Cholesterol esterification and Niemann-Pick disease: An approach to identifying the defect in fibroblasts
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience
Reference23 articles.
1. 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.
2. Rapid method for the isolation of lipoproteins from human serum by precipitation with polyanions
3. Defective activity of acyl-CoA:cholesterol O-acyltransferase in Niemann-Pick type C and type D fibroblasts
4. Identification of two lysosomal membrane glycoproteins.
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1. A comparative study of cytoplasmic granules imaged by the real-time microscope, Nile Red and Filipin in fibroblasts from patients with lipid storage diseases;Journal of Inherited Metabolic Disease;2005-12
2. Cholesterol-Enriched Membrane Microdomains Are Required for Inducing Host Cell Cytoskeleton Rearrangements in Response to Attaching-Effacing Escherichia coli;Infection and Immunity;2005-11
3. Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype;The American Journal of Human Genetics;1999-11
4. Spectrum of phenotypic variability in Niemann-Pick type C disease: A cause of delayed diagnosis;Paediatrics & Child Health;1998-09-01
5. Pulmonary infiltration in Niemann-Pick disease type C;Journal of Inherited Metabolic Disease;1996-11
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