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A novel µ-conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors. , Favreau P, Benoit E, Hocking HG, Carlier L, D' hoedt D, Leipold E, Markgraf R, Schlumberger S, Córdova MA, Gaertner H, Paolini-Bertrand M, Hartley O, Tytgat J, Heinemann SH, Bertrand D, Boelens R, Stöcklin R, Molgó J., Br J Pharmacol. July 1, 2012; 166 (5): 1654-68.
Differential state-dependent modification of inactivation-deficient Nav1.6 sodium channels by the pyrethroid insecticides S-bioallethrin, tefluthrin and deltamethrin. , McCavera SJ, Soderlund DM., Neurotoxicology. June 1, 2012; 33 (3): 384-90.
Pharmacological kinetics of BmK AS, a sodium channel site 4-specific modulator on Nav1.3. , Liu ZR, Tao J, Dong BQ, Ding G, Cheng ZJ, He HQ , Ji YH., Neurosci Bull. June 1, 2012; 28 (3): 209-21.
18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels. , Du YM, Xia CK, Zhao N, Dong Q, Lei M, Xia JH., Acta Pharmacol Sin. June 1, 2012; 33 (6): 752-60.
Infrared light excites cells by changing their electrical capacitance. , Shapiro MG, Homma K, Villarreal S, Richter CP, Bezanilla F., Nat Commun. March 13, 2012; 3 736.
JZTX-XIII, a Kv channel gating modifier toxin from Chinese tarantula Chilobrachys jingzhao. , Yuan C, Liu Z, Hu W , Gao T, Liang S., Toxicon. February 1, 2012; 59 (2): 265-71.
Transmembrane voltage potential controls embryonic eye patterning in Xenopus laevis. , Pai VP , Aw S, Shomrat T, Lemire JM , Levin M ., Development. January 1, 2012; 139 (2): 313-23.
Estimating the voltage-dependent free energy change of ion channels using the median voltage for activation. , Chowdhury S, Chanda B., J Gen Physiol. January 1, 2012; 139 (1): 3-17.
A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. , Gosselin-Badaroudine P, Keller DI, Huang H, Pouliot V, Chatelier A, Osswald S, Brink M, Chahine M., PLoS One. January 1, 2012; 7 (5): e38331.
Extracellular proton modulation of the cardiac voltage-gated sodium channel, Nav1.5. , Jones DK, Peters CH, Tolhurst SA, Claydon TW, Ruben PC., Biophys J. November 2, 2011; 101 (9): 2147-56.
Navβ subunits modulate the inhibition of Nav1.8 by the analgesic gating modifier μO-conotoxin MrVIB. , Wilson MJ, Zhang MM, Azam L, Olivera BM, Bulaj G, Yoshikami D., J Pharmacol Exp Ther. August 1, 2011; 338 (2): 687-93.
Functional properties and toxin pharmacology of a dorsal root ganglion sodium channel viewed through its voltage sensors. , Bosmans F, Puopolo M, Martin-Eauclaire MF, Bean BP, Swartz KJ., J Gen Physiol. July 1, 2011; 138 (1): 59-72.
μ-Conotoxins that differentially block sodium channels NaV1.1 through 1.8 identify those responsible for action potentials in sciatic nerve. , Wilson MJ, Yoshikami D, Azam L, Gajewiak J, Olivera BM, Bulaj G, Zhang MM., Proc Natl Acad Sci U S A. June 21, 2011; 108 (25): 10302-7.
Expression of the voltage- and Ca2+-dependent BK potassium channel subunits BKβ1 and BKβ4 in rodent astrocytes. , Seidel KN, Derst C, Salzmann M, Höltje M, Priller J, Markgraf R, Heinemann SH, Heilmann H, Skatchkov SN, Eaton MJ, Veh RW, Prüss H., Glia. June 1, 2011; 59 (6): 893-902.
Independent and joint modulation of rat Nav1.6 voltage-gated sodium channels by coexpression with the auxiliary β1 and β2 subunits. , Tan J, Soderlund DM., Biochem Biophys Res Commun. April 22, 2011; 407 (4): 788-92.
Localization of receptor site on insect sodium channel for depressant β-toxin BmK IT2. , He H , Liu Z, Dong B, Zhang J, Shu X, Zhou J, Ji Y., PLoS One. January 7, 2011; 6 (1): e14510.
Phyla- and Subtype-Selectivity of CgNa, a Na Channel Toxin from the Venom of the Giant Caribbean Sea Anemone Condylactis Gigantea. , Billen B, Debaveye S, Béress L, Garateix A, Tytgat J., Front Pharmacol. November 23, 2010; 1 133.
Molecular mechanism of allosteric modification of voltage-dependent sodium channels by local anesthetics. , Arcisio-Miranda M, Muroi Y, Chowdhury S, Chanda B., J Gen Physiol. November 1, 2010; 136 (5): 541-54.
Molecular determination of selectivity of the site 3 modulator ( BmK I) to sodium channels in the CNS: a clue to the importance of Nav1.6 in BmK I-induced neuronal hyperexcitability. , He H , Liu Z, Dong B, Zhou J, Zhu H, Ji Y., Biochem J. October 15, 2010; 431 (2): 289-98.
Induction of vertebrate regeneration by a transient sodium current. , Tseng AS , Beane WS, Lemire JM , Masi A, Levin M ., J Neurosci. September 29, 2010; 30 (39): 13192-200.
Pharmacological modulation of brain Nav1.2 and cardiac Nav1.5 subtypes by the local anesthetic ropivacaine. , Cheng HW, Yang HT, Zhou JJ , Ji YH, Zhu HY., Neurosci Bull. August 1, 2010; 26 (4): 289-96.
Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome. , Gui J, Wang T, Jones RP, Trump D, Zimmer T, Lei M., PLoS One. June 7, 2010; 5 (6): e10985.
Optogenetic localization and genetic perturbation of saccade-generating neurons in zebrafish. , Schoonheim PJ, Arrenberg AB, Del Bene F, Baier H., J Neurosci. May 19, 2010; 30 (20): 7111-20.
An in vivo tethered toxin approach for the cell-autonomous inactivation of voltage-gated sodium channel currents in nociceptors. , Stürzebecher AS, Hu J, Smith ES, Frahm S, Santos-Torres J, Kampfrath B, Auer S, Lewin GR, Ibañez-Tallon I., J Physiol. May 15, 2010; 588 (Pt 10): 1695-707.
Blocking effect of methylflavonolamine on human Na(V)1.5 channels expressed in Xenopus laevis oocytes and on sodium currents in rabbit ventricular myocytes. , Fan XR, Ma JH, Zhang PH, Xing JL., Acta Pharmacol Sin. March 1, 2010; 31 (3): 297-306.
Electric currents in Xenopus tadpole tail regeneration. , Reid B, Song B, Zhao M., Dev Biol. November 1, 2009; 335 (1): 198-207.
Membrane trauma and Na+ leak from Nav1.6 channels. , Wang JA , Lin W, Morris T, Banderali U, Juranka PF, Morris CE., Am J Physiol Cell Physiol. October 1, 2009; 297 (4): C823-34.
The external pore loop interacts with S6 and S3-S4 linker in domain 4 to assume an essential role in gating control and anticonvulsant action in the Na(+) channel. , Yang YC , Hsieh JY, Kuo CC., J Gen Physiol. August 1, 2009; 134 (2): 95-113.
Slow inactivation of the NaV1.4 sodium channel in mammalian cells is impeded by co-expression of the beta1 subunit. , Webb J, Wu FF, Cannon SC., Pflugers Arch. April 1, 2009; 457 (6): 1253-63.
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.
Synergistic and antagonistic interactions between tetrodotoxin and mu-conotoxin in blocking voltage-gated sodium channels. , Zhang MM, McArthur JR, Azam L, Bulaj G, Olivera BM, French RJ, Yoshikami D., Channels (Austin). January 1, 2009; 3 (1): 32-8.
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.
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.
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.
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.
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.
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.
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.
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.
Nav channel mechanosensitivity: activation and inactivation accelerate reversibly with stretch. , Morris CE, Juranka PF., Biophys J. August 1, 2007; 93 (3): 822-33.
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.
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.
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.
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.
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.
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.
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.
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.