Publications | Centre de recherche CERVO

Export 17 results:

Filtres: Keyword is Protein Binding [Enlever les filtres]

2017

Jiang Y, Loh Y-, Rajarajan P, Hirayama T, Liao W, Kassim BS, et al. The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain. Nat Genet. 2017;49(8):1239-1250.

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.

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.

Zakrys L, Ward RJ, Pediani JD, Godin AG, Graham GJ, Milligan G. Roundabout 1 exists predominantly as a basal dimeric complex and this is unaffected by binding of the ligand Slit2. Biochem J. 2014;461(1):61-73.

2012

Flynn R, Labrie-Dion É, Bernier N, Colicos MA, De Koninck P, Zamponi GW. Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα. PLoS ONE. 2012;7(7):e41185.

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.

Raingo J, Khvotchev M, Liu P, Darios F, Li YC, Ramirez DM, et al. VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission. Nat Neurosci. 2012;15(5):738-45.

2011

Rao MV, Mohan PS, Kumar A, Yuan A, Montagna L, Campbell J, et al. The myosin Va head domain binds to the neurofilament-L rod and modulates endoplasmic reticulum (ER) content and distribution within axons. PLoS ONE. 2011;6(2):e17087.

2007

Davidovic L, Jaglin XH, Lepagnol-Bestel A-, Tremblay S, Simonneau M, Bardoni B, et al. The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules. Hum Mol Genet. 2007;16(24):3047-58.

Ezzi SA, Urushitani M, J-P Julien. Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation. J Neurochem. 2007;102(1):170-8.

2006

K Bayer U, Lebel E, McDonald GL, O'Leary H, Schulman H, De Koninck P. Transition from reversible to persistent binding of CaMKII to postsynaptic sites and NR2B. J Neurosci. 2006;26(4):1164-74.

2005

Jung C, Lee S, Ortiz D, Zhu Q, J-P Julien, Shea TB. The high and middle molecular weight neurofilament subunits regulate the association of neurofilaments with kinesin: inhibition by phosphorylation of the high molecular weight subunit. Brain Res Mol Brain Res. 2005;141(2):151-5.

2003

Bardoni B, Castets M, Huot M-, Schenck A, Adinolfi S, Corbin F, et al. 82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization. Hum Mol Genet. 2003;12(14):1689-98.

Mazroui R, Huot M-, Tremblay S, Boilard N, Labelle Y, Khandjian EW. Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs. Hum Mol Genet. 2003;12(23):3087-96.

2001

Bayer KU, De Koninck P, Leonard AS, Hell JW, Schulman H. Interaction with the NMDA receptor locks CaMKII in an active conformation. Nature. 2001;411(6839):801-5.

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

Khandjian EW, Corbin F, Woerly S, Rousseau F. The fragile X mental retardation protein is associated with ribosomes. Nat Genet. 1996;12(1):91-3.

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