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Pascal Reynier

Showing results (171-180 of 245) with videos related to

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Antioxidants (Basel, Switzerland)|June 24, 2022
Altered Mitochondrial Opa1-Related Fusion in Mouse Promotes Endothelial Cell Dysfunction and AtherosclerosisAhmad Chehaitly, Anne-Laure Guihot, Coralyne Proux, et al.
Biomedicines|June 24, 2022
Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral SclerosisDébora Lanznaster, Clément Bruno, Jérôme Bourgeais, et al.
Brain : a Journal of Neurology|May 5, 2012
MFN2, a new gene responsible for mitochondrial DNA depletionFlorence Renaldo, Patrizia Amati-Bonneau, Abdelhamid Slama, et al.
Annals of Neurology|May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defectArnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2018
eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing dataDavid Goudenège, Celine Bris, Virginie Hoffmann, et al.
Scientific Reports|April 8, 2021
Ocular growth and metabolomics are dependent upon the spectral content of ambient white lightRaymond P Najjar, Juan Manuel Chao De La Barca, Veluchamy A Barathi, et al.
Scientific Data|August 6, 2021
ACO2 clinicobiological dataset with extensive phenotype ontology annotationKhadidja Guehlouz, Thomas Foulonneau, Patrizia Amati-Bonneau, et al.
Genes|July 27, 2022
Next-Generation Sequencing Identifies Novel <i>PMPCA</i> Variants in Patients with Late-Onset Dominant Optic AtrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Molecular Biology Reports|April 23, 2020
Mutations in aARS genes revealed by targeted next-generation sequencing in patients with mitochondrial diseasesRahma Felhi, Majida Charif, Lamia Sfaihi, et al.
Human Molecular Genetics|October 19, 2017
Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophyEmmanuelle Sarzi, Marie Seveno, Claire Angebault, et al.
Pageof 25

Showing results (171-180 of 245) with videos related to

Sort By:
Pageof 25
Antioxidants (Basel, Switzerland)|June 24, 2022
Altered Mitochondrial Opa1-Related Fusion in Mouse Promotes Endothelial Cell Dysfunction and AtherosclerosisAhmad Chehaitly, Anne-Laure Guihot, Coralyne Proux, et al.
Biomedicines|June 24, 2022
Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral SclerosisDébora Lanznaster, Clément Bruno, Jérôme Bourgeais, et al.
Brain : a Journal of Neurology|May 5, 2012
MFN2, a new gene responsible for mitochondrial DNA depletionFlorence Renaldo, Patrizia Amati-Bonneau, Abdelhamid Slama, et al.
Annals of Neurology|May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defectArnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 6, 2018
eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing dataDavid Goudenège, Celine Bris, Virginie Hoffmann, et al.
Scientific Reports|April 8, 2021
Ocular growth and metabolomics are dependent upon the spectral content of ambient white lightRaymond P Najjar, Juan Manuel Chao De La Barca, Veluchamy A Barathi, et al.
Scientific Data|August 6, 2021
ACO2 clinicobiological dataset with extensive phenotype ontology annotationKhadidja Guehlouz, Thomas Foulonneau, Patrizia Amati-Bonneau, et al.
Genes|July 27, 2022
Next-Generation Sequencing Identifies Novel <i>PMPCA</i> Variants in Patients with Late-Onset Dominant Optic AtrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
Molecular Biology Reports|April 23, 2020
Mutations in aARS genes revealed by targeted next-generation sequencing in patients with mitochondrial diseasesRahma Felhi, Majida Charif, Lamia Sfaihi, et al.
Human Molecular Genetics|October 19, 2017
Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophyEmmanuelle Sarzi, Marie Seveno, Claire Angebault, et al.
Pageof 25