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1 s a role in nonhomologous end joining in the double strand break repair pathway.
2 of the non-homologous end-joining (NHEJ) DNA-double strand break repair pathway.
3 ch identified USP11 as a component of the HR double-strand break repair pathway.
4 mponent of the nonhomologous end-joining DNA double-strand break repair pathway.
5 ns via the non-homologous end joining (NHEJ) double-strand break repair pathway.
6 -Mediated End Joining (TMEJ), an alternative double-strand break repair pathway.
7 referential use of the potentially mutagenic double-strand break repair pathway.
8 DNA methylation that utilizes endogenous DNA double strand break repair pathways.
9 er enzymes participate in minor, alternative double-strand break repair pathways.
10 pplications caused by the interplay with DNA double-strand break repair pathways.
11 s in CC-2931, are likely products of various double-strand break repair pathways.
12 is important for error-free DNA mismatch and double-strand break repair pathways.
13 rylation is a necessary component of the DNA double-stranded break repair pathway.
14 -PK disrupt both V(D)J recombination and DNA double-stranded break repair pathways.
15 mologous end-joining (NHEJ), the predominant double stranded break repair pathway active in somatic c
16  strand annealing rather than by a canonical double-strand break repair pathway and that resolution o
17 uced during the evolution of Oryza, and both double-strand break repair pathways and replication-base
18  for survival of cancer cells when other DNA double-stranded break repair pathways are impaired.
19 , and RTEL1 genes, which are involved in the double-strand break repair pathway, are associated with
20  plays critical roles in determining the DNA double-strand break repair pathway choice between nonhom
21 al. in this issue, provide insights into DNA double-strand break repair pathway choice in mammalian c
22 rhang structure is a critical determinant of double-strand break repair pathway choice.
23 and separable from 53BP1's regulation of DNA double-strand break repair pathway choice.
24                                Two major DNA double-strand break repair pathways exist in all eukaryo
25                                 Cellular DNA double-strand break-repair pathways have evolved to prot
26  a cell's ability to utilize the other major double-strand break repair pathway, HR.
27 to sequester the telomere from the prevalent double strand break repair pathway in mammals.
28 -homologous end joining (the predominant DNA double-strand break repair pathway in higher eukaryotes)
29  end joining (C-NHEJ) is the predominant DNA double-strand break repair pathway in humans.
30 s end-joining (cNHEJ) pathway is a major DNA double-strand break repair pathway in mammalian cells an
31          Processing of DNA damage by the DNA double-strand break repair pathway in mammalian cells is
32 mponent of the nonhomologous end joining DNA double-strand break repair pathway in mammalian cells.
33 eviously uncharacterized Rad50-dependent DNA double-strand break repair pathway in mammalian somatic
34 us end-joining (NHEJ) pathway is a major DNA double-strand break repair pathway in mammals and is ess
35 g is the primary deoxyribonucleic acid (DNA) double-strand break repair pathway in multicellular euka
36 ent methodologies to comprehensively profile double-strand break repair pathways in isogenic paired c
37 ologous end joining (NHEJ) are important DNA double-strand break repair pathways in many organisms.
38 ed with non-homologous end joining (NHEJ), a double-strand break repair pathway, in all kingdoms of l
39 nature associated with a backup, error-prone double-strand break repair pathway known as microhomolog
40 A ligase IV is a core component of the major double-strand break repair pathway, non-homologous end j
41               Cells deficient in a major DNA double-strand break repair pathway (nonhomologous DNA en
42  status had no impact on the other principal double-strand break repair pathway, nonhomologous end jo
43 promote spontaneous SCE by influencing which double-strand break repair pathway predominates during n
44                Homologous recombination is a double-strand break repair pathway required for resistan
45 translocations were likely mediated by a DNA double-strand break repair pathway termed nonhomologous
46 eta (Poltheta) plays a central role in a DNA double-strand break repair pathway termed theta-mediated
47         Break induced replication (BIR) is a double strand break repair pathway that can promote gene
48 homologous end-joining (NHEJ) is a major DNA double-strand break repair pathway that is conserved in
49     Break-induced replication (BIR) is a DNA double-strand break repair pathway that leads to genomic
50 s recombination (HR) is a template-based DNA double-strand break repair pathway that requires the sel
51                                 Fallible DNA double-strand break repair pathways were significantly a
52 e reconstitution of the initial steps of the double-strand break-repair pathway where joint molecule