A yeast-based screening assay identifies repurposed drugs that suppress mitochondrial fusion and mtDNA maintenance defects

por Delerue, Thomas, Tribouillard-Tanvier, Déborah, Daloyau, Marlène, Khosrobakhsh, Farnoosh, Emorine, Laurent Jean, Friocourt, Gaëlle, Belenguer, Pascale, Blondel, Marc, Arnauné-Pelloquin, Laetitia
Publicado 2019

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 2019

Mitochondrial OPA1 Deficiency Is Associated to Reversible Defects in Spatial Memory Related to Adult Neurogenesis in Mice

por Andraini, Trinovita, Moulédous, Lionel, Petsophonsakul, Petnoi, Florian, Cédrick, Gauzin, Sébastien, Botella-Daloyau, Marlène, Arrázola, Macarena, Nikolla, Kamela, Philip, Adam, Leydier, Alice, Marque, Manon, Arnauné-Pelloquin, Laetitia, Belenguer, Pascale, Rampon, Claire, Miquel, Marie-Christine
Publicado 2023