These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

276 related articles for article (PubMed ID: 20407424)

  • 1. TRF2/RAP1 and DNA-PK mediate a double protection against joining at telomeric ends.
    Bombarde O; Boby C; Gomez D; Frit P; Giraud-Panis MJ; Gilson E; Salles B; Calsou P
    EMBO J; 2010 May; 29(9):1573-84. PubMed ID: 20407424
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Both the classical and alternative non-homologous end joining pathways contribute to the fusion of drastically shortened telomeres induced by TRF2 overexpression.
    Nera B; Huang HS; Hendrickson EA; Xu L
    Cell Cycle; 2019 Apr; 18(8):880-888. PubMed ID: 30907229
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Human RAP1 inhibits non-homologous end joining at telomeres.
    Sarthy J; Bae NS; Scrafford J; Baumann P
    EMBO J; 2009 Nov; 28(21):3390-9. PubMed ID: 19763083
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple roles for MRE11 at uncapped telomeres.
    Deng Y; Guo X; Ferguson DO; Chang S
    Nature; 2009 Aug; 460(7257):914-8. PubMed ID: 19633651
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Biochemical evidence for Ku-independent backup pathways of NHEJ.
    Wang H; Perrault AR; Takeda Y; Qin W; Wang H; Iliakis G
    Nucleic Acids Res; 2003 Sep; 31(18):5377-88. PubMed ID: 12954774
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DNA ligase IV-dependent NHEJ of deprotected mammalian telomeres in G1 and G2.
    Smogorzewska A; Karlseder J; Holtgreve-Grez H; Jauch A; de Lange T
    Curr Biol; 2002 Oct; 12(19):1635-44. PubMed ID: 12361565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cell cycle-dependent role of MRN at dysfunctional telomeres: ATM signaling-dependent induction of nonhomologous end joining (NHEJ) in G1 and resection-mediated inhibition of NHEJ in G2.
    Dimitrova N; de Lange T
    Mol Cell Biol; 2009 Oct; 29(20):5552-63. PubMed ID: 19667071
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Removal of shelterin reveals the telomere end-protection problem.
    Sfeir A; de Lange T
    Science; 2012 May; 336(6081):593-7. PubMed ID: 22556254
    [TBL] [Abstract][Full Text] [Related]  

  • 9. BRCA1 and CtIP promote alternative non-homologous end-joining at uncapped telomeres.
    Badie S; Carlos AR; Folio C; Okamoto K; Bouwman P; Jonkers J; Tarsounas M
    EMBO J; 2015 Feb; 34(3):410-24. PubMed ID: 25582120
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A RAP1/TRF2 complex inhibits nonhomologous end-joining at human telomeric DNA ends.
    Bae NS; Baumann P
    Mol Cell; 2007 May; 26(3):323-34. PubMed ID: 17499040
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TRF2-Mediated Control of Telomere DNA Topology as a Mechanism for Chromosome-End Protection.
    Benarroch-Popivker D; Pisano S; Mendez-Bermudez A; Lototska L; Kaur P; Bauwens S; Djerbi N; Latrick CM; Fraisier V; Pei B; Gay A; Jaune E; Foucher K; Cherfils-Vicini J; Aeby E; Miron S; Londoño-Vallejo A; Ye J; Le Du MH; Wang H; Gilson E; Giraud-Panis MJ
    Mol Cell; 2016 Jan; 61(2):274-86. PubMed ID: 26774283
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. DNA processing is not required for ATM-mediated telomere damage response after TRF2 deletion.
    Celli GB; de Lange T
    Nat Cell Biol; 2005 Jul; 7(7):712-8. PubMed ID: 15968270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA-dependent protein kinase catalytic subunit is not required for dysfunctional telomere fusion and checkpoint response in the telomerase-deficient mouse.
    Maser RS; Wong KK; Sahin E; Xia H; Naylor M; Hedberg HM; Artandi SE; DePinho RA
    Mol Cell Biol; 2007 Mar; 27(6):2253-65. PubMed ID: 17145779
    [TBL] [Abstract][Full Text] [Related]  

  • 15. TRF2-RAP1 is required to protect telomeres from engaging in homologous recombination-mediated deletions and fusions.
    Rai R; Chen Y; Lei M; Chang S
    Nat Commun; 2016 Mar; 7():10881. PubMed ID: 26941064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DNA-dependent protein kinase in telomere maintenance and protection.
    Sui J; Zhang S; Chen BPC
    Cell Mol Biol Lett; 2020; 25():2. PubMed ID: 31988640
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The function of classical and alternative non-homologous end-joining pathways in the fusion of dysfunctional telomeres.
    Rai R; Zheng H; He H; Luo Y; Multani A; Carpenter PB; Chang S
    EMBO J; 2010 Aug; 29(15):2598-610. PubMed ID: 20588252
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Extensive ssDNA end formation at DNA double-strand breaks in non-homologous end-joining deficient cells during the S phase.
    Karlsson KH; Stenerlöw B
    BMC Mol Biol; 2007 Oct; 8():97. PubMed ID: 17963495
    [TBL] [Abstract][Full Text] [Related]  

  • 19. No overt nucleosome eviction at deprotected telomeres.
    Wu P; de Lange T
    Mol Cell Biol; 2008 Sep; 28(18):5724-35. PubMed ID: 18625717
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mechanisms of DNA double strand break repair and chromosome aberration formation.
    Iliakis G; Wang H; Perrault AR; Boecker W; Rosidi B; Windhofer F; Wu W; Guan J; Terzoudi G; Pantelias G
    Cytogenet Genome Res; 2004; 104(1-4):14-20. PubMed ID: 15162010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.