These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

143 related items for PubMed ID: 9134545

  • 1. 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]

  • 2. 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]

  • 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 30; 61(2):282-94. PubMed ID: 9311732
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 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 23; 358(1-2):75-80. PubMed ID: 15921673
    [Abstract] [Full Text] [Related]

  • 6. 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 Aug 23; 11(1):63-70. PubMed ID: 17286451
    [Abstract] [Full Text] [Related]

  • 7. 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 Aug 23; 59(4):248-52. PubMed ID: 1544317
    [Abstract] [Full Text] [Related]

  • 8. Delayed development of retinoblastoma associated with loss of a maternal allele on chromosome 13.
    Kato MV, Ishizaki K, Shimizu T, Toguchida J, Kaneko A, Sasaki MS.
    Int J Cancer; 1995 Feb 20; 64(1):3-8. PubMed ID: 7665245
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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]

  • 11. The polymerase chain reaction (PCR) in the routine genetic characterization of retinoblastoma: a tool for the clinical laboratory.
    Mastrangelo D, Squitieri N, Bruni S, Hadjistilianou T, Frezzotti R.
    Surv Ophthalmol; 1997 Jan 01; 41(4):331-40. PubMed ID: 9104770
    [Abstract] [Full Text] [Related]

  • 12. Loss of heterozygosity of the retinoblastoma gene is correlated with the altered pRb expression in human endometrial cancer.
    Semczuk A, Marzec B, Roessner A, Jakowicki JA, Wojcierowski J, Schneider-Stock R.
    Virchows Arch; 2002 Dec 01; 441(6):577-83. PubMed ID: 12461615
    [Abstract] [Full Text] [Related]

  • 13. The loss of heterozygosity in retinoblastoma and p53 suppressor genes as a prognostic indicator for head and neck cancer.
    Gleich LL, Li YQ, Biddinger PW, Gartside PS, Stambrook PJ, Pavelic ZP, Gluckman JL.
    Laryngoscope; 1996 Nov 01; 106(11):1378-81. PubMed ID: 8914904
    [Abstract] [Full Text] [Related]

  • 14. Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.
    Greger V, Debus N, Lohmann D, Höpping W, Passarge E, Horsthemke B.
    Hum Genet; 1994 Nov 01; 94(5):491-6. PubMed ID: 7959682
    [Abstract] [Full Text] [Related]

  • 15. [Prediction of retinoblastoma: linkage analysis of families with hereditary retinoblastoma by using polymorphic sites within the Rb gene].
    Yuan L, Gao Y, Lo S, Fang B, Ye J.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Oct 01; 17(5):338-42. PubMed ID: 8706167
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 94(3):357-62. PubMed ID: 19726429
    [Abstract] [Full Text] [Related]

  • 17. An association of the RB gene with osteosarcoma: molecular genetic evaluation of a case of hereditary retinoblastoma.
    Issing WJ, Wustrow TP, Oeckler R, Mezger J, Nerlich A.
    Eur Arch Otorhinolaryngol; 1993 Mar 01; 250(5):277-80. PubMed ID: 8217129
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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 01; 20(5):408. PubMed ID: 12402348
    [Abstract] [Full Text] [Related]

  • 20. Sex mutation ratio in retinoblastoma and retinoma: relevance to genetic counseling.
    Munier FL, Thonney F, Balmer A, Héon E, Pescia G, Schorderet DF.
    Klin Monbl Augenheilkd; 1996 May 01; 208(5):400-3. PubMed ID: 8766064
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.