In situ degradation of sphingomyelin by cultured normal fibroblasts and fibroblasts from patients with Niemann-Pick disease type A and C
- 29 October 1982
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 108 (3), 1101-1106
- https://doi.org/10.1016/0006-291x(82)92113-1
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
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- Partial Purification of Acid Sphingomyelinase from Normal and Pathological (M. Niemann‐Pick Type C) Human BrainJournal of Neurochemistry, 1980
- Niemann-Pick Disease, Type C: Evidence for the Deficiency of an Activating Factor Stimulating Sphingomyelin and Glucocerebroside DegradationHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1980
- Une micromethode simple pour la determination de l'activite sphingomyelinaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Resolution of tissue sphingomyelinase isoelectric profile in multiple components is extraction‐dependent: evidence for a component defect in Niemann‐Pick disease type C is spuriousJournal of Neurochemistry, 1977
- A Practical Chromogenic Procedure for the Detection of Homozygotes and Heterozygous Carriers of Niemann-Pick DiseaseNew England Journal of Medicine, 1975
- Isoenzymes of sphingomyelinase and the genetic defect in Niemann-Pick disease, type CBiochemical and Biophysical Research Communications, 1974
- A simple sphingomyelinase determination for Niemann‐Pick disease: differential diagnosis of types A, B and CJournal of Neurochemistry, 1973