I-cell disease: Deficiency of extracellular hydrolase phosphorylation
- 6 December 1979
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 91 (3), 976-981
- https://doi.org/10.1016/0006-291x(79)91975-2
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Human placental N-acetyl-β-d-hexosaminidase isozymesArchives of Biochemistry and Biophysics, 1978
- Evidence for lysosomal enzyme recognition by human fibroblasts via a phosphorylated carbohydrate moietyBiochemical Journal, 1978
- Recognition and receptor-mediated uptake of a lysosomal enzyme, α-l-iduronidase, by cultured human fibroblastsCell, 1977
- Phosphohexosyl recognition is a general characteristic of pinocytosis of lysosomal glycosidases by human fibroblasts.Journal of Clinical Investigation, 1977
- Abnormal ganglioside accumulation in cultured fibroblasts from patients with mucolipidosis IVBiochemical and Biophysical Research Communications, 1975
- Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis III (pseudo-Hurler polydystrophy)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomesBiochemical and Biophysical Research Communications, 1972
- I-cell disease: A clinical pictureThe Journal of Pediatrics, 1971
- I-CELL DISEASE : MULTIPLE LYSOSOMAL-ENZYME DEFECTThe Lancet, 1971
- Analytical fractionation of plant and animal proteins by gel electrofucingJournal of Chromatography A, 1968