190 related articles for article (PubMed ID: 12955724)
1. Mutational screening of the RB1 gene in Indian patients with retinoblastoma reveals eight novel and several recurrent mutations.
Kiran VS; Kannabiran C; Chakravarthi K; Vemuganti GK; Honavar SG
Hum Mutat; 2003 Oct; 22(4):339. PubMed ID: 12955724
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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; 167(1):43-6. PubMed ID: 16682285
[TBL] [Abstract][Full Text] [Related]
4. Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma.
Jakubowska A; Zajaczek S; Haus O; Limon J; Kostyk E; Krzystolik Z; Lubinski J
Hum Mutat; 2001 Nov; 18(5):459. PubMed ID: 11668642
[TBL] [Abstract][Full Text] [Related]
5. Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.
Nichols KE; Houseknecht MD; Godmilow L; Bunin G; Shields C; Meadows A; Ganguly A
Hum Mutat; 2005 Jun; 25(6):566-74. PubMed ID: 15884040
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. Identification of 26 new constitutional RB1 gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients.
Alonso J; Frayle H; Menéndez I; López A; García-Miguel P; Abelairas J; Sarret E; Vendrell MT; Navajas A; Artigas M; Indiano JM; Carbone A; Torrenteras C; Palacios I; Pestaña A
Hum Mutat; 2005 Jan; 25(1):99. PubMed ID: 15605413
[TBL] [Abstract][Full Text] [Related]
9. Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expression.
Albrecht P; Ansperger-Rescher B; Schüler A; Zeschnigk M; Gallie B; Lohmann DR
Hum Mutat; 2005 Nov; 26(5):437-45. PubMed ID: 16127685
[TBL] [Abstract][Full Text] [Related]
10. Twelve novel RB1 gene mutations in patients with hereditary retinoblastoma. Mutations in brief no. 206. Online.
Yilmaz S; Horsthemke B; Lohmann DR
Hum Mutat; 1998; 12(6):434. PubMed ID: 10671068
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Identification of four novel RB1 germline mutations in Korean retinoblastoma patients.
Yu YS; Kim IJ; Ku JL; Park JG
Hum Mutat; 2001 Sep; 18(3):252. PubMed ID: 11524739
[TBL] [Abstract][Full Text] [Related]
15. Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications.
Alonso J; García-Miguel P; Abelairas J; Mendiola M; Sarret E; Vendrell MT; Navajas A; Pestaña A
Hum Mutat; 2001 May; 17(5):412-22. PubMed ID: 11317357
[TBL] [Abstract][Full Text] [Related]
16. Mutational analysis of the RB1 gene in Indian patients with retinoblastoma.
Ata-ur-Rasheed M; Vemuganti Gk; Honavar Sg; Ahmed N; Hasnain Se; Kannabiran C
Ophthalmic Genet; 2002 Jun; 23(2):121-8. PubMed ID: 12187430
[TBL] [Abstract][Full Text] [Related]
17. RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations.
Ahani A; Behnam B; Khorshid HR; Akbari MT
Cancer Genet; 2011 Jun; 204(6):316-22. PubMed ID: 21763628
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation.
Dehainault C; Michaux D; Pagès-Berhouet S; Caux-Moncoutier V; Doz F; Desjardins L; Couturier J; Parent P; Stoppa-Lyonnet D; Gauthier-Villars M; Houdayer C
Eur J Hum Genet; 2007 Apr; 15(4):473-7. PubMed ID: 17299438
[TBL] [Abstract][Full Text] [Related]
20. [Spectrum and frequencies of RB1 gene structural defects in retinoblastoma].
Babenko OV; Saakian SV; Brovkina AF; Kozlova VM; Strel'nikov VV; Zaletaev DV; Nemtsova MV
Mol Biol (Mosk); 2002; 36(4):623-9. PubMed ID: 12173465
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]