HSD17B4 by Pubmed references

YEAR FIRST AUTHOR JOURNAL TITLE
2009 Bao Lige Mol. Biol. Cell Role of an ancestral d-bifunctional protein containing two sterol-carrier protein-2 domains in lipid uptake and trafficking in Toxoplasma.[Pubmed]
2007 Justyna Paprocka Clinical and neuropathological picture of familial encephalopathy with bifunctional protein deficiency.[Pubmed]
2006 Tam Nguyen J. Cell. Sci. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.[Pubmed]
2005 I Soorani-Lunsing J. Inherit. Metab. Dis. Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfall.[Pubmed]
2005 Shan Zha Prostate Peroxisomal branched chain fatty acid beta-oxidation pathway is upregulated in prostate cancer.[Pubmed]
2004 Johan Edqvist J. Biol. Chem. Plants express a lipid transfer protein with high similarity to mammalian sterol carrier protein-2.[Pubmed]
2004 Sacha Ferdinandusse J. Lipid Res. Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids.[Pubmed]
2004 V Schröder Acta Neuropathol. Optico-cochleo-dentate degeneration associated with severe peripheral neuropathy and caused by peroxisomal D-bifunctional protein deficiency.[Pubmed]
2003 Satomi Matsuoka Eukaryotic Cell MFE1, a member of the peroxisomal hydroxyacyl coenzyme A dehydrogenase family, affects fatty acid metabolism necessary for morphogenesis in Dictyostelium spp.[Pubmed]
2003 Jolein Gloerich J. Lipid Res. A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiency.[Pubmed]
2003 Sacha Ferdinandusse Mol. Genet. Metab. Evidence for increased oxidative stress in peroxisomal D-bifunctional protein deficiency.[Pubmed]
2003 Cristiano Rizzo Pediatr. Res. Characteristic acylcarnitine profiles in inherited defects of peroxisome biogenesis: a novel tool for screening diagnosis using tandem mass spectrometry.[Pubmed]
2002 Sacha Ferdinandusse Biochem. Biophys. Res. Commun. Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes.[Pubmed]
2002 S Ferdinandusse Am. J. Hum. Genet. Reinvestigation of peroxisomal 3-ketoacyl-CoA thiolase deficiency: identification of the true defect at the level of d-bifunctional protein.[Pubmed]
2002 Paton Paton Prenat. Diagn. Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency.[Pubmed]
2001 S Ferdinandusse J. Lipid Res. Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid.[Pubmed]
2001 Su Su J. Biol. Chem. Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis.[Pubmed]
2001 Clayton Clayton Biochem. Soc. Trans. Clinical consequences of defects in peroxisomal beta-oxidation.[Pubmed]
2000 M Baes J. Biol. Chem. Inactivation of the peroxisomal multifunctional protein-2 in mice impedes the degradation of not only 2-methyl-branched fatty acids and bile acid intermediates but also of very long chain fatty acids.[Pubmed]
2000 T Hashimoto Cell Biochem. Biophys. Peroxisomal beta-oxidation enzymes.[Pubmed]
2000 M Itoh Brain Res. Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome.[Pubmed]
2000 S Ferdinandusse J. Lipid Res. Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx). Activity measurements in liver and fibroblasts using a newly developed method.[Pubmed]
1999 N Shimozawa Biochem. Biophys. Res. Commun. Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.[Pubmed]
1999 P Mooijer Hum. Mol. Genet. Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency.[Pubmed]
1998 P Vreken J. Lipid Res. Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency.[Pubmed]
1998 E Ijlst Proc. Natl. Acad. Sci. U.S.A. Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.[Pubmed]
1997 T Jiang J. Biochem. Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.[Pubmed]
1990 Baker Baker FASEB J. A common ancestor for Candida tropicalis and dehydrogenases that synthesize antibiotics and steroids.[Pubmed]