| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2007 | M Casteels | Biochem. Soc. Trans. | The role of 2-hydroxyacyl-CoA lyase, a thiamin pyrophosphate-dependent enzyme, in the peroxisomal metabolism of 3-methyl-branched fatty acids and 2-hydroxy straight-chain fatty acids.[Pubmed] |
| 2001 | R Jansen | Biochem. Biophys. Res. Commun. | Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes.[Pubmed] |
| 2000 | S Jansen | J. Inherit. Metab. Dis. | Phytanic acid alpha-oxidation in man: identification of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal enzyme with normal activity in Zellweger syndrome.[Pubmed] |
| 1999 | S Jansen | Biochim. Biophys. Acta | Phytanic acid alpha-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomes.[Pubmed] |
| 1999 | V Foulon | Proc. Natl. Acad. Sci. U.S.A. | Purification, molecular cloning, and expression of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal thiamine pyrophosphate-dependent enzyme that catalyzes the carbon-carbon bond cleavage during alpha-oxidation of 3-methyl-branched fatty acids.[Pubmed] |