Deficiency of UDP-N-acetylglucosamine: Lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients
- 1 April 1982
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 105 (3), 1052-1058
- https://doi.org/10.1016/0006-291x(82)91076-2
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Synthesis and Processing of Arylsulfatase A in Human Skin FibroblastsHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1982
- Oligosaccharides in Lysosomal EnzymesEuropean Journal of Biochemistry, 1981
- Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5'-diphosphate-N-acetylglucosamine: glycoprotein N-acetylglucosaminylphosphotransferase activity.Journal of Clinical Investigation, 1981
- Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in l-cell fibroblastsBiochemical and Biophysical Research Communications, 1981
- β-Galactosidase in mucopolysaccharidoses and mucolipidoses. deficiency of GM1 β-galactosidase in liver and leukocytesClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- I-Cell disease (Mucolipidosis II)Acta Neuropathologica, 1975
- MUCOLIPIDOSIS II (I-CELL DISEASE) A Clinical and Biochemical StudyActa Paediatrica, 1974
- I-Cell disease, mucolipidosis IIEuropean Journal of Pediatrics, 1973
- I-Cell Disease: Biochemical StudiesPediatric Research, 1972
- Mutant Enzymatic and Cytological Phenotypes in Cultured Human FibroblastsScience, 1967