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1 e variation in the F-lectin domains of sperm bindin.
2 drift created the polymorphisms observed in bindin.
3 ombinant Strongylocentrotus purpuratus sperm bindin and a recombinant fragment of the putative egg bi
4 d by many observations in vivo and in vitro, bindin and the putative egg receptor display a specific
5 he interaction of the sperm adhesive protein,bindin, and a complementary receptor on the egg surface,
10 ion from neutrality has been detected in the bindin coding region and suggested in the intron, indica
13 clone the species-specific egg receptor for bindin, EBR1, from Strongylocentrotus franciscanus (Sf)
25 involvement of diversifying selection in the bindin intron evolution more data combining population g
29 ve selection at gamete recognition loci like bindin involves strong selection within species on mate
36 ir region located at the 5' end of the sperm bindin locus in 134 adult red sea urchins (Strongylocent
37 udied nucleotide variability in the complete bindin locus, including two exons and one intron, in the
39 he sea urchin genus Echinometra, the protein bindin mediates sperm attachment to eggs, evolves quickl
42 gigas oyster sperm acrosome react a ring of bindin protein is exposed that bonds the sperm to the eg
43 on followed by eight and one-half tandem egg bindin receptor (EBR) repeats that share 88% identity wi
44 Thus,the species-specific domains of egg bindin receptor 1 (EBR1) from both species function as t
45 d a recombinant fragment of the putative egg bindin receptor of the same species was measured in vitr
46 oxidase subunit I and nuclear gene encoding bindin, respectively, which is significantly below avera
49 oyster Crassostrea gigas contain the protein bindin that bonds sperm to egg during fertilization.
50 dase subunit I and the nuclear gene encoding bindin to evaluate the possibility of cryptic species wi
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