BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

191 related articles for article (PubMed ID: 19329795)

  • 41. Assembly of functional ALT-associated promyelocytic leukemia bodies requires Nijmegen Breakage Syndrome 1.
    Wu G; Jiang X; Lee WH; Chen PL
    Cancer Res; 2003 May; 63(10):2589-95. PubMed ID: 12750284
    [TBL] [Abstract][Full Text] [Related]  

  • 42. On BLM helicase in recombination-mediated telomere maintenance.
    Rezazadeh S
    Mol Biol Rep; 2013 Apr; 40(4):3049-64. PubMed ID: 23268311
    [TBL] [Abstract][Full Text] [Related]  

  • 43. FANCM, BRCA1, and BLM cooperatively resolve the replication stress at the ALT telomeres.
    Pan X; Drosopoulos WC; Sethi L; Madireddy A; Schildkraut CL; Zhang D
    Proc Natl Acad Sci U S A; 2017 Jul; 114(29):E5940-E5949. PubMed ID: 28673972
    [TBL] [Abstract][Full Text] [Related]  

  • 44. POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates.
    Opresko PL; Mason PA; Podell ER; Lei M; Hickson ID; Cech TR; Bohr VA
    J Biol Chem; 2005 Sep; 280(37):32069-80. PubMed ID: 16030011
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Telosome, a mammalian telomere-associated complex formed by multiple telomeric proteins.
    Liu D; O'Connor MS; Qin J; Songyang Z
    J Biol Chem; 2004 Dec; 279(49):51338-42. PubMed ID: 15383534
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Rif1 provides a new DNA-binding interface for the Bloom syndrome complex to maintain normal replication.
    Xu D; Muniandy P; Leo E; Yin J; Thangavel S; Shen X; Ii M; Agama K; Guo R; Fox D; Meetei AR; Wilson L; Nguyen H; Weng NP; Brill SJ; Li L; Vindigni A; Pommier Y; Seidman M; Wang W
    EMBO J; 2010 Sep; 29(18):3140-55. PubMed ID: 20711169
    [TBL] [Abstract][Full Text] [Related]  

  • 47. ALT-associated PML bodies are present in viable cells and are enriched in cells in the G(2)/M phase of the cell cycle.
    Grobelny JV; Godwin AK; Broccoli D
    J Cell Sci; 2000 Dec; 113 Pt 24():4577-85. PubMed ID: 11082050
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Depletion of Ku70/80 reduces the levels of extrachromosomal telomeric circles and inhibits proliferation of ALT cells.
    Li B; Reddy S; Comai L
    Aging (Albany NY); 2011 Apr; 3(4):395-406. PubMed ID: 21512205
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures.
    Barefield C; Karlseder J
    Nucleic Acids Res; 2012 Aug; 40(15):7358-67. PubMed ID: 22576367
    [TBL] [Abstract][Full Text] [Related]  

  • 50. TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA.
    Machwe A; Xiao L; Orren DK
    Oncogene; 2004 Jan; 23(1):149-56. PubMed ID: 14712220
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Geminin overexpression prevents the completion of topoisomerase IIα chromosome decatenation, leading to aneuploidy in human mammary epithelial cells.
    Gardner L; Malik R; Shimizu Y; Mullins N; ElShamy WM
    Breast Cancer Res; 2011 May; 13(3):R53. PubMed ID: 21595939
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Topoisomerase II inhibition suppresses the proliferation of telomerase-negative cancers.
    Hsieh MH; Tsai CH; Lin CC; Li TK; Hung TW; Chang LT; Hsin LW; Teng SC
    Cell Mol Life Sci; 2015 May; 72(9):1825-37. PubMed ID: 25430478
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Break-induced replication promotes fragile telomere formation.
    Yang Z; Takai KK; Lovejoy CA; de Lange T
    Genes Dev; 2020 Oct; 34(19-20):1392-1405. PubMed ID: 32883681
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Identification of candidate alternative lengthening of telomeres genes by methionine restriction and RNA interference.
    Jiang WQ; Zhong ZH; Henson JD; Reddel RR
    Oncogene; 2007 Jul; 26(32):4635-47. PubMed ID: 17297460
    [TBL] [Abstract][Full Text] [Related]  

  • 55. BLM and RMI1 alleviate RPA inhibition of TopoIIIα decatenase activity.
    Yang J; Bachrati CZ; Hickson ID; Brown GW
    PLoS One; 2012; 7(7):e41208. PubMed ID: 22911760
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase.
    Nora GJ; Buncher NA; Opresko PL
    Nucleic Acids Res; 2010 Jul; 38(12):3984-98. PubMed ID: 20215438
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Control of human telomere length by TRF1 and TRF2.
    Smogorzewska A; van Steensel B; Bianchi A; Oelmann S; Schaefer MR; Schnapp G; de Lange T
    Mol Cell Biol; 2000 Mar; 20(5):1659-68. PubMed ID: 10669743
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Lack of TRF2 in ALT cells causes PML-dependent p53 activation and loss of telomeric DNA.
    Stagno D'Alcontres M; Mendez-Bermudez A; Foxon JL; Royle NJ; Salomoni P
    J Cell Biol; 2007 Dec; 179(5):855-67. PubMed ID: 18056407
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Super-telomeres in transformed human fibroblasts.
    Chiodi I; Belgiovine C; Zongaro S; Ricotti R; Horard B; Lossani A; Focher F; Gilson E; Giulotto E; Mondello C
    Biochim Biophys Acta; 2013 Aug; 1833(8):1885-93. PubMed ID: 23570868
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Telomere repeat binding factors TRF1, TRF2, and hRAP1 modulate replication of Epstein-Barr virus OriP.
    Deng Z; Atanasiu C; Burg JS; Broccoli D; Lieberman PM
    J Virol; 2003 Nov; 77(22):11992-2001. PubMed ID: 14581536
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.