Peroxisomal cholesterol biosynthesis and Smith-Lemli-Opitz syndrome
- 23 June 2006
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 345 (1) , 205-209
- https://doi.org/10.1016/j.bbrc.2006.04.078
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Phosphomevalonate kinase is a cytosolic protein in humansJournal of Lipid Research, 2004
- Mevalonate kinase is a cytosolic enzyme in humansJournal of Cell Science, 2004
- Disturbed Cholesterol Homeostasis in a Peroxisome-Deficient PEX2 Knockout Mouse ModelMolecular and Cellular Biology, 2004
- Central role of peroxisomes in isoprenoid biosynthesisProgress in Lipid Research, 2002
- Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse modelBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 2001
- Mutations in the Δ7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndromeProceedings of the National Academy of Sciences, 1998
- Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz SyndromeAmerican Journal of Human Genetics, 1998
- Compartmentalization of Cholesterol BiosynthesisPublished by Elsevier ,1996
- Biosynthesis of dolichol by rat liver peroxisomesEuropean Journal of Biochemistry, 1989
- 3-Hydroxy-3-methylglutaryl coenzyme A reductase localization in rat liver peroxisomes and microsomes of control and cholestyramine-treated animals: quantitative biochemical and immunoelectron microscopical analyses.The Journal of cell biology, 1986