Molecular basis of d-bifunctional protein deficiency
- 29 January 2001
- journal article
- review article
- Published by Elsevier in Molecular and Cellular Endocrinology
- Vol. 171 (1-2) , 61-70
- https://doi.org/10.1016/s0303-7207(00)00388-9
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Evolution of 17β-HSD type 4, a multifunctional protein of β-oxidationMolecular and Cellular Endocrinology, 2001
- A guide to 17β-hydroxysteroid dehydrogenasesMolecular and Cellular Endocrinology, 2001
- 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 AcidsJournal of Biological Chemistry, 2000
- Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein importProceedings of the National Academy of Sciences, 1998
- Differential regulation by a peroxisome proliferator of the different multifunctional proteins in guinea pig: cDNA cloning of the guinea pig D-specific multifunctional protein 2Biochemical Journal, 1998
- Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal β-oxidation of pristanic acidBiochemical Journal, 1997
- Further Characterization of the Peroxisomal 3‐Hydroxyacyl‐Coa Dehydrogenases from Rat LiverEuropean Journal of Biochemistry, 1996
- New 17?-Hydroxysteroid Dehydrogenases.Annals of the New York Academy of Sciences, 1996
- Molecular cloning of a novel widely expressed human 80 kDa 17β-hydroxysteroid dehydrogenase IVBiochemical Journal, 1995
- Purification and properties of oestradiol 17β-dehydrogenase extracted from cytoplasmic vesicles of porcine endometrial cellsBiochemical Journal, 1992