79 related articles for article (PubMed ID: 23639616)
1. The C-terminal region of Rad52 is essential for Rad52 nuclear and nucleolar localization, and accumulation at DNA damage sites immediately after irradiation.
Koike M; Yutoku Y; Koike A
Biochem Biophys Res Commun; 2013 May; 435(2):260-6. PubMed ID: 23639616
[TBL] [Abstract][Full Text] [Related]
2. Dynamic changes in subcellular localization of cattle XLF during cell cycle, and focus formation of cattle XLF at DNA damage sites immediately after irradiation.
Koike M; Yutoku Y; Koike A
J Vet Med Sci; 2015 Sep; 77(9):1109-14. PubMed ID: 25947322
[TBL] [Abstract][Full Text] [Related]
3. Accumulation of p21 proteins at DNA damage sites independent of p53 and core NHEJ factors following irradiation.
Koike M; Yutoku Y; Koike A
Biochem Biophys Res Commun; 2011 Aug; 412(1):39-43. PubMed ID: 21787748
[TBL] [Abstract][Full Text] [Related]
4. Nuclear localization of mouse Ku70 in interphase cells and focus formation of mouse Ku70 at DNA damage sites immediately after irradiation.
Koike M; Yutoku Y; Koike A
J Vet Med Sci; 2015 Sep; 77(9):1137-42. PubMed ID: 25947323
[TBL] [Abstract][Full Text] [Related]
5. The role of nonhomologous DNA end joining, conservative homologous recombination, and single-strand annealing in the cell cycle-dependent repair of DNA double-strand breaks induced by H(2)O(2) in mammalian cells.
Frankenberg-Schwager M; Becker M; Garg I; Pralle E; Wolf H; Frankenberg D
Radiat Res; 2008 Dec; 170(6):784-93. PubMed ID: 19138034
[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. Cloning, localization and focus formation at DNA damage sites of canine XRCC4.
Koike M; Yutoku Y; Koike A
J Vet Med Sci; 2017 Jan; 78(12):1865-1871. PubMed ID: 27644316
[TBL] [Abstract][Full Text] [Related]
8. Homologous recombination protects mammalian cells from replication-associated DNA double-strand breaks arising in response to methyl methanesulfonate.
Nikolova T; Ensminger M; Löbrich M; Kaina B
DNA Repair (Amst); 2010 Oct; 9(10):1050-63. PubMed ID: 20708982
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Accumulation of Ku70 at DNA double-strand breaks in living epithelial cells.
Koike M; Yutoku Y; Koike A
Exp Cell Res; 2011 Oct; 317(17):2429-37. PubMed ID: 21820429
[TBL] [Abstract][Full Text] [Related]
11. Cloning, localization and focus formation at DNA damage sites of canine XLF.
Koike M; Yutoku Y; Koike A
J Vet Med Sci; 2017 Jan; 79(1):22-28. PubMed ID: 27746407
[TBL] [Abstract][Full Text] [Related]
12. Non-homologous DNA end joining.
Pastwa E; Błasiak J
Acta Biochim Pol; 2003; 50(4):891-908. PubMed ID: 14739985
[TBL] [Abstract][Full Text] [Related]
13. Ionizing radiation-induced foci formation of mammalian Rad51 and Rad54 depends on the Rad51 paralogs, but not on Rad52.
van Veelen LR; Essers J; van de Rakt MW; Odijk H; Pastink A; Zdzienicka MZ; Paulusma CC; Kanaar R
Mutat Res; 2005 Jul; 574(1-2):34-49. PubMed ID: 15914205
[TBL] [Abstract][Full Text] [Related]
14. Control of Rad52 recombination activity by double-strand break-induced SUMO modification.
Sacher M; Pfander B; Hoege C; Jentsch S
Nat Cell Biol; 2006 Nov; 8(11):1284-90. PubMed ID: 17013376
[TBL] [Abstract][Full Text] [Related]
15. Rad52 multimerization is important for its nuclear localization in Saccharomyces cerevisiae.
Plate I; Albertsen L; Lisby M; Hallwyl SC; Feng Q; Seong C; Rothstein R; Sung P; Mortensen UH
DNA Repair (Amst); 2008 Jan; 7(1):57-66. PubMed ID: 17888746
[TBL] [Abstract][Full Text] [Related]
16. The putative nuclear localization signal of the human RAD52 protein is a potential sumoylation site.
Saito K; Kagawa W; Suzuki T; Suzuki H; Yokoyama S; Saitoh H; Tashiro S; Dohmae N; Kurumizaka H
J Biochem; 2010 Jun; 147(6):833-42. PubMed ID: 20190268
[TBL] [Abstract][Full Text] [Related]
17. Increased repair of gamma-induced DNA double-strand breaks at lower dose-rate in CHO cells.
Boucher D; Hindo J; Averbeck D
Can J Physiol Pharmacol; 2004 Feb; 82(2):125-32. PubMed ID: 15052293
[TBL] [Abstract][Full Text] [Related]
18. The Escherichia coli RecA protein complements recombination defective phenotype of the Saccharomyces cerevisiae rad52 mutant cells.
Dudás A; Marková E; Vlasáková D; Kolman A; Bartosová Z; Brozmanová J; Chovanec M
Yeast; 2003 Apr; 20(5):389-96. PubMed ID: 12673622
[TBL] [Abstract][Full Text] [Related]
19. Novel function of HATs and HDACs in homologous recombination through acetylation of human RAD52 at double-strand break sites.
Yasuda T; Kagawa W; Ogi T; Kato TA; Suzuki T; Dohmae N; Takizawa K; Nakazawa Y; Genet MD; Saotome M; Hama M; Konishi T; Nakajima NI; Hazawa M; Tomita M; Koike M; Noshiro K; Tomiyama K; Obara C; Gotoh T; Ui A; Fujimori A; Nakayama F; Hanaoka F; Sugasawa K; Okayasu R; Jeggo PA; Tajima K
PLoS Genet; 2018 Mar; 14(3):e1007277. PubMed ID: 29590107
[TBL] [Abstract][Full Text] [Related]
20. Identification of sequences that target BRCA1 to nuclear foci following alkylative DNA damage.
Au WW; Henderson BR
Cell Signal; 2007 Sep; 19(9):1879-92. PubMed ID: 17531442
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
