Identification of the newly discovered 58kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: Implications for peroxisomal β-oxidation disorders-Reference-Cited by-同舟云学术

Identification of the newly discovered 58kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: Implications for peroxisomal β-oxidation disorders

Published:1998-06 Issue:3 Volume:21 Page:302-305
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Wanders R. J. A.,Denis S.,van Berkel E.,Wouters F.,Wirtz K. W. A.,Seedorf U.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005349028853/fullpdf

Reference8 articles.

1. A new peroxisomal β-oxidation disorder in twin neonates: defective oxidation of both cerotic and pristanic acids;Christensen;J Inher Metab Dis,1997

2. Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein;Jiang;J Biochem,1997

3. The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes;Miyazawa;Eur J Biochem,1980

4. Sterol carrier protein X is a peroxisomal 3-oxoacyl coenzyme A thiolase with intrinsic sterol carrier and lipid transfer activity;Seedorf;J Biol Chem,1994

5. Pre-and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography-mass spectrometry;Verhoeven;J Inher Metab Dis,1995

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