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

Rob Ofman

Showing results (11-20 of 39) with videos related to

Pageof 4
Sort By:
Journal of Biochemistry|September 19, 2008
The nudix hydrolase 7 is an Acyl-CoA diphosphatase involved in regulating peroxisomal coenzyme A homeostasisSarah-Jayne Reilly, Veronika Tillander, Rob Ofman, et al.
Biochimica Et Biophysica Acta|December 16, 2014
Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesisMartin J A Schackmann, Rob Ofman, Inge M E Dijkstra, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 1, 2017
Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophyMalu-Clair van de Beek, Rob Ofman, Inge Dijkstra, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Clinical Neurology and Neurosurgery|September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
American Journal of Medical Genetics. Part A|April 5, 2013
Intellectual disability and hemizygous GPD2 mutationDaniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Frontiers in Cell and Developmental Biology|April 19, 2021
Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis DefectFemke C C Klouwer, Kim D Falkenberg, Rob Ofman, et al.
Molecular Genetics and Metabolism|April 3, 2004
Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseasesBwee Tien Poll-The, Ronald J A Wanders, Jos P N Ruiter, et al.
The Biochemical Journal|April 12, 2011
Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expressionXuebin Zhang, Carine De Marcos Lousa, Nellie Schutte-Lensink, et al.
Plos One|August 23, 2012
Bezafibrate for X-linked adrenoleukodystrophyMarc Engelen, Luc Tran, Rob Ofman, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Journal of Biochemistry|September 19, 2008
The nudix hydrolase 7 is an Acyl-CoA diphosphatase involved in regulating peroxisomal coenzyme A homeostasisSarah-Jayne Reilly, Veronika Tillander, Rob Ofman, et al.
Biochimica Et Biophysica Acta|December 16, 2014
Enzymatic characterization of ELOVL1, a key enzyme in very long-chain fatty acid synthesisMartin J A Schackmann, Rob Ofman, Inge M E Dijkstra, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 1, 2017
Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophyMalu-Clair van de Beek, Rob Ofman, Inge Dijkstra, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Clinical Neurology and Neurosurgery|September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
American Journal of Medical Genetics. Part A|April 5, 2013
Intellectual disability and hemizygous GPD2 mutationDaniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Frontiers in Cell and Developmental Biology|April 19, 2021
Autophagy Inhibitors Do Not Restore Peroxisomal Functions in Cells With the Most Common Peroxisome Biogenesis DefectFemke C C Klouwer, Kim D Falkenberg, Rob Ofman, et al.
Molecular Genetics and Metabolism|April 3, 2004
Spastic diplegia and periventricular white matter abnormalities in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, a defect of isoleucine metabolism: differential diagnosis with hypoxic-ischemic brain diseasesBwee Tien Poll-The, Ronald J A Wanders, Jos P N Ruiter, et al.
The Biochemical Journal|April 12, 2011
Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expressionXuebin Zhang, Carine De Marcos Lousa, Nellie Schutte-Lensink, et al.
Plos One|August 23, 2012
Bezafibrate for X-linked adrenoleukodystrophyMarc Engelen, Luc Tran, Rob Ofman, et al.
Pageof 4