Reply from Naïg Gueguen, Louis Lefaucheur and Patrick Herpin

le Gueguen, Naïg, Lefaucheur, Louis, Herpin, Patrick
Foilsithe 2005

Iron Deficiency without Anemia Decreases Physical Endurance and Mitochondrial Complex I Activity of Oxidative Skeletal Muscle in the Mouse

le Rineau, Emmanuel, Gueguen, Naïg, Procaccio, Vincent, Geneviève, Franck, Reynier, Pascal, Henrion, Daniel, Lasocki, Sigismond
Foilsithe in Nutrients (2021)

Overexpression of the Mitochondrial T3 Receptor p43 Induces a Shift in Skeletal Muscle Fiber Types

le Casas, François, Pessemesse, Laurence, Grandemange, Stéphanie, Seyer, Pascal, Gueguen, Naïg, Baris, Olivier, Lepourry, Laurence, Cabello, Gérard, Wrutniak-Cabello, Chantal
Foilsithe 2008

Comparison of Spheroids Formed by Rat Glioma Stem Cells and Neural Stem Cells Reveals Differences in Glucose Metabolism and Promising Therapeutic Applications

le Morfouace, Marie, Lalier, Lisenn, Bahut, Muriel, Bonnamain, Virginie, Naveilhan, Philippe, Guette, Catherine, Oliver, Lisa, Gueguen, Naig, Reynier, Pascal, Vallette, Francois M.
Foilsithe 2012

Estrogen-Related Receptor Alpha Modulates Lactate Dehydrogenase Activity in Thyroid Tumors

le Mirebeau-Prunier, Delphine, Le Pennec, Soazig, Jacques, Caroline, Fontaine, Jean-Fred, Gueguen, Naig, Boutet-Bouzamondo, Nathalie, Donnart, Audrey, Malthièry, Yves, Savagner, Frédérique
Foilsithe 2013

Overexpression of the Mitochondrial T3 Receptor Induces Skeletal Muscle Atrophy during Aging

le Casas, François, Pessemesse, Laurence, Grandemange, Stéphanie, Seyer, Pascal, Baris, Olivier, Gueguen, Naïg, Ramonatxo, Christelle, Perrin, Florence, Fouret, Gilles, Lepourry, Laurence, Cabello, Gérard, Wrutniak-Cabello, Chantal
Foilsithe 2009

Metabolically induced heteroplasmy shifting and L-arginine treatment reduce the energetic defect in a neuronal-like model of MELAS

le Desquiret-Dumas, Valerie, Gueguen, Naig, Barth, Magalie, Chevrollier, Arnaud, Hancock, Saege, Wallace, Douglas C, Amati-Bonneau, Patrizia, Henrion, Daniel, Bonneau, Dominique, Reynier, Pascal, Procaccio, Vincent
Foilsithe 2012

Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged Mice

le Gueguen, Naïg, Desquiret-Dumas, Valérie, Leman, Géraldine, Chupin, Stéphanie, Baron, Stéphanie, Nivet-Antoine, Valérie, Vessières, Emilie, Ayer, Audrey, Henrion, Daniel, Lenaers, Guy, Reynier, Pascal, Procaccio, Vincent
Foilsithe in PLoS One (2015)

Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophy

le Kane, Mariame Selma, Alban, Jennifer, Desquiret‐Dumas, Valérie, Gueguen, Naïg, Ishak, Layal, Ferre, Marc, Amati‐Bonneau, Patrizia, Procaccio, Vincent, Bonneau, Dominique, Lenaers, Guy, Reynier, Pascal, Chevrollier, Arnaud
Foilsithe in J Cell Mol Med (2017)

Novel NDUFS4 gene mutation in an atypical late-onset mitochondrial form of multifocal dystonia

le Bris, Celine, Rouaud, Tiphaine, Desquiret-Dumas, Valerie, Gueguen, Naig, Goudenege, David, Barth, Magalie, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Lebre, Anne-Sophie, Procaccio, Vincent
Foilsithe in Neurol Genet (2017)

Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect

le Nochez, Yannick, Arsene, Sophie, Gueguen, Naig, Chevrollier, Arnaud, Ferré, Marc, Guillet, Virginie, Desquiret, Valérie, Toutain, Annick, Bonneau, Dominique, Procaccio, Vincent, Amati-Bonneau, Patrizia, Pisella, Pierre-Jean, Reynier, Pascal
Foilsithe 2009

Idebenone increases mitochondrial complex I activity in fibroblasts from LHON patients while producing contradictory effects on respiration

le Angebault, Claire, Gueguen, Naïg, Desquiret-Dumas, Valérie, Chevrollier, Arnaud, Guillet, Virginie, Verny, Christophe, Cassereau, Julien, Ferre, Marc, Milea, Dan, Amati-Bonneau, Patrizia, Bonneau, Dominique, Procaccio, Vincent, Reynier, Pascal, Loiseau, Dominique
Foilsithe 2011

Resveratrol Induces a Mitochondrial Complex I-dependent Increase in NADH Oxidation Responsible for Sirtuin Activation in Liver Cells

le Desquiret-Dumas, Valérie, Gueguen, Naïg, Leman, Géraldine, Baron, Stéphanie, Nivet-Antoine, Valérie, Chupin, Stéphanie, Chevrollier, Arnaud, Vessières, Emilie, Ayer, Audrey, Ferré, Marc, Bonneau, Dominique, Henrion, Daniel, Reynier, Pascal, Procaccio, Vincent
Foilsithe 2013

Increased Protein S-Glutathionylation in Leber’s Hereditary Optic Neuropathy (LHON)

le Zhou, Lei, Chan, James Chun Yip, Chupin, Stephanie, Gueguen, Naïg, Desquiret-Dumas, Valérie, Koh, Siew Kwan, Li, Jianguo, Gao, Yan, Deng, Lu, Verma, Chandra, Beuerman, Roger W, Chan, Eric Chun Yong, Milea, Dan, Reynier, Pascal
Foilsithe in Int J Mol Sci (2020)

DRP1 haploinsufficiency attenuates cardiac ischemia/reperfusion injuries

le Bouche, Laura, Kamel, Rima, Tamareille, Sophie, Garcia, Gabriel, Villedieu, Camille, Pillot, Bruno, Gueguen, Naïg, Chehaitly, Ahmad, Chao de la Barca, Juan Manuel, Beaumont, Justine, Baetz, Delphine, Ovize, Michel, Sesaki, Hiromi, Henrion, Daniel, Reynier, Pascal, Lenaers, Guy, Prunier, Fabrice, Mirebeau-Prunier, Delphine
Foilsithe in PLoS One (2021)

Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome

le Colin, Estelle, Huynh Cong, Evelyne, Mollet, Géraldine, Guichet, Agnès, Gribouval, Olivier, Arrondel, Christelle, Boyer, Olivia, Daniel, Laurent, Gubler, Marie-Claire, Ekinci, Zelal, Tsimaratos, Michel, Chabrol, Brigitte, Boddaert, Nathalie, Verloes, Alain, Chevrollier, Arnaud, Gueguen, Naig, Desquiret-Dumas, Valérie, Ferré, Marc, Procaccio, Vincent, Richard, Laurence, Funalot, Benoit, Moncla, Anne, Bonneau, Dominique, Antignac, Corinne
Foilsithe in Am J Hum Genet (2014)

Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy

le Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valérie, Leruez, Stéphanie, Colin, Estelle, Meunier, Audrey, Vignal, Catherine, Smirnov, Vasily, Defoort-Dhellemmes, Sabine, Drumare Bouvet, Isabelle, Goizet, Cyril, Votruba, Marcela, Jurkute, Neringa, Yu-Wai-Man, Patrick, Tagliavini, Francesca, Caporali, Leonardo, La Morgia, Chiara, Carelli, Valerio, Procaccio, Vincent, Zanlonghi, Xavier, Meunier, Isabelle, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy
Foilsithe in Neurol Genet (2020)

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

le Angebault, Claire, Guichet, Pierre-Olivier, Talmat-Amar, Yasmina, Charif, Majida, Gerber, Sylvie, Fares-Taie, Lucas, Gueguen, Naig, Halloy, François, Moore, David, Amati-Bonneau, Patrizia, Manes, Gael, Hebrard, Maxime, Bocquet, Béatrice, Quiles, Mélanie, Piro-Mégy, Camille, Teigell, Marisa, Delettre, Cécile, Rossel, Mireille, Meunier, Isabelle, Preising, Markus, Lorenz, Birgit, Carelli, Valerio, Chinnery, Patrick F., Yu-Wai-Man, Patrick, Kaplan, Josseline, Roubertie, Agathe, Barakat, Abdelhamid, Bonneau, Dominique, Reynier, Pascal, Rozet, Jean-Michel, Bomont, Pascale, Hamel, Christian P., Lenaers, Guy
Foilsithe in Am J Hum Genet (2015)

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

le Angebault, Claire, Guichet, Pierre-Olivier, Talmat-Amar, Yasmina, Charif, Majida, Gerber, Sylvie, Fares-Taie, Lucas, Gueguen, Naig, Halloy, François, Moore, David, Amati-Bonneau, Patrizia, Manes, Gael, Hebrard, Maxime, Bocquet, Béatrice, Quiles, Mélanie, Piro-Mégy, Camille, Teigell, Marisa, Delettre, Cécile, Rossel, Mireille, Meunier, Isabelle, Preising, Markus, Lorenz, Birgit, Carelli, Valerio, Chinnery, Patrick F., Yu-Wai-Man, Patrick, Kaplan, Josseline, Roubertie, Agathe, Barakat, Abdelhamid, Bonneau, Dominique, Reynier, Pascal, Rozet, Jean-Michel, Bomont, Pascale, Hamel, Christian P., Lenaers, Guy
Foilsithe in Am J Hum Genet (2015)

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

le Charif, Majida, Gueguen, Naïg, Ferré, Marc, Elkarhat, Zouhair, Khiati, Salim, LeMao, Morgane, Chevrollier, Arnaud, Desquiret-Dumas, Valerie, Goudenège, David, Bris, Céline, Kane, Selma, Alban, Jennifer, Chupin, Stéphanie, Wetterwald, Céline, Caporali, Leonardo, Tagliavini, Francesca, LaMorgia, Chiara, Carbonelli, Michele, Jurkute, Neringa, Barakat, Abdelhamid, Gohier, Philippe, Verny, Christophe, Barth, Magalie, Procaccio, Vincent, Bonneau, Dominique, Zanlonghi, Xavier, Meunier, Isabelle, Weisschuh, Nicole, Schimpf-Linzenbold, Simone, Tonagel, Felix, Kellner, Ulrich, Yu-Wai-Man, Patrick, Carelli, Valerio, Wissinger, Bernd, Amati-Bonneau, Patrizia, Reynier, Pascal, Lenaers, Guy
Foilsithe in Brain Commun (2021)