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Vincent Procaccio

Showing results (71-80 of 197) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesionsPhilippe Codron, Julien Cassereau, Patrick Vourc'h, et al.
Human Mutation|June 21, 2008
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequencesMarty C Brandon, Eduardo Ruiz-Pesini, Dan Mishmar, et al.
Neurogenetics|January 8, 2026
Dystonia-deafness syndrome 1 caused by ACTB p.(Arg183Trp) de novo variant: one novel case extending the phenotypic spectrumSilvestre Cuinat, Tiphaine Rouaud, Thomas Besnard, et al.
Plos One|December 20, 2015
Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged MiceNaïg Gueguen, Valérie Desquiret-Dumas, Géraldine Leman, et al.
Analytical Chemistry|December 20, 2016
A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic PreconditioningJudith Kouassi Nzoughet, Cinzia Bocca, Gilles Simard, et al.
Scientific Reports|June 17, 2021
Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex IFranziska Nuber, Johannes Schimpf, Jean-Paul di Rago, et al.
Plos One|January 7, 2016
Resveratrol Improved Flow-Mediated Outward Arterial Remodeling in Ovariectomized Rats with Hypertrophic Effect at High DoseMarie Petit, Anne-Laure Guihot, Linda Grimaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
Skeletal muscle transcriptional coactivator PGC-1α mediates mitochondrial, but not metabolic, changes during calorie restrictionLydia W S Finley, Jaewon Lee, Amanda Souza, et al.
Neurology. Genetics|December 22, 2017
Novel <i>NDUFS4</i> gene mutation in an atypical late-onset mitochondrial form of multifocal dystoniaCeline Bris, Tiphaine Rouaud, Valerie Desquiret-Dumas, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, et al.
Pageof 20

Showing results (71-80 of 197) with videos related to

Sort By:
Pageof 20
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 1, 2018
Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesionsPhilippe Codron, Julien Cassereau, Patrick Vourc'h, et al.
Human Mutation|June 21, 2008
MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequencesMarty C Brandon, Eduardo Ruiz-Pesini, Dan Mishmar, et al.
Neurogenetics|January 8, 2026
Dystonia-deafness syndrome 1 caused by ACTB p.(Arg183Trp) de novo variant: one novel case extending the phenotypic spectrumSilvestre Cuinat, Tiphaine Rouaud, Thomas Besnard, et al.
Plos One|December 20, 2015
Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged MiceNaïg Gueguen, Valérie Desquiret-Dumas, Géraldine Leman, et al.
Analytical Chemistry|December 20, 2016
A Nontargeted UHPLC-HRMS Metabolomics Pipeline for Metabolite Identification: Application to Cardiac Remote Ischemic PreconditioningJudith Kouassi Nzoughet, Cinzia Bocca, Gilles Simard, et al.
Scientific Reports|June 17, 2021
Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex IFranziska Nuber, Johannes Schimpf, Jean-Paul di Rago, et al.
Plos One|January 7, 2016
Resveratrol Improved Flow-Mediated Outward Arterial Remodeling in Ovariectomized Rats with Hypertrophic Effect at High DoseMarie Petit, Anne-Laure Guihot, Linda Grimaud, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
Skeletal muscle transcriptional coactivator PGC-1α mediates mitochondrial, but not metabolic, changes during calorie restrictionLydia W S Finley, Jaewon Lee, Amanda Souza, et al.
Neurology. Genetics|December 22, 2017
Novel <i>NDUFS4</i> gene mutation in an atypical late-onset mitochondrial form of multifocal dystoniaCeline Bris, Tiphaine Rouaud, Valerie Desquiret-Dumas, et al.
Journal of Cellular and Molecular Medicine|April 6, 2017
Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophyMariame Selma Kane, Jennifer Alban, Valérie Desquiret-Dumas, et al.
Pageof 20