Niemann-pick disease type C could result from a genetic deficiency of cholesterol egress from the lysosomes
- 1 December 1989
- journal article
- Published by Springer Nature in Journal of Inherited Metabolic Disease
- Vol. 12 (4) , 483-484
- https://doi.org/10.1007/bf01802046
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes.Proceedings of the National Academy of Sciences, 1988
- Type C Niemann-Pick disease. Lysosomal accumulation and defective intracellular mobilization of low density lipoprotein cholesterol.Journal of Biological Chemistry, 1988
- Type C Niemann-Pick disease. A parallel loss of regulatory responses in both the uptake and esterification of low density lipoprotein-derived cholesterol in cultured fibroblasts.Journal of Biological Chemistry, 1986
- The lysosome membraneTrends in Biochemical Sciences, 1986
- Role of acylcoenzyme A: Cholesterol o-acyltransferase in cholesterol metabolismProgress in Lipid Research, 1979