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Filtres: Author is Gros-Louis, François [Enlever les filtres]

2018

Paré B, Lehmann M, Beaudin M, Nordström U, Saikali S, J-P Julien, Gilthorpe JD, Marklund SL, Cashman NR, Andersen PM, Forsberg K, Dupré N, Gould P, Brännström T, Gros-Louis F. Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis. Sci Rep. 2018;8(1):14223.

2016

Ohta Y, Soucy G, Phaneuf D, Audet J-N, Gros-Louis F, Rouleau GA, Blasco H, Corcia P, Andersen PM, Nordin F, Yamashita T, Abe K, J-P Julien. Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. Hum Mol Genet. 2016.

Ohta Y, Soucy G, Phaneuf D, Audet J-N, Gros-Louis F, Rouleau GA, Blasco H, Corcia P, Andersen PM, Nordin F, Yamashita T, Abe K, J-P Julien. Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. Hum Mol Genet. 2016;25(21):4771-4786.

2013

Saxena S, Roselli F, Singh K, Leptien K, J-P Julien, Gros-Louis F, Caroni P. Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival. Neuron. 2013;80(1):80-96.

2010

Gros-Louis F, Soucy G, Larivière R, J-P Julien. 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. 2010;113(5):1188-99.

Bosco DA, Morfini G, N Karabacak M, Song Y, Gros-Louis F, Pasinelli P, Goolsby H, Fontaine BA, Lemay N, McKenna-Yasek D, Frosch MP, Agar JN, J-P Julien, Brady ST, Brown RH. Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS. Nat Neurosci. 2010;13(11):1396-403.

2009

Gros-Louis F, Andersen PM, Dupré N, Urushitani M, Dion P, Souchon F, D'Amour M, Camu W, Meininger V, Bouchard J-P, Rouleau GA, J-P Julien. Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis. Proc Natl Acad Sci USA. 2009;106(51):21777-82.

2008

Gros-Louis F, Kriz J, Kabashi E, McDearmid J, Millecamps S, Urushitani M, Lin L, Dion P, Zhu Q, Drapeau P, J-P Julien, Rouleau GA. Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish. Hum Mol Genet. 2008;17(17):2691-702.

2005

Millecamps S, Gentil BJ, Gros-Louis F, Rouleau G, J-P Julien. Alsin is partially associated with centrosome in human cells. Biochim Biophys Acta. 2005;1745(1):84-100.

2004

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard J-P, Meininger V, Rouleau GA, J-P Julien. A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis. J Biol Chem. 2004;279(44):45951-6.

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© Gouvernement du Québec, 2018