Sylvie Dirrig‐Grosch

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

Jelena Scekic‐Zahirovic, Oliver Sendscheid, Hajer El Oussini et al. · The EMBO Journal · 2016 · 242 citations · Full text

Life Sciences, Genetics, Neuroscience +17

A metabolic switch toward lipid use in glycolytic muscle is an early pathologic event in a mouse model of amyotrophic lateral sclerosis

Lavinia Palamiuc, A. Schlagowski, Shyuan T. Ngo et al. · EMBO Molecular Medicine · 2015 · 229 citations · Full text

Life Sciences, Biochemistry, Neuroscience +17

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

Jelena Scekic‐Zahirovic, Hajer El Oussini, Sina Mersmann et al. · Acta Neuropathologica · 2017 · 135 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Transmembrane Peptides as Inhibitors of ErbB Receptor Signaling

Amar Bennasroune, M Ficková, Anne Gardin et al. · Molecular Biology of the Cell · 2004 · 111 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

Amyotrophic lateral sclerosis and denervation alter sphingolipids and up-regulate glucosylceramide synthase

Alexandre Henriques, Vincent Croixmarie, David A. Priestman et al. · Human Molecular Genetics · 2015 · 94 citations · Full text

Life Sciences, Neurology, Neuroscience +17