BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

310 related articles for article (PubMed ID: 11668642)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. [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]  

  • 13. 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]  

  • 14. 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]  

  • 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. 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]  

  • 17. 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; 41(5):735-40. PubMed ID: 15763650
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathogenic validation of unique germline intronic variants of RB1 in retinoblastoma patients using minigenes.
    Gámez-Pozo A; Palacios I; Kontic M; Menéndez I; Camino I; García-Miguel P; Abelairas J; Pestaña A; Alonso J
    Hum Mutat; 2007 Dec; 28(12):1245. PubMed ID: 18000883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Two independent RB1-inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient.
    Alonso J; Menéndez I; López A; Frayle H; Ruisánchez N; Pestaña A
    Genes Chromosomes Cancer; 2004 Jul; 40(3):271-5. PubMed ID: 15139006
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.