Lysosomal storage diseases: mechanisms of enzyme replacement therapy
- 1 September 1993
- journal article
- review article
- Published by Springer Nature in Journal of Molecular Histology
- Vol. 25 (9), 593-605
- https://doi.org/10.1007/bf00157873
Abstract
No abstract availableKeywords
This publication has 112 references indexed in Scilit:
- Dose-dependent responses to macrophage-targeted glucocerebrosidase in a child with Gaucher diseaseThe Journal of Pediatrics, 1992
- Caveolin, a protein component of caveolae membrane coatsCell, 1992
- Sorting of mannose 6-phosphate receptors and lysosomal membrane proteins in endocytic vesicles.The Journal of cell biology, 1988
- Lymphocytes transfer only the lysosomal form of α-d-mannosidase during cell-to-cell contactExperimental Cell Research, 1988
- Cell-mediated cytotoxicity and the reorientation of effector cell granules towards the target cell are inhibited by the protonophore carbonylcyanide m-chlorophenylhydrazoneHuman Immunology, 1988
- The trans Golgi Network: Sorting at the Exit Site of the Golgi ComplexScience, 1986
- Fibroblasts acquire β-glucuronidase by direct and indirect transfer during co-culture with macrophagesExperimental Cell Research, 1985
- Direct enzyme transfer from lymphocytes corrects a lysosomal storage diseaseBiochemical and Biophysical Research Communications, 1985
- I-cell disease: Deficiency of extracellular hydrolase phosphorylationBiochemical and Biophysical Research Communications, 1979
- The uptake of native and desialylated glucocerebrosidase by rat hepatocytes and Kupffer cellsBiochemical and Biophysical Research Communications, 1978