BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

348 related articles for article (PubMed ID: 17442269)

  • 21. Mechanism of nonhomologous end-joining in mycobacteria: a low-fidelity repair system driven by Ku, ligase D and ligase C.
    Gong C; Bongiorno P; Martins A; Stephanou NC; Zhu H; Shuman S; Glickman MS
    Nat Struct Mol Biol; 2005 Apr; 12(4):304-12. PubMed ID: 15778718
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Role of budding yeast Rad18 in repair of HO-induced double-strand breaks.
    Hirano Y; Reddy J; Sugimoto K
    DNA Repair (Amst); 2009 Jan; 8(1):51-9. PubMed ID: 18824138
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Telomere maintenance is dependent on activities required for end repair of double-strand breaks.
    Nugent CI; Bosco G; Ross LO; Evans SK; Salinger AP; Moore JK; Haber JE; Lundblad V
    Curr Biol; 1998 May; 8(11):657-60. PubMed ID: 9635193
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DNA damage triggers disruption of telomeric silencing and Mec1p-dependent relocation of Sir3p.
    McAinsh AD; Scott-Drew S; Murray JA; Jackson SP
    Curr Biol; 1999 Sep; 9(17):963-6. PubMed ID: 10508591
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Repair of radiation induced DNA double strand breaks by backup NHEJ is enhanced in G2.
    Wu W; Wang M; Wu W; Singh SK; Mussfeldt T; Iliakis G
    DNA Repair (Amst); 2008 Feb; 7(2):329-38. PubMed ID: 18155970
    [TBL] [Abstract][Full Text] [Related]  

  • 27. PARP-1 and Ku compete for repair of DNA double strand breaks by distinct NHEJ pathways.
    Wang M; Wu W; Wu W; Rosidi B; Zhang L; Wang H; Iliakis G
    Nucleic Acids Res; 2006; 34(21):6170-82. PubMed ID: 17088286
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Lif1p targets the DNA ligase Lig4p to sites of DNA double-strand breaks.
    Teo SH; Jackson SP
    Curr Biol; 2000 Feb; 10(3):165-8. PubMed ID: 10679327
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double-strand break repair and serves as a barrier to error-prone DNA repair pathways.
    Boulton SJ; Jackson SP
    EMBO J; 1996 Sep; 15(18):5093-103. PubMed ID: 8890183
    [TBL] [Abstract][Full Text] [Related]  

  • 31. DNA damage-inducible and RAD52-independent repair of DNA double-strand breaks in Saccharomyces cerevisiae.
    Moore CW; McKoy J; Dardalhon M; Davermann D; Martinez M; Averbeck D
    Genetics; 2000 Mar; 154(3):1085-99. PubMed ID: 10757755
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations in two Ku homologs define a DNA end-joining repair pathway in Saccharomyces cerevisiae.
    Milne GT; Jin S; Shannon KB; Weaver DT
    Mol Cell Biol; 1996 Aug; 16(8):4189-98. PubMed ID: 8754818
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recruitment of Saccharomyces cerevisiae Dnl4-Lif1 complex to a double-strand break requires interactions with Yku80 and the Xrs2 FHA domain.
    Palmbos PL; Wu D; Daley JM; Wilson TE
    Genetics; 2008 Dec; 180(4):1809-19. PubMed ID: 18832348
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ku-dependent and Ku-independent end-joining pathways lead to chromosomal rearrangements during double-strand break repair in Saccharomyces cerevisiae.
    Yu X; Gabriel A
    Genetics; 2003 Mar; 163(3):843-56. PubMed ID: 12663527
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Mycobacterial nonhomologous end joining mediates mutagenic repair of chromosomal double-strand DNA breaks.
    Stephanou NC; Gao F; Bongiorno P; Ehrt S; Schnappinger D; Shuman S; Glickman MS
    J Bacteriol; 2007 Jul; 189(14):5237-46. PubMed ID: 17496093
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Ku: a multifunctional protein involved in telomere maintenance.
    Fisher TS; Zakian VA
    DNA Repair (Amst); 2005 Nov; 4(11):1215-26. PubMed ID: 15979949
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Requirement for end-joining and checkpoint functions, but not RAD52-mediated recombination, after EcoRI endonuclease cleavage of Saccharomyces cerevisiae DNA.
    Lewis LK; Kirchner JM; Resnick MA
    Mol Cell Biol; 1998 Apr; 18(4):1891-902. PubMed ID: 9528760
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 18.