ライフサイエンスコーパス: uncinate fasciculus

1 regulation and the processing of reward (the uncinate fasciculus).

2 sterior superior longitudinal fasciculus and uncinate fasciculus.

3 ts such as the anterior cingulum, fornix and uncinate fasciculus.

4 matter integrity) in the cingulum bundle and uncinate fasciculus.

5 everal association tracts, most commonly the uncinate fasciculus.

6 , the right arcuate fasciculus, and the left uncinate fasciculus.

7 erior limb of the internal capsule and right uncinate fasciculus.

8 als with reduced structural integrity of the uncinate fasciculus.

9 tal fasciculus, superior corona radiata, and uncinate fasciculus.

10 ornix, the parahippocampal cingulum, and the uncinate fasciculus.

11 e had significantly decreased FA in the left uncinate fasciculus.

12 terior commissure, corpus callosum and right uncinate fasciculus.

13 ion between memory performance and FA in the uncinate fasciculus.

14 ry performance and FA in a ROI placed in the uncinate fasciculus.

15 d to quantify the water diffusion within the uncinate fasciculus.

16 or cingulate cortex and the amygdala via the uncinate fasciculus.

17 medial frontal cortex via forceps minor and uncinate fasciculus; 2) rostral and dorsal cingulate cor

18 In addition, tractography analysis of the uncinate fasciculus, a tract associated with semantic pr

19 oved prediction model also included the left uncinate fasciculus, a white matter tract connecting the

20 ry analysis revealed that involvement of the uncinate fasciculus adjudicated between Broca's and glob

21 The uncinate fasciculus also is a conduit for vPFC fibers to

22 the white matter of the external capsule and uncinate fasciculus and a perisylvian division travellin

23 These findings suggest that abnormal uncinate fasciculus and cingulum WM structure may underl

24 rior cingulate, anterior thalamic radiation, uncinate fasciculus and hippocampal portion of the cingu

25 inferior fronto-occipital fasciculus and the uncinate fasciculus and in the left parietal regions tha

26 ex, and a white-matter index for the fornix, uncinate fasciculus and inferior longitudinal fasciculus

27 ed a significant increase in FA in bilateral uncinate fasciculus and right inferior longitudinal fasc

28 interest from the JHU ICBM atlas, including uncinate fasciculus and sagittal stratum as a control tr

29 The left uncinate fasciculus and the genu and splenium of the cor

30 l frontal cortex (via forceps minor and left uncinate fasciculus) and to the cingulate cortex (via le

31 motional regulation circuitry (ie, cingulum, uncinate fasciculus, and forceps minor) and (1) broader

32 nteraction for fractional anisotropy and for uncinate fasciculus area, derived from automatic segment

33 erminalis, ventral amygdalofugal pathway and uncinate fasciculus) as well as the internal and externa

34 onal anisotropy values in the left and right uncinate fasciculus, as measured by tract-based analysis

35 verging white matter bundles (forceps minor, uncinate fasciculus, cingulum and fronto-striatal fibers

36 I; compromised white-matter integrity of the uncinate fasciculus connecting the insula with the amygd

37 vPFC efferent axons travel through the uncinate fasciculus, connecting different vPFC regions a

38 h NMO, mainly located in the corona radiata, uncinate fasciculus, corpus callosum, optic radiation, i

39 and increased risk taking and reduced FA in uncinate fasciculus correlated significantly with increa

40 Conversely, damage to the uncinate fasciculus correlated with deficits in semantic

41 l fasciculus and from rostral to caudal, the uncinate fasciculus, extreme capsule and arcuate fascicu

42 nal fasciculus, fronto-occipital fasciculus, uncinate fasciculus, extreme capsule, and inferior longi

43 dinal fasciculus and arcuate fasciculus, the uncinate fasciculus, extreme capsule, middle longitudina

44 ate fasciculus (dorsal language pathway) and uncinate fasciculus/extreme capsule (ventral language pa

45 a lack of correlation between attention and uncinate fasciculus FA and the lack of correlation betwe

46 carriers had the greatest change within left uncinate fasciculus (FA: -7.9%/yr, p < 0.001; MD: 10.9%/

47 (t > 3.0, P <or= .05 corrected) in the right uncinate fasciculus (greater radial diffusivity).

48 Although abnormalities in the uncinate fasciculus have been associated with several ps

49 aphasia and further confirm the role of the uncinate fasciculus in semantic processing.

50 y and decreased axial diffusivity within the uncinate fasciculus in youth with emotional DDs vs those

51 ignificant WM differences bilaterally in the uncinate fasciculus (increased fractional anisotropy in

52 ractional anisotropy values in the bilateral uncinate fasciculus indicated reduced frontolimbic struc

53 The bidirectionality of the uncinate fasciculus information flow allows orbital fron

54 we identified a negative correlation between uncinate fasciculus integrity and subgenual ACC function

55 This reduction in uncinate fasciculus integrity was most pronounced for pa

56 The uncinate fasciculus is a bidirectional, long-range white

57 We propose that an overarching role of the uncinate fasciculus is to allow temporal lobe-based mnem

58 s in the left and right corona radiata, left uncinate fasciculus, left inferior fronto-occipital fasc

59 han right hemisphere stroke patients without uncinate fasciculus lesions in the emotional empathy tas

60 Participants with right uncinate fasciculus lesions were significantly more impa

61 tion of microstructure in the fornix and the uncinate fasciculus make critical but differential contr

62 In contrast, a decline in uncinate fasciculus microstructure was linked to impaire

63 the non-fluent/agrammatic variant and in the uncinate fasciculus of patients with the semantic varian

64 diagnosis by genotype interaction within the uncinate fasciculus (P0.05), with BD subjects carrying t

65 The right uncinate fasciculus plays an important role in the emoti

66 (t > 3.0, P <or= .05 corrected) in the left uncinate fasciculus (reduced radial diffusivity distally

67 and axial diffusivity in the left [P = .01] uncinate fasciculus, respectively).

68 al anisotropy (FA) was lower within the left uncinate fasciculus, right caudate and occipital regions

69 (FA) were measured in the following tracts: uncinate fasciculus, superior cingulum, temporal cingulu

70 e left superior longitudinal fasciculus, the uncinate fasciculus, the forceps minor, and in the genu

71 Anisotropic diffusion was assessed in the uncinate fasciculus, the most prominent white matter tra

72 th reduced structural integrity in the right uncinate fasciculus, the primary white matter connection

73 ies are present in association fibers of the uncinate fasciculus (UF) and cingulum bundle (CB) among

74 AF), inferior longitudinal fasciculus (ILF), uncinate fasciculus (UF) and cingulum bundle (CB).

75 had significantly decreased FA values in the uncinate fasciculus (UF) bilaterally (mean FA, 0.425; 95

76 The human brain uncinate fasciculus (UF) is an important cortico-cortica

77 ip between structural characteristics of the uncinate fasciculus (UF) measured by Diffusion Tensor Im

78 ckness and fractional anisotropy (FA) of the uncinate fasciculus (UF) were considered.

79 and a probabilistically defined tract of the uncinate fasciculus (UF), a WM pathway connecting the am

80 nd cerebellum; white matter integrity in the uncinate fasciculus, ventral frontal, and right cerebell

81 were included, of which the integrity of the uncinate fasciculus was assessed that connects the subge

82 l empathy, but only percentage damage to the uncinate fasciculus was independently associated with er

83 ts showed that white matter integrity of the uncinate fasciculus was reduced and that functional conn

84 cts--the extreme capsule fiber system or the uncinate fasciculus--was not associated with syntactic d

85 nix, parahippocampal white matter bundle and uncinate fasciculus were reconstructed, and scalar diffu