BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

405 related articles for article (PubMed ID: 14612421)

  • 1. Yeast Mre11 and Rad1 proteins define a Ku-independent mechanism to repair double-strand breaks lacking overlapping end sequences.
    Ma JL; Kim EM; Haber JE; Lee SE
    Mol Cell Biol; 2003 Dec; 23(23):8820-8. PubMed ID: 14612421
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Saccharomyces cerevisiae Sae2- and Tel1-dependent single-strand DNA formation at DNA break promotes microhomology-mediated end joining.
    Lee K; Lee SE
    Genetics; 2007 Aug; 176(4):2003-14. PubMed ID: 17565964
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Functional interplay of the Mre11 nuclease and Ku in the response to replication-associated DNA damage.
    Foster SS; Balestrini A; Petrini JH
    Mol Cell Biol; 2011 Nov; 31(21):4379-89. PubMed ID: 21876003
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Repair of endonuclease-induced double-strand breaks in Saccharomyces cerevisiae: essential role for genes associated with nonhomologous end-joining.
    Lewis LK; Westmoreland JW; Resnick MA
    Genetics; 1999 Aug; 152(4):1513-29. PubMed ID: 10430580
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the Yku80 C terminus and Xrs2 FHA domain specifically block yeast nonhomologous end joining.
    Palmbos PL; Daley JM; Wilson TE
    Mol Cell Biol; 2005 Dec; 25(24):10782-90. PubMed ID: 16314503
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Processing of DNA double-stranded breaks and intermediates of recombination and repair by Saccharomyces cerevisiae Mre11 and its stimulation by Rad50, Xrs2, and Sae2 proteins.
    Ghodke I; Muniyappa K
    J Biol Chem; 2013 Apr; 288(16):11273-86. PubMed ID: 23443654
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Overhang polarity of chromosomal double-strand breaks impacts kinetics and fidelity of yeast non-homologous end joining.
    Liang Z; Sunder S; Nallasivam S; Wilson TE
    Nucleic Acids Res; 2016 Apr; 44(6):2769-81. PubMed ID: 26773053
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Promotion of Dnl4-catalyzed DNA end-joining by the Rad50/Mre11/Xrs2 and Hdf1/Hdf2 complexes.
    Chen L; Trujillo K; Ramos W; Sung P; Tomkinson AE
    Mol Cell; 2001 Nov; 8(5):1105-15. PubMed ID: 11741545
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Telomere-related functions of yeast KU in the repair of bleomycin-induced DNA damage.
    Tam AT; Pike BL; Hammet A; Heierhorst J
    Biochem Biophys Res Commun; 2007 Jun; 357(3):800-3. PubMed ID: 17442269
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Recruitment and dissociation of nonhomologous end joining proteins at a DNA double-strand break in Saccharomyces cerevisiae.
    Wu D; Topper LM; Wilson TE
    Genetics; 2008 Mar; 178(3):1237-49. PubMed ID: 18245831
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Microhomology-mediated End Joining and Homologous Recombination share the initial end resection step to repair DNA double-strand breaks in mammalian cells.
    Truong LN; Li Y; Shi LZ; Hwang PY; He J; Wang H; Razavian N; Berns MW; Wu X
    Proc Natl Acad Sci U S A; 2013 May; 110(19):7720-5. PubMed ID: 23610439
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sae2 antagonizes Rad9 accumulation at DNA double-strand breaks to attenuate checkpoint signaling and facilitate end resection.
    Yu TY; Kimble MT; Symington LS
    Proc Natl Acad Sci U S A; 2018 Dec; 115(51):E11961-E11969. PubMed ID: 30510002
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Microhomology Selection for Microhomology Mediated End Joining in
    Lee K; Ji JH; Yoon K; Che J; Seol JH; Lee SE; Shim EY
    Genes (Basel); 2019 Apr; 10(4):. PubMed ID: 30965655
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Yeast Nej1 is a key participant in the initial end binding and final ligation steps of nonhomologous end joining.
    Chen X; Tomkinson AE
    J Biol Chem; 2011 Feb; 286(6):4931-40. PubMed ID: 21149442
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rad1, rad10 and rad52 mutations reduce the increase of microhomology length during radiation-induced microhomology-mediated illegitimate recombination in saccharomyces cerevisiae.
    Chan CY; Schiestl RH
    Radiat Res; 2009 Aug; 172(2):141-51. PubMed ID: 19630519
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 21.