Tremblay S - Search Results

1

Genetic testing for amyotrophic lateral sclerosis in Canada - an assessment of current practices.

Salmon K, Anoja N, Breiner A, Chum M, Dionne A, Dupré N, Fiander A, Fok D, Ghavanini A, Gosselin S, Izenberg A, Johnston W, Kalra S, Matte G, Melanson M, O'Connell C, Ritsma B, Schellenberg K, Shoesmith C, Tremblay S, Williams H, Genge A. Salmon K, et al. Among authors: tremblay s. Amyotroph Lateral Scler Frontotemporal Degener. 2022 May;23(3-4):305-312. doi: 10.1080/21678421.2021.1980890. Epub 2021 Sep 27. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34569363

2

Cook D, Sanchez-Carbente Mdel R, Lachance C, Radzioch D, Tremblay S, Khandjian EW, DesGroseillers L, Murai KK. Cook D, et al. Among authors: tremblay s. PLoS One. 2011;6(10):e26120. doi: 10.1371/journal.pone.0026120. Epub 2011 Oct 11. PLoS One. 2011. PMID: 22022532 Free PMC article.

3

Mapping of quantitative trait loci (QTL) of differential stress gene expression in rat recombinant inbred strains.

Dumas P, Sun Y, Corbeil G, Tremblay S, Pausova Z, Kren V, Krenova D, Pravenec M, Hamet P, Tremblay J. Dumas P, et al. Among authors: tremblay s, tremblay j. J Hypertens. 2000 May;18(5):545-51. doi: 10.1097/00004872-200018050-00006. J Hypertens. 2000. PMID: 10826556

4

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.

Mazroui R, Huot ME, Tremblay S, Filion C, Labelle Y, Khandjian EW. Mazroui R, et al. Among authors: tremblay s. Hum Mol Genet. 2002 Nov 15;11(24):3007-17. doi: 10.1093/hmg/11.24.3007. Hum Mol Genet. 2002. PMID: 12417522

5

Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.

Mazroui R, Huot ME, Tremblay S, Boilard N, Labelle Y, Khandjian EW. Mazroui R, et al. Among authors: tremblay s. Hum Mol Genet. 2003 Dec 1;12(23):3087-96. doi: 10.1093/hmg/ddg335. Epub 2003 Oct 7. Hum Mol Genet. 2003. PMID: 14532325

6

Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.

Khandjian EW, Huot ME, Tremblay S, Davidovic L, Mazroui R, Bardoni B. Khandjian EW, et al. Among authors: tremblay s. Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13357-62. doi: 10.1073/pnas.0405398101. Epub 2004 Aug 25. Proc Natl Acad Sci U S A. 2004. PMID: 15329415 Free PMC article.

7

The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.

Davidovic L, Jaglin XH, Lepagnol-Bestel AM, Tremblay S, Simonneau M, Bardoni B, Khandjian EW. Davidovic L, et al. Among authors: tremblay s. Hum Mol Genet. 2007 Dec 15;16(24):3047-58. doi: 10.1093/hmg/ddm263. Epub 2007 Sep 19. Hum Mol Genet. 2007. PMID: 17881655

8

Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].

El Fatimy R, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, Khandjian EW. El Fatimy R, et al. Among authors: tremblay s. PLoS One. 2012;7(6):e39338. doi: 10.1371/journal.pone.0039338. Epub 2012 Jun 21. PLoS One. 2012. PMID: 22737234 Free PMC article.

9

Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.

Dury AY, El Fatimy R, Tremblay S, Rose TM, Côté J, De Koninck P, Khandjian EW. Dury AY, et al. Among authors: tremblay s. PLoS Genet. 2013 Oct;9(10):e1003890. doi: 10.1371/journal.pgen.1003890. Epub 2013 Oct 31. PLoS Genet. 2013. PMID: 24204304 Free PMC article.

10

Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.

El Fatimy R, Davidovic L, Tremblay S, Jaglin X, Dury A, Robert C, De Koninck P, Khandjian EW. El Fatimy R, et al. Among authors: tremblay s. PLoS Genet. 2016 Jul 27;12(7):e1006192. doi: 10.1371/journal.pgen.1006192. eCollection 2016 Jul. PLoS Genet. 2016. PMID: 27462983 Free PMC article.

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