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Journal Abstract Search

95 related items for PubMed ID: 3730407

  • 1.
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  • 3. Specificity of human glucosylceramide beta-glucosidase towards synthetic glucosylsphingolipids inserted into liposomes. Kinetic studies in a detergent-free assay system.
    Sarmientos F, Schwarzmann G, Sandhoff K.
    Eur J Biochem; 1986 Nov 03; 160(3):527-35. PubMed ID: 3780720
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  • 4. Comparison of synthetic and natural glucosylceramides as substrate for glucosylceramidase assay.
    Vaccaro AM, Kobayashi T, Suzuki K.
    Clin Chim Acta; 1982 Jan 05; 118(1):1-7. PubMed ID: 7053901
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  • 6. Glucosylceramide and the level of the glucosidase-stimulating proteins.
    Datta SC, Radin NS.
    Lipids; 1986 Nov 05; 21(11):702-9. PubMed ID: 3099116
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  • 8. The fate of glucosylceramide (glucocerebroside) in genetically impaired (lysosomal beta-glucosidase deficient) Gaucher disease diploid human fibroblasts.
    Saito M, Rosenberg A.
    J Biol Chem; 1985 Feb 25; 260(4):2295-300. PubMed ID: 3919000
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  • 9. Mechanism of activation of glucocerebrosidase by co-beta-glucosidase (glucosidase activator protein).
    Berent SL, Radin NS.
    Biochim Biophys Acta; 1981 Jun 23; 664(3):572-82. PubMed ID: 6268176
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  • 11. Correlation between the activity of glucosylceramidase and its binding to glucosylceramide-containing liposomes. Role of acidic phospholipids and fatty acids.
    Vaccaro AM, Tatti M, Salvioli R, Ciaffoni F, Gallozzi E.
    Biochim Biophys Acta; 1990 Jan 29; 1033(1):73-9. PubMed ID: 2302413
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  • 12. Activation of membrane-bound glucosylceramide: beta-glucosidase in fibroblasts cultured from normal and glucosylceramidotic human skin.
    Mueller OT, Rosenberg A.
    J Biol Chem; 1979 May 10; 254(9):3521-5. PubMed ID: 429368
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  • 13. Presence of activator proteins for the enzymatic degradation of glucosylceramide in several human tissues.
    Vaccaro AM, Ciaffoni F, Mandara I, Suzuki K.
    Clin Chim Acta; 1988 Mar 15; 172(2-3):323-34. PubMed ID: 3370844
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  • 15. Biochemical studies in a patient with subacute neuropathic Gaucher disease without visceral glucosylceramide storage.
    Wenger DA, Roth S, Kudoh T, Grover WD, Tucker SH, Kaye EM, Ullman MD.
    Pediatr Res; 1983 May 15; 17(5):344-8. PubMed ID: 6856396
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  • 17. Gaucher disease. III. Substrate specificity of glucocerebrosidase and the use of nonlabeled natural substrates for the investigation of patients.
    Choy FY, Davidson RG.
    Am J Hum Genet; 1980 Sep 15; 32(5):670-80. PubMed ID: 6775530
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  • 18. Glycosphingolipid studies of visceral tissues and brain from type 1 Gaucher disease variants.
    Nilsson O, Grabowski GA, Ludman MD, Desnick RJ, Svennerholm L.
    Clin Genet; 1985 May 15; 27(5):443-50. PubMed ID: 3924448
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  • 19. Studies of the pathogenesis of Gaucher's disease: tissue distribution and biliary excretion of [14C]L-glucosylceramide in rats.
    Tokoro T, Gal AE, Gallo LL, Brady RO.
    J Lipid Res; 1987 Aug 15; 28(8):968-72. PubMed ID: 3668390
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  • 20. Salvage of glucosylceramide by recycling after internalization along the pathway of receptor-mediated endocytosis.
    Kok JW, Eskelinen S, Hoekstra K, Hoekstra D.
    Proc Natl Acad Sci U S A; 1989 Dec 15; 86(24):9896-900. PubMed ID: 2690077
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