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Bioscience Reports
|
January 1, 1984
Modern theories of metabolic control and their applications (review)
H V Westerhoff, A K Groen, R J Wanders
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 15, 1988
3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method
R J Wanders, R B Schutgens, P H Zoeters
Biochimica Et Biophysica Acta
|
October 26, 1991
Factors influencing the latency of the peroxisomal enzyme dihydroxyacetone-phosphate acyltransferase (DHAP-AT) in permeabilized human skin fibroblasts
E J Wolvetang, J M Tager, R J Wanders
European Journal of Biochemistry
|
September 1, 1980
Origin of the ammonia found in protein-free extracts of rat-liver mitochondria and rat hepatocytes
R J Wanders, J B Hoek, J M Tager
Progress in Clinical and Biological Research
|
January 1, 1992
Latency of peroxisomal palmitoyl-CoA beta-oxidation in digitonin permeabilized fibroblasts: the effect of ATP on peroxisomal permeability
E J Wolvetang, J M Tager, R J Wanders
Journal of Neuropathology and Experimental Neurology
|
November 15, 2001
Refsum disease, peroxisomes and phytanic acid oxidation: a review
R J Wanders, G A Jansen, O H Skjeldal
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1987
Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man
R J Wanders, R B Schutgens, H S Heymans
Journal of Inherited Metabolic Disease
|
January 1, 1988
Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method
R J Wanders, R B Schutgens, B H Zoeters
Biochimica Et Biophysica Acta
|
December 9, 2000
Biochemical and genetic aspects of mevalonate kinase and its deficiency
S M Houten, R J Wanders, H R Waterham
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mitochondrial oxidative phosphorylation in digitonin-permeabilized chorionic villus fibroblasts: a new method with potential for prenatal diagnosis
R J Wanders, J P Ruiter, F A Wijburg
Page
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Search research articles
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Showing results (41-50 of 497) with videos related to
Sort By:
Page
of 50
Bioscience Reports
|
January 1, 1984
Modern theories of metabolic control and their applications (review)
H V Westerhoff, A K Groen, R J Wanders
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 15, 1988
3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method
R J Wanders, R B Schutgens, P H Zoeters
Biochimica Et Biophysica Acta
|
October 26, 1991
Factors influencing the latency of the peroxisomal enzyme dihydroxyacetone-phosphate acyltransferase (DHAP-AT) in permeabilized human skin fibroblasts
E J Wolvetang, J M Tager, R J Wanders
European Journal of Biochemistry
|
September 1, 1980
Origin of the ammonia found in protein-free extracts of rat-liver mitochondria and rat hepatocytes
R J Wanders, J B Hoek, J M Tager
Progress in Clinical and Biological Research
|
January 1, 1992
Latency of peroxisomal palmitoyl-CoA beta-oxidation in digitonin permeabilized fibroblasts: the effect of ATP on peroxisomal permeability
E J Wolvetang, J M Tager, R J Wanders
Journal of Neuropathology and Experimental Neurology
|
November 15, 2001
Refsum disease, peroxisomes and phytanic acid oxidation: a review
R J Wanders, G A Jansen, O H Skjeldal
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 15, 1987
Deficient cholesterol side chain oxidation in patients without peroxisomes (Zellweger syndrome): evidence for the involvement of peroxisomes in bile acid synthesis in man
R J Wanders, R B Schutgens, H S Heymans
Journal of Inherited Metabolic Disease
|
January 1, 1988
Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method
R J Wanders, R B Schutgens, B H Zoeters
Biochimica Et Biophysica Acta
|
December 9, 2000
Biochemical and genetic aspects of mevalonate kinase and its deficiency
S M Houten, R J Wanders, H R Waterham
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mitochondrial oxidative phosphorylation in digitonin-permeabilized chorionic villus fibroblasts: a new method with potential for prenatal diagnosis
R J Wanders, J P Ruiter, F A Wijburg
Page
of 50