ライフサイエンスコーパス: anterior commissure

1 in a marsupial-like projection fate via the anterior commissure.

2 commissural bundles: the corpus callosum and anterior commissure.

3 ratum radiatum, the corpus callosum, and the anterior commissure.

4 f axons that form the posterior tract of the anterior commissure.

5 kinase expressed on axons projecting in the anterior commissure.

6 us callosum, hippocampal commissure, and the anterior commissure.

7 d, including the hippocampus, cerebellum and anterior commissure.

8 he pCC growth cone was redirected across the anterior commissure.

9 i lateralis was observed at the level of the anterior commissure.

10 internal capsule (ALIC) and anterior lateral anterior commissure.

11 s 39 and surroundings) via the posterior and anterior commissures.

12 +/- 0.03, P = .01) and white matter tracts (anterior commissure: 0.05 ug . g(-1) +/- 0.01, P = .002;

13 ormalities (70%), hypoplasia/agenesis of the anterior commissure (66%), short midbrain and small infe

14 nguage impairment was only detectable if the anterior commissure (a second temporal lobe commissural

15 The anterior commissure (AC) and the much smaller hippocampa

16 lopment: the postoptic commissure (POC), the anterior commissure (AC) and the optic nerve.

17 tralateral bulbectomy and transection of the anterior commissure (AC), (b) unilateral MD lesions plus

18 ozygote GAP-43 (-/-) mice failed to form the anterior commissure (AC), hippocampal commissure (HC), a

19 ng axon development and establishment of the anterior commissure (AC).

20 ctive to telencephalic neurons that form the anterior commissure (AC).

21 However, striatal regions caudal to the anterior commissure also receive inputs from the amygdal

22 the number of myelinated nerve fibers in the anterior commissure, an increase in the frequency of str

23 ralateral optic nerve, rostrally towards the anterior commissure and along the ipsilateral optic trac

24 stitial nucleus of the posterior limb of the anterior commissure and central and medial nuclei of the

25 missural projection that courses through the anterior commissure and innervates mainly the contralate

26 anterior commissure or the area between the anterior commissure and midposterior MA (P < .005 versus

27 ting reveal the absence or hypoplasia of the anterior commissure and reduced olfaction in a large pro

28 ction is required for the development of the anterior commissure and the corticothalamic, corticospin

29 eocortex results in lack of corpus callosum, anterior commissure, and corticospinal tract formation.

30 erves and dysgenesis of the corpus callosum, anterior commissure, and corticospinal tracts.

31 including internal capsule, corpus callosum, anterior commissure, and fimbria hippocampi, were invest

32 elencephalic VZ at the levels of area X, the anterior commissure, and high vocal center (HVC) reveale

33 roimaging reveals a thin corpus callosum and anterior commissure, and hypoplastic to absent olfactory

34 ral alterations of the bilateral PaVN, right anterior commissure, and left fornix (FX).

35 u-fibers, the corpus callosum forceps minor/anterior commissure, and the left middle cerebellar pedu

36 ss through the contralateral bulb, cross the anterior commissure, and then run to the ipsilateral olf

37 halamic, and nigrostriatal tracts and of the anterior commissure, and they show a variable loss of th

38 midline at the level of the hippocampal and anterior commissures, and more caudally at the medial pr

39 tely 13%), fimbria ( approximately 18%), and anterior commissure ( approximately 10%).

40 In all, 90-95% of the nerve fibers in the anterior commissure are myelinated.

41 The most common neuroglial cells in the anterior commissure are oligodendrocytes.

42 corpus callosum were transected, leaving the anterior commissure as the only path for cortical interh

43 correlated with parahippocampal cingulum and anterior commissure atrophy, indicating an effect of the

44 st rostral to the midline convergence of the anterior commissure back to the transition zone between

45 llosum, fornix, and posterior portion of the anterior commissure, but not in the lateral olfactory tr

46 r greatly reduced in the Fz3(-/-) brain: the anterior commissure, cerebral peduncle (corticospinal tr

47 scores to FA values in the cingulum, fornix, anterior commissure, corpus callosum and right uncinate

48 r relationships to the vertical plane at the anterior commissure, corpus callosum, and cingulate sulc

49 The diminutive telencephalic commissures (anterior commissure, corpus callosum, and hippocampal co

50 nd in crossing fiber pathways, including the anterior commissure, corpus callosum, and posterior comm

51 in fiber tracts such as the corpus callosum, anterior commissure, corticofugal fibers, lateral lemnis

52 sk allele was also associated with a smaller anterior commissure cross-sectional area (beta=-.167 mm2

53 the corpus callosum and the hippocampal and anterior commissures depriving one hemisphere of visual

54 mined stimulus intensity-response curves for anterior commissure-evoked hippocampal CA1 field potenti

55 area dorsalis (Dl) at about the level of the anterior commissure exhibits such a bilateral difference

56 ough the splenium of the corpus callosum and anterior commissure) explained 57% of the variance in la

57 the corpus callosum and the hippocampal and anterior commissures, fail to cross the midline.

58 ts-corpus callosum, ventral hippocampal, and anterior commissures-failed to cross the midline in mice

59 stitial nucleus of the posterior limb of the anterior commissure frequently and substantially disrupt

60 e matter, corpus callosum, internal capsule, anterior commissure), gray matter (globus pallidus, thal

61 jections of spinal sensory axons, and in the anterior commissure, habenulo-interpeduncular tract, and

62 ition, we found that a nonfrontal tract, the anterior commissure, had a smaller volume fraction in hu

63 lfactory tract, hippocamposeptal projection, anterior commissure, hippocampal commissure, and medial

64 ts of the VZ at the levels of area X and the anterior commissure in juveniles but not adults.

65 onal Sema3F in the normal development of the anterior commissure in the ventral forebrain and infrapy

66 phere and transected the corpus callosum and anterior commissure in two macaques.

67 with transection of the corpus callosum and anterior commissure in two macaques.

68 connected to the temporal lobe (such as the anterior commissure, inferior fronto-occipital fasciculu

69 all anatomical structures (corpus callosum, anterior commissure, internal capsule, thalamus, caudopu

70 stitial nucleus of the posterior limb of the anterior commissure (IPAC), a nucleus of the central ext

71 stitial nucleus of the posterior limb of the anterior commissure (IPAC), a subregion of the extended

72 stitial nucleus of the posterior limb of the anterior commissure (IPAC, 56%), bed nucleus of the stri

73 ean number of myelinated nerve fibers in the anterior commissure is 2.2 x 10(6), while in the old mon

74 e lateralized through naris occlusion as the anterior commissure is not yet functional.

75 TLJ) are two BSTL regions that lie above the anterior commissure, near the ventral striatum.

76 stitial nucleus of the posterior limb of the anterior commissure nucleus, and bed nucleus of the stri

77 the effects of age on the composition of the anterior commissure of the rhesus monkey.

78 The anterior commissures of nine young (5-10 years), five mi

79 toward the opposite side of the MA near the anterior commissure or the area between the anterior com

80 riented to standard position parallel to the anterior commissure-posterior commissure line and segmen

81 above a standard radiologic horizontal line (anterior commissure-posterior commissure line; ACPC line

82 frontal white matter regions 15 mm above the anterior commissure-posterior commissure plane was assoc

83 2) caudal to the posterior commissure in the anterior commissure-posterior commissure plane.

84 there was a reduction of the diameter of the anterior commissure produced by the asphyxia that was pr

85 uced several congruent phenotypes, including anterior commissure reduction in heterozygotes, which wa

86 commissural neurons instead project via the anterior commissure, similar to egg-laying monotreme mam

87 cific zone of dorsomedial VS, just above the anterior commissure; stimulation of more ventrolateral s

88 onal defects, affecting the corpus callosum, anterior commissure, subcortical fiber tracts, and inter

89 netic defects and neuropathological targets (anterior commissure, thalamus).

90 ivity in the corpus callosum compared to the anterior commissure that was not consistently seen follo

91 ntal cortex, the interstitial nucleus of the anterior commissure, the nucleus of the lateral olfactor

92 Jnk1(-/-) mice exhibit disrupted anterior commissure tract formation and a progressive lo

93 However, the anterior commissure was absent, and the corpus callosal

94 ly, this effect was greatly mitigated if the anterior commissure was left intact.

95 Critically, the nucleus accumbens proper and anterior commissure were associated with beneficial but

96 e same cell group (dorsal and ventral to the anterior commissure), which plays a role in coordinating