These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 8651278)

  • 1. The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.
    Lohmann DR; Brandt B; Höpping W; Passarge E; Horsthemke B
    Am J Hum Genet; 1996 May; 58(5):940-9. PubMed ID: 8651278
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma.
    Blanquet V; Turleau C; Gross-Morand MS; Sénamaud-Beaufort C; Doz F; Besmond C
    Hum Mol Genet; 1995 Mar; 4(3):383-8. PubMed ID: 7795591
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing.
    Zou Y; Li J; Hua P; Liang T; Ji X; Zhao P
    Mol Vis; 2021; 27():1-16. PubMed ID: 33456302
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastoma.
    Szijan I; Lohmann DR; Parma DL; Brandt B; Horsthemke B
    J Med Genet; 1995 Jun; 32(6):475-9. PubMed ID: 7666401
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Spectrum of RB1 mutations in argentine patients: 20-years experience in the molecular diagnosis of retinoblastoma.
    Ottaviani D; Parma D; Giliberto F; Ferrer M; Fandino A; Davila MT; Chantada G; Szijan I
    Ophthalmic Genet; 2013 Dec; 34(4):189-98. PubMed ID: 23301675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of small length germline mutations in the RB1 gene.
    Lohmann DR; Brandt B; Höpping W; Passarge E; Horsthemke B
    Hum Mol Genet; 1994 Dec; 3(12):2187-93. PubMed ID: 7881418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Frequent constitutional C to T mutations in CGA-arginine codons in the RB1 gene produce premature stop codons in patients with bilateral (hereditary) retinoblastoma.
    Cowell JK; Smith T; Bia B
    Eur J Hum Genet; 1994; 2(4):281-90. PubMed ID: 7704558
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RB1 gene mutations in retinoblastoma.
    Lohmann DR
    Hum Mutat; 1999; 14(4):283-8. PubMed ID: 10502774
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mechanisms of oncogenesis in patients with familial retinoblastoma.
    Onadim Z; Hogg A; Cowell JK
    Br J Cancer; 1993 Nov; 68(5):958-64. PubMed ID: 8217609
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Impact of RB1 gene mutation type in retinoblastoma patients on clinical presentation and management outcome.
    Mehyar M; Mosallam M; Tbakhi A; Saab A; Sultan I; Deebajah R; Jaradat I; AlJabari R; Mohammad M; AlNawaiseh I; Al-Hussaini M; Yousef YA
    Hematol Oncol Stem Cell Ther; 2020 Sep; 13(3):152-159. PubMed ID: 32222358
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of germline mutations in the RB1 gene by denaturant gradient gel electrophoresis and polymerase chain reaction direct sequencing.
    Blanquet V; Turleau C; Gross MS; Goossens M; Besmond C
    Hum Mol Genet; 1993 Jul; 2(7):975-9. PubMed ID: 8364580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exon-by-exon screening for RB germline mutations using Heteroduplex-SSCP analysis.
    Zhang Q; Minoda K; Zeng R; Wu Z; Xiao X; Li S; Zhang F
    Yan Ke Xue Bao; 1997 Mar; 13(1):5-11. PubMed ID: 11189328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.