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Journal Abstract Search

159 related items for PubMed ID: 6959123

  • 21. Restoration of hexosaminidase A activity in human Tay-Sachs fibroblasts via adenoviral vector-mediated gene transfer.
    Akli S, Guidotti JE, Vigne E, Perricaudet M, Sandhoff K, Kahn A, Poenaru L.
    Gene Ther; 1996 Sep; 3(9):769-74. PubMed ID: 8875224
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  • 22. Different mutations in Ashkenazi Jewish and non-Jewish French Canadians with Tay-Sachs disease.
    Myerowitz R, Hogikyan ND.
    Science; 1986 Jun 27; 232(4758):1646-8. PubMed ID: 3754980
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  • 23. Identification of an active acidic residue in the catalytic site of beta-hexosaminidase.
    Tse R, Vavougios G, Hou Y, Mahuran DJ.
    Biochemistry; 1996 Jun 11; 35(23):7599-607. PubMed ID: 8652542
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  • 24. Cultured skin fibroblasts in lipidoses. Enzymatic, histochemical, and ultrastructural relationship in Fabry's Tay-Sachs, and Sandhoff's diseases.
    Yuasa T, Fukuma M, Takashima S, Takaki R.
    Arch Pathol Lab Med; 1980 Jun 11; 104(6):321-7. PubMed ID: 6246846
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  • 27. Proteolytic processing of the beta-subunit of the lysosomal enzyme, beta-hexosaminidase, in normal human fibroblasts.
    Quon DV, Proia RL, Fowler AV, Bleibaum J, Neufeld EF.
    J Biol Chem; 1989 Feb 25; 264(6):3380-4. PubMed ID: 2521634
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  • 38. The expression of hex A and hex B isozymes of hexosaminidase in parental and experimental human fibroblast cells and their components.
    Bladon MT.
    Biochem Genet; 1981 Oct 25; 19(9-10):971-86. PubMed ID: 7332532
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  • 39. Hexosaminidase A deficiency in adults.
    Navon R, Argov Z, Frisch A.
    Am J Med Genet; 1986 May 25; 24(1):179-96. PubMed ID: 2939718
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