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1 he mitochondrial-containing midpiece and the principal piece.
2 cts of the proximal segment of the flagellar principal piece.
3 present only in the proximal portion of the principal piece.
4 AKAP82 localized to the entire length of the principal piece.
5 re co-localized by immunofluorescence to the principal piece.
6 The longest part of the sperm flagellum, the principal piece, contains the fibrous sheath, a cytoskel
7 and assemble into the fibrous sheath of the principal piece; however, calcium binding occurs only to
8 82 was localized to the entire length of the principal piece in testicular sperm, while in epididymal
9 quadrilateral structure along the flagellum principal piece, in the vicinity of AKAP4 and the CatSpe
10 imilar to CatSper, Cdc42 distribution in the principal piece is confined to four linear domains and t
12 CABYR: (1) the protein was localized to the principal piece of mouse epididymal spermatozoa; (2) mou
13 is-specific transcripts, localization in the principal piece of tail and occurrence of homologous spl
14 Moreover, cAMP dynamics in the midpiece and principal piece of the flagellum are distinctively diffe
15 ferent in connecting piece, middle piece and principal piece of the flagellum between testicular and
16 heath supports a growing literature that the principal piece of the flagellum is capable of generatin
17 compartmentalized glycolytic pathway in the principal piece of the flagellum, as opposed to ATP gene
18 ocalizes only to the proximal portion of the principal piece of the flagellum, pro-hAKAP82 localized
20 on X-100-insoluble and were localized to the principal piece of the flagellum, the region where the c
24 +) binding isoforms, and localization to the principal piece of the human sperm tail suggest that CAB
29 superfamily is specifically localized to the principal piece of the sperm tail and is required for sp
36 n sperm, we find that CAII is located in the principal piece, whereas CAIV is present in the plasma m