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Journal Abstract Search

331 related items for PubMed ID: 17210724

  • 1. Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
    Gratias S, Rieder H, Ullmann R, Klein-Hitpass L, Schneider S, Bölöni R, Kappler M, Lohmann DR.
    Cancer Res; 2007 Jan 01; 67(1):408-16. PubMed ID: 17210724
    [Abstract] [Full Text] [Related]

  • 2. Loss at chromosome arm 16q in retinoblastoma: confirmation of the association with diffuse vitreous seeding and refinement of the recurrently deleted region.
    Gustmann S, Klein-Hitpass L, Stephan H, Weber S, Bornfeld N, Kaulisch M, Lohmann DR, Dünker N.
    Genes Chromosomes Cancer; 2011 May 01; 50(5):327-37. PubMed ID: 21305643
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  • 3. Minimal 16q genomic loss implicates cadherin-11 in retinoblastoma.
    Marchong MN, Chen D, Corson TW, Lee C, Harmandayan M, Bowles E, Chen N, Gallie BL.
    Mol Cancer Res; 2004 Sep 01; 2(9):495-503. PubMed ID: 15383628
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  • 4. Loss of heterozygosity at chromosome 16q in prostate adenocarcinoma: identification of three independent regions.
    Latil A, Cussenot O, Fournier G, Driouch K, Lidereau R.
    Cancer Res; 1997 Mar 15; 57(6):1058-62. PubMed ID: 9067271
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  • 5. Loss of heterozygosity and mutations are the major mechanisms of RB1 gene inactivation in Chinese with sporadic retinoblastoma.
    Choy KW, Pang CP, Yu CB, Wong HL, Ng JS, Fan DS, Lo KW, Chai JT, Wang J, Fu W, Lam DS.
    Hum Mutat; 2002 Nov 15; 20(5):408. PubMed ID: 12402348
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  • 11. Deletions of chromosome 13q, mutations in Retinoblastoma 1, and retinoblastoma protein state in human hepatocellular carcinoma.
    Zhang X, Xu HJ, Murakami Y, Sachse R, Yashima K, Hirohashi S, Hu SX, Benedict WF, Sekiya T.
    Cancer Res; 1994 Aug 01; 54(15):4177-82. PubMed ID: 8033150
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  • 12. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
    Lillington DM, Kingston JE, Coen PG, Price E, Hungerford J, Domizio P, Young BD, Onadim Z.
    Genes Chromosomes Cancer; 2003 Feb 01; 36(2):121-8. PubMed ID: 12508240
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  • 14. Involvement of H-cadherin (CDH13) on 16q in the region of frequent deletion in ovarian cancer.
    Kawakami M, Staub J, Cliby W, Hartmann L, Smith DI, Shridhar V.
    Int J Oncol; 1999 Oct 01; 15(4):715-20. PubMed ID: 10493953
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  • 15. Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions.
    Cleton-Jansen AM, Callen DF, Seshadri R, Goldup S, Mccallum B, Crawford J, Powell JA, Settasatian C, van Beerendonk H, Moerland EW, Smit VT, Harris WH, Millis R, Morgan NV, Barnes D, Mathew CG, Cornelisse CJ.
    Cancer Res; 2001 Feb 01; 61(3):1171-7. PubMed ID: 11221848
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  • 16. [RB1 and CDKN2A functional defects resulting in retinoblastoma].
    Babenko OV, Zemliakova VV, Saakian SV, Brovkina AF, Strel'nikov VV, Zaletaev DV, Nemtsova MV.
    Mol Biol (Mosk); 2002 Feb 01; 36(5):777-83. PubMed ID: 12391839
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  • 17. Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinoma.
    Saffroy R, Riou P, Soler G, Azoulay D, Emile JF, Debuire B, Lemoine A.
    Eur J Hum Genet; 2002 Apr 01; 10(4):239-44. PubMed ID: 12032731
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  • 18. Three distinct commonly deleted regions of chromosome arm 16q in human primary and metastatic prostate cancers.
    Suzuki H, Komiya A, Emi M, Kuramochi H, Shiraishi T, Yatani R, Shimazaki J.
    Genes Chromosomes Cancer; 1996 Dec 01; 17(4):225-33. PubMed ID: 8946204
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  • 19. Allele loss on chromosome 16q24.2-qter occurs frequently in breast cancers irrespectively of differences in phenotype and extent of spread.
    Tsuda H, Callen DF, Fukutomi T, Nakamura Y, Hirohashi S.
    Cancer Res; 1994 Jan 15; 54(2):513-7. PubMed ID: 8275489
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