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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 10486322)

  • 1. Temperature-sensitive RB mutations linked to incomplete penetrance of familial retinoblastoma in 12 families.
    Otterson GA; Modi S; Nguyen K; Coxon AB; Kaye FJ
    Am J Hum Genet; 1999 Oct; 65(4):1040-6. PubMed ID: 10486322
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function.
    Otterson GA; Chen Wd; Coxon AB; Khleif SN; Kaye FJ
    Proc Natl Acad Sci U S A; 1997 Oct; 94(22):12036-40. PubMed ID: 9342358
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial inactivation of the RB product in a family with incomplete penetrance of familial retinoblastoma and benign retinal tumors.
    Kratzke RA; Otterson GA; Hogg A; Coxon AB; Geradts J; Cowell JK; Kaye FJ
    Oncogene; 1994 May; 9(5):1321-6. PubMed ID: 8152792
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Low-penetrant RB allele in small-cell cancer shows geldanamycin instability and discordant expression with mutant ras.
    Park Y; Kubo A; Komiya T; Coxon A; Beebe K; Neckers L; Meltzer PS; Kaye FJ
    Cell Cycle; 2008 Aug; 7(15):2384-91. PubMed ID: 18677112
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis of low-penetrance retinoblastoma.
    Harbour JW
    Arch Ophthalmol; 2001 Nov; 119(11):1699-704. PubMed ID: 11709023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1.
    Eloy P; Dehainault C; Sefta M; Aerts I; Doz F; Cassoux N; Lumbroso le Rouic L; Stoppa-Lyonnet D; Radvanyi F; Millot GA; Gauthier-Villars M; Houdayer C
    PLoS Genet; 2016 Feb; 12(2):e1005888. PubMed ID: 26925970
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.
    Mitter D; Rushlow D; Nowak I; Ansperger-Rescher B; Gallie BL; Lohmann DR
    Fam Cancer; 2009; 8(1):55-8. PubMed ID: 18509746
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Distinct Rb gene point mutations in families showing low penetrance of hereditary retinoblastoma].
    Huang Q; Dryja TP; Yandell DW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Jun; 15(3):139-42. PubMed ID: 9621119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Low penetrance hereditary retinoblastoma in a family: what should we consider in the genetic counselling process and follow up?
    Serrano C; Alonso J; Gómez-Mariano G; Aguirre E; Diez O; Gadea N; Bosch N; Balmaña J; Graña B
    Fam Cancer; 2011 Sep; 10(3):617-21. PubMed ID: 21538077
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genotype-phenotype correlations in hereditary familial retinoblastoma.
    Taylor M; Dehainault C; Desjardins L; Doz F; Levy C; Sastre X; Couturier J; Stoppa-Lyonnet D; Houdayer C; Gauthier-Villars M
    Hum Mutat; 2007 Mar; 28(3):284-93. PubMed ID: 17096365
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germline mutations in retinoma patients: relevance to low-penetrance and low-expressivity molecular basis.
    Abouzeid H; Schorderet DF; Balmer A; Munier FL
    Mol Vis; 2009; 15():771-7. PubMed ID: 19390654
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Overview of RB gene mutations in patients with retinoblastoma. Implications for clinical genetic screening.
    Harbour JW
    Ophthalmology; 1998 Aug; 105(8):1442-7. PubMed ID: 9709755
    [TBL] [Abstract][Full Text] [Related]  

  • 13. RB1 germ-line deletions in Argentine retinoblastoma patients.
    Fernández C; Repetto K; Dalamon V; Bergonzi F; Ferreiro V; Szijan I
    Mol Diagn Ther; 2007; 11(1):55-61. PubMed ID: 17286450
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice].
    Lohmann DR; Brandt B; Passarge E; Horsthemke B
    Ophthalmologe; 1997 Apr; 94(4):263-7. PubMed ID: 9229493
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic testing in Tunisian families with heritable retinoblastoma using a low cost approach permits accurate risk prediction in relatives and reveals incomplete penetrance in adults.
    Ayari Jeridi H; Bouguila H; Ansperger-Rescher B; Baroudi O; Mdimegh I; Omran I; Charradi K; Bouzayene H; Benammar-Elgaaïed A; Lohmann DR
    Exp Eye Res; 2014 Jul; 124():48-55. PubMed ID: 24810223
    [TBL] [Abstract][Full Text] [Related]  

  • 16. RB1 gene mutations in retinoblastoma.
    Lohmann DR
    Hum Mutat; 1999; 14(4):283-8. PubMed ID: 10502774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Retinoblastoma.
    Lohmann D
    Adv Exp Med Biol; 2010; 685():220-7. PubMed ID: 20687510
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Disruption of retinoblastoma protein function by coexpression of its C pocket fragment.
    Welch PJ; Wang JY
    Genes Dev; 1995 Jan; 9(1):31-46. PubMed ID: 7828850
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Attenuation of disease phenotype through alternative translation initiation in low-penetrance retinoblastoma.
    Sánchez-Sánchez F; Ramírez-Castillejo C; Weekes DB; Beneyto M; Prieto F; Nájera C; Mittnacht S
    Hum Mutat; 2007 Feb; 28(2):159-67. PubMed ID: 16988938
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A splicing mutation in RB1 in low penetrance retinoblastoma.
    Schubert EL; Strong LC; Hansen MF
    Hum Genet; 1997 Oct; 100(5-6):557-63. PubMed ID: 9341870
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.