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1 ir, the glycosylase, to the second step, the apurinic endonuclease.
2 7 bp apart, even in the absence of the major apurinic endonucleases.
3 he essential base excision DNA repair enzyme apurinic endonuclease 1 (Ape1) in response to sodium ars
4  the role of a critical histidine residue of apurinic endonuclease 1 (Ape1), a human DNA repair enzym
5 ity and increased mRNA and protein levels of apurinic endonuclease 1 (APE1).
6 bound thymine DNA glycosylase prevents human apurinic endonuclease 1 (HAP1) cutting the apurinic site
7 and the apurinic endonuclease redox factor 1/apurinic endonuclease 1 (REF1/APE1), in human breast car
8                   The multifunctional enzyme apurinic endonuclease 1/redox enhancing factor 1 (Ape1/r
9 limiting enzyme of DNA base excision repair, apurinic endonuclease-1 (Ape1), which is also known as r
10 cate that RECQL4 specifically stimulates the apurinic endonuclease activity of APE1, the DNA strand d
11 racil DNA glycosylase (UDG) and apyrimidinic/apurinic endonuclease (APE) digest G:U mismatches to com
12 C1), poly(ADP-ribose) polymerase (PARP), and apurinic endonuclease (Ape) proteins.
13 e determined that the DNA glycosylase hNTH1, apurinic endonuclease (APE), and DNA polymerase beta (Po
14 n uracil DNA glycosylase (UDG), apyrimidinic/apurinic endonuclease (APE), and DNA polymerase beta (po
15  zinc-containing DNA-repair proteins p53 and apurinic endonuclease (APE).
16 ity, genetic inactivation of all known yeast apurinic endonucleases does not increase the sensitivity
17 s confirmed by digestion of plasmid DNA with apurinic endonuclease IV, followed by primer extension a
18 he more "modern" non-LTR lineages possess an apurinic endonuclease-like domain and generally lack sit
19  truncating the amino 150 amino acids of the apurinic endonuclease portion of the O6-methylguanine DN
20 f the O6-methylguanine DNA methyltransferase-apurinic endonuclease protein resulted in the retention
21 f O6-methylguanine DNA methyltransferase and apurinic endonuclease proteins into a combined single re
22 se (OGG1), the DNA glycosylase NTH1, and the apurinic endonuclease redox factor 1/apurinic endonuclea
23 uanine DNA methyltransferase coupled with an apurinic endonuclease, resulting in a fully functional p

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