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1 ndonucleases Nth (endonuclease III) and Fpg (formamidopyrimidine DNA glycosylase).
2 dative stress and are efficiently excised by formamidopyrimidine DNA glycosylase.
3 ndo III), endonuclease VIII (endo VIII), and formamidopyrimidine DNA glycosylase.
4 igestion by the enzymes endonuclease III and formamidopyrimidine DNA glycosylase.
5 with the repair enzymes endonuclease III and formamidopyrimidine DNA glycosylase.
6 ares structural and functional homology with formamidopyrimidine-DNA glycosylase.
8 fferent damage products sensitive to E. coli formamidopyrimidine DNA glycosylase and hot piperidine,
9 at oxidized bases with endonuclease III and formamidopyrimidine DNA glycosylase and then using the l
10 sylases of the base excision repair pathway: formamidopyrimidine-DNA glycosylase and 8-oxoguanine DNA
11 ing oxidative DNA damage (sites sensitive to formamidopyrimidine-DNA glycosylase and single-strand br
14 amage was quantitated using Escherichia coli formamidopyrimidine DNA glycosylase (Fpg) in a gene-spec
15 approach was based on digestion of DNA with formamidopyrimidine DNA glycosylase (FPG) to convert 8-o
18 oxoG), is processed by two DNA glycosylases, formamidopyrimidine DNA glycosylase (Fpg), which removes
23 es have been identified for Escherichia coli formamidopyrimidine-DNA glycosylase (Fpg) and Drosophila
24 alf-life of Schiff bases formed when E. coli formamidopyrimidine-DNA glycosylase (Fpg) and endonuclea
26 is initiated by DNA glycosylases such as the formamidopyrimidine-DNA glycosylase (Fpg) in Escherichia
30 ed by treatment with either Escherichia coli formamidopyrimidine-DNA glycosylase (Fpg), Escherichia c
31 counterpart, guanine, by the repair enzyme, formamidopyrimidine-DNA glycosylase (Fpg), likely involv
32 and comet analysis revealed introduction of formamidopyrimidine-DNA glycosylase (Fpg)-sensitive oxid
36 on (lactoglyglutathione lyase gene), repair (formamidopyrimidine-DNA glycosylase gene), osmotic prote
37 Endo VIII do not serve as back up enzymes to formamidopyrimidine DNA glycosylase in the repair of for
38 ybrids were used as substrates for bacterial formamidopyrimidine-DNA glycosylase, Nth protein (endonu
39 displayed subtle biases in damage chemistry (formamidopyrimidine DNA glycosylase/piperidine ratio).
40 t Ug was a better substrate for endo III and formamidopyrimidine DNA glycosylase than Tg; for endonuc
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