Gros-Louis F - Search Results

1

Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis.

Paré B, Lehmann M, Beaudin M, Nordström U, Saikali S, Julien JP, Gilthorpe JD, Marklund SL, Cashman NR, Andersen PM, Forsberg K, Dupré N, Gould P, Brännström T, Gros-Louis F. Paré B, et al. Sci Rep. 2018 Sep 21;8(1):14223. doi: 10.1038/s41598-018-31773-z. Sci Rep. 2018. PMID: 30242181 Free PMC article.

2

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Hand CK, Khoris J, Salachas F, Gros-Louis F, Lopes AA, Mayeux-Portas V, Brewer CG, Brown RH Jr, Meininger V, Camu W, Rouleau GA. Hand CK, et al. Am J Hum Genet. 2002 Jan;70(1):251-6. doi: 10.1086/337945. Epub 2001 Nov 9. Am J Hum Genet. 2002. PMID: 11706389 Free PMC article.

3

A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis.

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard JP, Meininger V, Rouleau GA, Julien JP. Gros-Louis F, et al. J Biol Chem. 2004 Oct 29;279(44):45951-6. doi: 10.1074/jbc.M408139200. Epub 2004 Aug 17. J Biol Chem. 2004. PMID: 15322088 Free article.

4

Alsin is partially associated with centrosome in human cells.

Millecamps S, Gentil BJ, Gros-Louis F, Rouleau G, Julien JP. Millecamps S, et al. Biochim Biophys Acta. 2005 Aug 15;1745(1):84-100. doi: 10.1016/j.bbamcr.2004.12.008. Epub 2005 Jan 19. Biochim Biophys Acta. 2005. PMID: 16085057 Free article.

5

Genetics of familial and sporadic amyotrophic lateral sclerosis.

Gros-Louis F, Gaspar C, Rouleau GA. Gros-Louis F, et al. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):956-72. doi: 10.1016/j.bbadis.2006.01.004. Epub 2006 Feb 10. Biochim Biophys Acta. 2006. PMID: 16503123 Free article. Review.

6

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.

Dupré N, Gros-Louis F, Chrestian N, Verreault S, Brunet D, de Verteuil D, Brais B, Bouchard JP, Rouleau GA. Dupré N, et al. Ann Neurol. 2007 Jul;62(1):93-8. doi: 10.1002/ana.21143. Ann Neurol. 2007. PMID: 17503513

7

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

Gros-Louis F, Kriz J, Kabashi E, McDearmid J, Millecamps S, Urushitani M, Lin L, Dion P, Zhu Q, Drapeau P, Julien JP, Rouleau GA. Gros-Louis F, et al. Hum Mol Genet. 2008 Sep 1;17(17):2691-702. doi: 10.1093/hmg/ddn171. Epub 2008 Jun 16. Hum Mol Genet. 2008. PMID: 18558633

8

Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.

Gros-Louis F, Andersen PM, Dupre N, Urushitani M, Dion P, Souchon F, D'Amour M, Camu W, Meininger V, Bouchard JP, Rouleau GA, Julien JP. Gros-Louis F, et al. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21777-82. doi: 10.1073/pnas.0902174106. Epub 2009 Dec 9. Proc Natl Acad Sci U S A. 2009. PMID: 20007371 Free PMC article.

9

Intracerebroventricular infusion of monoclonal antibody or its derived Fab fragment against misfolded forms of SOD1 mutant delays mortality in a mouse model of ALS.

Gros-Louis F, Soucy G, Larivière R, Julien JP. Gros-Louis F, et al. J Neurochem. 2010 Jun;113(5):1188-99. doi: 10.1111/j.1471-4159.2010.06683.x. Epub 2010 Mar 14. J Neurochem. 2010. PMID: 20345765 Free article.

10

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS.

Bosco DA, Morfini G, Karabacak NM, Song Y, Gros-Louis F, Pasinelli P, Goolsby H, Fontaine BA, Lemay N, McKenna-Yasek D, Frosch MP, Agar JN, Julien JP, Brady ST, Brown RH Jr. Bosco DA, et al. Nat Neurosci. 2010 Nov;13(11):1396-403. doi: 10.1038/nn.2660. Epub 2010 Oct 17. Nat Neurosci. 2010. PMID: 20953194 Free PMC article.

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