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1 ution could convert SCCA2 into a more potent cysteine proteinase inhibitor.
2 rees C for 30 min or by treating them with a cysteine proteinase inhibitor.
3 containing structural motifs in common with cysteine proteinase inhibitors.
4 nd both were inhibited by treatment with the cysteine proteinase inhibitor (2S,3S)-transepoxysuccinyl
6 sgenic expression of a biosafe, anti-feedant cysteine proteinase inhibitor and an anti-root invasion,
9 ons for three soybean (Glycine max L. Merr.) cysteine proteinase inhibitors (CysPIs) are inferred fro
11 se genes, in turn, reduced the production of cysteine proteinase inhibitors (CystPIs), which are spec
18 The incubation of cultured parasites with cysteine proteinase inhibitors inhibited the denaturatio
20 ssion of a cysteine proteinase, instead of a cysteine proteinase inhibitor, may be a novel insect def
21 heir proteolytic activity was blocked by the cysteine proteinase inhibitor N-alpha-p-tosyl-L-lysine c
23 t region surface architecture of the soybean cysteine proteinase inhibitor (soyacystatin N, scN) was
24 Verge protein is dramatically increased by cysteine proteinase inhibitors, suggesting rapid turnove
25 ost are one-use suicide substrate serine and cysteine proteinase inhibitors that have evolved to fine
26 were similar; however, the concentrations of cysteine proteinase inhibitors were elevated under A- co
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