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2019
A. Leboucher, Pisani, D. F., Martinez-Gili, L., Chilloux, J., Bermudez-Martin, P., Van Dijck, A., Ganief, T., Macek, B., Becker, J. A. J., Le Merrer, J., R Kooy, F., Amri, E. - Z., Khandjian, E. W., Dumas, M. - E., and Davidovic, L., “The translational regulator FMRP controls lipid and glucose metabolism in mice and humans.”, Mol Metab, vol. 21, pp. 22-35, 2019.
2017
P. Adjibade, St-Sauveur, V. Grenier, Bergeman, J., Huot, M. - E., Khandjian, E. W., and Mazroui, R., “DDX3 regulates endoplasmic reticulum stress-induced ATF4 expression.”, Sci Rep, vol. 7, no. 1, p. 13832, 2017.
2016
A. D. Macaulay, Gilbert, I., Scantland, S., Fournier, E., Ashkar, F., Bastien, A., Saadi, H. A. Shojaei, Gagné, D., Sirard, M. - A., Khandjian, E. W., Richard, F. J., Hyttel, P., and Robert, C., “Cumulus Cell Transcripts Transit to the Bovine Oocyte in Preparation for Maturation.”, Biol Reprod, vol. 94, no. 1, p. 16, 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.
2015
P. Adjibade, St-Sauveur, V. Grenier, Huberdeau, M. Quevillon, Fournier, M. - J., Savard, A., Coudert, L., Khandjian, E. W., and Mazroui, R., “Sorafenib, a multikinase inhibitor, induces formation of stress granules in hepatocarcinoma cells.”, Oncotarget, vol. 6, no. 41, pp. 43927-43, 2015.
2014
A. D. Macaulay, Gilbert, I., Caballero, J., Barreto, R., Fournier, E., Tossou, P., Sirard, M. - A., Clarke, H. J., Khandjian, E. W., Richard, F. J., Hyttel, P., and Robert, C., “The gametic synapse: RNA transfer to the bovine oocyte.”, Biol Reprod, vol. 91, no. 4, p. 90, 2014.
M. Taha Moutaoufik, Fatimy, R. El, Nassour, H., Gareau, C., Lang, J., Tanguay, R. M., Mazroui, R., and Khandjian, E. W., “UVC-induced stress granules in mammalian cells.”, PLoS One, vol. 9, no. 11, p. e112742, 2014.
2013
G. Sanchez, Dury, A. Y., Murray, L. M., Biondi, O., Tadesse, H., Fatimy, R. El, Kothary, R., Charbonnier, F., Khandjian, E. W., and Côté, J., “A novel function for the survival motoneuron protein as a translational regulator.”, Hum Mol Genet, vol. 22, no. 4, pp. 668-84, 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.
M. - E. Huot, Bisson, N., Moss, T., and Khandjian, E. W., “Manipulating the fragile X mental retardation proteins in the frog.”, Results Probl Cell Differ, vol. 54, pp. 165-79, 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.
S. Scantland, Grenon, J. - P., Desrochers, M. - H., Sirard, M. - A., Khandjian, E. W., and Robert, C., “Method to isolate polyribosomal mRNA from scarce samples such as mammalian oocytes and early embryos.”, BMC Dev Biol, vol. 11, p. 8, 2011.
2009
E. G. Bechara, Didiot, M. Cecile, Melko, M., Davidovic, L., Bensaid, M., Martin, P., Castets, M., Pognonec, P., Khandjian, E. W., Moine, H., and Bardoni, B., “A novel function for fragile X mental retardation protein in translational activation.”, PLoS Biol, vol. 7, no. 1, p. e16, 2009.
2008
A. Iacoangeli, Rozhdestvensky, T. S., Dolzhanskaya, N., Tournier, B., Schütt, J., Brosius, J., Denman, R. B., Khandjian, E. W., Kindler, S., and Tiedge, H., “On BC1 RNA and the fragile X mental retardation protein.”, Proc Natl Acad Sci U S A, vol. 105, no. 2, pp. 734-9, 2008.
A. Iacoangeli, Rozhdestvensky, T. S., Dolzhanskaya, N., Tournier, B., Schütt, J., Brosius, J., Denman, R. B., Khandjian, E. W., Kindler, S., and Tiedge, H., “Reply to Bagni: On BC1 RNA and the fragile X mental retardation protein.”, Proc Natl Acad Sci U S A, vol. 105, no. 22, p. E29, 2008.
K. E. Lukong, Chang, K. -wei, Khandjian, E. W., and Richard, S., “RNA-binding proteins in human genetic disease.”, Trends Genet, vol. 24, no. 8, pp. 416-25, 2008.
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.
B. Bardoni, Davidovic, L., Bensaid, M., and Khandjian, E. W., “The fragile X syndrome: exploring its molecular basis and seeking a treatment.”, Expert Rev Mol Med, vol. 8, no. 8, pp. 1-16, 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.
2005
R. Ivanyi-Nagy, Davidovic, L., Khandjian, E. W., and Darlix, J. - L., “Disordered RNA chaperone proteins: from functions to disease.”, Cell Mol Life Sci, vol. 62, no. 13, pp. 1409-17, 2005.
M. Castets, Schaeffer, C., Bechara, E., Schenck, A., Khandjian, E. W., Luche, S., Moine, H., Rabilloud, T., Mandel, J. - L., and Bardoni, B., “FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.”, Hum Mol Genet, vol. 14, no. 6, pp. 835-44, 2005.

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