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Journal Abstract Search

159 related items for PubMed ID: 6959123

  • 1. Synthesis of beta-hexosaminidase in cell-free translation and in intact fibroblasts: an insoluble precursor alpha chain in a rare form of Tay-Sachs disease.
    Proia RL, Neufeld EF.
    Proc Natl Acad Sci U S A; 1982 Oct; 79(20):6360-4. PubMed ID: 6959123
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  • 2. cDNA clone for the alpha-chain of human beta-hexosaminidase: deficiency of alpha-chain mRNA in Ashkenazi Tay-Sachs fibroblasts.
    Myerowitz R, Proia RL.
    Proc Natl Acad Sci U S A; 1984 Sep; 81(17):5394-8. PubMed ID: 6236461
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  • 3. Hexosaminidase A deficient adults: presence of alpha chain precursor in cultured skin fibroblasts.
    Frisch A, Baram D, Navon R.
    Biochem Biophys Res Commun; 1984 Feb 29; 119(1):101-7. PubMed ID: 6231027
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  • 4. Normal transcription of the beta-hexosaminidase alpha-chain gene in the Ashkenazi Tay-Sachs mutation.
    Paw BH, Neufeld EF.
    J Biol Chem; 1988 Feb 25; 263(6):3012-5. PubMed ID: 2449434
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  • 7. The mutation mechanism causing juvenile-onset Tay-Sachs disease among Lebanese.
    Hechtman P, Boulay B, Bayleran J, Andermann E.
    Clin Genet; 1989 May 25; 35(5):364-75. PubMed ID: 2527097
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  • 9. Characterization of polypeptides serologically and structurally related to hexosaminidase in cultured fibroblasts.
    Tsui F, Mahuran DJ, Lowden JA, Mosmann T, Gravel RA.
    J Clin Invest; 1983 Apr 25; 71(4):965-73. PubMed ID: 6833496
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  • 10. Association of alpha- and beta-subunits during the biosynthesis of beta-hexosaminidase in cultured human fibroblasts.
    Proia RL, d'Azzo A, Neufeld EF.
    J Biol Chem; 1984 Mar 10; 259(5):3350-4. PubMed ID: 6230359
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  • 11. [Genetic study of GM2 gangliosidosis (Tay-Sachs and Sandhoff) by the study of the hexosaminidases of the Sandhoff-rodents hybrids (mouse and hamster)].
    Weil D, Van Cong N, Rebourcet R, Frézal J.
    Ann Genet; 1975 Sep 10; 18(3):163-8. PubMed ID: 810067
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  • 13. Segregation of Tay-Sachs and Sandhoff alleles in a non-Jewish family.
    Lane AB, Young E, Jenkins T.
    Am J Hum Genet; 1980 Nov 10; 32(6):920-6. PubMed ID: 7446530
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  • 14. Splice junction mutation in some Ashkenazi Jews with Tay-Sachs disease: evidence against a single defect within this ethnic group.
    Myerowitz R.
    Proc Natl Acad Sci U S A; 1988 Jun 10; 85(11):3955-9. PubMed ID: 3375249
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  • 15. Tay-Sachs disease and normal cerebellar cells in culture: elevated levels of lysosomal enzymes in Tay-Sachs disease cells.
    Hoffman LM, Brooks SE, Schneck L.
    J Neurosci Res; 1982 Jun 10; 8(1):49-55. PubMed ID: 6816949
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  • 17. [Tay-Sachs disease].
    Tanaka A.
    Nihon Rinsho; 1993 Sep 10; 51(9):2281-5. PubMed ID: 8411703
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  • 18. Cleavage of the (1 goes to 3)-2-acetamido-2-deoxy-beta-D-glucopyranosyl linkage present in keratan sulfate. The A and B isoenzymes of human liver hexosaminidase (EC 3.2.1.30).
    Toma S, Coppa G, Donnelly PV, Ricci R, Di Ferrante N, Srivastava SK.
    Carbohydr Res; 1981 Oct 16; 96(2):271-90. PubMed ID: 6458358
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  • 19. Genetic cause of a juvenile form of Tay-Sachs disease in a Lebanese child.
    Boustany RM, Tanaka A, Nishimoto J, Suzuki K.
    Ann Neurol; 1991 Jan 16; 29(1):104-7. PubMed ID: 1996872
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  • 20. Processing of human acid sphingomyelinase in normal and I-cell fibroblasts.
    Hurwitz R, Ferlinz K, Vielhaber G, Moczall H, Sandhoff K.
    J Biol Chem; 1994 Feb 18; 269(7):5440-5. PubMed ID: 8106525
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