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1 s in development of the infundibulum and the posterior lobe.
2 the pituitary, irBC was noted mainly in the posterior lobe.
3 -R2 transcripts were expressed mainly in the posterior lobe.
4 he anterior lobe and in limited areas of the posterior lobe.
5 f strong directional selection acting on the posterior lobe.
6 sed primarily in Purkinje cells (PCs) of the posterior lobe.
7 ut to the hindlimb C1 zone in the cerebellar posterior lobe.
8 n the anterior lobe or, unexpectedly, in the posterior lobe.
9 ts a history of directional selection on the posterior lobe.
10 anterior lobe but involves a portion of the posterior lobe.
11 nd preferential loss of granule cells in the posterior lobes.
12 elopment and in the prospective anterior and posterior lobes.
13 he primary fissure, between the anterior and posterior lobes.
14 lso significantly fewer granule cells in the posterior lobe (20-30%) without a concomitant loss of Pu
15 ritiana differ markedly in morphology of the posterior lobe, a male-specific genitalic structure.
18 ant intrinsically for the development of the posterior lobe and pituitary stalk, and it has significa
19 complex, with staining observed primarily in posterior lobes and considerably lower amounts of staini
20 be may be more severe than that of the three posterior lobes and may account for the prominence of pr
22 ivation of climbing fibres projecting to the posterior lobe cerebellar cortex by focal stimulation of
23 s and Purkinje cells in Crus I and II of the posterior lobe cerebellar hemisphere to activation of pe
24 tial expression of BETA2/NeuroD1 and TrkC in posterior lobes explains the earlier start of cell apopt
28 inant rostral pons projections to cerebellar posterior lobe, is consistent with new hypotheses regard
29 gests a mechanism whereby development of the posterior lobe may affect the development of the anterio
30 al introgressions that have large effects on posterior lobe morphology and that posterior lobe size a
31 c inputs to establish differences in overall posterior lobe morphology between D. mauritiana and D. s
34 e-supplementary motor area and the bilateral posterior lobe of cerebellum, compared to young subjects
35 inent in patients with lesions involving the posterior lobe of the cerebellum and the vermis, and in
36 d simultaneously from two or more PCs in the posterior lobe of the ketamine/xylazine-anaesthetized ra
41 ex to the cerebellar cortical C1 zone in the posterior lobe of the rat cerebellum was investigated us
43 midsagittal area and volume of the inferior posterior lobe remained significantly smaller in the sch
44 morphology and that posterior lobe size and posterior lobe shape can be separated genetically for so
46 ffects on posterior lobe morphology and that posterior lobe size and posterior lobe shape can be sepa
48 found that Purkinje cells recorded from the posterior lobe vermis and hemisphere have high simple sp
49 folia of the paramedian lobule (PML) in the posterior lobe were investigated in cats by using a comb
50 rebellum, the anterior lobe and the superior posterior lobe were profoundly reduced in both vermis an
51 expression appeared mostly restricted to the posterior lobe, where it followed a caudal-to-rostral gr
52 intermediate lobe, and by pituicytes in the posterior lobe, whereas GLT-1 is expressed only by the a
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