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Peter Bross

Showing results (31-40 of 94) with videos related to

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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.
Cell Stress & Chaperones|July 1, 2011
A cell model to study different degrees of Hsp60 deficiency in HEK293 cellsAnne Sigaard Bie, Johan Palmfeldt, Jakob Hansen, et al.
Proteome Science|May 30, 2009
Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stressJohan Palmfeldt, Søren Vang, Vibeke Stenbroen, et al.
JIMD Reports|September 26, 2015
Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited DisordersPaula Fernandez-Guerra, M Lund, T J Corydon, et al.
Biochimica Et Biophysica Acta|October 5, 2011
Cofactors and metabolites as potential stabilizers of mitochondrial acyl-CoA dehydrogenasesTânia G Lucas, Bárbara J Henriques, João V Rodrigues, 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.
Journal of Agricultural and Food Chemistry|May 1, 2010
NMR-based metabonomic investigation of heat stress in myotubes reveals a time-dependent change in the metabolitesIda K Straadt, Jette F Young, Peter Bross, 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.
Human Mutation|July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic diseaseBent N Terp, David N Cooper, Inge T Christensen, et al.
Pageof 10

Showing results (31-40 of 94) with videos related to

Sort By:
Pageof 10
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.
Cell Stress & Chaperones|July 1, 2011
A cell model to study different degrees of Hsp60 deficiency in HEK293 cellsAnne Sigaard Bie, Johan Palmfeldt, Jakob Hansen, et al.
Proteome Science|May 30, 2009
Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stressJohan Palmfeldt, Søren Vang, Vibeke Stenbroen, et al.
JIMD Reports|September 26, 2015
Application of an Image Cytometry Protocol for Cellular and Mitochondrial Phenotyping on Fibroblasts from Patients with Inherited DisordersPaula Fernandez-Guerra, M Lund, T J Corydon, et al.
Biochimica Et Biophysica Acta|October 5, 2011
Cofactors and metabolites as potential stabilizers of mitochondrial acyl-CoA dehydrogenasesTânia G Lucas, Bárbara J Henriques, João V Rodrigues, 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.
Journal of Agricultural and Food Chemistry|May 1, 2010
NMR-based metabonomic investigation of heat stress in myotubes reveals a time-dependent change in the metabolitesIda K Straadt, Jette F Young, Peter Bross, 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.
Human Mutation|July 19, 2002
Assessing the relative importance of the biophysical properties of amino acid substitutions associated with human genetic diseaseBent N Terp, David N Cooper, Inge T Christensen, et al.
Pageof 10