Reply from Naïg Gueguen, Louis Lefaucheur and Patrick Herpin

Por Gueguen, Naïg, Lefaucheur, Louis, Herpin, Patrick
Publicado em 2005

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

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

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

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

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

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

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

Por 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
Publicado em 2009

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

Por 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
Publicado em 2012

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

Por 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
Publicado no PLoS One (2015)

Autophagy controls the pathogenicity of OPA1 mutations in dominant optic atrophy

Por 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
Publicado no J Cell Mol Med (2017)

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

Por 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
Publicado no Neurol Genet (2017)

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

Por 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
Publicado em 2009

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

Por 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
Publicado em 2011

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

Por 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
Publicado em 2013

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

Por 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
Publicado no Int J Mol Sci (2020)

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

Por 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
Publicado no Am J Hum Genet (2014)

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

Por 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
Publicado no Neurol Genet (2020)

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

Por 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
Publicado no Am J Hum Genet (2015)

Recessive Mutations in RTN4IP1 Cause Isolated and Syndromic Optic Neuropathies

Por 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
Publicado no Am J Hum Genet (2015)