BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

326 related articles for article (PubMed ID: 22265791)

  • 1. [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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Genetic screening in Iranian patients with retinoblastoma.
    Shahraki K; Ahani A; Sharma P; Faranoush M; Bahoush G; Torktaz I; Gahl WA; Naseripour M; Behnam B
    Eye (Lond); 2017 Apr; 31(4):620-627. PubMed ID: 27983729
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Comprehensive screening for constitutional RB1 mutations by DHPLC and QMPSF.
    Houdayer C; Gauthier-Villars M; Laugé A; Pagès-Berhouet S; Dehainault C; Caux-Moncoutier V; Karczynski P; Tosi M; Doz F; Desjardins L; Couturier J; Stoppa-Lyonnet D
    Hum Mutat; 2004 Feb; 23(2):193-202. PubMed ID: 14722923
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutational analysis of the RB1 gene in Moroccan patients with retinoblastoma.
    Abidi O; Knari S; Sefri H; Charif M; Senechal A; Hamel C; Rouba H; Zaghloul K; El Kettani A; Lenaers G; Barakat A
    Mol Vis; 2011; 17():3541-7. PubMed ID: 22219649
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational screening of germline
    Nguyen HH; Nguyen HTT; Vu NP; Le QT; Pham CM; Huyen TT; Manh H; Pham HLB; Nguyen TD; Le HTT; Van Nong H
    Mol Vis; 2018; 24():231-238. PubMed ID: 29568217
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14.
    Fang X; Chen J; Wang Y; Zhao M; Zhang X; Yang L; Ni X; Zhao J; Gallie BL
    Ophthalmic Genet; 2021 Oct; 42(5):593-599. PubMed ID: 34190019
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Alterations in the RB1 gene in Pakistani patients with retinoblastoma using direct sequencing analysis.
    Kalsoom S; Wasim M; Afzal S; Shahzad MS; Ramzan S; Awan AR; Anjum AA; Ramzan K
    Mol Vis; 2015; 21():1085-92. PubMed ID: 26396485
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Uncommon RB1 somatic mutations in a unilateral retinoblastoma patient.
    Ottaviani D; Alonso C; Szijan I
    Medicina (B Aires); 2015; 75(3):137-41. PubMed ID: 26117602
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Screening for RB1 mutations in tumor tissue using denaturing high performance liquid chromatography, multiplex ligation-dependent probe amplification, and loss of heterozygosity analysis.
    Sellner LN; Edkins E; Smith N
    Pediatr Dev Pathol; 2006; 9(1):31-7. PubMed ID: 16808635
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
    Chai P; Luo Y; Yu J; Li Y; Yang J; Zhuang A; Fan J; Han M; Jia R
    Exp Eye Res; 2021 Apr; 205():108456. PubMed ID: 33493472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.