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Journal Abstract Search

61 related items for PubMed ID: 16007206

  • 1. 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]

  • 2. 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]

  • 3. The incidence of chromosome 9p21 abnormalities and deletions of tumor suppressor genes p15(INK4b)/p16(INK4a)/p14(ARF) in patients with acute lymphoblastic leukemia.
    Faderl S, Estrov Z, Kantarjian HM, Thomas D, Cortes J, Manshouri T, Chan CC, Hays KJ, Pierce S, Albitar M.
    Cytokines Cell Mol Ther; 1999 Sep 08; 5(3):159-63. PubMed ID: 10641574
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Fine-mapping loss of gene architecture at the CDKN2B (p15INK4b), CDKN2A (p14ARF, p16INK4a), and MTAP genes in head and neck squamous cell carcinoma.
    Worsham MJ, Chen KM, Tiwari N, Pals G, Schouten JP, Sethi S, Benninger MS.
    Arch Otolaryngol Head Neck Surg; 2006 Apr 12; 132(4):409-15. PubMed ID: 16618910
    [Abstract] [Full Text] [Related]

  • 6. Aberrations of p16INK4A, p14ARF and p15INK4B genes in pediatric solid tumors.
    Obana K, Yang HW, Piao HY, Taki T, Hashizume K, Hanada R, Yamamoto K, Tanaka Y, Toyoda Y, Takita J, Tsuchida Y, Hayashi Y.
    Int J Oncol; 2003 Oct 12; 23(4):1151-7. PubMed ID: 12963998
    [Abstract] [Full Text] [Related]

  • 7. Differential effect of epigenetic alterations and genomic deletions of CDK inhibitors [p16(INK4a), p15(INK4b), p14(ARF)] in mantle cell lymphoma.
    Hutter G, Scheubner M, Zimmermann Y, Kalla J, Katzenberger T, Hübler K, Roth S, Hiddemann W, Ott G, Dreyling M.
    Genes Chromosomes Cancer; 2006 Feb 12; 45(2):203-10. PubMed ID: 16258956
    [Abstract] [Full Text] [Related]

  • 8. Preferentially different mechanisms of inactivation of 9p21 gene cluster in liver fluke-related cholangiocarcinoma.
    Chinnasri P, Pairojkul C, Jearanaikoon P, Sripa B, Bhudhisawasdi V, Tantimavanich S, Limpaiboon T.
    Hum Pathol; 2009 Jun 12; 40(6):817-26. PubMed ID: 19200577
    [Abstract] [Full Text] [Related]

  • 9. Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.
    Weber RG, Hoischen A, Ehrler M, Zipper P, Kaulich K, Blaschke B, Becker AJ, Weber-Mangal S, Jauch A, Radlwimmer B, Schramm J, Wiestler OD, Lichter P, Reifenberger G.
    Oncogene; 2007 Feb 15; 26(7):1088-97. PubMed ID: 16909113
    [Abstract] [Full Text] [Related]

  • 10. Genomic instability, mutations and expression analysis of the tumour suppressor genes p14(ARF), p15(INK4b), p16(INK4a) and p53 in actinic keratosis.
    Kanellou P, Zaravinos A, Zioga M, Stratigos A, Baritaki S, Soufla G, Zoras O, Spandidos DA.
    Cancer Lett; 2008 Jun 08; 264(1):145-61. PubMed ID: 18331779
    [Abstract] [Full Text] [Related]

  • 11. Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells.
    Florl AR, Schulz WA.
    Genes Chromosomes Cancer; 2003 Jun 08; 37(2):141-8. PubMed ID: 12696062
    [Abstract] [Full Text] [Related]

  • 12. Deregulation of the tumour suppressor genes p14(ARF), p15(INK4b), p16(INK4a) and p53 in basal cell carcinoma.
    Kanellou P, Zaravinos A, Zioga M, Spandidos DA.
    Br J Dermatol; 2009 Jun 08; 160(6):1215-21. PubMed ID: 19298278
    [Abstract] [Full Text] [Related]

  • 13. Ionizing radiation and genetic risks XIV. Potential research directions in the post-genome era based on knowledge of repair of radiation-induced DNA double-strand breaks in mammalian somatic cells and the origin of deletions associated with human genomic disorders.
    Sankaranarayanan K, Wassom JS.
    Mutat Res; 2005 Oct 15; 578(1-2):333-70. PubMed ID: 16084534
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  • 15. Risk prediction of gastric cancer by analysis of aberrant DNA methylation in non-neoplastic gastric epithelium.
    Tahara T, Arisawa T, Shibata T, Wang FY, Nakamura M, Sakata M, Nagasaka M, Takagi T, Kamiya Y, Fujita H, Nakamura M, Hasegawa S, Iwata M, Takahama K, Watanabe M, Hirata I, Nakano H.
    Digestion; 2007 Oct 15; 75(1):54-61. PubMed ID: 17438355
    [Abstract] [Full Text] [Related]

  • 16. Genome-wide profiling of promoter methylation in human.
    Hatada I, Fukasawa M, Kimura M, Morita S, Yamada K, Yoshikawa T, Yamanaka S, Endo C, Sakurada A, Sato M, Kondo T, Horii A, Ushijima T, Sasaki H.
    Oncogene; 2006 May 18; 25(21):3059-64. PubMed ID: 16407832
    [Abstract] [Full Text] [Related]

  • 17. Frequent epigenetic inactivation of Rb1 in addition to p15 and p16 in mantle cell and follicular lymphoma.
    Chim CS, Wong KY, Loong F, Lam WW, Srivastava G.
    Hum Pathol; 2007 Dec 18; 38(12):1849-57. PubMed ID: 17900658
    [Abstract] [Full Text] [Related]

  • 18. Differing effects of T4 DNA ligase in the modulation of the damage induced in mammalian cells by either X-rays or restriction endonucleases.
    Ortiz T, Piñero J.
    Chemotherapy; 2007 Dec 18; 53(1):14-20. PubMed ID: 17192708
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  • 20. Promoter hypermethylation profile of ovarian epithelial neoplasms.
    Makarla PB, Saboorian MH, Ashfaq R, Toyooka KO, Toyooka S, Minna JD, Gazdar AF, Schorge JO.
    Clin Cancer Res; 2005 Aug 01; 11(15):5365-9. PubMed ID: 16061849
    [Abstract] [Full Text] [Related]

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