367 related articles for article (PubMed ID: 10611310)
21. Maintenance of double-stranded telomeric repeats as the critical determinant for cell viability in yeast cells lacking Ku.
Gravel S; Wellinger RJ
Mol Cell Biol; 2002 Apr; 22(7):2182-93. PubMed ID: 11884605
[TBL] [Abstract][Full Text] [Related]
22. Yeast Ku as a regulator of chromosomal DNA end structure.
Gravel S; Larrivée M; Labrecque P; Wellinger RJ
Science; 1998 May; 280(5364):741-4. PubMed ID: 9563951
[TBL] [Abstract][Full Text] [Related]
23. Chromosomal double-strand break repair in Ku80-deficient cells.
Liang F; Romanienko PJ; Weaver DT; Jeggo PA; Jasin M
Proc Natl Acad Sci U S A; 1996 Aug; 93(17):8929-33. PubMed ID: 8799130
[TBL] [Abstract][Full Text] [Related]
24. Human LIGIV is synthetically lethal with the loss of Rad54B-dependent recombination and is required for certain chromosome fusion events induced by telomere dysfunction.
Oh S; Wang Y; Zimbric J; Hendrickson EA
Nucleic Acids Res; 2013 Feb; 41(3):1734-49. PubMed ID: 23275564
[TBL] [Abstract][Full Text] [Related]
25. The fission yeast Taz1 protein protects chromosomes from Ku-dependent end-to-end fusions.
Ferreira MG; Cooper JP
Mol Cell; 2001 Jan; 7(1):55-63. PubMed ID: 11172711
[TBL] [Abstract][Full Text] [Related]
26. Ku must load directly onto the chromosome end in order to mediate its telomeric functions.
Lopez CR; Ribes-Zamora A; Indiviglio SM; Williams CL; Haricharan S; Bertuch AA
PLoS Genet; 2011 Aug; 7(8):e1002233. PubMed ID: 21852961
[TBL] [Abstract][Full Text] [Related]
27. Chromosomal end-to-end fusions in immortalized mouse embryonic fibroblasts deficient in the DNA-dependent protein kinase catalytic subunit.
Rebuzzini P; Lisa A; Giulotto E; Mondello C
Cancer Lett; 2004 Jan; 203(1):79-86. PubMed ID: 14670620
[TBL] [Abstract][Full Text] [Related]
28. Telomeres--unsticky ends.
Shore D
Science; 1998 Sep; 281(5384):1818-9. PubMed ID: 9776685
[No Abstract] [Full Text] [Related]
29. Ku70 stimulates fusion of dysfunctional telomeres yet protects chromosome ends from homologous recombination.
Celli GB; Denchi EL; de Lange T
Nat Cell Biol; 2006 Aug; 8(8):885-90. PubMed ID: 16845382
[TBL] [Abstract][Full Text] [Related]
30. The function of a stem-loop in telomerase RNA is linked to the DNA repair protein Ku.
Peterson SE; Stellwagen AE; Diede SJ; Singer MS; Haimberger ZW; Johnson CO; Tzoneva M; Gottschling DE
Nat Genet; 2001 Jan; 27(1):64-7. PubMed ID: 11138000
[TBL] [Abstract][Full Text] [Related]
31. DNA processing is not required for ATM-mediated telomere damage response after TRF2 deletion.
Celli GB; de Lange T
Nat Cell Biol; 2005 Jul; 7(7):712-8. PubMed ID: 15968270
[TBL] [Abstract][Full Text] [Related]
32. A central region of Ku80 mediates interaction with Ku70 in vivo.
Cary RB; Chen F; Shen Z; Chen DJ
Nucleic Acids Res; 1998 Feb; 26(4):974-9. PubMed ID: 9461456
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Novel functional requirements for non-homologous DNA end joining in Schizosaccharomyces pombe.
Manolis KG; Nimmo ER; Hartsuiker E; Carr AM; Jeggo PA; Allshire RC
EMBO J; 2001 Jan; 20(1-2):210-21. PubMed ID: 11226171
[TBL] [Abstract][Full Text] [Related]
35. The absence of the dna-dependent protein kinase catalytic subunit in mice results in anaphase bridges and in increased telomeric fusions with normal telomere length and G-strand overhang.
Goytisolo FA; Samper E; Edmonson S; Taccioli GE; Blasco MA
Mol Cell Biol; 2001 Jun; 21(11):3642-51. PubMed ID: 11340158
[TBL] [Abstract][Full Text] [Related]
36. Double-strand break repair by Ku70 requires heterodimerization with Ku80 and DNA binding functions.
Jin S; Weaver DT
EMBO J; 1997 Nov; 16(22):6874-85. PubMed ID: 9362500
[TBL] [Abstract][Full Text] [Related]
37. DNA double-strand break repair.
Featherstone C; Jackson SP
Curr Biol; 1999 Oct; 9(20):R759-61. PubMed ID: 10531043
[No Abstract] [Full Text] [Related]
38. The Ku heterodimer performs separable activities at double-strand breaks and chromosome termini.
Bertuch AA; Lundblad V
Mol Cell Biol; 2003 Nov; 23(22):8202-15. PubMed ID: 14585978
[TBL] [Abstract][Full Text] [Related]
39. Induction and repair of chromosome aberrations in scid cells measured by premature chromosome condensation.
Evans JW; Liu XF; Kirchgessner CU; Brown JM
Radiat Res; 1996 Jan; 145(1):39-46. PubMed ID: 8532835
[TBL] [Abstract][Full Text] [Related]
40. Telomeric DNA ends are essential for the localization of Ku at telomeres in fission yeast.
Miyoshi T; Sadaie M; Kanoh J; Ishikawa F
J Biol Chem; 2003 Jan; 278(3):1924-31. PubMed ID: 12424244
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
