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1 nts phenylmethylsulfonyl fluoride (PMSF) and diisopropylfluorophosphate.
2 deduced by specific labeling with tritiated-diisopropylfluorophosphate.
3 aoxon, diethylphenylphosphate, acephate, and diisopropylfluorophosphate.
4 r by SOD plus catalase, but was inhibited by diisopropylfluorophosphate.
5 nds chlorpyrifosmethyl oxon, dichlorvos, and diisopropylfluorophosphate (20-min IC(50) values of 18.3
6 eagents echothiophate (nonaged and aged) and diisopropylfluorophosphate (aged) were solved and refine
7 inhibited by two serine protease inhibitors, diisopropylfluorophosphate and aprotinin, but not by soy
8 rotein was identified by labeling with [(3)H]diisopropylfluorophosphate and subjected to tryptic dige
9 ition, an increased rate of incorporation of diisopropylfluorophosphate, and an enhanced fraction of
10 inase activity, 36-kDa protein labeled by 3H-diisopropylfluorophosphate, and immunologically detectab
12 nhibited by 0.1 mM echothiophate or 0.001 mM diisopropylfluorophosphate, but human BChE mutants G117H
14 rmine whether chlorpyrifos oxon, dichlorvos, diisopropylfluorophosphate (DFP), and sarin covalently b
16 eated with either chlorpyrifos oxon (CPO) or diisopropylfluorophosphate (DFP): human serum albumin (K
17 4-(2-Aminoethyl)benzenesulfonylfluoride and diisopropylfluorophosphate, killing by neutrophils was i
19 ptide hydrolase, was isolated as a tritiated-diisopropylfluorophosphate-reactive protein from porcine
20 es for the mutants tested with the substrate diisopropylfluorophosphate showed an increase in all cas
22 by the covalently reactive hapten probe and diisopropylfluorophosphate, suggesting a serine protease
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