386 related articles for article (PubMed ID: 15175261)
1. 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]
2. The non-homologous end-joining pathway is not involved in the radiosensitization of mammalian cells by heat shock.
Dynlacht JR; Bittner ME; Bethel JA; Beck BD
J Cell Physiol; 2003 Sep; 196(3):557-64. PubMed ID: 12891712
[TBL] [Abstract][Full Text] [Related]
3. Homologous recombination and non-homologous end-joining pathways of DNA double-strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells.
Takata M; Sasaki MS; Sonoda E; Morrison C; Hashimoto M; Utsumi H; Yamaguchi-Iwai Y; Shinohara A; Takeda S
EMBO J; 1998 Sep; 17(18):5497-508. PubMed ID: 9736627
[TBL] [Abstract][Full Text] [Related]
4. DNA Double Strand Break Response and Limited Repair Capacity in Mouse Elongated Spermatids.
Ahmed EA; Scherthan H; de Rooij DG
Int J Mol Sci; 2015 Dec; 16(12):29923-35. PubMed ID: 26694360
[TBL] [Abstract][Full Text] [Related]
5. Rad54 and DNA Ligase IV cooperate to maintain mammalian chromatid stability.
Mills KD; Ferguson DO; Essers J; Eckersdorff M; Kanaar R; Alt FW
Genes Dev; 2004 Jun; 18(11):1283-92. PubMed ID: 15175260
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Hypersensitivity of Ku80-deficient cell lines and mice to DNA damage: the effects of ionizing radiation on growth, survival, and development.
Nussenzweig A; Sokol K; Burgman P; Li L; Li GC
Proc Natl Acad Sci U S A; 1997 Dec; 94(25):13588-93. PubMed ID: 9391070
[TBL] [Abstract][Full Text] [Related]
8. Mechanisms of DNA double strand break repair and chromosome aberration formation.
Iliakis G; Wang H; Perrault AR; Boecker W; Rosidi B; Windhofer F; Wu W; Guan J; Terzoudi G; Pantelias G
Cytogenet Genome Res; 2004; 104(1-4):14-20. PubMed ID: 15162010
[TBL] [Abstract][Full Text] [Related]
9. Paradoxical decrease in mutant frequencies and chromosomal rearrangements in a transgenic lacZ reporter gene in Ku80 null mice deficient in DNA double strand break repair.
Rockwood LD; Nussenzweig A; Janz S
Mutat Res; 2003 Aug; 529(1-2):51-8. PubMed ID: 12943919
[TBL] [Abstract][Full Text] [Related]
10. After double-strand break induction by UV-A, homologous recombination and nonhomologous end joining cooperate at the same DSB if both systems are available.
Rapp A; Greulich KO
J Cell Sci; 2004 Oct; 117(Pt 21):4935-45. PubMed ID: 15367581
[TBL] [Abstract][Full Text] [Related]
11. Radiation-induced genomic rearrangements formed by nonhomologous end-joining of DNA double-strand breaks.
Rothkamm K; Kühne M; Jeggo PA; Löbrich M
Cancer Res; 2001 May; 61(10):3886-93. PubMed ID: 11358801
[TBL] [Abstract][Full Text] [Related]
12. Involvement of Ku80 in microhomology-mediated end joining for DNA double-strand breaks in vivo.
Katsura Y; Sasaki S; Sato M; Yamaoka K; Suzukawa K; Nagasawa T; Yokota J; Kohno T
DNA Repair (Amst); 2007 May; 6(5):639-48. PubMed ID: 17236818
[TBL] [Abstract][Full Text] [Related]
13. Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells.
Verkaik NS; Esveldt-van Lange RE; van Heemst D; Brüggenwirth HT; Hoeijmakers JH; Zdzienicka MZ; van Gent DC
Eur J Immunol; 2002 Mar; 32(3):701-9. PubMed ID: 11870614
[TBL] [Abstract][Full Text] [Related]
14. Non-homologous end joining, but not homologous recombination, enables survival for cells exposed to a histone deacetylase inhibitor.
Yaneva M; Li H; Marple T; Hasty P
Nucleic Acids Res; 2005; 33(16):5320-30. PubMed ID: 16177181
[TBL] [Abstract][Full Text] [Related]
15. Ku affects the CHK1-dependent G(2) checkpoint after ionizing radiation.
Wang X; Li GC; Iliakis G; Wang Y
Cancer Res; 2002 Nov; 62(21):6031-4. PubMed ID: 12414624
[TBL] [Abstract][Full Text] [Related]
16. A quantitative model of the major pathways for radiation-induced DNA double-strand break repair.
Belov OV; Krasavin EA; Lyashko MS; Batmunkh M; Sweilam NH
J Theor Biol; 2015 Feb; 366():115-30. PubMed ID: 25261728
[TBL] [Abstract][Full Text] [Related]
17. A comparison of response to cisplatin, radiation and combined treatment for cells deficient in recombination repair pathways.
Raaphorst GP; Leblanc M; Li LF
Anticancer Res; 2005; 25(1A):53-8. PubMed ID: 15816518
[TBL] [Abstract][Full Text] [Related]
18. Evidence of an adaptive response targeting DNA nonhomologous end joining and its transmission to bystander cells.
Klammer H; Kadhim M; Iliakis G
Cancer Res; 2010 Nov; 70(21):8498-506. PubMed ID: 20861183
[TBL] [Abstract][Full Text] [Related]
19. DNA double-strand break repair in cell-free extracts from Ku80-deficient cells: implications for Ku serving as an alignment factor in non-homologous DNA end joining.
Feldmann E; Schmiemann V; Goedecke W; Reichenberger S; Pfeiffer P
Nucleic Acids Res; 2000 Jul; 28(13):2585-96. PubMed ID: 10871410
[TBL] [Abstract][Full Text] [Related]
20. Defining functional domains of Ku80: DNA end binding and survival after radiation.
Osipovich O; Duhe RJ; Hasty P; Durum SK; Muegge K
Biochem Biophys Res Commun; 1999 Aug; 261(3):802-7. PubMed ID: 10441505
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
