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Biochimica Et Biophysica Acta
|
November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemia
G A Jansen, R J Wanders
Biochemical and Biophysical Research Communications
|
August 15, 1991
Conclusive evidence that very-long-chain fatty acids are oxidized exclusively in peroxisomes in human skin fibroblasts
B S Jakobs, R J Wanders
Molecular Aspects of Medicine
|
November 25, 1998
Lipid metabolism in peroxisomes in relation to human disease
R J Wanders, J M Tager
Annals of Clinical Biochemistry
|
July 1, 1994
Re-evaluation of conditions required for measurement of true alanine:glyoxylate aminotransferase activity in human liver: implications for the diagnosis of hyperoxaluria type I
V A Horváth, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1994
Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferase
V A Horváth, R J Wanders
Developmental Neuroscience
|
January 1, 1991
Peroxisomal fatty acid beta-oxidation in relation to adrenoleukodystrophy
R J Wanders, J M Tager
Biochemistry
|
October 4, 1988
Sigmoidal relation between mitochondrial respiration and log ([ATP]/[ADP])out under conditions of extramitochondrial ATP utilization. Implications for the control and thermodynamics of oxidative phosphorylation
R J Wanders, H V Westerhoff
Biochemical and Biophysical Research Communications
|
August 24, 1995
Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondria
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1996
Impaired peroxisomal fatty acid oxidation in human skin fibroblasts with a mitochondrial acylcarnitine/carnitine translocase deficiency
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1996
Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liver
R J Wanders, G J Romeijn
Page
of 50
Search research articles
Search
Showing results (21-30 of 497) with videos related to
Sort By:
Page
of 50
Biochimica Et Biophysica Acta
|
November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemia
G A Jansen, R J Wanders
Biochemical and Biophysical Research Communications
|
August 15, 1991
Conclusive evidence that very-long-chain fatty acids are oxidized exclusively in peroxisomes in human skin fibroblasts
B S Jakobs, R J Wanders
Molecular Aspects of Medicine
|
November 25, 1998
Lipid metabolism in peroxisomes in relation to human disease
R J Wanders, J M Tager
Annals of Clinical Biochemistry
|
July 1, 1994
Re-evaluation of conditions required for measurement of true alanine:glyoxylate aminotransferase activity in human liver: implications for the diagnosis of hyperoxaluria type I
V A Horváth, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1994
Rapid identification of primary hyperoxaluria type I patients using a novel, fully automated method for measurement of hepatic alanine: glyoxylate aminotransferase
V A Horváth, R J Wanders
Developmental Neuroscience
|
January 1, 1991
Peroxisomal fatty acid beta-oxidation in relation to adrenoleukodystrophy
R J Wanders, J M Tager
Biochemistry
|
October 4, 1988
Sigmoidal relation between mitochondrial respiration and log ([ATP]/[ADP])out under conditions of extramitochondrial ATP utilization. Implications for the control and thermodynamics of oxidative phosphorylation
R J Wanders, H V Westerhoff
Biochemical and Biophysical Research Communications
|
August 24, 1995
Fatty acid beta-oxidation in peroxisomes and mitochondria: the first, unequivocal evidence for the involvement of carnitine in shuttling propionyl-CoA from peroxisomes to mitochondria
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1996
Impaired peroxisomal fatty acid oxidation in human skin fibroblasts with a mitochondrial acylcarnitine/carnitine translocase deficiency
B S Jakobs, R J Wanders
Journal of Inherited Metabolic Disease
|
January 1, 1996
Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liver
R J Wanders, G J Romeijn
Page
of 50