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1 n than the wild-type strain during growth in complete medium.
2 he absence of serum, followed by a return to complete medium.
3 nfluence or continuous cell proliferation in complete medium.
4 d will form outgrowths when transferred into complete medium.
5 nesis of endothelial cells cultured in EGM-2 complete medium.
6 activity was the same in the cells grown in complete medium, after serum starvation, and subsequent
9 ever, the eIF-2 kinase in the cells grown in complete medium and also after mitogen activation of the
10 exhibited significant growth deficiencies in complete medium and an inability to grow on glycerol as
11 sduced HUVEC have equivalent growth rates in complete medium and both show contact inhibition of grow
14 selenium or on the commonly used yeast-based complete medium at about twice the rate as those on a me
15 ble mutants were unable to grow on synthetic complete medium, but were able to grow on rich medium.
18 udied in KRC-7 cells (rat hepatoma) grown in complete medium, during serum starvation, and mitogen ac
20 each treated for 6, 12, 24, or 48 hours with complete medium or complete medium containing 25% vitreo
21 the extracts from either the cells grown in complete medium or mitogen-activated cells were used.
23 Delta mutant grows less rapidly in a defined complete medium, TC abundance increases threefold withou
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