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C W van Roermund

Showing results (11-20 of 63) with videos related to

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European Journal of Biochemistry|July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondriaR J Wanders, A K Groen, C W Van Roermund, et al.
The EMBO Journal|July 17, 1995
The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditionsC W van Roermund, Y Elgersma, N Singh, et al.
European Journal of Biochemistry|August 1, 1997
Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiaeN Verleur, Y Elgersma, C W Van Roermund, et al.
European Journal of Biochemistry|December 12, 1997
Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell systemN Verleur, E H Hettema, C W van Roermund, et al.
Progress in Clinical and Biological Research|January 1, 1990
Inborn errors of peroxisomal beta-oxidation: biochemical identification using enzymic and immunological methodsR J Wanders, C W van Roermund, A Schelen, et al.
Biochimica Et Biophysica Acta|May 8, 1992
Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liverR J Wanders, S Denis, C W van Roermund, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysisR J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndromeC W van Roermund, S Brul, J M Tager, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Biochimica Et Biophysica Acta|November 29, 1994
2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Pageof 7

Showing results (11-20 of 63) with videos related to

Sort By:
Pageof 7
European Journal of Biochemistry|July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondriaR J Wanders, A K Groen, C W Van Roermund, et al.
The EMBO Journal|July 17, 1995
The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditionsC W van Roermund, Y Elgersma, N Singh, et al.
European Journal of Biochemistry|August 1, 1997
Cytosolic aspartate aminotransferase encoded by the AAT2 gene is targeted to the peroxisomes in oleate-grown Saccharomyces cerevisiaeN Verleur, Y Elgersma, C W Van Roermund, et al.
European Journal of Biochemistry|December 12, 1997
Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell systemN Verleur, E H Hettema, C W van Roermund, et al.
Progress in Clinical and Biological Research|January 1, 1990
Inborn errors of peroxisomal beta-oxidation: biochemical identification using enzymic and immunological methodsR J Wanders, C W van Roermund, A Schelen, et al.
Biochimica Et Biophysica Acta|May 8, 1992
Characteristics and subcellular localization of pristanoyl-CoA synthetase in rat liverR J Wanders, S Denis, C W van Roermund, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysisR J Wanders, C W van Roermund, S Brul, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndromeC W van Roermund, S Brul, J M Tager, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Biochimica Et Biophysica Acta|November 29, 1994
2-Hydroxyphytanic acid oxidase activity in rat and human liver and its deficiency in the Zellweger syndromeR J Wanders, C W van Roermund, D S Schor, et al.
Pageof 7