242 related articles for article (PubMed ID: 11709023)
1. Molecular basis of low-penetrance retinoblastoma.
Harbour JW
Arch Ophthalmol; 2001 Nov; 119(11):1699-704. PubMed ID: 11709023
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Retinoblastoma: the disease, gene and protein provide critical leads to understand cancer.
DiCiommo D; Gallie BL; Bremner R
Semin Cancer Biol; 2000 Aug; 10(4):255-69. PubMed ID: 10966849
[TBL] [Abstract][Full Text] [Related]
8. Role of the retinoblastoma protein in the pathogenesis of human cancer.
Sellers WR; Kaelin WG
J Clin Oncol; 1997 Nov; 15(11):3301-12. PubMed ID: 9363859
[TBL] [Abstract][Full Text] [Related]
9. A novel constitutional mutation affecting splicing of retinoblastoma tumor suppressor gene intron 23 causes partial loss of pRB activity.
Sánchez-Sánchez F; Kruetzfeldt M; Nájera C; Mittnacht S
Hum Mutat; 2005 Feb; 25(2):223. PubMed ID: 15643604
[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. [From gene to disease; retinoblastoma and the RB1 gene].
Scheffer H; Imhof SM; Moll AC
Ned Tijdschr Geneeskd; 2001 Jun; 145(26):1245-7. PubMed ID: 11455690
[TBL] [Abstract][Full Text] [Related]
12. [Low-penetrance retinoblastoma due to exons 24 and 25 deletions in the Rb1 gene].
Du C; Jiang Y; Gallie BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):370-4. PubMed ID: 12362308
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. The molecular biology of retinoblastoma.
Brantley MA; Harbour JW
Ocul Immunol Inflamm; 2001 Mar; 9(1):1-8. PubMed ID: 11262663
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. 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]
19. Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.
Ottaviani D; Alonso C; Szijan I
Medicina (B Aires); 2015; 75(3):137-41. PubMed ID: 26117602
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
