BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 23500596)

  • 1. The 50th anniversary of gene therapy: beginnings and present realities.
    Szybalski W
    Gene; 2013 Aug; 525(2):151-4. PubMed ID: 23500596
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hypoxanthine guanine phosphoribosyl transferase deficiency; Lesch-Nyhan syndrome].
    Ogasawara N
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):601-5. PubMed ID: 3270871
    [No Abstract]   [Full Text] [Related]  

  • 3. Gene therapy for inherited neurological disorders: towards therapeutic intervention in the Lesch-Nyhan syndrome.
    Lowenstein PR; Southgate TD; Smith-Arica JR; Smith J; Castro MG
    Prog Brain Res; 1998; 117():485-501. PubMed ID: 9932427
    [No Abstract]   [Full Text] [Related]  

  • 4. Animal models point the way to human clinical trials.
    Kolberg R
    Science; 1992 May; 256(5058):772-3. PubMed ID: 1589756
    [No Abstract]   [Full Text] [Related]  

  • 5. History of gene therapy.
    Wirth T; Parker N; Ylä-Herttuala S
    Gene; 2013 Aug; 525(2):162-9. PubMed ID: 23618815
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetics of hypoxanthine-guanine phosphoribosyltransferase deficiency in man.
    Wilson JM; Kelley WN
    Arch Intern Med; 1985 Oct; 145(10):1895-1900. PubMed ID: 3899038
    [No Abstract]   [Full Text] [Related]  

  • 7. Lesch-Nyhan syndrome: mutation, prevention, and therapy.
    Caskey CT
    Res Publ Assoc Res Nerv Ment Dis; 1987; 65():187-94. PubMed ID: 3330841
    [No Abstract]   [Full Text] [Related]  

  • 8. Linkage between HPRTB STR alleles and Lesch-Nyhan syndrome inside a family: Implications in forensic casework.
    Gil A; Castillo A; Rodríguez F; Amorim A; Gusmão L
    Forensic Sci Int Genet; 2013 Jan; 7(1):e5-6. PubMed ID: 23063963
    [No Abstract]   [Full Text] [Related]  

  • 9. Molecular characterization of a deletion in the HPRT1 gene in a patient with Lesch-Nyhan syndrome.
    Taniguchi A; Yamada Y; Hakoda M; Sekita C; Kawamoto M; Kaneko H; Yamanaka H
    Nucleosides Nucleotides Nucleic Acids; 2011 Dec; 30(12):1266-71. PubMed ID: 22132985
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetics of HPRT deficiency.
    Caskey CT; Stout JT
    Semin Nephrol; 1989 Jun; 9(2):162-7. PubMed ID: 2672223
    [No Abstract]   [Full Text] [Related]  

  • 11. HPRT gene organization and expression.
    Melton DW
    Oxf Surv Eukaryot Genes; 1987; 4():34-76. PubMed ID: 3334328
    [No Abstract]   [Full Text] [Related]  

  • 12. Lesch-Nyhan disease.
    Nyhan WL
    Nucleosides Nucleotides Nucleic Acids; 2008 Jun; 27(6):559-63. PubMed ID: 18600504
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Use of the HPRT gene and the HAT selection technique in DNA-mediated transformation of mammalian cells: first steps toward developing hybridoma techniques and gene therapy.
    Szybalski W
    Bioessays; 1992 Jul; 14(7):495-500. PubMed ID: 1445289
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lesch-Nyhan syndrome. Engineering mutant mice.
    Hogan B
    Nature; 1987 Mar 19-25; 326(6110):240-1. PubMed ID: 3469525
    [No Abstract]   [Full Text] [Related]  

  • 15. 50 years of gene therapy--a contribution of Wacław Szybalski to science and humanity.
    Dulak J; Uchto J; Jozkowicz A
    Gene; 2013 Aug; 525(2):149-50. PubMed ID: 23500591
    [No Abstract]   [Full Text] [Related]  

  • 16. [Complete and partial deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT)].
    Yamada Y
    Nihon Rinsho; 2003 Jan; 61 Suppl 1():288-93. PubMed ID: 12629733
    [No Abstract]   [Full Text] [Related]  

  • 17. A novel de novo mutation in HPRT gene responsible for Lesch-Nyhan syndrome (HPRT OSAKA).
    Yamada Y; Goto H; Shiomi M; Yamamoto T; Higashino K; Ogasawara N
    Jpn J Hum Genet; 1996 Dec; 41(4):427-30. PubMed ID: 9088115
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fluorescent approaches to diagnosis of Lesch-Nyhan syndrome and quantitative analysis of carrier status.
    Mansfield ES; Blasband A; Kronick MN; Wrabetz L; Kaplan P; Rappaport E; Sartore M; Parrella T; Surrey S; Fortina P
    Mol Cell Probes; 1993 Aug; 7(4):311-24. PubMed ID: 8232348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Automated DNA sequencing methods for detection and analysis of mutations: applications to the Lesch-Nyhan syndrome.
    Edwards A; Gibbs RA; Nguyen PN; Ansorge W; Caskey CT
    Trans Assoc Am Physicians; 1989; 102():185-94. PubMed ID: 2638525
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification of novel mutations in the human HPRT gene.
    Nguyen KV; Nyhan WL
    Nucleosides Nucleotides Nucleic Acids; 2013; 32(3):155-60. PubMed ID: 23473102
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.