Publications
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Filtres: Author is Gros-Louis, François [Enlever les filtres]
, « Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis. », Sci Rep, vol. 8, nᵒ 1, p. 14223, 2018.
, « Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. », Hum Mol Genet, 2016.
, « Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. », Hum Mol Genet, vol. 25, nᵒ 21, p. 4771-4786, 2016.
, « Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival. », Neuron, vol. 80, nᵒ 1, p. 80-96, 2013.
, « Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS. », J Neurochem, vol. 113, nᵒ 5, p. 1188-99, 2010.
, « Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS. », Nat Neurosci, vol. 13, nᵒ 11, p. 1396-403, 2010.
, « Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis. », Proc Natl Acad Sci U S A, vol. 106, nᵒ 51, p. 21777-82, 2009.
, « Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish. », Hum Mol Genet, vol. 17, nᵒ 17, p. 2691-702, 2008.
, « Alsin is partially associated with centrosome in human cells. », Biochim Biophys Acta, vol. 1745, nᵒ 1, p. 84-100, 2005.
, « A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis. », J Biol Chem, vol. 279, nᵒ 44, p. 45951-6, 2004.
