BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

320 related articles for article (PubMed ID: 9311732)

  • 1. Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.
    Lohmann DR; Gerick M; Brandt B; Oelschläger U; Lorenz B; Passarge E; Horsthemke B
    Am J Hum Genet; 1997 Aug; 61(2):282-94. PubMed ID: 9311732
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Prognostic factors associated with loss of heterozygosity at the RB1 locus in retinoblastoma.
    Munier FL; Thonney F; Balmer A; Uffer S; Héon E; Van Melle G; Rutz HP; Pescia G; Schorderet DF
    Ophthalmic Genet; 1997 Mar; 18(1):7-12. PubMed ID: 9134545
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequency and parental origin of hypermethylated RB1 alleles in retinoblastoma.
    Greger V; Debus N; Lohmann D; Höpping W; Passarge E; Horsthemke B
    Hum Genet; 1994 Nov; 94(5):491-6. PubMed ID: 7959682
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Molecular diagnosis in patients with retinoblastoma: Report of a series of cases.
    Ossandón D; Zanolli M; López JP; Benavides F; Pérez V; Repetto GM
    Arch Soc Esp Oftalmol; 2016 Aug; 91(8):379-84. PubMed ID: 27021801
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Preliminary report of molecular detection of retinoblastoma gene mutations.
    Zeng R; Jiang X; Zhang Q; Hu B; Chen Y
    Yan Ke Xue Bao; 1994 Mar; 10(1):1-5. PubMed ID: 7843377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetics of retinoblastoma].
    Minoda K
    Nihon Rinsho; 1995 Nov; 53(11):2774-8. PubMed ID: 8538043
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum of RB1 gene mutations and loss of heterozygosity in Mexican patients with retinoblastoma: identification of six novel mutations.
    Macías M; Dean M; Atkinson A; Jiménez-Morales S; García-Vazquez FJ; Saldaña-Alvarez Y; Ramírez-Bello J; Chávez M; Orozco L
    Cancer Biomark; 2008; 4(2):93-9. PubMed ID: 18503160
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Next-Generation Sequencing of Retinoblastoma Identifies Pathogenic Alterations beyond RB1 Inactivation That Correlate with Aggressive Histopathologic Features.
    Afshar AR; Pekmezci M; Bloomer MM; Cadenas NJ; Stevers M; Banerjee A; Roy R; Olshen AB; Van Ziffle J; Onodera C; Devine WP; Grenert JP; Bastian BC; Solomon DA; Damato BE
    Ophthalmology; 2020 Jun; 127(6):804-813. PubMed ID: 32139107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Retinoblastoma in India : microsatellite analysis and its application in genetic counseling.
    Ramprasad VL; Madhavan J; Murugan S; Sujatha J; Suresh S; Sharma T; Kumaramanickavel G
    Mol Diagn Ther; 2007; 11(1):63-70. PubMed ID: 17286451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mechanisms of loss of heterozygosity in retinoblastoma.
    Zhu X; Dunn JM; Goddard AD; Squire JA; Becker A; Phillips RA; Gallie BL
    Cytogenet Cell Genet; 1992; 59(4):248-52. PubMed ID: 1544317
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.