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1                  We propose that D76 affects replicational accuracy by mediating interaction between
2  nonpolar (D76V and D76I) residues increased replicational accuracy, while substitutions with negativ
3 able in understanding the molecular bases of replicational accuracy.
4  valylation provides a small but significant replicational advantage to both PCV RNAs.
5 formation, and the various components of the replicational and transcriptional machinery may be inter
6  substitutions displayed transcriptional and replicational asymmetries consistent with mutations resu
7  and delta, respectively, and show that post-replicational bypass of UV-damaged DNA is severely inhib
8               The major role is likely to be replicational, dependent on features present in tymovira
9 tions favour the view that the process is co-replicational: DNA replication forks are anchored at the
10 recombination and sex has been selection for replicational fidelity and viability; without the recomb
11 sitive determinants of both dNTP binding and replicational fidelity within the highly conserved motif
12 appear symmetrical in both replichores (i.e. replicational halves of circular chromosomes) and most s
13                         To determine whether replicational mutagenesis in the yeast genome is influen
14   Our findings suggest the possibility of co-replicational or co-transcriptional folding of G-quadrup
15                          Consistent with its replicational origin, ttsgR accumulation required a 5' t
16 nalogies between the genome organization and replicational requirements of plant closteroviruses and
17  distinct activities directly involved in co-replicational segregation dynamics.
18                                              Replicational selection is responsible for the higher nu
19             Cds1 is required for survival of replicational stress caused by agents that stall replica
20 ighlight the potential importance of chronic replicational stress in promoting cancer development.
21 the ATR/Chk1- and 53BP1-mediated signal from replicational stress is received, BLM functions in multi
22                                        Since replicational stress leads to clonal selection of cells
23 own that exposure of cells to high levels of replicational stress leads to permanent proliferation ar
24 y of mutant p53 to prevent arrest induced by replicational stress per se is primarily dependent on pr
25  pathway(s) important for DNA repair and the replicational stress response.
26 erate in homologous recombination repair and replicational stress response.
27 uggests that FANCJ helicase functions in the replicational stress response.
28 es to therapeutically relevant low levels of replicational stress that allow limited proliferation.
29 the ERCC1-XPF endonuclease, is important for replicational stress tolerance in both budding and fissi
30                           Cds1 also controls replicational stress tolerance mechanisms.
31 ests that, in response to DNA damage and DNA replicational stress, Chk1 and Chk2 may phosphorylate Cd
32  Rnr2 and Rnr4 in response to DNA damage and replicational stress.
33 mutations in DNA polymerase alpha and to DNA replicational stresses.
34                             Moreover, the co-replicational synthesis of scaffold and staple strands b
35                                         Post-replicational telomere end processing involves both exte
36                                              Replicational-transcriptional selection, therefore, has