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A Wanders

Showing results (161-170 of 480) with videos related to

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Orphanet Journal of Rare Diseases|December 3, 2015
Zellweger spectrum disorders: clinical overview and management approachFemke C C Klouwer, Kevin Berendse, Sacha Ferdinandusse, et al.
Human Mutation|October 30, 2010
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorderMerel S Ebberink, Petra A W Mooijer, Jeannette Gootjes, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 5, 2012
Improving the description of metabolic networks: the TCA cycle as exampleMiranda D Stobbe, Sander M Houten, Antoine H C van Kampen, et al.
Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.
Journal of Gastroenterology and Hepatology|January 10, 2003
Examination of small bowel enzymes in chronic diarrheaMarcellus Simadibrata, Ronald J A Wanders, Gerrit Jan, et al.
Progress in Lipid Research|June 20, 2003
The chemical biology of branched-chain lipid metabolismMridul Mukherji, Christopher J Schofield, Anthony S Wierzbicki, et al.
Orphanet Journal of Rare Diseases|September 11, 2013
Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorderKevin Berendse, Merel S Ebberink, Lodewijk Ijlst, et al.
Aging Cell|June 13, 2013
The significance of peroxisome function in chronological aging of Saccharomyces cerevisiaeSophie D Lefevre, Carlo W van Roermund, Ronald J A Wanders, et al.
Biochimica Et Biophysica Acta|January 22, 2008
Cholesterol-deprivation increases mono-unsaturated very long-chain fatty acids in skin fibroblasts from patients with X-linked adrenoleukodystrophyM Engelen, R Ofman, P A W Mooijer, et al.
Molecular Genetics and Metabolism|December 16, 2006
Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) geneKeitaro Yamada, Toshiyuki Fukao, Gaixiu Zhang, et al.
Pageof 48

Showing results (161-170 of 480) with videos related to

Sort By:
Pageof 48
Orphanet Journal of Rare Diseases|December 3, 2015
Zellweger spectrum disorders: clinical overview and management approachFemke C C Klouwer, Kevin Berendse, Sacha Ferdinandusse, et al.
Human Mutation|October 30, 2010
Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorderMerel S Ebberink, Petra A W Mooijer, Jeannette Gootjes, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 5, 2012
Improving the description of metabolic networks: the TCA cycle as exampleMiranda D Stobbe, Sander M Houten, Antoine H C van Kampen, et al.
Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.
Journal of Gastroenterology and Hepatology|January 10, 2003
Examination of small bowel enzymes in chronic diarrheaMarcellus Simadibrata, Ronald J A Wanders, Gerrit Jan, et al.
Progress in Lipid Research|June 20, 2003
The chemical biology of branched-chain lipid metabolismMridul Mukherji, Christopher J Schofield, Anthony S Wierzbicki, et al.
Orphanet Journal of Rare Diseases|September 11, 2013
Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorderKevin Berendse, Merel S Ebberink, Lodewijk Ijlst, et al.
Aging Cell|June 13, 2013
The significance of peroxisome function in chronological aging of Saccharomyces cerevisiaeSophie D Lefevre, Carlo W van Roermund, Ronald J A Wanders, et al.
Biochimica Et Biophysica Acta|January 22, 2008
Cholesterol-deprivation increases mono-unsaturated very long-chain fatty acids in skin fibroblasts from patients with X-linked adrenoleukodystrophyM Engelen, R Ofman, P A W Mooijer, et al.
Molecular Genetics and Metabolism|December 16, 2006
Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) geneKeitaro Yamada, Toshiyuki Fukao, Gaixiu Zhang, et al.
Pageof 48