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227 related items for PubMed ID: 7959682

  • 1. 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; 94(5):491-6. PubMed ID: 7959682
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Identification of three new mutations in the RB1 gene in patients with sporadic retinoblastoma in Colombia.
    Serrano ML, Yunis JJ.
    Biomedica; 2013 Aug; 33(1):53-61. PubMed ID: 23715307
    [Abstract] [Full Text] [Related]

  • 4. Methylation status of the retinoblastoma gene (RB1) in osteosarcoma: no evidence for hypermethylation.
    Otte C, Scholz R, Werner M, Weber B, Delling G, Kabisch H.
    Pediatr Hematol Oncol; 2004 Aug; 21(1):57-65. PubMed ID: 14660307
    [Abstract] [Full Text] [Related]

  • 5. Epigenetic changes may contribute to the formation and spontaneous regression of retinoblastoma.
    Greger V, Passarge E, Höpping W, Messmer E, Horsthemke B.
    Hum Genet; 1989 Sep; 83(2):155-8. PubMed ID: 2550354
    [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; 20(5):408. PubMed ID: 12402348
    [Abstract] [Full Text] [Related]

  • 7. Extensive DNA methylation spanning the Rb promoter in retinoblastoma tumors.
    Stirzaker C, Millar DS, Paul CL, Warnecke PM, Harrison J, Vincent PC, Frommer M, Clark SJ.
    Cancer Res; 1997 Jun 01; 57(11):2229-37. PubMed ID: 9187126
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 18(1):7-12. PubMed ID: 9134545
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Methylation status of RB1 promoter in Indian retinoblastoma patients.
    Joseph B, Mamatha G, Raman G, Shanmugam MP, Kumaramanickavel G.
    Cancer Biol Ther; 2004 Feb 27; 3(2):184-7. PubMed ID: 14726655
    [Abstract] [Full Text] [Related]

  • 11. Hypermethylation in the retinoblastoma gene is associated with unilateral, sporadic retinoblastoma.
    Ohtani-Fujita N, Dryja TP, Rapaport JM, Fujita T, Matsumura S, Ozasa K, Watanabe Y, Hayashi K, Maeda K, Kinoshita S, Matsumura T, Ohnishi Y, Hotta Y, Takahashi R, Kato MV, Ishizaki K, Sasaki MS, Horsthemke B, Minoda K, Sakai T.
    Cancer Genet Cytogenet; 1997 Oct 01; 98(1):43-9. PubMed ID: 9309117
    [Abstract] [Full Text] [Related]

  • 12. [Genetics of retinoblastoma].
    Minoda K.
    Nihon Rinsho; 1995 Nov 01; 53(11):2774-8. PubMed ID: 8538043
    [Abstract] [Full Text] [Related]

  • 13. Distinct RB1 gene mutations with low penetrance in hereditary retinoblastoma.
    Lohmann DR, Brandt B, Höpping W, Passarge E, Horsthemke B.
    Hum Genet; 1994 Oct 01; 94(4):349-54. PubMed ID: 7927327
    [Abstract] [Full Text] [Related]

  • 14. A molecular study of first and second RB1 mutational hits in retinoblastoma patients.
    de Andrade AF, da Hora Barbosa R, Vargas FR, Ferman S, Eisenberg AL, Fernandes L, Bonvicino CR.
    Cancer Genet Cytogenet; 2006 May 01; 167(1):43-6. PubMed ID: 16682285
    [Abstract] [Full Text] [Related]

  • 15. Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.
    Sakai T, Toguchida J, Ohtani N, Yandell DW, Rapaport JM, Dryja TP.
    Am J Hum Genet; 1991 May 01; 48(5):880-8. PubMed ID: 1673287
    [Abstract] [Full Text] [Related]

  • 16. Mutations in the RB1 gene and their effects on transcription.
    Dunn JM, Phillips RA, Zhu X, Becker A, Gallie BL.
    Mol Cell Biol; 1989 Nov 01; 9(11):4596-604. PubMed ID: 2601691
    [Abstract] [Full Text] [Related]

  • 17. Detection of mutations of the RB1 gene in retinoblastoma patients by using exon-by-exon PCR-SSCP analysis.
    Shimizu T, Toguchida J, Kato MV, Kaneko A, Ishizaki K, Sasaki MS.
    Am J Hum Genet; 1994 May 01; 54(5):793-800. PubMed ID: 8178820
    [Abstract] [Full Text] [Related]

  • 18. 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 May 01; 11(1):63-70. PubMed ID: 17286451
    [Abstract] [Full Text] [Related]

  • 19. Detection of mutations in the RB1 gene by single strand conformation polymorphism (SSCP) analysis, amplification mismatch detection (AMD) analysis and polymerase chain reaction sequencing.
    Dundar M, Lanyon GW, Connor MJ.
    Proc Natl Sci Counc Repub China B; 2001 Jul 01; 25(3):166-73. PubMed ID: 11480772
    [Abstract] [Full Text] [Related]

  • 20. Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
    Schüler A, Weber S, Neuhäuser M, Jurklies C, Lehnert T, Heimann H, Rudolph G, Jöckel KH, Bornfeld N, Lohmann DR.
    Eur J Cancer; 2005 Mar 01; 41(5):735-40. PubMed ID: 15763650
    [Abstract] [Full Text] [Related]

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