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Peter Bross

Showing results (11-20 of 94) with videos related to

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APMIS. Supplementum|July 24, 2003
Protein quality control in the endoplasmic reticulumMalene Munk Jørgensen, Peter Bross, Niels Gregersen
Current Topics in Medicinal Chemistry|January 24, 2013
Molecular chaperone disorders: defective Hsp60 in neurodegenerationPeter Bross, Raffaella Magnoni, Anne Sigaard Bie
European Journal of Biochemistry|January 20, 2004
Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationshipsNiels Gregersen, Peter Bross, Brage S Andresen
Ugeskrift for Laeger|March 11, 2003
[Conformational diseases]Niels Gregersen, Peter Bross, Lars A Bolund
Methods in Molecular Biology (Clifton, N.J.)|October 21, 2018
A Cell Model for HSP60 Deficiencies: Modeling Different Levels of Chaperonopathies Leading to Oxidative Stress and Mitochondrial DysfunctionCagla Cömert, Paula Fernandez-Guerra, Peter Bross
Biochimica Et Biophysica Acta|August 3, 2010
Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiencyBárbara J Henriques, Peter Bross, Cláudio M Gomes
Assay and Drug Development Technologies|July 22, 2020
Optimized High-Contrast Brightfield Microscopy Application for Noninvasive Proliferation Assays of Human Cell CulturesJasper Carlsen, Cagla Cömert, Peter Bross, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 4, 2003
Investigation of folding and degradation of in vitro synthesized mutant proteins in mitochondriaPeter Bross, Vibeke Winter, Christina Bak Pedersen, et al.
Annual Review of Genomics and Human Genetics|May 26, 2006
Protein misfolding and human diseaseNiels Gregersen, Peter Bross, Søren Vang, et al.
Molecular Genetics and Metabolism|June 2, 2005
Down-regulation of Hsp60 expression by RNAi impairs folding of medium-chain acyl-CoA dehydrogenase wild-type and disease-associated proteinsThomas J Corydon, Jakob Hansen, Peter Bross, et al.
Pageof 10

Showing results (11-20 of 94) with videos related to

Sort By:
Pageof 10
APMIS. Supplementum|July 24, 2003
Protein quality control in the endoplasmic reticulumMalene Munk Jørgensen, Peter Bross, Niels Gregersen
Current Topics in Medicinal Chemistry|January 24, 2013
Molecular chaperone disorders: defective Hsp60 in neurodegenerationPeter Bross, Raffaella Magnoni, Anne Sigaard Bie
European Journal of Biochemistry|January 20, 2004
Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationshipsNiels Gregersen, Peter Bross, Brage S Andresen
Ugeskrift for Laeger|March 11, 2003
[Conformational diseases]Niels Gregersen, Peter Bross, Lars A Bolund
Methods in Molecular Biology (Clifton, N.J.)|October 21, 2018
A Cell Model for HSP60 Deficiencies: Modeling Different Levels of Chaperonopathies Leading to Oxidative Stress and Mitochondrial DysfunctionCagla Cömert, Paula Fernandez-Guerra, Peter Bross
Biochimica Et Biophysica Acta|August 3, 2010
Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiencyBárbara J Henriques, Peter Bross, Cláudio M Gomes
Assay and Drug Development Technologies|July 22, 2020
Optimized High-Contrast Brightfield Microscopy Application for Noninvasive Proliferation Assays of Human Cell CulturesJasper Carlsen, Cagla Cömert, Peter Bross, et al.
Methods in Molecular Biology (Clifton, N.J.)|July 4, 2003
Investigation of folding and degradation of in vitro synthesized mutant proteins in mitochondriaPeter Bross, Vibeke Winter, Christina Bak Pedersen, et al.
Annual Review of Genomics and Human Genetics|May 26, 2006
Protein misfolding and human diseaseNiels Gregersen, Peter Bross, Søren Vang, et al.
Molecular Genetics and Metabolism|June 2, 2005
Down-regulation of Hsp60 expression by RNAi impairs folding of medium-chain acyl-CoA dehydrogenase wild-type and disease-associated proteinsThomas J Corydon, Jakob Hansen, Peter Bross, et al.
Pageof 10