J. Sinniger

发表

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

Y. Larmet, A. Ludolph, M. Shy, 2013, Neurobiology of Disease.

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

Ying Sun, A. Ludolph, C. Haass, 2017, Acta Neuropathologica.

Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis.

V. Meininger, G. Rouleau, P. Drapeau, 2013, Human molecular genetics.

Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis

P. Wong, L. H. van den Berg, J. Veldink, 2016, Acta Neuropathologica.

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

Xiang-Dong Fu, Hai-Ri Li, A. Ludolph, 2016, The EMBO journal.

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

P. Wong, V. Rasche, J. Kassubek, 2015, Human molecular genetics.

Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis.

J. Dreyhaupt, J. Kassubek, A. Ludolph, 2016, Brain : a journal of neurology.

Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis

P. Wong, L. H. van den Berg, J. Veldink, 2016, Acta Neuropathologica.

Loss of hypothalamic MCH decreases food intake in amyotrophic lateral sclerosis

D. Thal, S. Kuwabara, K. Arai, 2023, Acta Neuropathologica.

Degeneration of serotonin neurons triggers spasticity in amyotrophic lateral sclerosis

C. Rouaux, L. Dupuis, S. Dirrig‐Grosch, 2017, Annals of neurology.

H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating

S. Brun, O. Taleb, B. Ludes, 2021, International journal of molecular sciences.

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

P. Wong, V. Rasche, J. Kassubek, 2015, Human Molecular Genetics.

Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis.

J. Dreyhaupt, J. Kassubek, A. Ludolph, 2016, Brain : a journal of neurology.

Cortical hyperexcitability in mouse models and patients with amyotrophic lateral sclerosis is linked to noradrenaline deficiency

V. Marchand-Pauvert, C. Rouaux, Y. Goumon, 2024, Science Translational Medicine.