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

Rikke K J Olsen

Showing results (1-10 of 25) with videos related to

Pageof 3
Sort By:
Journal of Inherited Metabolic Disease|February 13, 2010
Disease mechanisms and protein structures in fatty acid oxidation defectsNiels Gregersen, Rikke K J Olsen
Journal of Inherited Metabolic Disease|May 31, 2015
Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolismRikke K J Olsen, Nanna Cornelius, Niels Gregersen
Human Molecular Genetics|April 5, 2014
Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblastsNanna Cornelius, Thomas J Corydon, Niels Gregersen, et al.
Molecular Genetics and Metabolism|March 3, 2006
Electron transfer flavoprotein deficiency: functional and molecular aspectsManuel Schiff, Roseline Froissart, Rikke K J Olsen, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|November 10, 2022
Odd- and even-numbered medium-chained fatty acids protect against glutathione depletion in very long-chain acyl-CoA dehydrogenase deficiencyMartin Lund, Robert Heaton, Iain P Hargreaves, et al.
Human Mutation|June 20, 2003
Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 7, 2021
Bezafibrate activation of PPAR drives disturbances in mitochondrial redox bioenergetics and decreases the viability of cells from patients with VLCAD deficiencyMartin Lund, Kathrine G Andersen, Robert Heaton, et al.
Journal of Inherited Metabolic Disease|October 7, 2008
Mitochondrial fatty acid oxidation defects--remaining challengesNiels Gregersen, Brage S Andresen, Christina B Pedersen, et al.
Human Molecular Genetics|May 22, 2012
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiencyNanna Cornelius, Frank E Frerman, Thomas J Corydon, et al.
Molecular Genetics and Metabolism|February 4, 2014
Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiencyAnders V Edhager, Vibeke Stenbroen, Nadia Sukusu Nielsen, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Journal of Inherited Metabolic Disease|February 13, 2010
Disease mechanisms and protein structures in fatty acid oxidation defectsNiels Gregersen, Rikke K J Olsen
Journal of Inherited Metabolic Disease|May 31, 2015
Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolismRikke K J Olsen, Nanna Cornelius, Niels Gregersen
Human Molecular Genetics|April 5, 2014
Cellular consequences of oxidative stress in riboflavin responsive multiple acyl-CoA dehydrogenation deficiency patient fibroblastsNanna Cornelius, Thomas J Corydon, Niels Gregersen, et al.
Molecular Genetics and Metabolism|March 3, 2006
Electron transfer flavoprotein deficiency: functional and molecular aspectsManuel Schiff, Roseline Froissart, Rikke K J Olsen, et al.
Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids|November 10, 2022
Odd- and even-numbered medium-chained fatty acids protect against glutathione depletion in very long-chain acyl-CoA dehydrogenase deficiencyMartin Lund, Robert Heaton, Iain P Hargreaves, et al.
Human Mutation|June 20, 2003
Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiencyRikke K J Olsen, Brage S Andresen, Ernst Christensen, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 7, 2021
Bezafibrate activation of PPAR drives disturbances in mitochondrial redox bioenergetics and decreases the viability of cells from patients with VLCAD deficiencyMartin Lund, Kathrine G Andersen, Robert Heaton, et al.
Journal of Inherited Metabolic Disease|October 7, 2008
Mitochondrial fatty acid oxidation defects--remaining challengesNiels Gregersen, Brage S Andresen, Christina B Pedersen, et al.
Human Molecular Genetics|May 22, 2012
Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiencyNanna Cornelius, Frank E Frerman, Thomas J Corydon, et al.
Molecular Genetics and Metabolism|February 4, 2014
Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiencyAnders V Edhager, Vibeke Stenbroen, Nadia Sukusu Nielsen, et al.
Pageof 3