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1 biochemically that HpxO is an FAD-dependent urate oxidase.
2 tes were examined as potential inhibitors of urate oxidase.
3 hat there is no covalently bound cofactor in urate oxidase.
4 rate monoanion is the species which binds to urate oxidase.
5 rum UA levels to 0 by infusing a recombinant urate oxidase.
6 tration on the second virial coefficient for urate oxidase.
8 e and stand in contrast to the mechanisms of urate oxidase and (1H)-3-hydroxy-4-oxoquinaldine 2,4-dio
9 of hydroxyisourate hydrolase matched that of urate oxidase, and supports the hypothesis that hydroxyi
10 observed upon binding of 8-nitroxanthine to urate oxidase are consistent with increased anionic char
12 the enzyme active site, and Raman spectra of urate oxidase-bound 8-nitroxanthine suggest that both th
15 beta-galactosidase reporter gene or to a rat urate oxidase cDNA and establishing stably transfected A
16 ase kinase kinase in Magnaporthe oryzae, and urate oxidase (designated ClUrase) were functionally cha
17 AD), contrasting with all previously studied urate oxidase enzymes, which have no cofactor requiremen
19 lymphoma in the United States is the use of urate oxidase for prevention of tumor lysis syndrome and
21 binding of the inhibitor 8-nitroxanthine to urate oxidase has been investigated by Raman and UV-visi
22 rate concentration (PUA), related to loss of urate oxidase in evolution, is postulated to protect hum
25 sed that oxidation of the substrate urate by urate oxidase is facilitated by formation of the substra
27 avenous (IV) PEGylated recombinant mammalian urate oxidase (PEG-uricase) for the treatment of severe
33 jugation assay, two sites (W160 and D112) of urate oxidase (Uox), a model therapeutic protein, were s
36 nsformation, a full-length cDNA encoding rat urate oxidase (UOX), which oxidizes uric acid to allanto
39 The oxidation of urate catalyzed by soybean urate oxidase was studied under single-turnover conditio
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