Purification and characterization of I-cell disease alpha-L-fucosidase.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference56 articles.
1. Inherited Disorders of Lysosomal Metabolism
2. Increased levels of sialic acid associated with a sialidase deficiency in I-cell disease (mucolipidosis II) fibroblasts
3. I-Cell Disease: Biochemical Studies
4. Studies on the Pathogenetic Mechanism of I-Cell Disease in Cultured Fibroblasts
5. Mucolipidosis II and III: different residual activity of beta-galactosidase in cultured fibroblasts*
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1. Regioselective synthesis of α-L-fucosyl-containing benzyl disaccharides by use of α-L-fucosidases ofAspergillus niger;Archives of Pharmacal Research;1996-08
2. The effect of carbohydrate removal on the properties of human liver α-l-fucosidase;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1992-02
3. The identification of type 1 Gaucher disease patients, asymptomatic cases and carriers in The Netherlands using urine samples: An evaluation;Clinica Chimica Acta;1991-12
4. Mammalian α-l-fucosidases;Comparative Biochemistry and Physiology Part B: Comparative Biochemistry;1991-01
5. The basic isoelectric form of α-l-fucosidase from the hepatopancreas of the shrimp Penaeus monodon (crustacea: decapoda);Comparative Biochemistry and Physiology Part B: Comparative Biochemistry;1991-01
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