1. Research
  2. Publications

Publications

Export 28 results:
Filters: Keyword is Gene Expression Regulation  [Clear All Filters]
2021
C. Ducrot, Bourque, M. - J., Delmas, C. V. L., Racine, A. - S., Bello, D. Guadarrama, Delignat-Lavaud, B., Lycas, M. Domenic, Fallon, A., Michaud-Tardif, C., Nanni, S. Burke, Herborg, F., Gether, U., Nanci, A., Takahashi, H., Parent, M., and Trudeau, L. - E., “Dopaminergic neurons establish a distinctive axonal arbor with a majority of non-synaptic terminals.”, FASEB J, vol. 35, no. 8, p. e21791, 2021.
2017
P. Gosselin-Badaroudine and Chahine, M., “Biophysical characterization of the Varroa destructor NaV1 sodium channel and its affinity for τ-fluvalinate insecticide.”, FASEB J, vol. 31, no. 7, pp. 3066-3071, 2017.
Y. Jiang, Loh, Y. - H. Eddie, Rajarajan, P., Hirayama, T., Liao, W., Kassim, B. S., Javidfar, B., Hartley, B. J., Kleofas, L., Park, R. B., Labonte, B., Ho, S. - M., Chandrasekaran, S., Do, C., Ramirez, B. R., Peter, C. J., W, J. T. C., Safaie, B. M., Morishita, H., Roussos, P., Nestler, E. J., Schaefer, A., Tycko, B., Brennand, K. J., Yagi, T., Shen, L., and Akbarian, S., “The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain.”, Nat Genet, vol. 49, no. 8, pp. 1239-1250, 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.
2015
H. Doucet-Beaupré, Ang, S. - L., and Lévesque, M., “Cell fate determination, neuronal maintenance and disease state: The emerging role of transcription factors Lmx1a and Lmx1b.”, FEBS Lett, vol. 589, no. 24 Pt A, pp. 3727-38, 2015.
2014
M. E. Ward, Taubes, A., Chen, R., Miller, B. L., Sephton, C. F., Gelfand, J. M., Minami, S., Boscardin, J., Martens, L. Herl, Seeley, W. W., Yu, G., Herz, J., Filiano, A. J., Arrant, A. E., Roberson, E. D., Kraft, T. W., Farese, R. V., Green, A., and Gan, L., “Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLD.”, J Exp Med, vol. 211, no. 10, pp. 1937-45, 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.
F. A. Wright, Sullivan, P. F., Brooks, A. I., Zou, F., Sun, W., Xia, K., Madar, V., Jansen, R., Chung, W., Zhou, Y. - H., Abdellaoui, A., Batista, S., Butler, C., Chen, G., Chen, T. - H., D'Ambrosio, D., Gallins, P., Ha, M. Jin, Hottenga, J. Jan, Huang, S., Kattenberg, M., Kochar, J., Middeldorp, C. M., Qu, A., Shabalin, A., Tischfield, J., Todd, L., Tzeng, J. - Y., van Grootheest, G., Vink, J. M., Wang, Q., Wang, W., Wang, W., Willemsen, G., Smit, J. H., de Geus, E. J., Yin, Z., Penninx, B. W. J. H., and Boomsma, D. I., “Heritability and genomics of gene expression in peripheral blood.”, Nat Genet, vol. 46, no. 5, pp. 430-7, 2014.
P. Jourdain, Becq, F., Lengacher, S., Boinot, C., Magistretti, P. J., and Marquet, P., “The human CFTR protein expressed in CHO cells activates aquaporin-3 in a cAMP-dependent pathway: study by digital holographic microscopy.”, J Cell Sci, vol. 127, no. Pt 3, pp. 546-56, 2014.
2013
S. Grade, Weng, Y. C., Snapyan, M., Kriz, J., Malva, J. O., and Saghatelyan, A., “Brain-derived neurotrophic factor promotes vasculature-associated migration of neuronal precursors toward the ischemic striatum.”, PLoS One, vol. 8, no. 1, p. e55039, 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. Flynn, Labrie-Dion, É., Bernier, N., Colicos, M. A., De Koninck, P., and Zamponi, G. W., “Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα.”, PLoS One, vol. 7, no. 7, p. e41185, 2012.
2011
K. V. Danilenko, Plisov, I. L., Cooper, H. M., Wirz-Justice, A., and Hébert, M., “Human cone light sensitivity and melatonin rhythms following 24-hour continuous illumination.”, Chronobiol Int, vol. 28, no. 5, pp. 407-14, 2011.
J. Zhao, O'Leary, M. E., and Chahine, M., “Regulation of Nav1.6 and Nav1.8 peripheral nerve Na+ channels by auxiliary β-subunits.”, J Neurophysiol, vol. 106, no. 2, pp. 608-19, 2011.
2010
J. McLean, Liu, H. - N., Miletic, D., Weng, Y. Cheng, Rogaeva, E., Zinman, L., Kriz, J., and Robertson, J., “Distinct biochemical signatures characterize peripherin isoform expression in both traumatic neuronal injury and motor neuron disease.”, J Neurochem, vol. 114, no. 4, pp. 1177-92, 2010.
S. Takeuchi, Fujiwara, N., Ido, A., Oono, M., Takeuchi, Y., Tateno, M., Suzuki, K., Takahashi, R., Tooyama, I., Taniguchi, N., J-P Julien, and Urushitani, M., “Induction of protective immunity by vaccination with wild-type apo superoxide dismutase 1 in mutant SOD1 transgenic mice.”, J Neuropathol Exp Neurol, vol. 69, no. 10, pp. 1044-56, 2010.
S. Abou Ezzi, Larivière, R., Urushitani, M., and J-P Julien, “Neuronal over-expression of chromogranin A accelerates disease onset in a mouse model of ALS.”, J Neurochem, vol. 115, no. 5, pp. 1102-11, 2010.
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.
T. A. Klempan, Rujescu, D., Mérette, C., Himmelman, C., Sequeira, A., Canetti, L., Fiori, L. M., Schneider, B., Bureau, A., and Turecki, G., “Profiling brain expression of the spermidine/spermine N1-acetyltransferase 1 (SAT1) gene in suicide.”, Am J Med Genet B Neuropsychiatr Genet, vol. 150B, no. 7, pp. 934-43, 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.
2007
S. Millecamps, Gowing, G., Corti, O., Mallet, J., and J-P Julien, “Conditional NF-L transgene expression in mice for in vivo analysis of turnover and transport rate of neurofilaments.”, J Neurosci, vol. 27, no. 18, pp. 4947-56, 2007.
J. Zhao, Ziane, R., Chatelier, A., O'Leary, M. E., and Chahine, M., “Lidocaine promotes the trafficking and functional expression of Na(v)1.8 sodium channels in mammalian cells.”, J Neurophysiol, vol. 98, no. 1, pp. 467-77, 2007.
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
J. Garnon, Lachance, C., Di Marco, S., Hel, Z., Marion, D., Ruiz, M. C., Newkirk, M. M., Khandjian, E. W., and Radzioch, D., “Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level.”, J Biol Chem, vol. 280, no. 7, pp. 5750-63, 2005.

Funding / Support / Partners

logo FRQ-S logo ctrn logo fci logo cihr irsc logo nserc logo MESISentinelle nord