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A Wanders

Showing results (181-190 of 480) with videos related to

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FEBS Letters|May 9, 2006
Identification and characterization of human cardiolipin synthaseRiekelt H Houtkooper, Hana Akbari, Henk van Lenthe, et al.
The Journal of Pediatrics|July 25, 2006
Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometryIna Schymik, Michaela Liebig, Martina Mueller, et al.
Molecular Genetics and Metabolism|December 14, 2007
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidationMalika Chegary, Heleen Te Brinke, Mirjam Doolaard, et al.
FEBS Letters|March 21, 2006
Peroxisomal trans-2-enoyl-CoA reductase is involved in phytol degradationJ Gloerich, J P N Ruiter, D M van den Brink, et al.
Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.
Annals of the Rheumatic Diseases|October 13, 2005
Combining information obtained from magnetic resonance imaging and conventional radiographs to detect sacroiliitis in patients with recent onset inflammatory back painL Heuft-Dorenbosch, R Landewé, R Weijers, et al.
Journal of Medicinal Chemistry|May 5, 2007
Design, synthesis, and in vitro testing of alpha-methylacyl-CoA racemase inhibitorsAndrew J Carnell, Ian Hale, Simone Denis, et al.
Journal of Human Genetics|May 31, 2007
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees CAvraham Zeharia, Merel S Ebberink, Ronald J A Wanders, et al.
Cold Spring Harbor Molecular Case Studies|February 26, 2022
A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classificationIngeborg Hauth, Hans R Waterham, Ronald J A Wanders, et al.
FEBS Letters|October 28, 2020
The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co-imports CoASH into the peroxisomeCarlo W T van Roermund, Lodewijk IJlst, Alison Baker, et al.
Pageof 48

Showing results (181-190 of 480) with videos related to

Sort By:
Pageof 48
FEBS Letters|May 9, 2006
Identification and characterization of human cardiolipin synthaseRiekelt H Houtkooper, Hana Akbari, Henk van Lenthe, et al.
The Journal of Pediatrics|July 25, 2006
Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometryIna Schymik, Michaela Liebig, Martina Mueller, et al.
Molecular Genetics and Metabolism|December 14, 2007
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidationMalika Chegary, Heleen Te Brinke, Mirjam Doolaard, et al.
FEBS Letters|March 21, 2006
Peroxisomal trans-2-enoyl-CoA reductase is involved in phytol degradationJ Gloerich, J P N Ruiter, D M van den Brink, et al.
Placenta|November 23, 2005
L-carnitine is synthesized in the human fetal-placental unit: potential roles in placental and fetal metabolismN A Oey, N van Vlies, F A Wijburg, et al.
Annals of the Rheumatic Diseases|October 13, 2005
Combining information obtained from magnetic resonance imaging and conventional radiographs to detect sacroiliitis in patients with recent onset inflammatory back painL Heuft-Dorenbosch, R Landewé, R Weijers, et al.
Journal of Medicinal Chemistry|May 5, 2007
Design, synthesis, and in vitro testing of alpha-methylacyl-CoA racemase inhibitorsAndrew J Carnell, Ian Hale, Simone Denis, et al.
Journal of Human Genetics|May 31, 2007
A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees CAvraham Zeharia, Merel S Ebberink, Ronald J A Wanders, et al.
Cold Spring Harbor Molecular Case Studies|February 26, 2022
A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classificationIngeborg Hauth, Hans R Waterham, Ronald J A Wanders, et al.
FEBS Letters|October 28, 2020
The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co-imports CoASH into the peroxisomeCarlo W T van Roermund, Lodewijk IJlst, Alison Baker, et al.
Pageof 48