Dion PA - Search Results

1

Identification of rare protein disulfide isomerase gene variants in amyotrophic lateral sclerosis patients.

Gonzalez-Perez P, Woehlbier U, Chian RJ, Sapp P, Rouleau GA, Leblond CS, Daoud H, Dion PA, Landers JE, Hetz C, Brown RH. Gonzalez-Perez P, et al. Among authors: dion pa. Gene. 2015 Jul 25;566(2):158-65. doi: 10.1016/j.gene.2015.04.035. Epub 2015 Apr 22. Gene. 2015. PMID: 25913742 Free PMC article.

2

CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation.

Gaspar C, Jannatipour M, Dion P, Laganière J, Sequeiros J, Brais B, Rouleau GA. Gaspar C, et al. Hum Mol Genet. 2000 Aug 12;9(13):1957-66. doi: 10.1093/hmg/9.13.1957. Hum Mol Genet. 2000. PMID: 10942424

3

PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophy.

Shanmugam V, Dion P, Rochefort D, Laganière J, Brais B, Rouleau GA. Shanmugam V, et al. Ann Neurol. 2000 Nov;48(5):798-802. Ann Neurol. 2000. PMID: 11079546

4

Schwannomin isoform-1 interacts with syntenin via PDZ domains.

Jannatipour M, Dion P, Khan S, Jindal H, Fan X, Laganière J, Chishti AH, Rouleau GA. Jannatipour M, et al. J Biol Chem. 2001 Aug 31;276(35):33093-100. doi: 10.1074/jbc.M105792200. Epub 2001 Jun 29. J Biol Chem. 2001. PMID: 11432873 Free article.

5

Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death.

Fan X, Dion P, Laganiere J, Brais B, Rouleau GA. Fan X, et al. Hum Mol Genet. 2001 Oct 1;10(21):2341-51. doi: 10.1093/hmg/10.21.2341. Hum Mol Genet. 2001. PMID: 11689481

6

HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy.

Fan X, Messaed C, Dion P, Laganiere J, Brais B, Karpati G, Rouleau GA. Fan X, et al. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

7

Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.

Toulouse A, Au-Yeung F, Gaspar C, Roussel J, Dion P, Rouleau GA. Toulouse A, et al. Hum Mol Genet. 2005 Sep 15;14(18):2649-60. doi: 10.1093/hmg/ddi299. Epub 2005 Aug 8. Hum Mol Genet. 2005. PMID: 16087686

8

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

Gros-Louis F, Dupré N, Dion P, Fox MA, Laurent S, Verreault S, Sanes JR, Bouchard JP, Rouleau GA. Gros-Louis F, et al. Nat Genet. 2007 Jan;39(1):80-5. doi: 10.1038/ng1927. Epub 2006 Dec 10. Nat Genet. 2007. PMID: 17159980

9

Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.

Valdmanis PN, Meijer IA, Reynolds A, Lei A, MacLeod P, Schlesinger D, Zatz M, Reid E, Dion PA, Drapeau P, Rouleau GA. Valdmanis PN, et al. Among authors: dion pa. Am J Hum Genet. 2007 Jan;80(1):152-61. doi: 10.1086/510782. Epub 2006 Dec 1. Am J Hum Genet. 2007. PMID: 17160902 Free PMC article.

10

Purification of the NF2 tumor suppressor protein from human erythrocytes.

Jindal HK, Yoshinaga K, Seo PS, Lutchman M, Dion PA, Rouleau GA, Hanada T, Chishti AH. Jindal HK, et al. Among authors: dion pa. Can J Neurol Sci. 2006 Nov;33(4):394-402. doi: 10.1017/s0317167100005357. Can J Neurol Sci. 2006. PMID: 17168165

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