151 related articles for article (PubMed ID: 16447266)
21. Assessment of DNA double-strand breaks and gammaH2AX induced by the topoisomerase II poisons etoposide and mitoxantrone.
Smart DJ; Halicka HD; Schmuck G; Traganos F; Darzynkiewicz Z; Williams GM
Mutat Res; 2008 May; 641(1-2):43-7. PubMed ID: 18423498
[TBL] [Abstract][Full Text] [Related]
22. The absence of Ku but not defects in classical non-homologous end-joining is required to trigger PARP1-dependent end-joining.
Mansour WY; Borgmann K; Petersen C; Dikomey E; Dahm-Daphi J
DNA Repair (Amst); 2013 Dec; 12(12):1134-42. PubMed ID: 24210699
[TBL] [Abstract][Full Text] [Related]
23. Evidence for a role of vertebrate Rad52 in the repair of topoisomerase II-mediated DNA damage.
Adachi N; Iiizumi S; Koyama H
DNA Cell Biol; 2005 Jun; 24(6):388-93. PubMed ID: 15941391
[TBL] [Abstract][Full Text] [Related]
24. Identification of a DNA nonhomologous end-joining complex in bacteria.
Weller GR; Kysela B; Roy R; Tonkin LM; Scanlan E; Della M; Devine SK; Day JP; Wilkinson A; d'Adda di Fagagna F; Devine KM; Bowater RP; Jeggo PA; Jackson SP; Doherty AJ
Science; 2002 Sep; 297(5587):1686-9. PubMed ID: 12215643
[TBL] [Abstract][Full Text] [Related]
25. KU70/80, DNA-PKcs, and Artemis are essential for the rapid induction of apoptosis after massive DSB formation.
Abe T; Ishiai M; Hosono Y; Yoshimura A; Tada S; Adachi N; Koyama H; Takata M; Takeda S; Enomoto T; Seki M
Cell Signal; 2008 Nov; 20(11):1978-85. PubMed ID: 18674614
[TBL] [Abstract][Full Text] [Related]
26. Yeast recombination pathways triggered by topoisomerase II-mediated DNA breaks.
Sabourin M; Nitiss JL; Nitiss KC; Tatebayashi K; Ikeda H; Osheroff N
Nucleic Acids Res; 2003 Aug; 31(15):4373-84. PubMed ID: 12888496
[TBL] [Abstract][Full Text] [Related]
27. Binding of double-strand breaks in DNA by human Rad52 protein.
Van Dyck E; Stasiak AZ; Stasiak A; West SC
Nature; 1999 Apr; 398(6729):728-31. PubMed ID: 10227297
[TBL] [Abstract][Full Text] [Related]
28. DNA damage response (DDR) induced by topoisomerase II poisons requires nuclear function of the small GTPase Rac.
Wartlick F; Bopp A; Henninger C; Fritz G
Biochim Biophys Acta; 2013 Dec; 1833(12):3093-3103. PubMed ID: 23999236
[TBL] [Abstract][Full Text] [Related]
29. Role of nucleotide excision repair proteins in response to DNA damage induced by topoisomerase II inhibitors.
Rocha JC; Busatto FF; Guecheva TN; Saffi J
Mutat Res Rev Mutat Res; 2016; 768():68-77. PubMed ID: 27234564
[TBL] [Abstract][Full Text] [Related]
30. Differential cytotoxic pathways of topoisomerase I and II anticancer agents after overexpression of the E2F-1/DP-1 transcription factor complex.
Hofland K; Petersen BO; Falck J; Helin K; Jensen PB; Sehested M
Clin Cancer Res; 2000 Apr; 6(4):1488-97. PubMed ID: 10778981
[TBL] [Abstract][Full Text] [Related]
31. Involvement of human polynucleotide kinase in double-strand break repair by non-homologous end joining.
Chappell C; Hanakahi LA; Karimi-Busheri F; Weinfeld M; West SC
EMBO J; 2002 Jun; 21(11):2827-32. PubMed ID: 12032095
[TBL] [Abstract][Full Text] [Related]
32. DNA-PK-dependent phosphorylation of Ku70/80 is not required for non-homologous end joining.
Douglas P; Gupta S; Morrice N; Meek K; Lees-Miller SP
DNA Repair (Amst); 2005 Aug; 4(9):1006-18. PubMed ID: 15941674
[TBL] [Abstract][Full Text] [Related]
33. Proteasomal inhibition potentiates drugs targeting DNA topoisomerase II.
Lee KC; Bramley RL; Cowell IG; Jackson GH; Austin CA
Biochem Pharmacol; 2016 Mar; 103():29-39. PubMed ID: 26794000
[TBL] [Abstract][Full Text] [Related]
34. Non-homologous end joining is the responsible pathway for the repair of fludarabine-induced DNA double strand breaks in mammalian cells.
de Campos-Nebel M; Larripa I; González-Cid M
Mutat Res; 2008 Nov; 646(1-2):8-16. PubMed ID: 18812179
[TBL] [Abstract][Full Text] [Related]
35. Influence of different metal ions on the ultrastructure, biochemical properties, and protein localization of the K562 cell nuclear matrix.
Neri LM; Bortul R; Zweyer M; Tabellini G; Borgatti P; Marchisio M; Bareggi R; Capitani S; Martelli AM
J Cell Biochem; 1999 Jun; 73(3):342-54. PubMed ID: 10321834
[TBL] [Abstract][Full Text] [Related]
36. FEN1 participates in repair of the 5'-phosphotyrosyl terminus of DNA single-strand breaks.
Kametani Y; Takahata C; Narita T; Tanaka K; Iwai S; Kuraoka I
Carcinogenesis; 2016 Jan; 37(1):56-62. PubMed ID: 26581212
[TBL] [Abstract][Full Text] [Related]
37. KARP-1 works as a heterodimer with Ku70, but the function of KARP-1 cannot perfectly replace that of Ku80 in DSB repair.
Koike M; Yutoku Y; Koike A
Exp Cell Res; 2011 Oct; 317(16):2267-75. PubMed ID: 21756904
[TBL] [Abstract][Full Text] [Related]
38. The efficacy of topoisomerase II-targeted anticancer agents reflects the persistence of drug-induced cleavage complexes in cells.
Bandele OJ; Osheroff N
Biochemistry; 2008 Nov; 47(45):11900-8. PubMed ID: 18922022
[TBL] [Abstract][Full Text] [Related]
39. Collaboration of homologous recombination and nonhomologous end-joining factors for the survival and integrity of mice and cells.
Couëdel C; Mills KD; Barchi M; Shen L; Olshen A; Johnson RD; Nussenzweig A; Essers J; Kanaar R; Li GC; Alt FW; Jasin M
Genes Dev; 2004 Jun; 18(11):1293-304. PubMed ID: 15175261
[TBL] [Abstract][Full Text] [Related]
40. The requirement of Artemis in double-strand break repair depends on the type of DNA damage.
Kurosawa A; Koyama H; Takayama S; Miki K; Ayusawa D; Fujii M; Iiizumi S; Adachi N
DNA Cell Biol; 2008 Jan; 27(1):55-61. PubMed ID: 17941805
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]