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1 s on adhesion between the blastoderm and the vitelline envelope.
2 ently in the absence of the eggshell and the vitelline envelope.
3 in used by sperm to create a hole in the egg vitelline envelope.
4 receptor (gp69/64) in the Xenopus laevis egg vitelline envelope.
5 n is exposed that bonds the sperm to the egg vitelline envelope.
8 o the egg, its action required an intact egg vitelline envelope, and its action was independent of la
10 de that the gp69/64 glycoproteins in the egg vitelline envelope mediate sperm-egg binding, an initial
11 Conversely, after fertilization, when the vitelline envelope of the egg is converted to the fertil
12 iotemporal pattern of tissue adhesion to the vitelline envelope provides controllable, counteracting
13 telline coat lysin (VCL) and female-specific vitelline envelope receptor for lysin (VERL) could ident
15 versity of the amino-terminal end of the egg vitelline envelope receptor for lysin has been promoted
18 ring the conversion from the coelomic to the vitelline envelope, the gp69/64 sperm receptors become e
19 -specificity in dissolving a hole in the egg vitelline envelope through which the sperm swims to reac
20 use 16 kDa lysin to create a hole in the egg vitelline envelope (VE) by a species-specific, nonenzyma
22 pecies selectively creates a hole in the egg vitelline envelope (VE) through which the sperm passes t
23 6-kDa protein that creates a hole in the egg vitelline envelope (VE) through which the sperm swims to
24 molecular basis of sperm binding to the egg vitelline envelope (VE), a competition assay was used an
26 ze the constituent proteins of the egg coat [vitelline envelope (VE)] of abalone eggs and to provide