Publications | Cervo Brain Research Centre

Export 13 results:

Filters: Author is Tremblay, Sandra [Clear All Filters]

2016

R. El Fatimy, Davidovic, L., Tremblay, S., Jaglin, X., Dury, A., Robert, C., De Koninck, P., and Khandjian, E. W., “Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.”, PLoS Genet, vol. 12, no. 7, p. e1006192, 2016.

2013

A. Y. Dury, Fatimy, R. El, Tremblay, S., Rose, T. M., Côté, J., De Koninck, P., and Khandjian, E. W., “Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.”, PLoS Genet, vol. 9, no. 10, p. e1003890, 2013.

2012

R. El Fatimy, Tremblay, S., Dury, A. Y., Solomon, S., De Koninck, P., Schrader, J. W., and Khandjian, E. W., “Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].”, PLoS One, vol. 7, no. 6, p. e39338, 2012.

2011

D. Cook, Sanchez-Carbente, Mdel Rayo, Lachance, C., Radzioch, D., Tremblay, S., Khandjian, E. W., DesGroseillers, L., and Murai, K. K., “Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus.”, PLoS One, vol. 6, no. 10, p. e26120, 2011.

2007

L. Davidovic, Jaglin, X. H., Lepagnol-Bestel, A. - M., Tremblay, S., Simonneau, M., Bardoni, B., and Khandjian, E. W., “The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.”, Hum Mol Genet, vol. 16, no. 24, pp. 3047-58, 2007.

E. Bechara, Davidovic, L., Melko, M., Bensaid, M., Tremblay, S., Grosgeorge, J., Khandjian, E. W., Lalli, E., and Bardoni, B., “Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure.”, Nucleic Acids Res, vol. 35, no. 1, pp. 299-306, 2007.

2006

I. Plante, Davidovic, L., Ouellet, D. L., Gobeil, L. - A., Tremblay, S., Khandjian, E. W., and Provost, P., “Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs.”, J Biomed Biotechnol, vol. 2006, no. 4, p. 64347, 2006.

L. Davidovic, Tremblay, S., Gravel, M., De Koninck, P., and Khandjian, E. W., “[The fragile X syndrome: one protein missing and 1001 disoriented mRNAs].”, Med Sci (Paris), vol. 22, no. 1, pp. 41-6, 2006.

L. Davidovic, Bechara, E., Gravel, M., Jaglin, X. H., Tremblay, S., Sík, A., Bardoni, B., and Khandjian, E. W., “The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.”, Hum Mol Genet, vol. 15, no. 9, pp. 1525-38, 2006.

2004

E. W. Khandjian, Huot, M. - E., Tremblay, S., Davidovic, L., Mazroui, R., and Bardoni, B., “Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.”, Proc Natl Acad Sci U S A, vol. 101, no. 36, pp. 13357-62, 2004.

C. Gabus, Mazroui, R., Tremblay, S., Khandjian, E. W., and Darlix, J. - L., “The fragile X mental retardation protein has nucleic acid chaperone properties.”, Nucleic Acids Res, vol. 32, no. 7, pp. 2129-37, 2004.

2003

R. Mazroui, Huot, M. - E., Tremblay, S., Boilard, N., Labelle, Y., and Khandjian, E. W., “Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.”, Hum Mol Genet, vol. 12, no. 23, pp. 3087-96, 2003.

2002

R. Mazroui, Huot, M. - E., Tremblay, S., Filion, C., Labelle, Y., and Khandjian, E. W., “Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.”, Hum Mol Genet, vol. 11, no. 24, pp. 3007-17, 2002.

Funding / Support / Partners

© Gouvernement du Québec