Publications
Export 27 results:
Filtres: Keyword is Molecular Sequence Data [Enlever les filtres]
, « Characterization of the honeybee AmNaV1 channel and tools to assess the toxicity of insecticides. », Sci Rep, vol. 5, p. 12475, 2015.
, « Gating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy. », J Gen Physiol, vol. 145, nᵒ 2, p. 93-106, 2015.
, « Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics. », Mol Pharmacol, vol. 86, nᵒ 4, p. 378-89, 2014.
, « Rhomboid proteases in mitochondria and plastids: keeping organelles in shape. », Biochim Biophys Acta, vol. 1833, nᵒ 2, p. 371-80, 2013.
, « Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. », PLoS One, vol. 7, nᵒ 6, p. e39338, 2012.
, « Gating pore currents and the resting state of Nav1.4 voltage sensor domains. », Proc Natl Acad Sci U S A, vol. 109, nᵒ 47, p. 19250-5, 2012.
, « Manipulating the fragile X mental retardation proteins in the frog. », Results Probl Cell Differ, vol. 54, p. 165-79, 2012.
, « A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. », PLoS One, vol. 7, nᵒ 5, p. e38331, 2012.
, « TDP-43 is directed to stress granules by sorbitol, a novel physiological osmotic and oxidative stressor. », Mol Cell Biol, vol. 31, nᵒ 5, p. 1098-108, 2011.
, « Wild-type human SOD1 overexpression does not accelerate motor neuron disease in mice expressing murine Sod1 G86R. », Neurobiol Dis, vol. 40, nᵒ 1, p. 245-50, 2010.
, « Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure. », Nucleic Acids Res, vol. 35, nᵒ 1, p. 299-306, 2007.
, « 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, p. 1525-38, 2006.
, « Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification. », Am J Hum Genet, vol. 77, nᵒ 3, p. 477-83, 2005.
, « The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis. », Mol Biol Cell, vol. 16, nᵒ 9, p. 4350-61, 2005.
, « The fragile X mental retardation protein has nucleic acid chaperone properties. », Nucleic Acids Res, vol. 32, nᵒ 7, p. 2129-37, 2004.
, « Role of arginine residues on the S4 segment of the Bacillus halodurans Na+ channel in voltage-sensing. », J Membr Biol, vol. 201, nᵒ 1, p. 9-24, 2004.
, « Alternative splicing modulates the frequency-dependent response of CaMKII to Ca(2+) oscillations. », EMBO J, vol. 21, nᵒ 14, p. 3590-7, 2002.
, « Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation. », Ophthalmology, vol. 109, nᵒ 10, p. 1862-70, 2002.
, « Implication of the C-terminal region of the alpha-subunit of voltage-gated sodium channels in fast inactivation. », J Membr Biol, vol. 183, nᵒ 2, p. 103-14, 2001.
, « Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast. », BMC Genet, vol. 1, p. 4, 2000.
, « Expression of dopamine D1-receptor mRNA in the carotid body of adult rabbits, cats and rats. », Neurosci Res, vol. 31, nᵒ 2, p. 147-54, 1998.
, « Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis. », Hum Mol Genet, vol. 7, nᵒ 13, p. 2121-8, 1998.
, « Sensitivity of CaM kinase II to the frequency of Ca2+ oscillations. », Science, vol. 279, nᵒ 5348, p. 227-30, 1998.
, « Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region. », Hum Mol Genet, vol. 6, nᵒ 12, p. 2051-60, 1997.
, « Electrophysiological characteristics of cloned skeletal and cardiac muscle sodium channels. », Am J Physiol, vol. 271, nᵒ 2 Pt 2, p. H498-506, 1996.
