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Developmental expression of the novel voltage-gated sodium channel auxiliary subunit beta3, in rat CNS. , Shah BS, Stevens EB, Pinnock RD, Dixon AK, Lee K., J Physiol. August 1, 2001; 534 (Pt 3): 763-76.
Nav1.3 sodium channels: rapid repriming and slow closed-state inactivation display quantitative differences after expression in a mammalian cell line and in spinal sensory neurons. , Cummins TR, Aglieco F, Renganathan M, Herzog RI, Dib-Hajj SD, Waxman SG., J Neurosci. August 15, 2001; 21 (16): 5952-61.
Gating properties of Na(v)1.7 and Na(v)1.8 peripheral nerve sodium channels. , Vijayaragavan K, O'Leary ME, Chahine M., J Neurosci. October 15, 2001; 21 (20): 7909-18.
Point mutations in homology domain II modify the sensitivity of rat Nav1.8 sodium channels to the pyrethroid insecticide cismethrin. , Soderlun DM, Lee SH., Neurotoxicology. December 1, 2001; 22 (6): 755-65.
Repressor element-1 silencing transcription/ neuron-restrictive silencer factor is required for neural sodium channel expression during development of Xenopus. , Armisén R, Fuentes R, Olguín P, Cabrejos ME, Kukuljan M ., J Neurosci. October 1, 2002; 22 (19): 8347-51.
Sodium channel heterologous expression in mammalian cells and the role of the endogenous beta1-subunits. , Moran O, Conti F, Tammaro P., Neurosci Lett. January 23, 2003; 336 (3): 175-9.
Lidocaine block of neonatal Nav1.3 is differentially modulated by co-expression of beta1 and beta3 subunits. , Lenkowski PW, Shah BS, Dinn AE, Lee K, Patel MK., Eur J Pharmacol. April 25, 2003; 467 (1-3): 23-30.
Importance of the conserved aromatic residues in the scorpion alpha-like toxin BmK M1: the hydrophobic surface region revisited. , Sun YM, Bosmans F, Zhu RH, Goudet C, Xiong YM, Tytgat J, Wang DC., J Biol Chem. June 27, 2003; 278 (26): 24125-31.
Inhibition of cardiac sodium currents by toluene exposure. , Cruz SL, Orta-Salazar G, Gauthereau MY, Millan-Perez Peña L, Salinas-Stefanón EM., Br J Pharmacol. October 1, 2003; 140 (4): 653-60.
Closing and inactivation potentiate the cocaethylene inhibition of cardiac sodium channels by distinct mechanisms. , O'Leary ME, Digregorio M, Chahine M., Mol Pharmacol. December 1, 2003; 64 (6): 1575-85.
Molecular cloning and functional expression of the human sodium channel beta1B subunit, a novel splicing variant of the beta1 subunit. , Qin N, D'Andrea MR, Lubin ML, Shafaee N, Codd EE, Correa AM., Eur J Biochem. December 1, 2003; 270 (23): 4762-70.
Modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by protein kinase A and protein kinase C. , Vijayaragavan K, Boutjdir M, Chahine M., J Neurophysiol. April 1, 2004; 91 (4): 1556-69.
Differential modulation of Nav1.7 and Nav1.8 peripheral nerve sodium channels by the local anesthetic lidocaine. , Chevrier P, Vijayaragavan K, Chahine M., Br J Pharmacol. June 1, 2004; 142 (3): 576-84.
Role of auxiliary beta1-, beta2-, and beta3-subunits and their interaction with Na(v)1.8 voltage-gated sodium channel. , Vijayaragavan K, Powell AJ, Kinghorn IJ, Chahine M., Biochem Biophys Res Commun. June 25, 2004; 319 (2): 531-40.
Occurrence of a tetrodotoxin-sensitive calcium current in rat ventricular myocytes after long-term myocardial infarction. , Alvarez JL, Salinas-Stefanon E, Orta G, Ferrer T, Talavera K, Galán L, Vassort G., Cardiovasc Res. September 1, 2004; 63 (4): 653-61.
Cyclosporin A and deltamethrin block the downregulation of Nav1.8 sodium channels expressed in Xenopus oocytes. , Choi JS, Soderlund DM., Neurosci Lett. September 9, 2004; 367 (3): 389-93.
State-dependent trapping of flecainide in the cardiac sodium channel. , Ramos E, O'leary ME., J Physiol. October 1, 2004; 560 (Pt 1): 37-49.
The poison Dart frog's batrachotoxin modulates Nav1.8. , Bosmans F, Maertens C, Verdonck F, Tytgat J., FEBS Lett. November 5, 2004; 577 (1-2): 245-8.
Use-dependent potentiation of the Nav1.6 sodium channel. , Zhou W, Goldin AL., Biophys J. December 1, 2004; 87 (6): 3862-72.
A role for the carbohydrate portion of ginsenoside Rg3 in Na+ channel inhibition. , Kim JH , Hong YH, Lee JH , Lee JH , Kim DH, Nam G, Jeong SM, Lee BH, Lee SM, Nah SY., Mol Cells. February 28, 2005; 19 (1): 137-42.
Molecular basis of the mammalian potency of the scorpion alpha-like toxin, BmK M1. , Liu LH, Bosmans F, Maertens C, Zhu RH, Wang DC, Tytgat J., FASEB J. April 1, 2005; 19 (6): 594-6.
State-dependent block of rat Nav1.4 sodium channels expressed in xenopus oocytes by pyrazoline-type insecticides. , Silver K, Soderlund DM., Neurotoxicology. June 1, 2005; 26 (3): 397-406.
A new type of scorpion Na+-channel-toxin-like polypeptide active on K+ channels. , Srairi-Abid N, Guijarro JI, Benkhalifa R, Mantegazza M, Cheikh A, Ben Aissa M, Haumont PY, Delepierre M, El Ayeb M., Biochem J. June 1, 2005; 388 (Pt 2): 455-64.
Distribution and functional characterization of human Nav1.3 splice variants. , Thimmapaya R, Neelands T, Niforatos W, Davis-Taber RA, Choi W, Putman CB, Kroeger PE, Packer J, Gopalakrishnan M, Faltynek CR, Surowy CS, Scott VE., Eur J Neurosci. July 1, 2005; 22 (1): 1-9.
Structural basis for the voltage-gated Na+ channel selectivity of the scorpion alpha-like toxin BmK M1. , Ye X, Bosmans F, Li C, Zhang Y , Wang DC, Tytgat J., J Mol Biol. November 4, 2005; 353 (4): 788-803.
A mutation in the local anaesthetic binding site abolishes toluene effects in sodium channels. , Gauthereau MY, Salinas-Stefanon EM, Cruz SL., Eur J Pharmacol. December 28, 2005; 528 (1-3): 17-26.
RE-1 silencer of transcription/neural restrictive silencer factor modulates ectodermal patterning during Xenopus development. , Olguín P, Oteíza P, Gamboa E, Gómez-Skármeta JL, Kukuljan M ., J Neurosci. March 8, 2006; 26 (10): 2820-9.
An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability. , Barela AJ, Waddy SP, Lickfett JG, Hunter J, Anido A, Helmers SL, Goldin AL, Escayg A., J Neurosci. March 8, 2006; 26 (10): 2714-23.
GLUT8 is dispensable for embryonic development but influences hippocampal neurogenesis and heart function. , Membrez M, Hummler E, Beermann F, Haefliger JA, Savioz R, Pedrazzini T, Thorens B., Mol Cell Biol. June 1, 2006; 26 (11): 4268-76.
Potent modulation of the voltage-gated sodium channel Nav1.7 by OD1, a toxin from the scorpion Odonthobuthus doriae. , Maertens C, Cuypers E, Amininasab M, Jalali A, Vatanpour H, Tytgat J., Mol Pharmacol. July 1, 2006; 70 (1): 405-14.
Augmentation of Cav3.2 T-type calcium channel activity by cAMP-dependent protein kinase A. , Kim JA , Park JY , Kang HW, Huh SU, Jeong SW, Lee JH , Lee JH ., J Pharmacol Exp Ther. July 1, 2006; 318 (1): 230-7.
muO-conotoxin MrVIB selectively blocks Nav1.8 sensory neuron specific sodium channels and chronic pain behavior without motor deficits. , Ekberg J, Jayamanne A, Vaughan CW, Aslan S, Thomas L, Mould J, Drinkwater R, Baker MD, Abrahamsen B, Wood JN, Adams DJ, Christie MJ, Lewis RJ., Proc Natl Acad Sci U S A. November 7, 2006; 103 (45): 17030-5.
Isolation and structure-activity of mu-conotoxin TIIIA, a potent inhibitor of tetrodotoxin-sensitive voltage-gated sodium channels. , Lewis RJ, Schroeder CI, Ekberg J, Nielsen KJ, Loughnan M, Thomas L, Adams DA, Drinkwater R, Adams DJ, Alewood PF., Mol Pharmacol. March 1, 2007; 71 (3): 676-85.
A cation-pi interaction discriminates among sodium channels that are either sensitive or resistant to tetrodotoxin block. , Santarelli VP, Eastwood AL, Dougherty DA, Horn R, Ahern CA., J Biol Chem. March 16, 2007; 282 (11): 8044-51.
H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration. , Adams DS , Masi A, Levin M ., Development. April 1, 2007; 134 (7): 1323-35.
Modulatory effect of auxiliary beta1 subunit on Nav1.3 voltage-gated sodium channel expressed in Xenopus oocyte. , Wang YW, Cheng ZJ, Tan H, Xia YM, Ren RR, Ding YQ ., Chin Med J (Engl). April 20, 2007; 120 (8): 721-3.
Effects of dextrorotatory morphinans on brain Na+ channels expressed in Xenopus oocytes. , Lee JH , Lee JH , Shin EJ, Jeong SM, Lee BH, Yoon IS, Lee JH , Lee JH , Choi SH, Kim YH, Pyo MK, Lee SM, Chae JS, Rhim H, Oh JW, Kim HC , Nah SY., Eur J Pharmacol. June 14, 2007; 564 (1-3): 7-17.
A Na+ channel mutation linked to hypokalemic periodic paralysis exposes a proton-selective gating pore. , Struyk AF, Cannon SC., J Gen Physiol. July 1, 2007; 130 (1): 11-20.
Solution structure of Jingzhaotoxin-III, a peptide toxin inhibiting both Nav1.5 and Kv2.1 channels. , Liao Z, Yuan C, Peng K, Xiao Y, Liang S., Toxicon. July 1, 2007; 50 (1): 135-43.
Nav channel mechanosensitivity: activation and inactivation accelerate reversibly with stretch. , Morris CE, Juranka PF., Biophys J. August 1, 2007; 93 (3): 822-33.
Structure and sodium channel activity of an excitatory I1-superfamily conotoxin. , Buczek O, Wei D, Babon JJ, Yang X, Fiedler B, Chen P, Yoshikami D, Olivera BM, Bulaj G, Norton RS., Biochemistry. September 4, 2007; 46 (35): 9929-40.
Concentration-dependent accumulation of [3H]-deltamethrin in sodium channel Nav1.2/beta1 expressing Xenopus laevis oocytes. , Watkins JA, Meacham CA, Crofton KM, Shafer TJ., Toxicol In Vitro. December 1, 2007; 21 (8): 1672-7.
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel. , Surber R, Hensellek S, Prochnau D, Werner GS, Benndorf K, Figulla HR, Zimmer T., Cardiovasc Res. March 1, 2008; 77 (4): 740-8.
Modifications of aliphatic side chain of 20(S)-ginsenoside RG3 cause an enhancement or loss of brain Na+ channel current inhibitions. , Lee JH , Lee JH , Choi SH, Lee BH, Yoon IS, Shin TJ, Pyo MK, Lee SM, Rhim H, Park MH, Park TY, Nah SY., Biol Pharm Bull. March 1, 2008; 31 (3): 480-6.
Effects of BmK AS on Nav1.2 expressed in Xenopus laevis oocytes. , Tan M, Zhu MM, Liu Y , Cheng HW, Ji YH., Cell Biol Toxicol. April 1, 2008; 24 (2): 143-9.
Involvement of batrachotoxin binding sites in ginsenoside-mediated voltage-gated Na+ channel regulation. , Lee JH , Lee BH, Choi SH, Yoon IS, Shin TJ, Pyo MK, Lee SM, Kim HC , Nah SY., Brain Res. April 8, 2008; 1203 61-7.
An extracellular Cu2+ binding site in the voltage sensor of BK and Shaker potassium channels. , Ma Z, Wong KY, Horrigan FT., J Gen Physiol. May 1, 2008; 131 (5): 483-502.
Alpha-scorpion toxin impairs a conformational change that leads to fast inactivation of muscle sodium channels. , Campos FV, Chanda B, Beirão PS, Bezanilla F., J Gen Physiol. August 1, 2008; 132 (2): 251-63.
Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channel. , Zhang Y , Wang T, Ma A, Zhou X , Gui J, Wan H, Shi R, Huang C, Grace AA, Huang CL, Trump D, Zhang H , Zimmer T, Lei M., Acta Physiol (Oxf). December 1, 2008; 194 (4): 311-23.
Human and rat Nav1.3 voltage-gated sodium channels differ in inactivation properties and sensitivity to the pyrethroid insecticide tefluthrin. , Tan J, Soderlund DM., Neurotoxicology. January 1, 2009; 30 (1): 81-9.