Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases
- 1 October 1977
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 80 (1), 79-86
- https://doi.org/10.1016/0009-8981(77)90266-2
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- GLYCOSIDASES IN HUMAN SKIN FIBROBLAST CULTURESActa Paediatrica, 1975
- Studies on the Pathogenetic Mechanism of I-Cell Disease in Cultured FibroblastsPediatric Research, 1974
- Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis III (pseudo-Hurler polydystrophy)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblastsBiochemical and Biophysical Research Communications, 1974
- MUCOLIPIDOSIS II (I-CELL DISEASE) A Clinical and Biochemical StudyActa Paediatrica, 1974
- PROPERTIES OF FIVE ACID HYDROLASES IN HUMAN SKIN FIBROBLAST CULTURES Possible Use in the Diagnosis of Inborn Lysosomal DiseasesActa Paediatrica, 1973
- A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomesBiochemical and Biophysical Research Communications, 1972
- I-CELL DISEASE : MULTIPLE LYSOSOMAL-ENZYME DEFECTThe Lancet, 1971
- Functions of LysosomesAnnual Review of Physiology, 1966