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 *

135 related articles for article (PubMed ID: 9285025)

  • 1. Molecular studies of loss of heterozygosity in retinoblastoma.
    Chiu LL; Lai PS; Low PS; Ling YL; Cheong PY; Chee CK; Wong PK; Lim AS
    Ann Acad Med Singap; 1997 May; 26(3):315-9. PubMed ID: 9285025
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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. Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm.
    Tran HV; Schorderet DF; Gaillard MC; Balmer A; Munier FL
    Ophthalmic Genet; 2012 Mar; 33(1):6-11. PubMed ID: 22103627
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Preferential germline mutation of the paternal allele in retinoblastoma.
    Zhu XP; Dunn JM; Phillips RA; Goddard AD; Paton KE; Becker A; Gallie BL
    Nature; 1989 Jul; 340(6231):312-3. PubMed ID: 2568588
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Molecular studies of loss of heterozygosity in Chinese sporadic retinoblastoma patients.
    Zhang XL; Fu WL; Zhao HX; Zhou LX; Huang JF; Wang JH
    Clin Chim Acta; 2005 Aug; 358(1-2):75-80. PubMed ID: 15921673
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A microsatellite fluorescent method for linkage analysis in familial retinoblastoma and deletion detection at the RB1 locus in retinoblastoma and osteosarcoma.
    Alonso J; García-Miguel P; Abelairas J; Mendiola M; Pestaña A
    Diagn Mol Pathol; 2001 Mar; 10(1):9-14. PubMed ID: 11277399
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. "Monoallelic germline methylation and sequence variant in the promoter of the RB1 gene: a possible constitutive epimutation in hereditary retinoblastoma".
    Quiñonez-Silva G; Dávalos-Salas M; Recillas-Targa F; Ostrosky-Wegman P; Aranda DA; Benítez-Bribiesca L
    Clin Epigenetics; 2016; 8():1. PubMed ID: 26753011
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Linkage analysis and detection of somatic, postzygous RB1 mutations in Serbian retinoblastoma patients.
    Kontic M; Palacios I; Kontic M; Alonso J; Pestana A
    J BUON; 2011; 16(1):142-6. PubMed ID: 21674866
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Age at diagnosis of isolated unilateral retinoblastoma does not distinguish patients with and without a constitutional RB1 gene mutation but is influenced by a parent-of-origin effect.
    Schüler A; Weber S; Neuhäuser M; Jurklies C; Lehnert T; Heimann H; Rudolph G; Jöckel KH; Bornfeld N; Lohmann DR
    Eur J Cancer; 2005 Mar; 41(5):735-40. PubMed ID: 15763650
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. [Early diagnosis of retinoblastoma: usefulness of searching for RB1 gene mutations].
    Nájera C; Sánchez F; Mateu E; Prieto F; Beneyto M
    Med Clin (Barc); 2001 Mar; 116(10):365-72. PubMed ID: 11333669
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PCR detection of Xbal polymorphism in the human Rb gene of retinoblastoma patients.
    Costanzi E; Erwenne CM; Armelin MC
    Braz J Med Biol Res; 1993 Oct; 26(10):1031-6. PubMed ID: 7906172
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Spectrum and frequencies of RB1 gene structural defects in retinoblastoma].
    Babenko OV; Saakian SV; Brovkina AF; Kozlova VM; Strel'nikov VV; Zaletaev DV; Nemtsova MV
    Mol Biol (Mosk); 2002; 36(4):623-9. PubMed ID: 12173465
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular karyotype of sporadic unilateral retinoblastoma tumors.
    Ganguly A; Nichols KE; Grant G; Rappaport E; Shields C
    Retina; 2009; 29(7):1002-12. PubMed ID: 19491728
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A Parent-of-Origin Effect Impacts the Phenotype in Low Penetrance Retinoblastoma Families Segregating the c.1981C>T/p.Arg661Trp Mutation of RB1.
    Eloy P; Dehainault C; Sefta M; Aerts I; Doz F; Cassoux N; Lumbroso le Rouic L; Stoppa-Lyonnet D; Radvanyi F; Millot GA; Gauthier-Villars M; Houdayer C
    PLoS Genet; 2016 Feb; 12(2):e1005888. PubMed ID: 26925970
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.