Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

R J Wanders

Showing results (141-150 of 497) with videos related to

Pageof 50
Sort By:
Biochimica Et Biophysica Acta|June 20, 1998
Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disordersR J Wanders, L Ijlst, E van Elk, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Molecular and Biochemical Parasitology|November 12, 1996
Identification of 2-enoyl coenzyme A hydratase and NADP(+)-dependent 3-hydroxyacyl-CoA dehydrogenase activity in glycosomes of procyclic Trypanosoma bruceiE A Wiemer, L IJlst, J van Roy, et al.
Annals of Clinical Biochemistry|March 1, 1994
Heterogeneity in di/trihydroxycholestanoic acidaemiaH J ten Brink, R J Wanders, E Christensen, et al.
Journal of Medical Genetics|July 25, 2000
Incidence and molecular mechanism of aberrant splicing owing to a G-->C splice acceptor site mutation causing Smith-Lemli-Opitz syndromeH R Waterham, W Oostheim, G J Romeijn, 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.
The New England Journal of Medicine|July 18, 1985
Rhizomelic chondrodysplasia punctata: another peroxisomal disorderH S Heymans, J W Oorthuys, G Nelck, et al.
Neuropediatrics|April 25, 2000
2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduriaR J Dunckelmann, F Ebinger, A Schulze, et al.
Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.
Pageof 50

Showing results (141-150 of 497) with videos related to

Sort By:
Pageof 50
Biochimica Et Biophysica Acta|June 20, 1998
Pristanic acid beta-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disordersR J Wanders, L Ijlst, E van Elk, et al.
Biochimica Et Biophysica Acta|December 31, 1997
Phytanic acid alpha-oxidation in peroxisomal disorders: studies in cultured human fibroblastsN M Verhoeven, D S Schor, C R Roe, et al.
Molecular and Biochemical Parasitology|November 12, 1996
Identification of 2-enoyl coenzyme A hydratase and NADP(+)-dependent 3-hydroxyacyl-CoA dehydrogenase activity in glycosomes of procyclic Trypanosoma bruceiE A Wiemer, L IJlst, J van Roy, et al.
Annals of Clinical Biochemistry|March 1, 1994
Heterogeneity in di/trihydroxycholestanoic acidaemiaH J ten Brink, R J Wanders, E Christensen, et al.
Journal of Medical Genetics|July 25, 2000
Incidence and molecular mechanism of aberrant splicing owing to a G-->C splice acceptor site mutation causing Smith-Lemli-Opitz syndromeH R Waterham, W Oostheim, G J Romeijn, 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.
The New England Journal of Medicine|July 18, 1985
Rhizomelic chondrodysplasia punctata: another peroxisomal disorderH S Heymans, J W Oorthuys, G Nelck, et al.
Neuropediatrics|April 25, 2000
2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduriaR J Dunckelmann, F Ebinger, A Schulze, et al.
Journal of Lipid Research|November 4, 2000
Subcellular localization and physiological role of alpha-methylacyl-CoA racemaseS Ferdinandusse, S Denis, L IJlst, et al.
Pageof 50