BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 30965655)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings.
    McVey M; Lee SE
    Trends Genet; 2008 Nov; 24(11):529-38. PubMed ID: 18809224
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DNA polymerases δ and λ cooperate in repairing double-strand breaks by microhomology-mediated end-joining in Saccharomyces cerevisiae.
    Meyer D; Fu BX; Heyer WD
    Proc Natl Acad Sci U S A; 2015 Dec; 112(50):E6907-16. PubMed ID: 26607450
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RPA antagonizes microhomology-mediated repair of DNA double-strand breaks.
    Deng SK; Gibb B; de Almeida MJ; Greene EC; Symington LS
    Nat Struct Mol Biol; 2014 Apr; 21(4):405-12. PubMed ID: 24608368
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Microhomology-mediated end joining in fission yeast is repressed by pku70 and relies on genes involved in homologous recombination.
    Decottignies A
    Genetics; 2007 Jul; 176(3):1403-15. PubMed ID: 17483423
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microhomology-mediated end joining induces hypermutagenesis at breakpoint junctions.
    Sinha S; Li F; Villarreal D; Shim JH; Yoon S; Myung K; Shim EY; Lee SE
    PLoS Genet; 2017 Apr; 13(4):e1006714. PubMed ID: 28419093
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homology and enzymatic requirements of microhomology-dependent alternative end joining.
    Sharma S; Javadekar SM; Pandey M; Srivastava M; Kumari R; Raghavan SC
    Cell Death Dis; 2015 Mar; 6(3):e1697. PubMed ID: 25789972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Secondary structure forming sequences drive SD-MMEJ repair of DNA double-strand breaks.
    Khodaverdian VY; Hanscom T; Yu AM; Yu TL; Mak V; Brown AJ; Roberts SA; McVey M
    Nucleic Acids Res; 2017 Dec; 45(22):12848-12861. PubMed ID: 29121353
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assays for DNA double-strand break repair by microhomology-based end-joining repair mechanisms.
    Kostyrko K; Mermod N
    Nucleic Acids Res; 2016 Apr; 44(6):e56. PubMed ID: 26657630
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Contribution of Microhomology to Genome Instability: Connection between DNA Repair and Replication Stress.
    Jiang Y
    Int J Mol Sci; 2022 Oct; 23(21):. PubMed ID: 36361724
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Efficient ligase 3-dependent microhomology-mediated end joining repair of DNA double-strand breaks in zebrafish embryos.
    He MD; Zhang FH; Wang HL; Wang HP; Zhu ZY; Sun YH
    Mutat Res; 2015 Oct; 780():86-96. PubMed ID: 26318124
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis-dependent microhomology-mediated end joining accounts for multiple types of repair junctions.
    Yu AM; McVey M
    Nucleic Acids Res; 2010 Sep; 38(17):5706-17. PubMed ID: 20460465
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Microhomology-mediated deletion and gene conversion in African trypanosomes.
    Glover L; Jun J; Horn D
    Nucleic Acids Res; 2011 Mar; 39(4):1372-80. PubMed ID: 20965968
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Involvement of Ku80 in microhomology-mediated end joining for DNA double-strand breaks in vivo.
    Katsura Y; Sasaki S; Sato M; Yamaoka K; Suzukawa K; Nagasawa T; Yokota J; Kohno T
    DNA Repair (Amst); 2007 May; 6(5):639-48. PubMed ID: 17236818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Microhomology-mediated end joining: Good, bad and ugly.
    Seol JH; Shim EY; Lee SE
    Mutat Res; 2018 May; 809():81-87. PubMed ID: 28754468
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.