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Journal Abstract Search

180 related items for PubMed ID: 848490

  • 21. Protein catabolism in fibroblasts cultured from patients with mucolipidosis II and other lysosomal disorders.
    Kopitz J, Arnold A, Meissner T, Cantz M.
    Biochem J; 1993 Oct 15; 295 ( Pt 2)(Pt 2):577-80. PubMed ID: 8240260
    [Abstract] [Full Text] [Related]

  • 22. Multiple molecular forms of lysosomal enzymes in mucolipidosis II.
    Farrell DF, MacMartin MP.
    Hum Genet; 1981 Oct 15; 58(3):317-21. PubMed ID: 7327554
    [No Abstract] [Full Text] [Related]

  • 23. Mucolipidosis III is genetically heterogeneous.
    Honey NK, Mueller OT, Little LE, Miller AL, Shows TB.
    Proc Natl Acad Sci U S A; 1982 Dec 15; 79(23):7420-4. PubMed ID: 6961420
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  • 24. Light and heavy lysosomes: characterization of N-acetyl-beta-D-hexosaminidase isolated from normal and I-cell disease lymphoblasts.
    Miller AL, Norton V, Robertson R, Jenks M, Yeh RY, Wright D.
    Glycobiology; 1993 Aug 15; 3(4):313-8. PubMed ID: 8400547
    [Abstract] [Full Text] [Related]

  • 25. Phosphorylation of lysosomal enzymes in fibroblasts. Marked deficiency of N-acetylglucosamine-1-phosphotransferase in fibroblasts of patients with mucolipidosis III.
    Waheed A, Hasilik A, Cantz M, von Figura K.
    Hoppe Seylers Z Physiol Chem; 1982 Feb 15; 363(2):169-78. PubMed ID: 6460679
    [Abstract] [Full Text] [Related]

  • 26. Metabolism of lysosomal enzymes in the protein-deficient weanling rat.
    Glew RH, Diven WF, Zidian JL, Rankin BB, Czuczman M, Axelrod AE.
    Am J Clin Nutr; 1982 Feb 15; 35(2):236-49. PubMed ID: 7064885
    [Abstract] [Full Text] [Related]

  • 27. Comparison of the alpha-mannosidases in fibroblast cultures from patients with mannosidosis and mucolipidosis II and from controls.
    Halley DJ, Winchester BG, Burditt LJ, d'Azzo A, Robinson D, Galjaard H.
    Biochem J; 1980 May 01; 187(2):541-3. PubMed ID: 7396862
    [Abstract] [Full Text] [Related]

  • 28. Lysosomal enzyme activities during ageing of adult human liver cell lines.
    Le Gall JY, Khoi TD, Glaise D, Le treut A, Brissot P, Guillouzo A.
    Mech Ageing Dev; 1979 Nov 01; 11(4):287-93. PubMed ID: 522513
    [Abstract] [Full Text] [Related]

  • 29. Demonstration of the heterozygous state for I-cell disease and pseudo-Hurler polydystrophy by assay of N-acetylglucosaminylphosphotransferase in white blood cells and fibroblasts.
    Varki A, Reitman ML, Vannier A, Kornfeld S, Grubb JH, Sly WS.
    Am J Hum Genet; 1982 Sep 01; 34(5):717-29. PubMed ID: 6289658
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  • 35. Demonstration of altered acidic hydrolases in fibroblasts from patients with mucolipidosis II by lectin titration.
    Rousson R, Ben-Yoseph Y, Fiddler MB, Nadler HL.
    Biochem J; 1979 Jun 15; 180(3):501-5. PubMed ID: 486128
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  • 36. Immunocytochemical localization of lysosomal acid phosphatase in normal and "I-cell" fibroblasts.
    Parenti G, Willemsen R, Hoogeveen AT, Verleun-Mooyman M, Van Dongen JM, Galjaard H.
    Eur J Cell Biol; 1987 Feb 15; 43(1):121-7. PubMed ID: 3552677
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  • 37. Oligosaccharides in lysosomal enzymes. Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase.
    Hasilik A, Von Figura K.
    Eur J Biochem; 1981 Dec 15; 121(1):125-9. PubMed ID: 6459926
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  • 39. I-cell disease: intracellular desialylation of lysosomal enzymes using an influenza virus vector.
    Spritz RA, Coates PM, Lief FS.
    Biochim Biophys Acta; 1979 Jan 04; 582(1):164-71. PubMed ID: 760815
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  • 40. Lysosomal enzyme activities in cultured lymphoid cell lines.
    Matsuda I, Yamamoto J, Nagata N, Ninomiya N, Akaboshi I.
    Clin Chim Acta; 1977 Nov 01; 80(3):483-6. PubMed ID: 410567
    [Abstract] [Full Text] [Related]

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