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Journal Abstract Search

116 related items for PubMed ID: 7085649

  • 1. Normalization of intracellular lysosomal hydrolases in I-cell disease fibroblasts with sucrose loading.
    Kato T, Okada S, Ohshima T, Inui K, Yutaka T, Yabuuchi H.
    J Biol Chem; 1982 Jul 10; 257(13):7814-9. PubMed ID: 7085649
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  • 2. The effects of sucrose loading on lysosomal hydrolases.
    Kato T, Okada S, Yutaka T, Yabuuchi H.
    Mol Cell Biochem; 1984 Jul 10; 60(1):83-98. PubMed ID: 6708943
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  • 3. Multiple transfer of lysosomal enzymes from normal lymphocytes to I-cell disease fibroblasts.
    Olsen I, Hand C, Muir H.
    Cell Biol Int Rep; 1987 Feb 10; 11(2):131-40. PubMed ID: 3829132
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  • 4. Heterogeneity in mucolipidosis II (I-cell disease).
    Okada S, Kato T, Oshima T, Yutaka T, Yabuuchi H.
    Clin Genet; 1983 Feb 10; 23(2):155-9. PubMed ID: 6839528
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  • 5. Biochemical studies on lymphoblastoid cells with inherited N-acetyl-glucosamine 1-phosphotransferase deficiency (I-cell disease).
    Okada S, Handa M, Hashimoto T, Nishimoto J, Inui K, Furukawa M, Furuyama J, Yabuuchi H, Tate M, Gasa S.
    Biochem Int; 1988 Aug 10; 17(2):375-83. PubMed ID: 2847740
    [Abstract] [Full Text] [Related]

  • 6. Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases.
    Hultberg B, Sjöblad S.
    Clin Chim Acta; 1977 Oct 01; 80(1):79-86. PubMed ID: 409577
    [Abstract] [Full Text] [Related]

  • 7. Cystic fibrosis: leakage of lysosomal enzymes and of alkaline phosphatase into the extracellular space.
    Hösli P, Vogt E.
    Biochem Biophys Res Commun; 1977 Dec 07; 79(3):741-8. PubMed ID: 597304
    [No Abstract] [Full Text] [Related]

  • 8. Genetic heterogeneity of I-cell disease is demonstrated by complementation of lysosomal enzyme processing mutants.
    Shows TB, Mueller OT, Honey NK, Wright CE, Miller AL.
    Am J Med Genet; 1982 Jul 07; 12(3):343-53. PubMed ID: 6287841
    [Abstract] [Full Text] [Related]

  • 9. Biochemical heterogeneity in I-cell disease. Sucrose-loading test classifies two distinct subtypes.
    Okada S, Inui K, Furukawa M, Midorikawa M, Nishimoto J, Yabuuchi H, Kato T, Watanabe M, Gasa S, Makita A.
    Enzyme; 1987 Jul 07; 38(1-4):267-72. PubMed ID: 2831041
    [Abstract] [Full Text] [Related]

  • 10. 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 07; 3(4):313-8. PubMed ID: 8400547
    [Abstract] [Full Text] [Related]

  • 11. The role of lysosomal enzymes in killing of mammalian cells by the lysosomotropic detergent N-dodecylimidazole.
    Wilson PD, Firestone RA, Lenard J.
    J Cell Biol; 1987 May 07; 104(5):1223-9. PubMed ID: 3571330
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  • 13. I--cell disease: nine lysosomal enzyme levels in lymphocytes and granulocytes.
    Tanaka T, Kobayashi M, Fukuda T, Tsuzi Y, Usui T.
    Hiroshima J Med Sci; 1979 Dec 07; 28(4):189-93. PubMed ID: 536230
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  • 19. Effect of bacterial endotoxin on lysosomal enzyme activities of normal and mucolipidosis III fibroblasts.
    Di Natale P, Stabile M, Ronsisvalle L, Utili R.
    Biomedicine; 1981 May 07; 35(2):46-9. PubMed ID: 7260237
    [Abstract] [Full Text] [Related]

  • 20. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.
    den Tandt WR, Schaberg A.
    Pathol Eur; 1973 May 07; 8(1):3-11. PubMed ID: 4269628
    [No Abstract] [Full Text] [Related]

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