrus is critical for both episodic simulation a

67 In contrast, the left angular gyrus is functionally disconnected from these re

68 , we found that the degree of atrophy in the angular gyrus is specifically related to impaired perfor

69 trated that temporary disruption of the left angular gyrus leads to impairments in simulation and mem

70 raphy scans showed regions in left and right angular gyrus, left mid-temporal gyrus, and left middle

71 etrosplenial cortex, lateral parietal cortex/angular gyrus, medial prefrontal cortex, superior fronta

72 hology averaged from three cerebral regions (angular gyrus, mid-frontal cortex, and anterior cingulat

73 ivation in anterior and posterior cingulate, angular gyrus, middle frontal gyrus, and cuneus.

74 pecifically modulates neural activity in the angular gyrus of healthy adults, independent of the moda

75 rea involved in all neglect patients was the angular gyrus of the inferior parietal lobe (IPL).

76 e inferior parietal lobule, particularly the angular gyrus of the inferior parietal lobule, and the p

77 y associated with hypoperfusion of the right angular gyrus (p < 0.0001).

78 in areas including the left parietal cortex [angular gyrus/parallel sulcus (area 39)], left anterior

79 or supramarginal gyrus and adjacent anterior angular gyrus, planum temporale, and posterior superior

80 oral lobe, lateral inferior parietal cortex (angular gyrus), posterior cingulate cortex, dorsomedial

81 ior frontal gyrus, medial prefrontal cortex, angular gyrus, posterior MTG, and medial temporal lobes.

82 s of individual regions demonstrated thinner angular gyrus, precuneus and superior parietal lobule in

83 lso regionally specific; connectivity of the angular gyrus predicted poorer performance in both group

84 y tasks also increased after TMS to the left angular gyrus relative to the vertex.

85 ivity in the superior temporal gyrus and the angular gyrus, respectively.

86 bank of the intraparietal sulcus and on the angular gyrus, responds selectively to cues for differen

87 of the error: this network, including right angular gyrus, right supplementary motor area, and bilat

88 e. episodic memory: medial temporal lobe and angular gyrus; semantic memory: left anterior temporal r

89 ocessing areas such as superior temporal and angular gyrus showed no delay or width difference for ro

90 other set, including the hippocampus and the angular gyrus, showed a nonmonotonic response profile tr

91 hat regional cerebral blood flow in the left angular gyrus shows strong within-task, across-subjects

92 ontrol site (vertex), disruption of the left angular gyrus significantly reduced the number of intern

93 Within the IPL, although supramarginal and angular gyrus (SMG; AG) regions both demonstrated invali

94 tures (dorsal and ventral PFC, amygdala, and angular gyrus) subserving moral cognition and emotion.

95 erior parietal areas located anterior to the angular gyrus such as AIP and VIP are less medially disp

96 a subregion of lateral parietal cortex, the angular gyrus, supported successful reconstruction of pe

97 , white matter region proximate to the right angular gyrus (Tailerach coordinates 35, -71, 19) and wh

98 ombined stimulation of the supramarginal and angular gyrus than an isolated PFm stimulation.

99 sociated with increased activity in the left angular gyrus, the medial and left lateral prefrontal co

100 ng that recollection-related activity in the angular gyrus tracked the period over which recollected

101 r middle/inferior temporal gyrus (pMTG/ITG), angular gyrus, ventral temporal cortex, posterior cingul

102 tween inferior prefrontal region volumes and angular gyrus volumes.

103 cortex, orbital prefrontal cortex, and left angular gyrus, was involved in the neural interaction be

104 On the other hand, lesions in the angular gyrus were associated with persistent allocentri

105 rietal region, area 45 is connected with the angular gyrus, whereas area 44 is connected with the sup

106 GG-homozygotes) in the right middle temporal/angular gyrus while subjects were viewing negative versu

107 ation by nicotine in posterior cingulate and angular gyrus with performance improvements under INT(hi

108 ion of heteromodal association cortex in the angular gyrus would be critical for conceptual combinati

109 ess whether temporary disruption of the left angular gyrus would impair both episodic simulation and