Molecular defect in processing α-fucosidase in fucosidosis
Authors:
- Karl JohnsonKJKarl Johnson
- Glyn DawsonGDGlyn Dawson
- 1 November 1985
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 133 (1) , 90-97
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Carboxyl-terminal proteolytic processing during biosynthesis of the lysosomal enzymes .beta.-glucuronidase and cathepsin DBiochemistry, 1983
- [58] Studies of lysosomal enzyme biosynthesis in cultured cells1983
- Radioimmunoassay determinations of decreased amounts of α-L-fucosidase protein in fucosidosisBiochimica et Biophysica Acta (BBA) - General Subjects, 1982
- Purification and properties of two forms of human α-l-fucosidaseBiochimica et Biophysica Acta (BBA) - Enzymology, 1980
- Substrate specificity of human α-l-fucosidaseArchives of Biochemistry and Biophysics, 1977
- Structure of the accumulating oligosaccharide in fucosidosis.Journal of Biological Chemistry, 1976
- Human liver alpha-L-fucosidase. Purification, characterization, and immunochemical studies.Journal of Biological Chemistry, 1975
- Glycosphingolipids in Cultured Human Skin FibroblastsJournal of Biological Chemistry, 1972
- Deficiency of α-L-FucosidaseScience, 1972
- FucosidosisThe Journal of Pediatrics, 1969