Wolfram syndrome: MAMs’ connection?

Por Delprat, Benjamin, Maurice, Tangui, Delettre, Cécile
Publicado no Cell Death Dis (2018)

Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus

Por Delettre, Cécile, Lenaers, Guy, Belenguer, Pascale, Hamel, Christian P
Publicado em 2003

Impairment of Visual Function and Retinal ER Stress Activation in Wfs1-Deficient Mice

Por Bonnet Wersinger, Delphine, Benkafadar, Nesrine, Jagodzinska, Jolanta, Hamel, Christian, Tanizawa, Yukio, Lenaers, Guy, Delettre, Cécile
Publicado em 2014

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo

Por Jagodzinska, Jolanta, Sarzi, Emmanuelle, Cavalier, Mélanie, Seveno, Marie, Baecker, Volker, Hamel, Christian, Péquignot, Marie, Delettre, Cecile
Publicado no J Vis Exp (2017)

Dominant optic atrophy

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

OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model

Por Sarzi, Emmanuelle, Seveno, Marie, Piro-Mégy, Camille, Elzière, Lucie, Quilès, Mélanie, Péquignot, Marie, Müller, Agnès, Hamel, Christian P., Lenaers, Guy, Delettre, Cécile
Publicado no Sci Rep (2018)

ACO2 mutations: A novel phenotype associating severe optic atrophy and spastic paraplegia

Por Marelli, Cecilia, Hamel, Christian, Quiles, Melanie, Carlander, Bertrand, Larrieu, Lise, Delettre, Cecile, Sarzi, Emmanuelle, Chretien, Dominique, Rustin, Pierre, Koenig, Michel, Guissart, Claire
Publicado no Neurol Genet (2018)

OPA1 links human mitochondrial genome maintenance to mtDNA replication and distribution

Por Elachouri, Ghizlane, Vidoni, Sara, Zanna, Claudia, Pattyn, Alexandre, Boukhaddaoui, Hassan, Gaget, Karen, Yu-Wai-Man, Patrick, Gasparre, Giuseppe, Sarzi, Emmanuelle, Delettre, Cécile, Olichon, Aurélien, Loiseau, Dominique, Reynier, Pascal, Chinnery, Patrick F., Rotig, Agnès, Carelli, Valerio, Hamel, Christian P., Rugolo, Michela, Lenaers, Guy
Publicado em 2011

Mitochondrial Complex I activity signals antioxidant response through ERK5

Por Khan, Abrar Ul Haq, Allende-Vega, Nerea, Gitenay, Delphine, Garaude, Johan, Vo, Dang-Nghiem, Belkhala, Sana, Gerbal-Chaloin, Sabine, Gondeau, Claire, Daujat-Chavanieu, Martine, Delettre, Cécile, Orecchioni, Stefania, Talarico, Giovanna, Bertolini, Francesco, Anel, Alberto, Cuezva, José M., Enriquez, Jose A., Cartron, Guillaume, Lecellier, Charles-Henri, Hernandez, Javier, Villalba, Martin
Publicado no Sci Rep (2018)

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)