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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,
8 nding Protein Cytoplasmic 4 (PABPC4), Serine/Cysteine Proteinase Inhibitor Clade G Member 1 (SERPING1
9 s: 2.0-fold to 3.4-fold increase) and serine/cysteine proteinase inhibitor clade G member 1 (transcri
11 ons for three soybean (Glycine max L. Merr.) cysteine proteinase inhibitors (CysPIs) are inferred fro
13 se genes, in turn, reduced the production of cysteine proteinase inhibitors (CystPIs), which are spec
20 The incubation of cultured parasites with cysteine proteinase inhibitors inhibited the denaturatio
22 ssion of a cysteine proteinase, instead of a cysteine proteinase inhibitor, may be a novel insect def
23 heir proteolytic activity was blocked by the cysteine proteinase inhibitor N-alpha-p-tosyl-L-lysine c
25 t region surface architecture of the soybean cysteine proteinase inhibitor (soyacystatin N, scN) was
26 Verge protein is dramatically increased by cysteine proteinase inhibitors, suggesting rapid turnove
27 ost are one-use suicide substrate serine and cysteine proteinase inhibitors that have evolved to fine
28 were similar; however, the concentrations of cysteine proteinase inhibitors were elevated under A- co