BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 31835688)

  • 1. Next-Generation Technologies and Strategies for the Management of Retinoblastoma.
    Gudiseva HV; Berry JL; Polski A; Tummina SJ; O'Brien JM
    Genes (Basel); 2019 Dec; 10(12):. PubMed ID: 31835688
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enhanced sensitivity for detection of low-level germline mosaic RB1 mutations in sporadic retinoblastoma cases using deep semiconductor sequencing.
    Chen Z; Moran K; Richards-Yutz J; Toorens E; Gerhart D; Ganguly T; Shields CL; Ganguly A
    Hum Mutat; 2014 Mar; 35(3):384-91. PubMed ID: 24282159
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. Spectrum of germ-line RB1 gene mutations in Malaysian patients with retinoblastoma.
    Mohd Khalid MK; Yakob Y; Md Yasin R; Wee Teik K; Siew CG; Rahmat J; Ramasamy S; Alagaratnam J
    Mol Vis; 2015; 21():1185-90. PubMed ID: 26539030
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Simultaneous identification of clinically relevant
    Xu L; Shen L; Polski A; Prabakar RK; Shah R; Jubran R; Kim JW; Biegel J; Kuhn P; Cobrinik D; Hicks J; Gai X; Berry JL
    Ophthalmic Genet; 2020 Dec; 41(6):526-532. PubMed ID: 32799607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microarray analysis and biochemical correlations of oxidative stress responsive genes in retinoblastoma.
    Vandhana S; Lakshmi TS; Indra D; Deepa PR; Krishnakumar S
    Curr Eye Res; 2012 Sep; 37(9):830-41. PubMed ID: 22668346
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Next-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.
    Singh J; Mishra A; Pandian AJ; Mallipatna AC; Khetan V; Sripriya S; Kapoor S; Agarwal S; Sankaran S; Katragadda S; Veeramachaneni V; Hariharan R; Subramanian K; Mannan AU
    Mol Vis; 2016; 22():1036-47. PubMed ID: 27582626
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Clinical findings and molecular diagnosis of retinoblastoma in older children.
    Sheck LH; Ng YS; Watson M; Vincent AL
    Ophthalmic Genet; 2013 Dec; 34(4):238-42. PubMed ID: 23289805
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Screening of RB1 alterations in Brazilian patients with retinoblastoma and relatives with retinoma: phenotypic and genotypic associations.
    Barbosa RH; Aguiar FC; Silva MF; Costa RA; Vargas FR; Lucena E; Carvalho de Souza M; de Almeida LM; Bittar C; Ashton Prolla P; Bonvicino CR; Seuánez HN
    Invest Ophthalmol Vis Sci; 2013 May; 54(5):3184-94. PubMed ID: 23532519
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.