BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

747 related articles for article (PubMed ID: 9501103)

  • 1. 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]  

  • 2. Yeast Ku protein plays a direct role in telomeric silencing and counteracts inhibition by rif proteins.
    Mishra K; Shore D
    Curr Biol; 1999 Oct; 9(19):1123-6. PubMed ID: 10531008
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Role of yeast SIR genes and mating type in directing DNA double-strand breaks to homologous and non-homologous repair paths.
    Lee SE; Pâques F; Sylvan J; Haber JE
    Curr Biol; 1999 Jul; 9(14):767-70. PubMed ID: 10421582
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Telomerase, Ku, and telomeric silencing in Saccharomyces cerevisiae.
    Evans SK; Sistrunk ML; Nugent CI; Lundblad V
    Chromosoma; 1998 Dec; 107(6-7):352-8. PubMed ID: 9914366
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Differential suppression of DNA repair deficiencies of Yeast rad50, mre11 and xrs2 mutants by EXO1 and TLC1 (the RNA component of telomerase).
    Lewis LK; Karthikeyan G; Westmoreland JW; Resnick MA
    Genetics; 2002 Jan; 160(1):49-62. PubMed ID: 11805044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rap1-Sir4 binding independent of other Sir, yKu, or histone interactions initiates the assembly of telomeric heterochromatin in yeast.
    Luo K; Vega-Palas MA; Grunstein M
    Genes Dev; 2002 Jun; 16(12):1528-39. PubMed ID: 12080091
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A genetic screen for ribosomal DNA silencing defects identifies multiple DNA replication and chromatin-modulating factors.
    Smith JS; Caputo E; Boeke JD
    Mol Cell Biol; 1999 Apr; 19(4):3184-97. PubMed ID: 10082585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Silencing factors participate in DNA repair and recombination in Saccharomyces cerevisiae.
    Tsukamoto Y; Kato J; Ikeda H
    Nature; 1997 Aug; 388(6645):900-3. PubMed ID: 9278054
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ku-deficient yeast strains exhibit alternative states of silencing competence.
    Maillet L; Gaden F; Brevet V; Fourel G; Martin SG; Dubrana K; Gasser SM; Gilson E
    EMBO Rep; 2001 Mar; 2(3):203-10. PubMed ID: 11266361
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sir-Ku-itous routes to make ends meet.
    Haber JE
    Cell; 1999 Jun; 97(7):829-32. PubMed ID: 10399911
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres.
    Laroche T; Martin SG; Gotta M; Gorham HC; Pryde FE; Louis EJ; Gasser SM
    Curr Biol; 1998 May; 8(11):653-6. PubMed ID: 9635192
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae.
    Lewis LK; Resnick MA
    Mutat Res; 2000 Jun; 451(1-2):71-89. PubMed ID: 10915866
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Non-homologous end-joining proteins are required for Agrobacterium T-DNA integration.
    van Attikum H; Bundock P; Hooykaas PJ
    EMBO J; 2001 Nov; 20(22):6550-8. PubMed ID: 11707425
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence that a complex of SIR proteins interacts with the silencer and telomere-binding protein RAP1.
    Moretti P; Freeman K; Coodly L; Shore D
    Genes Dev; 1994 Oct; 8(19):2257-69. PubMed ID: 7958893
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 38.