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1 ge of the gamma-glutamyl bond and release of cysteinylglycine.
2 ne, releasing glutamic acid or glutamine and cysteinylglycine.
3 tubules perfused with mercuric conjugates of cysteinylglycine.
4 se) to yield the S-benzfurazan derivative of cysteinylglycine.
5 rexpression also significantly lowered serum cysteinylglycine (3.6 versus 2.8 micromol/L; P<0.003) le
7 thiol glutathione amide, gamma-L-glutamyl-L-cysteinylglycine amide (GASH), when grown photoheterotro
8 dditional four metabolites (22% of Tp dose): cysteinylglycine and cysteine derivatives of glutathione
10 thiols (glutathione, cysteine, homocysteine, cysteinylglycine, and beta-mercaptoethanol) and human se
11 sulted in significant increases in cysteine, cysteinylglycine, and glutathione concentrations (P < 0.
12 ne, glutamylcysteine, total glutathione, and cysteinylglycine; capillary electrophoresis) were collec
13 coli and shown to catalyze the hydrolysis of cysteinylglycine (Cys-Gly) with the same kinetics as the
14 ne, S-adenosylmethionine (AdoMet), cysteine, cysteinylglycine (cys-gly), and glutathione (GSH) were m
15 thione, vitamin B-6, homocysteine, cysteine, cysteinylglycine (CysGly), and glutamylcysteine (GluCys)
17 binding properties of 5 different peptides (cysteinylglycine, glutathione, Cys-Ile-His-Asn-Pro, Cys-
18 oding the first enzyme in gamma-l-glutamyl-l-cysteinylglycine (GSH) biosynthesis, cannot grow in its
19 fluid (ELF), glutathione (L-alpha-glutamyl-L-cysteinylglycine, GSH) is essential for adequate protect
20 racterization of glutathione (gamma-glutamyl-cysteinylglycine, GSH)-trapped reactive metabolites usin
25 glycyl-(S-4-nitrobenzo-2-oxa- 1,3-diazole)-L-cysteinylglycine [NO2ZGly(S-NBD)CysGly] with an absorpti
26 en mercuric conjugates of glutathione (GSH), cysteinylglycine or cysteine (containing 203Hg2+) were p
31 t catalyst for the oxidation of cysteine and cysteinylglycine to cystine and bis(-S-cysteinylglycine)
34 rved associations between serum cysteine and cysteinylglycine with upper gastrointestinal cancer risk
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