185 related articles for article (PubMed ID: 17202845)
1. Decreased expression of DNA repair proteins Ku70 and Mre11 is associated with aging and may contribute to the cellular senescence.
Ju YJ; Lee KH; Park JE; Yi YS; Yun MY; Ham YH; Kim TJ; Choi HM; Han GJ; Lee JH; Lee J; Han JS; Lee KM; Park GH
Exp Mol Med; 2006 Dec; 38(6):686-93. PubMed ID: 17202845
[TBL] [Abstract][Full Text] [Related]
2. Effects of double-strand break repair proteins on vertebrate telomere structure.
Wei C; Skopp R; Takata M; Takeda S; Price CM
Nucleic Acids Res; 2002 Jul; 30(13):2862-70. PubMed ID: 12087170
[TBL] [Abstract][Full Text] [Related]
3. Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing.
Boulton SJ; Jackson SP
EMBO J; 1998 Mar; 17(6):1819-28. PubMed ID: 9501103
[TBL] [Abstract][Full Text] [Related]
4. Mre11 and Ku70 interact in somatic cells, but are differentially expressed in early meiosis.
Goedecke W; Eijpe M; Offenberg HH; van Aalderen M; Heyting C
Nat Genet; 1999 Oct; 23(2):194-8. PubMed ID: 10508516
[TBL] [Abstract][Full Text] [Related]
5. Disruption of DNA-PK in Ku80 mutant xrs-6 and the implications in DNA double-strand break repair.
Chen F; Peterson SR; Story MD; Chen DJ
Mutat Res; 1996 Jan; 362(1):9-19. PubMed ID: 8538653
[TBL] [Abstract][Full Text] [Related]
6. The Ku70-binding site of Ku80 is required for the stabilization of Ku70 in the cytoplasm, for the nuclear translocation of Ku80, and for Ku80-dependent DNA repair.
Koike M; Koike A
Exp Cell Res; 2005 May; 305(2):266-76. PubMed ID: 15817152
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Clinicopathological significance of KU70/KU80, a key DNA damage repair protein in breast cancer.
Alshareeda AT; Negm OH; Albarakati N; Green AR; Nolan C; Sultana R; Madhusudan S; Benhasouna A; Tighe P; Ellis IO; Rakha EA
Breast Cancer Res Treat; 2013 Jun; 139(2):301-10. PubMed ID: 23624778
[TBL] [Abstract][Full Text] [Related]
9. Identification of a Saccharomyces cerevisiae Ku80 homologue: roles in DNA double strand break rejoining and in telomeric maintenance.
Boulton SJ; Jackson SP
Nucleic Acids Res; 1996 Dec; 24(23):4639-48. PubMed ID: 8972848
[TBL] [Abstract][Full Text] [Related]
10. Ku70 is required for DNA repair but not for T cell antigen receptor gene recombination In vivo.
Ouyang H; Nussenzweig A; Kurimasa A; Soares VC; Li X; Cordon-Cardo C; Li Wh; Cheong N; Nussenzweig M; Iliakis G; Chen DJ; Li GC
J Exp Med; 1997 Sep; 186(6):921-9. PubMed ID: 9294146
[TBL] [Abstract][Full Text] [Related]
11. Delayed kinetics of DNA double-strand break processing in normal and pathological aging.
Sedelnikova OA; Horikawa I; Redon C; Nakamura A; Zimonjic DB; Popescu NC; Bonner WM
Aging Cell; 2008 Jan; 7(1):89-100. PubMed ID: 18005250
[TBL] [Abstract][Full Text] [Related]
12. The Ku heterodimer: function in DNA repair and beyond.
Fell VL; Schild-Poulter C
Mutat Res Rev Mutat Res; 2015; 763():15-29. PubMed ID: 25795113
[TBL] [Abstract][Full Text] [Related]
13. Ku70/80 gene expression and DNA-dependent protein kinase (DNA-PK) activity do not correlate with double-strand break (dsb) repair capacity and cellular radiosensitivity in normal human fibroblasts.
Kasten U; Plottner N; Johansen J; Overgaard J; Dikomey E
Br J Cancer; 1999 Mar; 79(7-8):1037-41. PubMed ID: 10098733
[TBL] [Abstract][Full Text] [Related]
14. Bax-induced apoptosis shortens the life span of DNA repair defect Ku70-knockout mice by inducing emphysema.
Matsuyama S; Palmer J; Bates A; Poventud-Fuentes I; Wong K; Ngo J; Matsuyama M
Exp Biol Med (Maywood); 2016 Jun; 241(12):1265-71. PubMed ID: 27302174
[TBL] [Abstract][Full Text] [Related]
15. DNA repair factors and telomere-chromosome integrity in mammalian cells.
Hande MP
Cytogenet Genome Res; 2004; 104(1-4):116-22. PubMed ID: 15162024
[TBL] [Abstract][Full Text] [Related]
16. In normal human fibroblasts variation in DSB repair capacity cannot be ascribed to radiation-induced changes in the localisation, expression or activity of major NHEJ proteins.
Kasten-Pisula U; Vronskaja S; Overgaard J; Dikomey E
Radiother Oncol; 2008 Mar; 86(3):321-8. PubMed ID: 18158193
[TBL] [Abstract][Full Text] [Related]
17. SIRT1 promotes DNA repair activity and deacetylation of Ku70.
Jeong J; Juhn K; Lee H; Kim SH; Min BH; Lee KM; Cho MH; Park GH; Lee KH
Exp Mol Med; 2007 Feb; 39(1):8-13. PubMed ID: 17334224
[TBL] [Abstract][Full Text] [Related]
18. Noncanonical functions of Ku may underlie essentiality in human cells.
Kelly RD; Parmar G; Bayat L; Maitland MER; Lajoie GA; Edgell DR; Schild-Poulter C
Sci Rep; 2023 Jul; 13(1):12162. PubMed ID: 37500706
[TBL] [Abstract][Full Text] [Related]
19. Accumulation of Ku80 proteins at DNA double-strand breaks in living cells.
Koike M; Koike A
Exp Cell Res; 2008 Mar; 314(5):1061-70. PubMed ID: 18164703
[TBL] [Abstract][Full Text] [Related]
20. Mre11 and Blm-Dependent Formation of ALT-Like Telomeres in Ku-Deficient Ustilago maydis.
Yu EY; Pérez-Martín J; Holloman WK; Lue NF
PLoS Genet; 2015 Oct; 11(10):e1005570. PubMed ID: 26492073
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]