J. Heikoop

Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder

R. J. A. Wanders, Herbert Schumacher, J. Heikoop et al. · Journal of Inherited Metabolic Disease · 1992 · 130 citations

Mendelian Disorder, Biochemistry, Genetic Disorder +8

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.

Ronald J. A. Wanders, C W van Roermund, M J van Wijland et al. · Journal of Clinical Investigation · 1987 · 87 citations · Full text

Metabolic Disorder, Lipid Peroxidation, Pathology +17

Autophagic degradation of peroxisomes in isolated rat hepatocytes

Joost J. F. P. Luiken, Marlene van den Berg, J. Heikoop et al. · FEBS Letters · 1992 · 72 citations

Peroxisomal Enzymes, Lipid Peroxidation, Redox Biology +19

Peroxisomal very long-chain fatty acid β-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders

Ronald J. A. Wanders, Carlo W.T. van Roermund, M.J.A. van Wijland et al. · Clinica Chimica Acta · 1987 · 58 citations

Skin Development, Biochemistry, Cutaneous Biology +8

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

J. Heikoop, C W van Roermund, Wilhelm W. Just et al. · Journal of Clinical Investigation · 1990 · 58 citations · Full text

Genetics, Lipid Peroxidation, Pathology +17