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1 pathways, including the DNA glycosylase gene 3-MethylAdenine DNA Glycosylase 1 (MAG1), which is part
2 rom DNA suggests an age-dependent decline in 3-methyladenine DNA glycosylase, a BER enzyme responsibl
7 UC with increases in the DNA repair enzymes 3-methyladenine DNA glycosylase and apurinic/apyrimidini
8 base excision-repair enzymes, AAG, the major 3-methyladenine DNA glycosylase, and APE1, the major apu
10 Methylpurine-DNA glycosylases (MPG proteins, 3-methyladenine-DNA glycosylases) excise numerous damage
11 nt of the DNA with uracil-DNA glycosylase or 3-methyladenine DNA glycosylase failed to reveal additio
13 NA excision repair genes (including the MAG1 3-methyladenine DNA glycosylase gene) and a large select
19 is approximately 0.3 in strains deficient in 3-methyladenine DNA glycosylases I and II, FAPY DNA glyc
20 e DNA glycosylase (AAG) and Escherichia coli 3-methyladenine DNA glycosylase II (AlkA) bind tightly t
24 monofunctional DNA glycosylase AlkA (E. coli 3-methyladenine-DNA glycosylase II) reveals a large hydr
27 n between ERalpha and the DNA repair protein 3-methyladenine DNA glycosylase (MPG) thereby providing
30 study was made possible by the generation of 3-methyladenine DNA glycosylase null mutant cells by tar