Publications | Cervo Brain Research Centre

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Filters: Keyword is Ribonucleoproteins [Clear All Filters]

2015

Y. Yue, Castrichini, M., Srivastava, U., Fabris, F., Shah, K., Li, Z., Qu, Y., El-Sherif, N., Zhou, Z., January, C., M Hussain, M., Jiang, X. - C., Sobie, E. A., Wahren-Herlenius, M., Chahine, M., Capecchi, P. - L., Laghi-Pasini, F., Lazzerini, P. - E., and Boutjdir, M., “Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome.”, Circulation, vol. 132, no. 4, pp. 230-40, 2015.

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.

C. F. Sephton, Cenik, B., Cenik, B. Kutluk, Herz, J., and Yu, G., “TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration.”, Biol Chem, vol. 393, no. 7, pp. 589-94, 2012.

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.

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.

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.

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.

1976

E. W. Khandjian and Turian, G., “Release of RNA--DNA-protein complex during differentiation of the water mould Allomyces arbuscula.”, Cell Differ, vol. 5, no. 3, pp. 171-88, 1976.

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