A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K

Por Cassereau, Julien, Chevrollier, Arnaud, Bonneau, Dominique, Verny, Christophe, Procaccio, Vincent, Reynier, Pascal, Ferré, Marc
Publicado em 2011

Increase of mitochondrial DNA content and transcripts in early bovine embryogenesis associated with upregulation of mtTFA and NRF1 transcription factors

Por May-Panloup, Pascale, Vignon, Xavier, Chrétien, Marie-Françoise, Heyman, Yvan, Tamassia, Manoel, Malthièry, Yves, Reynier, Pascal
Publicado em 2005

How Can a Ketogenic Diet Improve Motor Function?

Por Veyrat-Durebex, Charlotte, Reynier, Pascal, Procaccio, Vincent, Hergesheimer, Rudolf, Corcia, Philippe, Andres, Christian R., Blasco, Hélène
Publicado no Front Mol Neurosci (2018)

Dominant optic atrophy

Por Lenaers, Guy, Hamel, Christian, Delettre, Cécile, Amati-Bonneau, Patrizia, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, Milea, Dan
Publicado em 2012

Early compaction at day 3 may be a useful additional criterion for embryo transfer

Por Le Cruguel, Sébastien, Ferré-L’Hôtellier, Véronique, Morinière, Catherine, Lemerle, Sophie, Reynier, Pascal, Descamps, Philippe, May-Panloup, Pascale
Publicado em 2013

OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background

Por Pierron, Denis, Ferré, Marc, Rocher, Christophe, Chevrollier, Arnaud, Murail, Pascal, Thoraval, Didier, Amati-Bonneau, Patrizia, Reynier, Pascal, Letellier, Thierry
Publicado em 2009

Is ABCC6 a genuine mitochondrial protein?

Por Ferré, Marc, Reynier, Pascal, Chevrollier, Arnaud, Prunier-Mirebeau, Delphine, Lefthériotis, Georges, Henrion, Daniel, Bonneau, Dominique, Procaccio, Vincent, Martin, Ludovic
Publicado em 2013

Metabolomic Approach in STEMI-Patients Undergoing Left Ventricular Remodeling

Por Garcia, Gabriel, Chao de la Barca, Juan Manuel, Mirebeau-Prunier, Delphine, Reynier, Pascal, Furber, Alain, Prunier, Fabrice, Bière, Loïc
Publicado no Int J Mol Sci (2019)

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

Loss of functional OPA1 unbalances redox state: implications in dominant optic atrophy pathogenesis

Por Millet, Aurélie M. C., Bertholet, Ambre M., Daloyau, Marlène, Reynier, Pascal, Galinier, Anne, Devin, Anne, Wissinguer, Bernd, Belenguer, Pascale, Davezac, Noélie
Publicado no Ann Clin Transl Neurol (2016)

Endometriosis Lowers the Cumulative Live Birth Rates in IVF by Decreasing the Number of Embryos but Not Their Quality

Por Boucret, Lisa, Bouet, Pierre-Emmanuel, Riou, Jérémie, Legendre, Guillaume, Delbos, Léa, Hachem, Hady El, Descamps, Philippe, Reynier, Pascal, May-Panloup, Pascale
Publicado no J Clin Med (2020)

Bioinformatics Tools and Databases to Assess the Pathogenicity of Mitochondrial DNA Variants in the Field of Next Generation Sequencing

Por Bris, Céline, Goudenege, David, Desquiret-Dumas, Valérie, Charif, Majida, Colin, Estelle, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy, Reynier, Pascal, Procaccio, Vincent
Publicado no Front Genet (2018)

Are zona pellucida genes involved in recurrent oocyte lysis observed during in vitro fertilization?

Por Ferré, Marc, Amati-Bonneau, Patrizia, Morinière, Catherine, Ferré-L’Hôtellier, Véronique, Lemerle, Sophie, Przyrowski, Daniel, Procaccio, Vincent, Descamps, Philippe, Reynier, Pascal, May-Panloup, Pascale
Publicado em 2013

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

Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics

Por de la Barca, Juan Manuel Chao, Huang, Nuan-Ting, Jiao, Haihan, Tessier, Lydie, Gadras, Cédric, Simard, Gilles, Natoli, Riccardo, Tcherkez, Guillaume, Reynier, Pascal, Valter, Krisztina
Publicado no Metabolomics (2017)

The Metabolomic Signature of Opa1 Deficiency in Rat Primary Cortical Neurons Shows Aspartate/Glutamate Depletion and Phospholipids Remodeling

Por Chao de la Barca, Juan Manuel, Arrázola, Macarena S., Bocca, Cinzia, Arnauné-Pelloquin, Laetitia, Iuliano, Olga, Tcherkez, Guillaume, Lenaers, Guy, Simard, Gilles, Belenguer, Pascale, Reynier, Pascal
Publicado no Sci Rep (2019)

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)

Familial Dysalbuminemic Hyperthyroxinemia: An Underdiagnosed Entity

Por Dieu, Xavier, Bouzamondo, Nathalie, Briet, Claire, Illouz, Frédéric, Moal, Valérie, Boux de Casson, Florence, Bouhours-Nouet, Natacha, Reynier, Pascal, Coutant, Régis, Rodien, Patrice, Mirebeau-Prunier, Delphine
Publicado no J Clin Med (2020)

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)