Publications | Cervo Brain Research Centre

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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, 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

Lee S-, Srinivasan B, Sephton CF, Dries DR, Wang B, Yu C, et al. Gamma-secretase-regulated proteolysis of the Notch receptor by mitochondrial intermediate peptidase. J Biol Chem. 2011;286(31):27447-53.

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.

2009

Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, et al. Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome. FEBS Lett. 2009;583(5):890-6.

2005

Millecamps S, Gentil BJ, Gros-Louis F, Rouleau G, J-P Julien. Alsin is partially associated with centrosome in human cells. Biochim Biophys Acta. 2005;1745(1):84-100.

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

Gros-Louis F, Larivière R, Gowing G, Laurent S, Camu W, Bouchard J-, et al. A frameshift deletion in peripherin gene associated with amyotrophic lateral sclerosis. J Biol Chem. 2004;279(44):45951-6.

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.

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.

Chahine M, Sirois J, Marcotte P, Chen L, Kallen RG. Extrapore residues of the S5-S6 loop of domain 2 of the voltage-gated skeletal muscle sodium channel (rSkM1) contribute to the mu-conotoxin GIIIA binding site. Biophys J. 1998;75(1):236-46.

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

Marcotte P, Chen LQ, Kallen RG, Chahine M. Effects of Tityus serrulatus scorpion toxin gamma on voltage-gated Na+ channels. Circ Res. 1997;80(3):363-9.

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.

1995

Rousseau F, Rouillard P, Morel ML, Khandjian EW, 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. 1995;57(5):1006-18.

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