BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 14729978)

  • 1. Microhomology-dependent end joining and repair of transposon-induced DNA hairpins by host factors in Saccharomyces cerevisiae.
    Yu J; Marshall K; Yamaguchi M; Haber JE; Weil CF
    Mol Cell Biol; 2004 Feb; 24(3):1351-64. PubMed ID: 14729978
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Mre11/Rad50/Xrs2 complex and non-homologous end-joining of incompatible ends in S. cerevisiae.
    Zhang X; Paull TT
    DNA Repair (Amst); 2005 Nov; 4(11):1281-94. PubMed ID: 16043424
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nonhomologous End-Joining with Minimal Sequence Loss Is Promoted by the Mre11-Rad50-Nbs1-Ctp1 Complex in
    Li Y; Wang J; Zhou G; Lajeunesse M; Le N; Stawicki BN; Corcino YL; Berkner KL; Runge KW
    Genetics; 2017 May; 206(1):481-496. PubMed ID: 28292918
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Ku complex suppresses recombination in the absence of MRX activity during budding yeast meiosis.
    Yun H; Kim K
    BMB Rep; 2019 Oct; 52(10):607-612. PubMed ID: 30940321
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Role of Dnl4-Lif1 in nonhomologous end-joining repair complex assembly and suppression of homologous recombination.
    Zhang Y; Hefferin ML; Chen L; Shim EY; Tseng HM; Kwon Y; Sung P; Lee SE; Tomkinson AE
    Nat Struct Mol Biol; 2007 Jul; 14(7):639-46. PubMed ID: 17589524
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Physiological protein blocks direct the Mre11-Rad50-Xrs2 and Sae2 nuclease complex to initiate DNA end resection.
    Reginato G; Cannavo E; Cejka P
    Genes Dev; 2017 Dec; 31(23-24):2325-2330. PubMed ID: 29321179
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nej1 interacts with Sae2 at DNA double-stranded breaks to inhibit DNA resection.
    Mojumdar A; Adam N; Cobb JA
    J Biol Chem; 2022 Jun; 298(6):101937. PubMed ID: 35429499
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Ku DNA End-Binding Activity Promotes Repair Fidelity and Influences End-Processing During Nonhomologous End-Joining in
    Emerson CH; Lopez CR; Ribes-Zamora A; Polleys EJ; Williams CL; Yeo L; Zaneveld JE; Chen R; Bertuch AA
    Genetics; 2018 May; 209(1):115-128. PubMed ID: 29500182
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Role of the nuclease activity of Saccharomyces cerevisiae Mre11 in repair of DNA double-strand breaks in mitotic cells.
    Lewis LK; Storici F; Van Komen S; Calero S; Sung P; Resnick MA
    Genetics; 2004 Apr; 166(4):1701-13. PubMed ID: 15126391
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Stepwise 5' DNA end-specific resection of DNA breaks by the Mre11-Rad50-Xrs2 and Sae2 nuclease ensemble.
    Cannavo E; Reginato G; Cejka P
    Proc Natl Acad Sci U S A; 2019 Mar; 116(12):5505-5513. PubMed ID: 30819891
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CDK targets Sae2 to control DNA-end resection and homologous recombination.
    Huertas P; Cortés-Ledesma F; Sartori AA; Aguilera A; Jackson SP
    Nature; 2008 Oct; 455(7213):689-92. PubMed ID: 18716619
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The non-homologous end-joining factor Nej1 inhibits resection mediated by Dna2-Sgs1 nuclease-helicase at DNA double strand breaks.
    Sorenson KS; Mahaney BL; Lees-Miller SP; Cobb JA
    J Biol Chem; 2017 Sep; 292(35):14576-14586. PubMed ID: 28679532
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Requirement of POL3 and POL4 on non-homologous and microhomology-mediated end joining in rad50/xrs2 mutants of Saccharomyces cerevisiae.
    Galli A; Chan CY; Parfenova L; Cervelli T; Schiestl RH
    Mutagenesis; 2015 Nov; 30(6):841-9. PubMed ID: 26122113
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Chromosome aberrations resulting from double-strand DNA breaks at a naturally occurring yeast fragile site composed of inverted ty elements are independent of Mre11p and Sae2p.
    Casper AM; Greenwell PW; Tang W; Petes TD
    Genetics; 2009 Oct; 183(2):423-39, 1SI-26SI. PubMed ID: 19635935
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.