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Journal Abstract Search

211 related items for PubMed ID: 16931177

  • 1. Molecular processes of chromosome 9p21 deletions causing inactivation of the p16 tumor suppressor gene in human cancer: deduction from structural analysis of breakpoints for deletions.
    Kohno T, Yokota J.
    DNA Repair (Amst); 2006 Sep 08; 5(9-10):1273-81. PubMed ID: 16931177
    [Abstract] [Full Text] [Related]

  • 2. Molecular processes of chromosome 9p21 deletions in human cancers.
    Sasaki S, Kitagawa Y, Sekido Y, Minna JD, Kuwano H, Yokota J, Kohno T.
    Oncogene; 2003 Jun 12; 22(24):3792-8. PubMed ID: 12802286
    [Abstract] [Full Text] [Related]

  • 3. Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells.
    Florl AR, Schulz WA.
    Genes Chromosomes Cancer; 2003 Jun 12; 37(2):141-8. PubMed ID: 12696062
    [Abstract] [Full Text] [Related]

  • 4. Non-homologous end-joining for repairing I-SceI-induced DNA double strand breaks in human cells.
    Honma M, Sakuraba M, Koizumi T, Takashima Y, Sakamoto H, Hayashi M.
    DNA Repair (Amst); 2007 Jun 01; 6(6):781-8. PubMed ID: 17296333
    [Abstract] [Full Text] [Related]

  • 5. Homozygous deletions of CDKN2A caused by alternative mechanisms in various human cancer cell lines.
    Raschke S, Balz V, Efferth T, Schulz WA, Florl AR.
    Genes Chromosomes Cancer; 2005 Jan 01; 42(1):58-67. PubMed ID: 15495191
    [Abstract] [Full Text] [Related]

  • 6. Probing the chromosome 9p21 region susceptible to DNA double-strand breaks in human cells in vivo by restriction enzyme transfer.
    Sato M, Sasaki H, Kazui T, Yokota J, Kohno T.
    Oncogene; 2005 Sep 08; 24(40):6108-18. PubMed ID: 16007206
    [Abstract] [Full Text] [Related]

  • 7. Distinct mechanisms of nonhomologous end joining in the repair of site-directed chromosomal breaks with noncomplementary and complementary ends.
    Willers H, Husson J, Lee LW, Hubbe P, Gazemeier F, Powell SN, Dahm-Daphi J.
    Radiat Res; 2006 Oct 08; 166(4):567-74. PubMed ID: 17007549
    [Abstract] [Full Text] [Related]

  • 8. Two regions of homozygous deletion clusters at chromosome band 9p21 in human lung cancer.
    Hamada K, Kohno T, Takahashi M, Yamazaki M, Yamazaki M, Tashiro H, Sugawara C, Ohwada S, Sekido Y, Minna JD, Yokota J.
    Genes Chromosomes Cancer; 2000 Mar 08; 27(3):308-18. PubMed ID: 10679921
    [Abstract] [Full Text] [Related]

  • 9. Chromatin structural elements and chromosomal translocations in leukemia.
    Zhang Y, Rowley JD.
    DNA Repair (Amst); 2006 Sep 08; 5(9-10):1282-97. PubMed ID: 16893685
    [Abstract] [Full Text] [Related]

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  • 11. Biochemical mechanisms of chromosomal translocations resulting from DNA double-strand breaks.
    Povirk LF.
    DNA Repair (Amst); 2006 Sep 08; 5(9-10):1199-212. PubMed ID: 16822725
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  • 13. Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors.
    Morelli C, Karayianni E, Magnanini C, Mungall AJ, Thorland E, Negrini M, Smith DI, Barbanti-Brodano G.
    Oncogene; 2002 Oct 17; 21(47):7266-76. PubMed ID: 12370818
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  • 15. Checkpoint kinase 2-mediated phosphorylation of BRCA1 regulates the fidelity of nonhomologous end-joining.
    Zhuang J, Zhang J, Willers H, Wang H, Chung JH, van Gent DC, Hallahan DE, Powell SN, Xia F.
    Cancer Res; 2006 Feb 01; 66(3):1401-8. PubMed ID: 16452195
    [Abstract] [Full Text] [Related]

  • 16. Deletion, rearrangement, and gene conversion; genetic consequences of chromosomal double-strand breaks in human cells.
    Honma M, Izumi M, Sakuraba M, Tadokoro S, Sakamoto H, Wang W, Yatagai F, Hayashi M.
    Environ Mol Mutagen; 2003 Feb 01; 42(4):288-98. PubMed ID: 14673874
    [Abstract] [Full Text] [Related]

  • 17. Modeling oncogenic translocations: distinct roles for double-strand break repair pathways in translocation formation in mammalian cells.
    Weinstock DM, Richardson CA, Elliott B, Jasin M.
    DNA Repair (Amst); 2006 Sep 08; 5(9-10):1065-74. PubMed ID: 16815104
    [Abstract] [Full Text] [Related]

  • 18. Molecular analysis of deletions in human chromosome 3p21 and the role of resident cancer genes in disease.
    Angeloni D.
    Brief Funct Genomic Proteomic; 2007 Mar 08; 6(1):19-39. PubMed ID: 17525073
    [Abstract] [Full Text] [Related]

  • 19. Premature chromosome condensation reveals DNA-PK independent pathways of chromosome break repair.
    Terzoudi GI, Singh SK, Pantelias GE, Iliakis G.
    Int J Oncol; 2008 Oct 08; 33(4):871-9. PubMed ID: 18813802
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