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Journal Abstract Search

88 related items for PubMed ID: 2438102

  • 1. Efficient in vitro and in vivo expression of human glucocerebrosidase cDNA.
    Reiner O, Wilder S, Givol D, Horowitz M.
    DNA; 1987 Apr; 6(2):101-8. PubMed ID: 2438102
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  • 2. Structural analysis of the human glucocerebrosidase genes.
    Reiner O, Wigderson M, Horowitz M.
    DNA; 1988 Mar; 7(2):107-16. PubMed ID: 3359914
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  • 3. Retrovirus-mediated transfer of the human glucocerebrosidase gene to Gaucher fibroblasts.
    Choudary PV, Barranger JA, Tsuji S, Mayor J, LaMarca ME, Cepko CL, Mulligan RC, Ginns EI.
    Mol Biol Med; 1986 Jun; 3(3):293-9. PubMed ID: 3736391
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  • 7. Gaucher disease: functional expression of the normal glucocerebrosidase and Gaucher T1366G and G1604A alleles in Baculovirus-transfected Spodoptera frugiperda cells.
    Choy FY, Wei C, Levin D.
    Am J Med Genet; 1996 Oct 28; 65(3):184-9. PubMed ID: 9240741
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  • 8. Isozymes of beta-glucosidase: determination of Gaucher's disease phenotypes.
    Ginns EI, Erickson A, Tegelaers FP, Barneveld R, Reuser AJ, Brady RO, Tager JM, Barranger JA.
    Isozymes Curr Top Biol Med Res; 1983 Oct 28; 11():83-93. PubMed ID: 6417048
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  • 9. A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorder.
    Zimran A, Sorge J, Gross E, Kubitz M, West C, Beutler E.
    J Clin Invest; 1990 Jan 28; 85(1):219-22. PubMed ID: 2295698
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  • 11. Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidase.
    Dahl N, Erikson A, Hammarström-Heeroma K, Pettersson U.
    Genomics; 1988 Nov 28; 3(4):296-8. PubMed ID: 2468600
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  • 13. Complete correction of the enzymatic defect of type I Gaucher disease fibroblasts by retroviral-mediated gene transfer.
    Sorge J, Kuhl W, West C, Beutler E.
    Proc Natl Acad Sci U S A; 1987 Feb 28; 84(4):906-9. PubMed ID: 3547401
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  • 14. Isolation of cDNA clones for human beta-glucocerebrosidase using the lambda gt11 expression system.
    Ginns EI, Choudary PV, Martin BM, Winfield S, Stubblefield B, Mayor J, Merkle-Lehman D, Murray GJ, Bowers LA, Barranger JA.
    Biochem Biophys Res Commun; 1984 Sep 17; 123(2):574-80. PubMed ID: 6091633
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  • 16. Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.
    Ginns EI, Brady RO, Pirruccello S, Moore C, Sorrell S, Furbish FS, Murray GJ, Tager J, Barranger JA.
    Proc Natl Acad Sci U S A; 1982 Sep 17; 79(18):5607-10. PubMed ID: 6957882
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  • 18. Gene mapping and leader polypeptide sequence of human glucocerebrosidase: implications for Gaucher disease.
    Ginns EI, Choudary PV, Tsuji S, Martin B, Stubblefield B, Sawyer J, Hozier J, Barranger JA.
    Proc Natl Acad Sci U S A; 1985 Oct 17; 82(20):7101-5. PubMed ID: 3863141
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  • 19. Novel frameshift mutation (Pro171fsX21) in neonatal type 2 Gaucher's disease.
    Park HW, Lee Y, Kim GH, Lee BS, Kim KS, Yoo HW, Kim EA.
    Gene; 2012 Oct 10; 507(2):170-3. PubMed ID: 22772462
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