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Filters: Keyword is Molecular Sequence Data  [Clear All Filters]
2015
Gosselin-Badaroudine P, Moreau A, Delemotte L, Cens T, Collet C, Rousset M, et al. Characterization of the honeybee AmNaV1 channel and tools to assess the toxicity of insecticides. Sci Rep. 2015;5:12475.
Moreau A, Gosselin-Badaroudine P, Delemotte L, Klein ML, Chahine M. Gating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy. J Gen Physiol. 2015;145(2):93-106.
2014
Poulin H, Bruhova I, Timour Q, Thériault O, Beaulieu J-, Frassati D, et al. Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics. Mol Pharmacol. 2014;86(4):378-89.
2013
Jeyaraju DV, Sood A, Laforce-Lavoie A, Pellegrini L. Rhomboid proteases in mitochondria and plastids: keeping organelles in shape. Biochim Biophys Acta. 2013;1833(2):371-80.
2012
Fatimy RE, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, et al. Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. PLoS ONE. 2012;7(6):e39338.
Gosselin-Badaroudine P, Delemotte L, Moreau A, Klein ML, Chahine M. Gating pore currents and the resting state of Nav1.4 voltage sensor domains. Proc Natl Acad Sci USA. 2012;109(47):19250-5.
Huot M-, Bisson N, Moss T, Khandjian EW. Manipulating the fragile X mental retardation proteins in the frog. Results Probl Cell Differ. 2012;54:165-79.
Gosselin-Badaroudine P, Keller DI, Huang H, Pouliot V, Chatelier A, Osswald S, et al. A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. PLoS ONE. 2012;7(5):e38331.
2011
Dewey CM, Cenik B, Sephton CF, Dries DR, Mayer P, Good SK, et al. TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor. Mol Cell Biol. 2011;31(5):1098-108.
2010
Audet J-, Gowing G, J-P Julien. Wild-type human SOD1 overexpression does not accelerate motor neuron disease in mice expressing murine Sod1 G86R. Neurobiol Dis. 2010;40(1):245-50.
2007
Bechara E, Davidovic L, Melko M, Bensaid M, Tremblay S, Grosgeorge J, et al. Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure. Nucleic Acids Res. 2007;35(1):299-306.
2006
Davidovic L, Bechara E, Gravel M, Jaglin XH, Tremblay S, Sík A, et al. 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. 2006;15(9):1525-38.
2005
Boycott KM, Flavelle S, Bureau A, Glass HC, T Fujiwara M, Wirrell E, et al. Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. Am J Hum Genet. 2005;77(3):477-83.
Huot M-, Bisson N, Davidovic L, Mazroui R, Labelle Y, Moss T, et al. The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis. Mol Biol Cell. 2005;16(9):4350-61.
2004
Gabus C, Mazroui R, Tremblay S, Khandjian EW, Darlix J-. The fragile X mental retardation protein has nucleic acid chaperone properties. Nucleic Acids Res. 2004;32(7):2129-37.
Chahine M, Pilote S, Pouliot V, Takami H, Sato C. Role of arginine residues on the S4 segment of the Bacillus halodurans Na+ channel in voltage-sensing. J Membr Biol. 2004;201(1):9-24.
2002
K Bayer U, De Koninck P, Schulman H. Alternative splicing modulates the frequency-dependent response of CaMKII to Ca(2+) oscillations. EMBO J. 2002;21(14):3590-7.
Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM. Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. Ophthalmology. 2002;109(10):1862-70.
2001
Deschênes I, Trottier E, Chahine M. Implication of the C-terminal region of the alpha-subunit of voltage-gated sodium channels in fast inactivation. J Membr Biol. 2001;183(2):103-14.
2000
Dubé M, Huot ME, Khandjian EW. Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast. BMC Genet. 2000;1:4.
1998
Bairam A, Frenette J, Dauphin C, Carroll JL, Khandjian EW. Expression of dopamine D1-receptor mRNA in the carotid body of adult rabbits, cats and rats. Neurosci Res. 1998;31(2):147-54.
Khandjian EW, Bardoni B, Corbin F, Sittler A, Giroux S, Heitz D, et al. Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis. Hum Mol Genet. 1998;7(13):2121-8.
De Koninck P, Schulman H. Sensitivity of CaM kinase II to the frequency of Ca2+ oscillations. Science. 1998;279(5348):227-30.
1997
Drouin R, Angers M, Dallaire N, Rose TM, Khandjian EW, Rousseau F. Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region. Hum Mol Genet. 1997;6(12):2051-60.
1996
Chahine M, Deschene I, Chen LQ, Kallen RG. Electrophysiological characteristics of cloned skeletal and cardiac muscle sodium channels. Am J Physiol. 1996;271(2 Pt 2):H498-506.

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