Niemann–Pick C disease: cholesterol handling gone awry
Open Access
- 1 December 1998
- journal article
- review article
- Published by Elsevier in Molecular Medicine Today
- Vol. 4 (12) , 525-531
- https://doi.org/10.1016/s1357-4310(98)01374-4
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis GeneScience, 1997
- Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol HomeostasisScience, 1997
- The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterolBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1994
- A clinical staging classification for type C Niemann‐Pick diseaseNeurology, 1992
- Clinical spectrum of Niemann‐Pick disease type CNeurology, 1989
- The intracellular transport of low density lipoprotein-derived cholesterol is defective in Niemann-Pick type C fibroblasts.The Journal of cell biology, 1989
- 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
- Group C Niemann‐Pick disease: faulty regulation of low‐density lipoprotein uptake and cholesterol storage in cultured fibroblastsThe FASEB Journal, 1987
- A Receptor-Mediated Pathway for Cholesterol HomeostasisScience, 1986
- A defect in cholesterol esterification in Niemann-Pick disease (type C) patients.Proceedings of the National Academy of Sciences, 1985