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133 related items for PubMed ID: 1544317

  • 1. Mechanisms of loss of heterozygosity in retinoblastoma.
    Zhu X, Dunn JM, Goddard AD, Squire JA, Becker A, Phillips RA, Gallie BL.
    Cytogenet Cell Genet; 1992; 59(4):248-52. PubMed ID: 1544317
    [Abstract] [Full Text] [Related]

  • 2. Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma.
    Munier FL, Thonney F, Balmer A, Uffer S, Héon E, Van Melle G, Rutz HP, Pescia G, Schorderet DF.
    Ophthalmic Genet; 1997 Mar; 18(1):7-12. PubMed ID: 9134545
    [Abstract] [Full Text] [Related]

  • 3. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
    Lohmann DR, Gerick M, Brandt B, Oelschläger U, Lorenz B, Passarge E, Horsthemke B.
    Am J Hum Genet; 1997 Aug; 61(2):282-94. PubMed ID: 9311732
    [Abstract] [Full Text] [Related]

  • 4. Loss of heterozygosity on chromosome 13 and its association with delayed growth of retinoblastoma.
    Kato MV, Ishizaki K, Ejima Y, Kaneko A, Tanooka H, Sasaki MS.
    Int J Cancer; 1993 Jul 30; 54(6):922-6. PubMed ID: 8335400
    [Abstract] [Full Text] [Related]

  • 5. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
    Zhang XL, Fu WL, Zhao HX, Zhou LX, Huang JF, Wang JH.
    Clin Chim Acta; 2005 Aug 30; 358(1-2):75-80. PubMed ID: 15921673
    [Abstract] [Full Text] [Related]

  • 6. 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 30; 20(5):408. PubMed ID: 12402348
    [Abstract] [Full Text] [Related]

  • 7. Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma.
    Toguchida J, Ishizaki K, Sasaki MS, Ikenaga M, Sugimoto M, Kotoura Y, Yamamuro T.
    Cancer Res; 1988 Jul 15; 48(14):3939-43. PubMed ID: 2898286
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Loss of retinoblastoma gene function and heterozygosity at the RB locus in renal cortical neoplasms.
    Lai S, Benedict WF, Silver SA, El-Naggar AK.
    Hum Pathol; 1997 Jun 01; 28(6):693-7. PubMed ID: 9191003
    [Abstract] [Full Text] [Related]

  • 10. Loss of heterozygosity at the RB locus is frequent and correlates with muscle invasion in bladder carcinoma.
    Cairns P, Proctor AJ, Knowles MA.
    Oncogene; 1991 Dec 01; 6(12):2305-9. PubMed ID: 1766677
    [Abstract] [Full Text] [Related]

  • 11. Alterations of the retinoblastoma gene in clinically localized, stage B prostate adenocarcinomas.
    Ittmann MM, Wieczorek R.
    Hum Pathol; 1996 Jan 01; 27(1):28-34. PubMed ID: 8543307
    [Abstract] [Full Text] [Related]

  • 12. Human pituitary adenomas show no loss of heterozygosity at the retinoblastoma gene locus.
    Zhu J, Leon SP, Beggs AH, Busque L, Gilliland DG, Black PM.
    J Clin Endocrinol Metab; 1994 Apr 01; 78(4):922-7. PubMed ID: 8157722
    [Abstract] [Full Text] [Related]

  • 13. Evidence of functional RB protein in epithelial ovarian carcinomas despite loss of heterozygosity at the RB locus.
    Dodson MK, Cliby WA, Xu HJ, DeLacey KA, Hu SX, Keeney GL, Li J, Podratz KC, Jenkins RB, Benedict WF.
    Cancer Res; 1994 Feb 01; 54(3):610-3. PubMed ID: 8306318
    [Abstract] [Full Text] [Related]

  • 14. The retinoblastoma gene is involved in malignant progression of astrocytomas.
    Henson JW, Schnitker BL, Correa KM, von Deimling A, Fassbender F, Xu HJ, Benedict WF, Yandell DW, Louis DN.
    Ann Neurol; 1994 Nov 01; 36(5):714-21. PubMed ID: 7979217
    [Abstract] [Full Text] [Related]

  • 15. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
    Ramprasad VL, Madhavan J, Murugan S, Sujatha J, Suresh S, Sharma T, Kumaramanickavel G.
    Mol Diagn Ther; 2007 Nov 01; 11(1):63-70. PubMed ID: 17286451
    [Abstract] [Full Text] [Related]

  • 16. Preferential germline mutation of the paternal allele in retinoblastoma.
    Zhu XP, Dunn JM, Phillips RA, Goddard AD, Paton KE, Becker A, Gallie BL.
    Nature; 1989 Jul 27; 340(6231):312-3. PubMed ID: 2568588
    [Abstract] [Full Text] [Related]

  • 17. Allelic imbalance at 13q31 is associated with reduced GPC6 in Chinese with sporadic retinoblastoma.
    Lau CS, Yu CB, Wong HK, Fan DS, Mak HT, Wong KW, Lam DS, Pang CP, Choy KW.
    Br J Ophthalmol; 2010 Mar 27; 94(3):357-62. PubMed ID: 19726429
    [Abstract] [Full Text] [Related]

  • 18. Loss of heterozygosity on chromosome 17 and mutation of the p53 gene in retinoblastoma.
    Kato MV, Shimizu T, Ishizaki K, Kaneko A, Yandell DW, Toguchida J, Sasaki MS.
    Cancer Lett; 1996 Aug 23; 106(1):75-82. PubMed ID: 8827049
    [Abstract] [Full Text] [Related]

  • 19. Loss of heterozygosity of chromosome 13 in Merkel cell carcinoma.
    Leonard JH, Hayard N.
    Genes Chromosomes Cancer; 1997 Sep 23; 20(1):93-7. PubMed ID: 9290960
    [Abstract] [Full Text] [Related]

  • 20. High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma.
    Priya K, Jada SR, Quah BL, Quah TC, Lai PS.
    Cancer Biol Ther; 2009 Apr 23; 8(8):714-7. PubMed ID: 19252413
    [Abstract] [Full Text] [Related]

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