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Journal Abstract Search

169 related items for PubMed ID: 3530334

  • 1. Genetic relationship between lysosomal and lamellar body-specific alpha-glucosidases in human lung.
    de Vries AC, Schram AW, Tager JM, Batenburg JJ, van Golde LM.
    Biochim Biophys Acta; 1986 Sep 12; 878(2):288-91. PubMed ID: 3530334
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  • 2. A specific acid alpha-glucosidase in lamellar bodies of the human lung.
    de Vries AC, Schram AW, Tager JM, Batenburg JJ, van Golde LM.
    Biochim Biophys Acta; 1985 Dec 04; 837(3):230-8. PubMed ID: 3933564
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  • 3. An improved procedure for the isolation of lamellar bodies from human lung. Lamellar bodies free of lysosomes contain a spectrum of lysosomal-type hydrolases.
    de Vries AC, Schram AW, van den Berg M, Tager JM, Batenburg JJ, van Golde LM.
    Biochim Biophys Acta; 1987 Dec 14; 922(3):259-69. PubMed ID: 3689811
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  • 4. The molecular heterogeneity of purified human liver lysosomal alpha-glucosidase (acid alpha-glucosidase).
    Murray AK, Brown BI, Brown DH.
    Arch Biochem Biophys; 1978 Jan 30; 185(2):511-24. PubMed ID: 24417
    [No Abstract] [Full Text] [Related]

  • 5. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle.
    Van der Ploeg AT, Loonen MC, Bolhuis PA, Busch HM, Reuser AJ, Galjaard H.
    Pediatr Res; 1988 Jul 30; 24(1):90-4. PubMed ID: 2970619
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  • 7. Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type II.
    Pfister K, Gitzelmann R, Steinmann B.
    Clin Chim Acta; 1983 Nov 15; 134(3):307-15. PubMed ID: 6357553
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  • 8. Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease.
    Schram AW, Brouwer-Kelder B, Donker-Koopman WE, Loonen C, Hamers MN, Tager JM.
    Biochim Biophys Acta; 1979 Apr 12; 567(2):370-83. PubMed ID: 36157
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  • 9. Immunochemical studies of human acid alpha-1,4-glucosidase in type II glycogenosis.
    Bienvenu J, Mathieu M.
    Enzyme; 1981 Apr 12; 26(4):182-90. PubMed ID: 7018896
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  • 10. Immunohistochemical demonstration of acid alpha-glucosidase in muscle in Pompe's disease.
    Ninomiya N, Matsuda I, Fukuda S, Iwamasa T, Osame M.
    Histochem J; 1983 Jun 12; 15(6):601-4. PubMed ID: 6347982
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  • 13. Adult forms of glycogenosis type II. A defect in an early stage of acid alpha-glucosidase realization.
    Reuser AJ, Kroos M.
    FEBS Lett; 1982 Sep 20; 146(2):361-4. PubMed ID: 6754447
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  • 14. [Immunochemical study of acid alpha-1,4-glucosidase in 7 patients with type II glycogenosis].
    Bienvenu J, Mathieu M, Collombel C, Baltassat P, Divry P, Dorche C, Cotte J.
    Pediatrie; 1979 Sep 20; 34(6):659-76. PubMed ID: 388338
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  • 16. Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.
    Beratis NG, LaBadie GU, Hirschhorn K.
    J Clin Invest; 1978 Dec 20; 62(6):1264-74. PubMed ID: 34626
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  • 17. Cell-free translation of human lysosomal alpha-glucosidase: evidence for reduced precursor synthesis in an adult patient with glycogenosis type II.
    van der Horst GT, Hoefsloot EH, Kroos MA, Reuser AJ.
    Biochim Biophys Acta; 1987 Nov 20; 910(2):123-9. PubMed ID: 3315002
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  • 18. An investigation of the possible influence of neutral alpha-glucosidases on the clinical heterogeneity of glycogenosis type II.
    Van der Ploeg AT, Kroos MA, Swallow DM, Reuser AJ.
    Ann Hum Genet; 1989 May 20; 53(2):185-92. PubMed ID: 2688540
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