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Pascal Reynier

Showing results (91-100 of 245) with videos related to

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Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
American Journal of Physiology. Endocrinology and Metabolism|December 9, 2004
Maternal smoking is associated with mitochondrial DNA depletion and respiratory chain complex III deficiency in placentaNatacha Bouhours-Nouet, Pascale May-Panloup, Régis Coutant, et al.
Physiological Reports|July 5, 2025
Altered endothelial mitochondrial Opa1-related fusion in mouse accelerates age-associated vascular and kidney damageCarlotta Turnaturi, Loïck L'Hoste, Coralyne Proux, et al.
Annales De Biologie Clinique|October 27, 2025
[Clinical metabolomics in laboratory medicine: mapping of practices, state of the art, and proposals from the Société Française de Biologie Clinique Working Group]Marie Lenski, Thibaud Lefebvre, Karim Chikh, et al.
Frontiers in Immunology|July 31, 2023
An immuno-lipidomic signature revealed by metabolomic and machine-learning approaches in labial salivary gland to diagnose primary Sjögren's syndromeGeoffrey Urbanski, Floris Chabrun, Estelle Delattre, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
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.
Oncogene|April 5, 2005
Gene profiling reveals specific oncogenic mechanisms and signaling pathways in oncocytic and papillary thyroid carcinomaOlivier Baris, Delphine Mirebeau-Prunier, Frédérique Savagner, et al.
European Journal of Ophthalmology|May 31, 2011
Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome geneSalah Mohamed Cherif Titah, Isabelle Meunier, Catherine Blanchet, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Pageof 25

Showing results (91-100 of 245) with videos related to

Sort By:
Pageof 25
Journal of the Peripheral Nervous System : JPNS|October 6, 2016
Increased mitochondrial fusion in a autosomal recessive CMT2A family with mitochondrial GTPase mitofusin 2 mutationsPhilippe Codron, Arnaud Chevrollier, Mariame S Kane, et al.
American Journal of Physiology. Endocrinology and Metabolism|December 9, 2004
Maternal smoking is associated with mitochondrial DNA depletion and respiratory chain complex III deficiency in placentaNatacha Bouhours-Nouet, Pascale May-Panloup, Régis Coutant, et al.
Physiological Reports|July 5, 2025
Altered endothelial mitochondrial Opa1-related fusion in mouse accelerates age-associated vascular and kidney damageCarlotta Turnaturi, Loïck L'Hoste, Coralyne Proux, et al.
Annales De Biologie Clinique|October 27, 2025
[Clinical metabolomics in laboratory medicine: mapping of practices, state of the art, and proposals from the Société Française de Biologie Clinique Working Group]Marie Lenski, Thibaud Lefebvre, Karim Chikh, et al.
Frontiers in Immunology|July 31, 2023
An immuno-lipidomic signature revealed by metabolomic and machine-learning approaches in labial salivary gland to diagnose primary Sjögren's syndromeGeoffrey Urbanski, Floris Chabrun, Estelle Delattre, et al.
Biochimica Et Biophysica Acta|February 7, 2012
Metabolically induced heteroplasmy shifting and l-arginine treatment reduce the energetic defect in a neuronal-like model of MELASValerie Desquiret-Dumas, Naig Gueguen, Magalie Barth, et al.
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.
Oncogene|April 5, 2005
Gene profiling reveals specific oncogenic mechanisms and signaling pathways in oncocytic and papillary thyroid carcinomaOlivier Baris, Delphine Mirebeau-Prunier, Frédérique Savagner, et al.
European Journal of Ophthalmology|May 31, 2011
Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome geneSalah Mohamed Cherif Titah, Isabelle Meunier, Catherine Blanchet, et al.
Mitochondrion|November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicityVirginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Pageof 25