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A Wanders

Showing results (121-130 of 480) with videos related to

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Annals of the Rheumatic Diseases|June 17, 2005
Association between radiographic damage of the spine and spinal mobility for individual patients with ankylosing spondylitis: can assessment of spinal mobility be a proxy for radiographic evaluation?A Wanders, R Landewé, M Dougados, et al.
Biochemical and Biophysical Research Communications|March 14, 2002
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndromeNobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, et al.
Frontiers in Cell and Developmental Biology|January 28, 2021
Peroxisomal Metabolite and Cofactor Transport in HumansSerhii Chornyi, Lodewijk IJlst, Carlo W T van Roermund, et al.
Journal of Inherited Metabolic Disease|May 22, 2010
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening resultsRonald J A Wanders, Jos P N Ruiter, Lodewijk IJLst, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 9, 2004
Novel genotype of mevalonic aciduria with fatalities in premature siblingsP Raupp, E Varady, M Duran, et al.
Molecular Genetics and Metabolism|August 29, 2006
An improved enzyme assay for carnitine palmitoyl transferase I in fibroblasts using tandem mass spectrometryNaomi van Vlies, Jos P N Ruiter, Mirjam Doolaard, et al.
Journal of Inherited Metabolic Disease|January 11, 2024
Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylateSander F Garrelfs, Serhii Chornyi, Heleen Te Brinke, et al.
Frontiers in Cell and Developmental Biology|February 7, 2022
Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD TransportersCarlo W T van Roermund, Lodewijk IJlst, Nicole Linka, et al.
Journal of Lipid Research|February 4, 2003
A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiencyJolein Gloerich, Simone Denis, Elisabeth G van Grunsven, et al.
Biochimica Et Biophysica Acta|December 17, 2013
A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acidsCarlo W T van Roermund, Lodewijk Ijlst, Tom Wagemans, et al.
Pageof 48

Showing results (121-130 of 480) with videos related to

Sort By:
Pageof 48
Annals of the Rheumatic Diseases|June 17, 2005
Association between radiographic damage of the spine and spinal mobility for individual patients with ankylosing spondylitis: can assessment of spinal mobility be a proxy for radiographic evaluation?A Wanders, R Landewé, M Dougados, et al.
Biochemical and Biophysical Research Communications|March 14, 2002
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndromeNobuyuki Shimozawa, Tomoko Nagase, Yasuhiko Takemoto, et al.
Frontiers in Cell and Developmental Biology|January 28, 2021
Peroxisomal Metabolite and Cofactor Transport in HumansSerhii Chornyi, Lodewijk IJlst, Carlo W T van Roermund, et al.
Journal of Inherited Metabolic Disease|May 22, 2010
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening resultsRonald J A Wanders, Jos P N Ruiter, Lodewijk IJLst, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|January 9, 2004
Novel genotype of mevalonic aciduria with fatalities in premature siblingsP Raupp, E Varady, M Duran, et al.
Molecular Genetics and Metabolism|August 29, 2006
An improved enzyme assay for carnitine palmitoyl transferase I in fibroblasts using tandem mass spectrometryNaomi van Vlies, Jos P N Ruiter, Mirjam Doolaard, et al.
Journal of Inherited Metabolic Disease|January 11, 2024
Glyoxylate reductase: Definitive identification in human liver mitochondria, its importance for the compartment-specific detoxification of glyoxylateSander F Garrelfs, Serhii Chornyi, Heleen Te Brinke, et al.
Frontiers in Cell and Developmental Biology|February 7, 2022
Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD TransportersCarlo W T van Roermund, Lodewijk IJlst, Nicole Linka, et al.
Journal of Lipid Research|February 4, 2003
A novel HPLC-based method to diagnose peroxisomal D-bifunctional protein enoyl-CoA hydratase deficiencyJolein Gloerich, Simone Denis, Elisabeth G van Grunsven, et al.
Biochimica Et Biophysica Acta|December 17, 2013
A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acidsCarlo W T van Roermund, Lodewijk Ijlst, Tom Wagemans, et al.
Pageof 48