Rouleau GA - Search Results

1

Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family.

Noreau A, La Piana R, Marcoux C; FORGE Canada; Dion PA, Brais B, Bernard G, Rouleau GA. Noreau A, et al. Among authors: rouleau ga. Neurogenetics. 2015 Oct;16(4):315-8. doi: 10.1007/s10048-015-0455-z. Epub 2015 Aug 11. Neurogenetics. 2015. PMID: 26260654

2

Oculopharyngeal muscular dystrophy: What's new?

Codère F, Brais B, Rouleau G, Lafontaine E. Codère F, et al. Orbit. 2001 Dec;20(4):259-266. doi: 10.1076/orbi.20.4.259.2617. Orbit. 2001. PMID: 12045902

3

Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.

Abu-Baker A, Messaed C, Laganiere J, Gaspar C, Brais B, Rouleau GA. Abu-Baker A, et al. Among authors: rouleau ga. Hum Mol Genet. 2003 Oct 15;12(20):2609-23. doi: 10.1093/hmg/ddg293. Epub 2003 Aug 27. Hum Mol Genet. 2003. PMID: 12944420

4

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. Among authors: rouleau ga. Can J Neurol Sci. 2003 Aug;30(3):244-51. doi: 10.1017/s0317167100002675. Can J Neurol Sci. 2003. PMID: 12945950

5

Polymorphism, shared functions and convergent evolution of genes with sequences coding for polyalanine domains.

Lavoie H, Debeane F, Trinh QD, Turcotte JF, Corbeil-Girard LP, Dicaire MJ, Saint-Denis A, Pagé M, Rouleau GA, Brais B. Lavoie H, et al. Among authors: rouleau ga. Hum Mol Genet. 2003 Nov 15;12(22):2967-79. doi: 10.1093/hmg/ddg329. Epub 2003 Sep 30. Hum Mol Genet. 2003. PMID: 14519685

6

TAU mutations are not a predominant cause of frontotemporal dementia in Canadian patients.

Levchenko A, Robitaille Y, Strong MJ, Rouleau GA. Levchenko A, et al. Among authors: rouleau ga. Can J Neurol Sci. 2004 Aug;31(3):363-7. doi: 10.1017/s0317167100003450. Can J Neurol Sci. 2004. PMID: 15376481

7

Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.

Dion P, Shanmugam V, Gaspar C, Messaed C, Meijer I, Toulouse A, Laganiere J, Roussel J, Rochefort D, Laganiere S, Allen C, Karpati G, Bouchard JP, Brais B, Rouleau GA. Dion P, et al. Among authors: rouleau ga. Neurobiol Dis. 2005 Apr;18(3):528-36. doi: 10.1016/j.nbd.2004.09.021. Neurobiol Dis. 2005. PMID: 15755680

8

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. Among authors: rouleau ga. 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

9

Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophy.

Abu-Baker A, Laganiere S, Fan X, Laganiere J, Brais B, Rouleau GA. Abu-Baker A, et al. Among authors: rouleau ga. Traffic. 2005 Sep;6(9):766-79. doi: 10.1111/j.1600-0854.2005.00315.x. Traffic. 2005. PMID: 16101680 Free article.

10

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian population.

Dupré N, Bouchard JP, Brais B, Rouleau GA. Dupré N, et al. Among authors: rouleau ga. Can J Neurol Sci. 2006 May;33(2):149-57. doi: 10.1017/s031716710000490x. Can J Neurol Sci. 2006. PMID: 16736723 Review.

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