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1 commissural bundles: the corpus callosum and anterior commissure.
2 ratum radiatum, the corpus callosum, and the anterior commissure.
3 f axons that form the posterior tract of the anterior commissure.
4 kinase expressed on axons projecting in the anterior commissure.
5 us callosum, hippocampal commissure, and the anterior commissure.
6 d, including the hippocampus, cerebellum and anterior commissure.
7 he pCC growth cone was redirected across the anterior commissure.
8 i lateralis was observed at the level of the anterior commissure.
9 s 39 and surroundings) via the posterior and anterior commissures.
10 nguage impairment was only detectable if the anterior commissure (a second temporal lobe commissural
13 tralateral bulbectomy and transection of the anterior commissure (AC), (b) unilateral MD lesions plus
14 ozygote GAP-43 (-/-) mice failed to form the anterior commissure (AC), hippocampal commissure (HC), a
18 the number of myelinated nerve fibers in the anterior commissure, an increase in the frequency of str
19 ralateral optic nerve, rostrally towards the anterior commissure and along the ipsilateral optic trac
20 stitial nucleus of the posterior limb of the anterior commissure and central and medial nuclei of the
21 missural projection that courses through the anterior commissure and innervates mainly the contralate
22 anterior commissure or the area between the anterior commissure and midposterior MA (P < .005 versus
23 ting reveal the absence or hypoplasia of the anterior commissure and reduced olfaction in a large pro
24 ction is required for the development of the anterior commissure and the corticothalamic, corticospin
25 eocortex results in lack of corpus callosum, anterior commissure, and corticospinal tract formation.
27 including internal capsule, corpus callosum, anterior commissure, and fimbria hippocampi, were invest
28 elencephalic VZ at the levels of area X, the anterior commissure, and high vocal center (HVC) reveale
29 roimaging reveals a thin corpus callosum and anterior commissure, and hypoplastic to absent olfactory
30 ss through the contralateral bulb, cross the anterior commissure, and then run to the ipsilateral olf
31 halamic, and nigrostriatal tracts and of the anterior commissure, and they show a variable loss of th
32 midline at the level of the hippocampal and anterior commissures, and more caudally at the medial pr
36 corpus callosum were transected, leaving the anterior commissure as the only path for cortical interh
37 correlated with parahippocampal cingulum and anterior commissure atrophy, indicating an effect of the
38 st rostral to the midline convergence of the anterior commissure back to the transition zone between
39 llosum, fornix, and posterior portion of the anterior commissure, but not in the lateral olfactory tr
40 r greatly reduced in the Fz3(-/-) brain: the anterior commissure, cerebral peduncle (corticospinal tr
41 scores to FA values in the cingulum, fornix, anterior commissure, corpus callosum and right uncinate
42 r relationships to the vertical plane at the anterior commissure, corpus callosum, and cingulate sulc
43 The diminutive telencephalic commissures (anterior commissure, corpus callosum, and hippocampal co
44 nd in crossing fiber pathways, including the anterior commissure, corpus callosum, and posterior comm
45 in fiber tracts such as the corpus callosum, anterior commissure, corticofugal fibers, lateral lemnis
46 sk allele was also associated with a smaller anterior commissure cross-sectional area (beta=-.167 mm2
47 the corpus callosum and the hippocampal and anterior commissures depriving one hemisphere of visual
48 mined stimulus intensity-response curves for anterior commissure-evoked hippocampal CA1 field potenti
49 area dorsalis (Dl) at about the level of the anterior commissure exhibits such a bilateral difference
50 ough the splenium of the corpus callosum and anterior commissure) explained 57% of the variance in la
52 ts-corpus callosum, ventral hippocampal, and anterior commissures-failed to cross the midline in mice
53 stitial nucleus of the posterior limb of the anterior commissure frequently and substantially disrupt
54 jections of spinal sensory axons, and in the anterior commissure, habenulo-interpeduncular tract, and
55 lfactory tract, hippocamposeptal projection, anterior commissure, hippocampal commissure, and medial
57 onal Sema3F in the normal development of the anterior commissure in the ventral forebrain and infrapy
60 all anatomical structures (corpus callosum, anterior commissure, internal capsule, thalamus, caudopu
61 stitial nucleus of the posterior limb of the anterior commissure (IPAC, 56%), bed nucleus of the stri
62 ean number of myelinated nerve fibers in the anterior commissure is 2.2 x 10(6), while in the old mon
65 stitial nucleus of the posterior limb of the anterior commissure nucleus, and bed nucleus of the stri
68 toward the opposite side of the MA near the anterior commissure or the area between the anterior com
69 riented to standard position parallel to the anterior commissure-posterior commissure line and segmen
70 above a standard radiologic horizontal line (anterior commissure-posterior commissure line; ACPC line
71 frontal white matter regions 15 mm above the anterior commissure-posterior commissure plane was assoc
73 cific zone of dorsomedial VS, just above the anterior commissure; stimulation of more ventrolateral s
74 onal defects, affecting the corpus callosum, anterior commissure, subcortical fiber tracts, and inter
76 ivity in the corpus callosum compared to the anterior commissure that was not consistently seen follo
77 ntal cortex, the interstitial nucleus of the anterior commissure, the nucleus of the lateral olfactor
81 e same cell group (dorsal and ventral to the anterior commissure), which plays a role in coordinating
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