Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age

Por Eschbach, Judith, Sinniger, Jérome, Bouitbir, Jamal, Fergani, Anissa, Zoll, Joffrey, Geny, Bernard, Rene, Frédérique, Larmet, Yves, Baloh, Robert H., Harms, Matthew B., Shy, Michael E., Messadeq, Nadia, Weydt, Patrick, Loeffler, Jean-Philippe, Ludolph, Albert C., Dupuis, Luc
Publicado em 2013

Low dietary protein content alleviates motor symptoms in mice with mutant dynactin/dynein-mediated neurodegeneration

Por Wiesner, Diana, Sinniger, Jérome, Henriques, Alexandre, Dieterlé, Stéphane, Müller, Hans-Peter, Rasche, Volker, Ferger, Boris, Dirrig-Grosch, Sylvie, Soylu-Kucharz, Rana, Petersén, Asa, Walther, Paul, Linkus, Birgit, Kassubek, Jan, Wong, Philip C., Ludolph, Albert C., Dupuis, Luc
Publicado no Hum Mol Genet (2015)

Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis

Por Scekic-Zahirovic, Jelena, Oussini, Hajer El, Mersmann, Sina, Drenner, Kevin, Wagner, Marina, Sun, Ying, Allmeroth, Kira, Dieterlé, Stéphane, Sinniger, Jérôme, Dirrig-Grosch, Sylvie, René, Frédérique, Dormann, Dorothee, Haass, Christian, Ludolph, Albert C., Lagier-Tourenne, Clotilde, Storkebaum, Erik, Dupuis, Luc
Publicado no Acta Neuropathol (2017)

Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss

Por Scekic‐Zahirovic, Jelena, Sendscheid, Oliver, El Oussini, Hajer, Jambeau, Mélanie, Sun, Ying, Mersmann, Sina, Wagner, Marina, Dieterlé, Stéphane, Sinniger, Jérome, Dirrig‐Grosch, Sylvie, Drenner, Kevin, Birling, Marie‐Christine, Qiu, Jinsong, Zhou, Yu, Li, Hairi, Fu, Xiang‐Dong, Rouaux, Caroline, Shelkovnikova, Tatyana, Witting, Anke, Ludolph, Albert C, Kiefer, Friedemann, Storkebaum, Erik, Lagier‐Tourenne, Clotilde, Dupuis, Luc
Publicado no EMBO J (2016)