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2 ain, found in the small subunits of archaeal DNA polymerase II and eukaryotic DNA polymerases alpha a
4 nucleolytic proofreading by Escherichia coli DNA polymerase II and inhibits proofreading by E. coli D
5 o be determined why this new pathway prefers DNA polymerase II and why there are two pathways to repa
8 ia coli beta clamp is known to function with DNA polymerases II and V, indicating that beta also inte
9 om the cap guanosine 3'-OH primer by E. coli DNA polymerase II (B family) and E. coli DNA polymerase
10 ymerases tested, only DNA polymerase IV, not DNA polymerase II, could engage productively with the Es
15 We show that the intein interrupting the DNA polymerase II DP2 subunit in Pyrococcus abyssi, whic
16 Neither polA (DNA polymerase I) nor polB (DNA polymerase II) genes are required for the mutA pheno
17 e polA (encoding DNA polymerase I) and polB (DNA polymerase II) genes on inducible and constitutive s
19 receive lesion-free homologous DNA.) Herein, DNA polymerase II is shown to be in this new pathway, si
22 .e., DeltarecR), or impair the activities of DNA polymerase II or DNA polymerase V (i.e., DeltapolB o
25 We find that Escherichia coli translesion DNA polymerase II (Pol II) and polymerase IV (Pol IV) fu
26 ave investigated a role for Escherichia coli DNA polymerase II (Pol II) in copying chromosomal and ep
30 deficient in either recombination (recA) or DNA polymerase II (polB) are hypersensitive to nitrogen
31 i) the conventional reagent system using Taq DNA polymerase; (ii) the hot-start reagent system based
34 ibed DPB3 gene, which codes for a subunit of DNA polymerase II, with both transcripts showing peak ab
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