An animal model of human acid sphingomyelinase deficiency (Niemannpick disease) and the study of its enzyme replacement
- 1 June 1987
- journal article
- other
- Published by Springer Nature in Journal of Human Genetics
- Vol. 32 (2) , 55-69
- https://doi.org/10.1007/bf01893159
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Subcellular localization of acid sphingomyelinase and lipid in Niemann‐Pick miceJournal of Inherited Metabolic Disease, 1987
- Bone marrow transplantation in niemann-pick miceJournal of Inherited Metabolic Disease, 1986
- Lack of acid sphingomyelinase in the mitochondria‐lysosome fraction of brain from Niemann‐Pick miceJournal of Inherited Metabolic Disease, 1985
- Metabolism: Therapeutic Bone Marrow Transplantation in Niemann-Pick MicePediatrics International, 1985
- Bone marrow transplantation for Niemann-Pick miceBiochemical and Biophysical Research Communications, 1983
- A lysosomal storage disorder in mice: A model of Niemann‐Pick diseaseJournal of Inherited Metabolic Disease, 1982
- REVERSAL OF CLINICAL FEATURES OF HURLER'S DISEASE AND BIOCHEMICAL IMPROVEMENT AFTER TREATMENT BY BONE-MARROW TRANSPLANTATIONThe Lancet, 1981
- ASSAY AND SUBCELLULAR LOCALIZATION OF THE ARYLSULPHATASES IN RAT BRAINJournal of Neurochemistry, 1970
- Isoelectric Fractionation, Analysis, and Characterization of Ampholytes in Natural pH Gradients. IV. Further Studies on the Resolving Power in Connection with Separation of Myoglobins.Acta Chemica Scandinavica, 1966
- CHOLINERGIC AND NON‐CHOLINERGIC NERVE ENDINGS IN RAT BRAIN–IJournal of Neurochemistry, 1962