D. Cuebas

发表

3-Hydroxyacyl-CoA epimerases of rat liver peroxisomes and Escherichia coli function as auxiliary enzymes in the beta-oxidation of polyunsaturated fatty acids.

H. Schulz, S. Yang, D. Cuebas, 1986, The Journal of biological chemistry.

Epithelial cell specificity and apotope recognition by serum autoantibodies in primary biliary cirrhosis

G. Gores, R. Coppel, Xiao-Song He, 2011, Hepatology.

3-Mercaptopropionic acid, a potent inhibitor of fatty acid oxidation in rat heart mitochondria.

H. Schulz, E. Sabbagh, D. Cuebas, 1985, The Journal of biological chemistry.

Evidence for a modified pathway of linoleate degradation. Metabolism of 2,4-decadienoyl coenzyme A.

H. Schulz, D. Cuebas, 1982, The Journal of biological chemistry.

The role of α-methylacyl-CoA racemase in bile acid synthesis

C. Phillips, W. Schmitz, E. Conzelmann, 2002 .

The reactions catalyzed by the inducible bifunctional enzyme of rat liver peroxisomes cannot lead to the formation of bile acids.

R. Xu, D. Cuebas, 1996, Biochemical and biophysical research communications.

NADPH-dependent beta-oxidation of unsaturated fatty acids with double bonds extending from odd-numbered carbon atoms.

H. Schulz, M. Nada, D. Cuebas, 1992, Proceedings of the National Academy of Sciences of the United States of America.

The Human Liver-specific Homolog of Very Long-chain Acyl-CoA Synthetase Is Cholate:CoA Ligase*

P. Watkins, S. Mihalik, S. Steinberg, 2000, The Journal of Biological Chemistry.

Mitochondrial metabolism of 3-mercaptopropionic acid. Chemical synthesis of 3-mercaptopropionyl coenzyme A and some of its S-acyl derivatives.

H. Schulz, F. Frerman, D. Cuebas, 1985, The Journal of biological chemistry.

Mitochondrial Metabolism of 3-Mercaptopropionic Acid

H. Schulz, D. Cuebas, Joe D. BeckrnannSg, 1985 .

The 3-hydroxyacyl-CoA epimerase activity of rat liver peroxisomes is due to the combined actions of two enoyl-CoA hydratases: a revision of the epimerase-dependent pathway of unsaturated fatty acid oxidation.

H. Schulz, J. Li, D. Cuebas, 1989, Biochemical and biophysical research communications.

Epimerization of 3-hydroxy-4-trans-decenoyl coenzyme A by a dehydration/hydration mechanism catalyzed by the multienzyme complex of fatty acid oxidation from Escherichia coli.

H. Schulz, D. Cuebas, T. E. Smeland, 1991, The Journal of biological chemistry.

Analysis of carnitine biosynthesis metabolites in urine by HPLC-electrospray tandem mass spectrometry.

P. Vreken, R. Wanders, F. Vaz, 2002, Clinical chemistry.

Evidence for involvement of medium chain acyl-CoA dehydrogenase in the metabolism of phenylbutyrate.

J. Vockley, A. Mohsen, D. Cuebas, 2012, Molecular genetics and metabolism.

Channeling of 3-hydroxy-4-trans-decenoyl coenzyme A on the bifunctional beta-oxidation enzyme from rat liver peroxisomes and on the large subunit of the fatty acid oxidation complex from Escherichia coli.

H. Schulz, S. Yang, D. Cuebas, 1986, The Journal of biological chemistry.

The role of alpha-methylacyl-CoA racemase in bile acid synthesis.

C. Phillips, W. Schmitz, E. Conzelmann, 2002, The Biochemical journal.

Participation of Two Members of the Very Long-chain Acyl-CoA Synthetase Family in Bile Acid Synthesis and Recycling*

Georges Dacremont, G. Dacremont, R. Wanders, 2002, The Journal of Biological Chemistry.

Recombinant 2-enoyl-CoA hydratase derived from rat peroxisomal multifunctional enzyme 2: role of the hydratase reaction in bile acid synthesis.

J. Hiltunen, A. Haapalainen, D. Novikov, 1997, The Biochemical journal.

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.

P. Vreken, S. Denis, R. Wanders, 1998, Journal of lipid research.

The activity of 3-hydroxyacyl-CoA epimerase is insufficient to account for the rate of linoleate oxidation in rat heart mitochondria. Evidence for a modified pathway of linoleate degradation.

H. Schulz, L. Kushner, D. Cuebas, 1984, Biochemical and biophysical research communications.

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.

P. Vreken, R. Wanders, J. Adamski, 1998, Proceedings of the National Academy of Sciences of the United States of America.