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Biochimica Et Biophysica Acta
|
May 18, 1994
Purification of peroxisomal acyl-CoA: dihydroxyacetonephosphate acyltransferase from human placenta
R Ofman, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1992
Long-chain 3-hydroxyacyl-CoA dehydrogenase in leukocytes and chorionic villus fibroblasts: potential for pre- and postnatal diagnosis
R J Wanders, L Ijlst
Journal of Inherited Metabolic Disease
|
January 1, 1993
A simple, straightforward assay for long-chain 3-hydroxyacyl-CoA dehydrogenase based on the use of N-ethylmaleimide: potential for pre- and postnatal diagnosis
L Ijlst, R J Wanders
European Journal of Biochemistry
|
November 15, 1993
Permeability properties of peroxisomes in digitonin-permeabilized rat hepatocytes. Evidence for free permeability towards a variety of substrates
N Verleur, R J Wanders
Biochemical Pharmacology
|
July 6, 1993
Studies on the effect of fenoprofen on the activation and oxidation of long chain and very long chain fatty acids in hepatocytes and subcellular fractions from rat liver
W Lageweg, R J Wanders
Biochimica Et Biophysica Acta
|
December 9, 2000
Biochemical and genetic aspects of 7-dehydrocholesterol reductase and Smith-Lemli-Opitz syndrome
H R Waterham, R J Wanders
Journal of Inherited Metabolic Disease
|
March 1, 1997
Plasmalogens and oxidative stress: evidence against a major role of plasmalogens in protection against the superoxide anion radical
G A Jansen, R J Wanders
Progress in Clinical and Biological Research
|
January 1, 1992
Resolution of the subcellular site of very long-chain fatty acid beta-oxidation in human skin fibroblasts using a novel approach
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
August 1, 1998
Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata
R J Wanders, G J Romeijn
Biochemical and Biophysical Research Communications
|
July 2, 1998
Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis
R J Wanders, G J Romeijn
Page
of 50
Search research articles
Search
Showing results (11-20 of 497) with videos related to
Sort By:
Page
of 50
Biochimica Et Biophysica Acta
|
May 18, 1994
Purification of peroxisomal acyl-CoA: dihydroxyacetonephosphate acyltransferase from human placenta
R Ofman, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1992
Long-chain 3-hydroxyacyl-CoA dehydrogenase in leukocytes and chorionic villus fibroblasts: potential for pre- and postnatal diagnosis
R J Wanders, L Ijlst
Journal of Inherited Metabolic Disease
|
January 1, 1993
A simple, straightforward assay for long-chain 3-hydroxyacyl-CoA dehydrogenase based on the use of N-ethylmaleimide: potential for pre- and postnatal diagnosis
L Ijlst, R J Wanders
European Journal of Biochemistry
|
November 15, 1993
Permeability properties of peroxisomes in digitonin-permeabilized rat hepatocytes. Evidence for free permeability towards a variety of substrates
N Verleur, R J Wanders
Biochemical Pharmacology
|
July 6, 1993
Studies on the effect of fenoprofen on the activation and oxidation of long chain and very long chain fatty acids in hepatocytes and subcellular fractions from rat liver
W Lageweg, R J Wanders
Biochimica Et Biophysica Acta
|
December 9, 2000
Biochemical and genetic aspects of 7-dehydrocholesterol reductase and Smith-Lemli-Opitz syndrome
H R Waterham, R J Wanders
Journal of Inherited Metabolic Disease
|
March 1, 1997
Plasmalogens and oxidative stress: evidence against a major role of plasmalogens in protection against the superoxide anion radical
G A Jansen, R J Wanders
Progress in Clinical and Biological Research
|
January 1, 1992
Resolution of the subcellular site of very long-chain fatty acid beta-oxidation in human skin fibroblasts using a novel approach
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
August 1, 1998
Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata
R J Wanders, G J Romeijn
Biochemical and Biophysical Research Communications
|
July 2, 1998
Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis
R J Wanders, G J Romeijn
Page
of 50