Publications | Cervo Brain Research Centre

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Filters: Keyword is Molecular Sequence Data and Author is E W Khandjian [Clear All Filters]

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.

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

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

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

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.

2000

M. Dubé, Huot, M. E., and Khandjian, E. W., “Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast.”, BMC Genet, vol. 1, p. 4, 2000.

1998

A. Bairam, Frenette, J., Dauphin, C., Carroll, J. L., and Khandjian, E. W., “Expression of dopamine D1-receptor mRNA in the carotid body of adult rabbits, cats and rats.”, Neurosci Res, vol. 31, no. 2, pp. 147-54, 1998.

E. W. Khandjian, Bardoni, B., Corbin, F., Sittler, A., Giroux, S., Heitz, D., Tremblay, S., Pinset, C., Montarras, D., Rousseau, F., and Mandel, J., “Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.”, Hum Mol Genet, vol. 7, no. 13, pp. 2121-8, 1998.

1997

R. Drouin, Angers, M., Dallaire, N., Rose, T. M., Khandjian, E. W., and Rousseau, F., “Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.”, Hum Mol Genet, vol. 6, no. 12, pp. 2051-60, 1997.

1995

F. Rousseau, Rouillard, P., Morel, M. L., Khandjian, E. W., and Morgan, K., “Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.”, Am J Hum Genet, vol. 57, no. 5, pp. 1006-18, 1995.

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