BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

373 related articles for article (PubMed ID: 9709755)

  • 1. 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]  

  • 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. [Gene diagnosis and genetic counselling of Rb gene mutations in retinoblastoma patients and their family members].
    Huang Q; Dryja TP; Yandell DW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):65-8. PubMed ID: 9531640
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Improved clinical management of retinoblastoma through gene testing.
    Raizis A; Clemett R; Corbett R; McGaughran J; Evans J; George P
    N Z Med J; 2002 May; 115(1154):231-4. PubMed ID: 12117173
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. Rapid identification of germline mutations in retinoblastoma by protein truncation testing.
    Tsai T; Fulton L; Smith BJ; Mueller RL; Gonzalez GA; Uusitalo MS; O'Brien JM
    Arch Ophthalmol; 2004 Feb; 122(2):239-48. PubMed ID: 14769601
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. [The structure, function and mutation of Rb gene promoter in normal individuals and retinoblastoma patients].
    Huang Q; Wang J; Tao Y
    Zhonghua Zhong Liu Za Zhi; 1998 May; 20(3):165-7. PubMed ID: 10920996
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. 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]  

  • 19. [Molecular diagnosis of retinoblastoma. First experience in Russia].
    Babenko OV; Brovkina AF; Zaletaev DV; Kozlova VM; Saakian SV; Nemtsova MV
    Vestn Oftalmol; 2002; 118(1):28-31. PubMed ID: 11898356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 19.