359 related articles for article (PubMed ID: 16225399)
1. Constitutional and somatic RB1 mutation spectrum in nonfamilial unilateral and bilateral retinoblastoma in India.
Bamne MN; Ghule PN; Jose J; Banavali SD; Kurkure PA; Amare Kadam PS
Genet Test; 2005; 9(3):200-11. PubMed ID: 16225399
[TBL] [Abstract][Full Text] [Related]
2. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
Amare Kadam PS; Ghule P; Jose J; Bamne M; Kurkure P; Banavali S; Sarin R; Advani S
Cancer Genet Cytogenet; 2004 Apr; 150(1):33-43. PubMed ID: 15041221
[TBL] [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; 33(1):53-61. PubMed ID: 23715307
[TBL] [Abstract][Full Text] [Related]
4. p53 gene gets altered by various mechanisms: studies in childhood sarcomas and retinoblastoma.
Ghule P; Kadam PA; Jambhekar N; Bamne M; Pai S; Nair C; Banavali S; Puri A; Agarwal M
Med Sci Monit; 2006 Dec; 12(12):BR385-396. PubMed ID: 17136003
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Unilateral retinoblastoma, lack of familial history and older age does not exclude germline RB1 gene mutation.
Brichard B; Heusterspreute M; De Potter P; Chantrain C; Vermylen C; Sibille C; Gala JL
Eur J Cancer; 2006 Jan; 42(1):65-72. PubMed ID: 16343894
[TBL] [Abstract][Full Text] [Related]
7. 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; 25(3):166-73. PubMed ID: 11480772
[TBL] [Abstract][Full Text] [Related]
8. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling.
Parma D; Ferrer M; Luce L; Giliberto F; Szijan I
PLoS One; 2017; 12(12):e0189736. PubMed ID: 29261756
[TBL] [Abstract][Full Text] [Related]
9. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
[TBL] [Abstract][Full Text] [Related]
10. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
Hogg A; Onadim Z; Baird PN; Cowell JK
Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
[TBL] [Abstract][Full Text] [Related]
11. Independent constitutional germline mutations occurring in the RB1 gene in cousins with bilateral retinoblastoma.
Bia B; Cowell JK
Oncogene; 1995 Sep; 11(5):977-9. PubMed ID: 7675457
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of RB1 mutations identified in 403 retinoblastoma patients.
Price EA; Price K; Kolkiewicz K; Hack S; Reddy MA; Hungerford JL; Kingston JE; Onadim Z
J Med Genet; 2014 Mar; 51(3):208-14. PubMed ID: 24225018
[TBL] [Abstract][Full Text] [Related]
13. 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; 54(5):793-800. PubMed ID: 8178820
[TBL] [Abstract][Full Text] [Related]
14. Constitutional nonsense germline mutations in the RB1 gene detected in patients with early onset unilateral retinoblastoma.
Cowell JK; Cragg H
Eur J Cancer; 1996 Sep; 32A(10):1749-52. PubMed ID: 8983285
[TBL] [Abstract][Full Text] [Related]
15. Detection of mosaic RB1 mutations in families with retinoblastoma.
Rushlow D; Piovesan B; Zhang K; Prigoda-Lee NL; Marchong MN; Clark RD; Gallie BL
Hum Mutat; 2009 May; 30(5):842-51. PubMed ID: 19280657
[TBL] [Abstract][Full Text] [Related]
16. Spectrum of germline
Rojanaporn D; Boontawon T; Chareonsirisuthigul T; Thanapanpanich O; Attaseth T; Saengwimol D; Anurathapan U; Sujirakul T; Kaewkhaw R; Hongeng S
Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
[TBL] [Abstract][Full Text] [Related]
17. Two novel cases of trilateral retinoblastoma: genetics and review of the literature.
D'Elia G; Grotta S; Del Bufalo F; De Ioris MA; Surace C; Sirleto P; Romanzo A; Cozza R; Locatelli F; Angioni A
Cancer Genet; 2013 Nov; 206(11):398-401. PubMed ID: 24412019
[TBL] [Abstract][Full Text] [Related]
18. Ten novel RB1 gene mutations in patients with retinoblastoma.
Abouzeid H; Munier FL; Thonney F; Schorderet DF
Mol Vis; 2007 Sep; 13():1740-5. PubMed ID: 17960112
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Molecular study of retinoblastoma in the Algerian population. Screening of Rb gene in constitutional and tumoral level].
Boubekeur A; Louhibi L; Mahmoudi K; Boudjema A; Mehtar N
Bull Cancer; 2012 Feb; 99(2):127-35. PubMed ID: 22265791
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
