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238 results
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Deleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.
Kaneb HM, Folkmann AW, Belzil VV, Jao LE, Leblond CS, Girard SL, Daoud H, Noreau A, Rochefort D, Hince P, Szuto A, Levert A, Vidal S, André-Guimont C, Camu W, Bouchard JP, Dupré N, Rouleau GA, Wente SR, Dion PA. Kaneb HM, et al. Among authors: bouchard jp. Hum Mol Genet. 2015 Mar 1;24(5):1363-73. doi: 10.1093/hmg/ddu545. Epub 2014 Oct 24. Hum Mol Genet. 2015. PMID: 25343993 Free PMC article.
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, Rouleau GA. Leblond CS, et al. Among authors: bouchard jp. Neurobiol Aging. 2016 Jan;37:209.e17-209.e21. doi: 10.1016/j.neurobiolaging.2015.09.013. Epub 2015 Sep 28. Neurobiol Aging. 2016. PMID: 26493020
Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Belzil VV, Daoud H, St-Onge J, Desjarlais A, Bouchard JP, Dupre N, Lacomblez L, Salachas F, Pradat PF, Meininger V, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Amyotroph Lateral Scler. 2011 Mar;12(2):113-7. doi: 10.3109/17482968.2010.536840. Epub 2011 Jan 24. Amyotroph Lateral Scler. 2011. PMID: 21261515
Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.
Belzil VV, André-Guimont C, Atallah MR, Daoud H, Dupré N, Bouchard JP, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Neurobiol Aging. 2012 Aug;33(8):1845.e7-9. doi: 10.1016/j.neurobiolaging.2012.01.011. Epub 2012 Feb 22. Neurobiol Aging. 2012. PMID: 22361451
Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.
Belzil VV, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA. Belzil VV, et al. Among authors: bouchard jp. Neurobiol Aging. 2011 Mar;32(3):555.e13-4. doi: 10.1016/j.neurobiolaging.2010.10.001. Epub 2010 Nov 11. Neurobiol Aging. 2011. PMID: 21074290
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. Among authors: bouchard jp. 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.
50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis.
Broom WJ, Greenway M, Sadri-Vakili G, Russ C, Auwarter KE, Glajch KE, Dupre N, Swingler RJ, Purcell S, Hayward C, Sapp PC, McKenna-Yasek D, Valdmanis PN, Bouchard JP, Meininger V, Hosler BA, Glass JD, Polack M, Rouleau GA, Cha JH, Hardiman O, Brown RH Jr. Broom WJ, et al. Among authors: bouchard jp. Amyotroph Lateral Scler. 2008 Aug;9(4):229-37. doi: 10.1080/17482960802103107. Amyotroph Lateral Scler. 2008. PMID: 18608091
238 results