HPCL2 by Pubmed references

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]