Publications | Cervo Brain Research Centre

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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.

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.

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.

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

L. Davidovic, Huot, M. - E., and Khandjian, E. W., “Lost once, the Fragile X Mental Retardation protein is now back onto brain polyribosomes.”, RNA Biol, vol. 2, no. 1, pp. 1-3, 2005.

M. - E. Huot, Bisson, N., Davidovic, L., Mazroui, R., Labelle, Y., Moss, T., and Khandjian, E. W., “The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis.”, Mol Biol Cell, vol. 16, no. 9, pp. 4350-61, 2005.

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.

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