Molecular weight characterization of β-d-glucocerebrosidase in mononuclear white blood cells in Gaucher's disease
Author:
Publisher
Elsevier BV
Subject
Biochemistry
Reference25 articles.
1. The Metabolic Basis of Inherited Disease;Brady,1983
2. Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's disease
3. beta-Glucoside hydrolase activity of normal and glucosylceramidotic cultured human skin fibroblasts.
4. Deficiency of steroid β-glucosidase in Gaucher disease
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1. Glycolipid and Glycoprotein Degradation;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
2. Analyses of catalytic activity and inhibitor binding of human acid beta-glucosidase by site-directed mutagenesis. Identification of residues critical to catalysis and evidence for causality of two Ashkenazi Jewish Gaucher disease type 1 mutations.;Journal of Biological Chemistry;1990-04
3. Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzyme;Biochimica et Biophysica Acta (BBA) - Biomembranes;1986-12
4. A procedure for the rapid purification in high yield of human glucocerebrosidase using immunoaffinity chromatography with monoclonal antibodies;Analytical Biochemistry;1986-05
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