Publications
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, “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, pp. 93-106, 2015.
, “Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics.”, Mol Pharmacol, vol. 86, no. 4, pp. 378-89, 2014.
, “Rhomboid proteases in mitochondria and plastids: keeping organelles in shape.”, Biochim Biophys Acta, vol. 1833, no. 2, pp. 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, pp. 19250-5, 2012.
, “Manipulating the fragile X mental retardation proteins in the frog.”, Results Probl Cell Differ, vol. 54, pp. 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, pp. 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, pp. 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, pp. 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, pp. 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, pp. 477-83, 2005.
, “The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis.”, Mol Biol Cell, vol. 16, no. 9, pp. 4350-61, 2005.
, “The fragile X mental retardation protein has nucleic acid chaperone properties.”, Nucleic Acids Res, vol. 32, no. 7, pp. 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, pp. 9-24, 2004.
, “Alternative splicing modulates the frequency-dependent response of CaMKII to Ca(2+) oscillations.”, EMBO J, vol. 21, no. 14, pp. 3590-7, 2002.
, “Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.”, Ophthalmology, vol. 109, no. 10, pp. 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, pp. 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, pp. 147-54, 1998.
, “Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.”, Hum Mol Genet, vol. 7, no. 13, pp. 2121-8, 1998.
, “Sensitivity of CaM kinase II to the frequency of Ca2+ oscillations.”, Science, vol. 279, no. 5348, pp. 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, pp. 2051-60, 1997.
, “Electrophysiological characteristics of cloned skeletal and cardiac muscle sodium channels.”, Am J Physiol, vol. 271, no. 2 Pt 2, pp. H498-506, 1996.
