Suchergebnisse - Yves Larmet
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Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age von Judith Eschbach, Jérôme Sinniger, Jamal Bouitbir, Anissa Fergani, Anna-Isabel Schlagowski, Joffrey Zoll, Bernard Gény, Frédérique René, Yves Larmet, Vincent Marion, Robert H. Baloh, Matthew B. Harms, Michael E. Shy, Nadia Messadeq, Patrick Weydt, Jean‐Philippe Loeffler, Albert C. Ludolph, Luc Dupuis
Veröffentlicht 2013Artigo -
2
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons von Kerstin E. Braunstein, Judith Eschbach, Krisztina Ròna-Vörös, Rana Soylu-Kucharz, Elli Mikrouli, Yves Larmet, Frédérique René, José‐Luis González de Aguilar, Jean Philippe Loeffler, Hans-Peter Müller, Selina Bucher, Thomas Kaulisch, Heiko G. Niessen, Julia Tillmanns, Kristina Fischer, Birgit Schwalenstöcker, Jan Kassubek, Bernd J. Pichler, Detlef Stiller, Åsa Petersén, Albert C. Ludolph, Luc Dupuis
Veröffentlicht 2010Artigo -
3
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis von Hajer El Oussini, Hanna Bayer, Jelena Scekic‐Zahirovic, Pauline Vercruysse, Jérôme Sinniger, Sylvie Dirrig‐Grosch, Stéphane Dieterle, Andoni Echaniz‐Laguna, Yves Larmet, Kathrin Müller, Jochen H. Weishaupt, Dietmar Rudolf Thal, Wouter van Rheenen, Kristel van Eijk, Roland Lawson, Laurent Monassier, Luc Maroteaux, Anne Roumier, Philip C. Wong, Leonard H. van den Berg, Albert C. Ludolph, Jan H. Veldink, Anke Witting, Luc Dupuis
Veröffentlicht 2016Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Gene
Cell biology
Dynein
Genetics
Microtubule
Mutant
Neuroscience
Amyotrophic lateral sclerosis
Atrophy
Axoplasmic transport
Basal ganglia
Biochemistry
Central nervous system
Combinatorics
Disease
Dopamine
Dopaminergic
Downregulation and upregulation
Dynactin
Huntingtin
Immunology
In vitro
Inflammation
Mathematics
Medicine
Microglia
Mitochondrial DNA
Mitochondrial disease
Mitochondrion