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A Wanders

Showing results (171-180 of 480) with videos related to

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The Journal of Biological Chemistry|May 4, 2005
Characterization of the final step in the conversion of phytol into phytanic acidDaan M van den Brink, Joram N I van Miert, Georges Dacremont, et al.
Journal of Lipid Research|April 27, 2012
Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acidsSander M Houten, Simone Denis, Carmen A Argmann, et al.
Kidney International|July 16, 2004
Clinical implications of mutation analysis in primary hyperoxaluria type 1Christiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.
The Biochemical Journal|February 25, 2005
Demonstration and characterization of phosphate transport in mammalian peroxisomesWouter F Visser, Carlo W Van Roermund, Lodewijk Ijlst, et al.
JIMD Reports|August 26, 2016
Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum DisorderC Maxit, I Denzler, D Marchione, et al.
Molecular Microbiology|December 4, 2003
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndromeZhiming Gu, Fredoen Valianpour, Shuliang Chen, et al.
Annals of Neurology|July 12, 2002
Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiencyRegina Ensenauer, Helmut Niederhoff, Jos P N Ruiter, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Fatty acid oxidation in the human fetus: implications for fetal and adult diseaseNadia A Oey, Jos P N Ruiter, Tania Attié-Bitach, et al.
Journal of Inherited Metabolic Disease|December 15, 2022
Genetic defects in peroxisome morphogenesis (Pex11β, dynamin-like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid-phospholipid metabolismYuichi Abe, Ronald J A Wanders, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglyceridesA Muth, A Mosandl, R J A Wanders, et al.
Pageof 48

Showing results (171-180 of 480) with videos related to

Sort By:
Pageof 48
The Journal of Biological Chemistry|May 4, 2005
Characterization of the final step in the conversion of phytol into phytanic acidDaan M van den Brink, Joram N I van Miert, Georges Dacremont, et al.
Journal of Lipid Research|April 27, 2012
Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acidsSander M Houten, Simone Denis, Carmen A Argmann, et al.
Kidney International|July 16, 2004
Clinical implications of mutation analysis in primary hyperoxaluria type 1Christiaan S van Woerden, Jaap W Groothoff, Frits A Wijburg, et al.
The Biochemical Journal|February 25, 2005
Demonstration and characterization of phosphate transport in mammalian peroxisomesWouter F Visser, Carlo W Van Roermund, Lodewijk Ijlst, et al.
JIMD Reports|August 26, 2016
Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum DisorderC Maxit, I Denzler, D Marchione, et al.
Molecular Microbiology|December 4, 2003
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndromeZhiming Gu, Fredoen Valianpour, Shuliang Chen, et al.
Annals of Neurology|July 12, 2002
Clinical variability in 3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiencyRegina Ensenauer, Helmut Niederhoff, Jos P N Ruiter, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Fatty acid oxidation in the human fetus: implications for fetal and adult diseaseNadia A Oey, Jos P N Ruiter, Tania Attié-Bitach, et al.
Journal of Inherited Metabolic Disease|December 15, 2022
Genetic defects in peroxisome morphogenesis (Pex11β, dynamin-like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid-phospholipid metabolismYuichi Abe, Ronald J A Wanders, Hans R Waterham, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Stereoselective analysis of 2-hydroxysebacic acid in urine of patients with Zellweger syndrome and of premature infants fed with medium-chain triglyceridesA Muth, A Mosandl, R J A Wanders, et al.
Pageof 48