Publications
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Filtres: Keyword is Cell Line [Enlever les filtres]
The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain. Nat Genet. 2017;49(8):1239-1250.
Dynamic Regulation of Quaternary Organization of the M1 Muscarinic Receptor by Subtype-selective Antagonist Drugs. J Biol Chem. 2016;291(25):13132-46.
Oxidative stress at low levels can induce clustered DNA lesions leading to NHEJ mediated mutations. Oncotarget. 2016;7(18):25377-90.
The human CFTR protein expressed in CHO cells activates aquaporin-3 in a cAMP-dependent pathway: study by digital holographic microscopy. J Cell Sci. 2014;127(Pt 3):546-56.
Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1. Hum Mol Genet. 2013;22(19):3947-59.
Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα. PLoS ONE. 2012;7(7):e41185.
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.
QRS widening and QT prolongation under bupropion: a unique cardiac electrophysiological profile. Fundam Clin Pharmacol. 2012;26(5):599-608.
TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor. Mol Cell Biol. 2011;31(5):1098-108.
Involvement of TLR2 in recognition of acute gammaherpesvirus-68 infection. PLoS ONE. 2010;5(10):e13742.
Lipopolysaccharide-QD micelles induce marked induction of TLR2 and lipid droplet accumulation in olfactory bulb microglia. Mol Pharm. 2010;7(4):1183-94.
Microglial response to gold nanoparticles. ACS Nano. 2010;4(5):2595-606.
Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome. FEBS Lett. 2009;583(5):890-6.
Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A. J Neurophysiol. 2008;99(5):2241-50.
The endoplasmic reticulum-Golgi pathway is a target for translocation and aggregation of mutant superoxide dismutase linked to ALS. FASEB J. 2008;22(7):2476-87.
Protein kinase C activation inhibits alpha1D L-type Ca channel: a single-channel analysis. Pflugers Arch. 2008;455(5):913-9.
Accessibility of four arginine residues on the S4 segment of the Bacillus halodurans sodium channel. J Membr Biol. 2007;215(2-3):169-80.
Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot-Marie-Tooth disease mutants. Hum Mol Genet. 2006;15(6):943-52.
Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin. J Neurochem. 2006;98(3):926-38.
Transition from reversible to persistent binding of CaMKII to postsynaptic sites and NR2B. J Neurosci. 2006;26(4):1164-74.
Alsin is partially associated with centrosome in human cells. Biochim Biophys Acta. 2005;1745(1):84-100.
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts. Hum Mol Genet. 2005;14(6):835-44.
Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level. J Biol Chem. 2005;280(7):5750-63.
