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1 elevated levels of nitrogen mustard-induced forward mutation.
2 igh selection coefficient (s > 0.1) for each forward mutation.
3 sequences and raises the rate of spontaneous forward mutation.
4 -52, rth1Delta/rad27Delta) mutations in both forward mutation and repeat-tract instability assays.
5 c heat stress caused elevated frequencies of forward mutations and interchromosomal DNA recombination
6 e of base substitution mutations by the CAN1 forward mutation assay compared to the rate for the wild
9 ion of the mutational spectra generated by a forward mutation assay revealed that errors in DNA repai
11 We have developed an in vitro DNA polymerase forward mutation assay using damaged DNA templates that
13 Most of the R2 base substitutions in the forward mutation assay were caused by the misincorporati
16 sphoribosyltransferase (APRT(+)) --> APRT(-) forward mutation assay, we found that while Cr(VI) alone
30 In the experiments reported here, the SUP4-o forward-mutation assay was used to monitor GC --> TA mut
33 irement for this regulation, we employed two forward mutation assays to characterize PrimPol's replic
35 fidelity in both misincorporation assays and forward mutation assays, but display a substantially hig
38 hermophilic archaea, a quantitative assay of forward mutation at extremely high temperature was devel
40 pH 3.5 and 75 degrees C based on the rate of forward mutation at the pyrE gene and the nucleotide cha
43 Because of the large size of the LYS2 locus, forward mutations first were mapped to specific LYS2 sub
45 ic conditions showed a powerful induction of forward mutation frequencies compared to wild-type cells
48 ion assay to show that the mean frequency of forward mutations in primary mammary adenocarcinomas ari
51 ion, implying that impairment of [PSI(+)] by forward mutations is due to altered ability of the ATPas
55 transgene that selects for phage containing forward mutations only in the lambda cII gene, using an
56 This can be attributed largely to the low forward mutation rate and the propensity for closely lin
59 aize (Zea mays) afford the advantage of high forward mutation rates but pose a challenge for identify
60 L/F116Y/Q151M (VILYM) RTs, for their overall forward mutation rates in an M13 gapped-duplex assay tha
62 in vitro tropism (residues 317 and 321) and forward mutation residues (residues 399, 460, 553, and 5
63 we used the ampD system to observe the true forward-mutation sequence spectrum of DSBR-associated st
64 into the mechanism of TAM, we obtained LYS2 forward mutation spectra under low- versus high-transcri
65 A defect in mug also has little effect on forward mutations, suggesting that Mug does not play a r
66 Finally, we summarize those aspects of T4 forward-mutation systems which are relevant to optimal c
67 ant displays a higher rate of CAN1S to can1r forward mutations than the ogg1Delta or msh2Delta single
68 in DNA repair capacity, approximately 50% of forward mutations that arise in the CAN1 gene under high
69 act instability phenotype and a high rate of forward mutations to canavanine resistance that result p
70 e reversions arose significantly faster than forward mutations, with the most rapidly reverting mutat
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