E. van Berkel

Peroxisomal <scp>d</scp> -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

E.G. van Grunsven, E. van Berkel, Lodewijk IJlst et al. · Proceedings of the National Academy of Sciences · 1998 · 149 citations · Full text

Life Sciences, Biochemistry, Molecular Genetics +17

Peroxisomal Bifunctional Protein Deficiency Revisited: Resolution of Its True Enzymatic and Molecular Basis

E.G. van Grunsven, E. van Berkel, Petra A.W. Mooijer et al. · The American Journal of Human Genetics · 1999 · 107 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +16

Peroxisomal fatty acid oxidation disorders and 58 kDa sterol carrier protein X (SCPx): activity measurements in liver and fibroblasts using a newly developed method

Sacha Ferdinandusse, Simone Denis, E. van Berkel et al. · Journal of Lipid Research · 2000 · 39 citations · Full text

Life Sciences, Biochemistry, Cellular Metabolism +16

Fusagene vectors: a novel strategy for the expression of multiple genes from a single cistron

Joop Gäken, Jianping Jiang, E. van Berkel et al. · Gene Therapy · 2000 · 33 citations

Life Sciences, Biotechnology, Genetics +12

Identification of the newly discovered 58kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: Implications for peroxisomal β‐oxidation disorders

R. J. A. Wanders, Simone Denis, E. van Berkel et al. · Journal of Inherited Metabolic Disease · 1998 · 29 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17