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Pascal Reynier

Showing results (21-30 of 245) with videos related to

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Annales De Biologie Clinique|December 14, 2018
Alagille syndrome: a case reportYacine Benabed, Emilie Chaillou, Marie-Christine Denis, et al.
Antioxidants (Basel, Switzerland)|January 27, 2021
Embryo and Its MitochondriaPascale May-Panloup, Magalie Boguenet, Hady El Hachem, et al.
Experimental Cell Research|January 18, 2006
mtDNA controls expression of the Death Associated Protein 3Caroline Jacques, Arnaud Chevrollier, Dominique Loiseau, et al.
Journal of Cellular and Molecular Medicine|March 19, 2026
Nicotinamide (Vitamin B3) Deficiency in Follicular Fluid of Patients With Ovarian AgeingCinzia Bocca, Magalie Boguenet, Lisa Boucret, et al.
Nutrients|April 3, 2021
Iron Deficiency without Anemia Decreases Physical Endurance and Mitochondrial Complex I Activity of Oxidative Skeletal Muscle in the MouseEmmanuel Rineau, Naïg Gueguen, Vincent Procaccio, et al.
Orphanet Journal of Rare Diseases|December 28, 2011
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2KJulien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Molecular Carcinogenesis|April 7, 2009
Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapyDominique Loiseau, Daniel Morvan, Arnaud Chevrollier, et al.
Scientific Reports|August 1, 2025
Deep-learning model for embryo selection using time-lapse imaging of matched high-quality embryosLisa Boucret, Floris Chabrun, Magalie Boguenet, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
Pediatrics|September 2, 2016
Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase DeficiencyIsabelle Signolet, Rachel Chenouard, Florine Oca, et al.
Pageof 25

Showing results (21-30 of 245) with videos related to

Sort By:
Pageof 25
Annales De Biologie Clinique|December 14, 2018
Alagille syndrome: a case reportYacine Benabed, Emilie Chaillou, Marie-Christine Denis, et al.
Antioxidants (Basel, Switzerland)|January 27, 2021
Embryo and Its MitochondriaPascale May-Panloup, Magalie Boguenet, Hady El Hachem, et al.
Experimental Cell Research|January 18, 2006
mtDNA controls expression of the Death Associated Protein 3Caroline Jacques, Arnaud Chevrollier, Dominique Loiseau, et al.
Journal of Cellular and Molecular Medicine|March 19, 2026
Nicotinamide (Vitamin B3) Deficiency in Follicular Fluid of Patients With Ovarian AgeingCinzia Bocca, Magalie Boguenet, Lisa Boucret, et al.
Nutrients|April 3, 2021
Iron Deficiency without Anemia Decreases Physical Endurance and Mitochondrial Complex I Activity of Oxidative Skeletal Muscle in the MouseEmmanuel Rineau, Naïg Gueguen, Vincent Procaccio, et al.
Orphanet Journal of Rare Diseases|December 28, 2011
A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2KJulien Cassereau, Arnaud Chevrollier, Dominique Bonneau, et al.
Molecular Carcinogenesis|April 7, 2009
Mitochondrial bioenergetic background confers a survival advantage to HepG2 cells in response to chemotherapyDominique Loiseau, Daniel Morvan, Arnaud Chevrollier, et al.
Scientific Reports|August 1, 2025
Deep-learning model for embryo selection using time-lapse imaging of matched high-quality embryosLisa Boucret, Floris Chabrun, Magalie Boguenet, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
Pediatrics|September 2, 2016
Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase DeficiencyIsabelle Signolet, Rachel Chenouard, Florine Oca, et al.
Pageof 25