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Blockade of HERG and Kv1.5 by ketoconazole. , Dumaine R, Roy ML, Brown AM., J Pharmacol Exp Ther. August 1, 1998; 286 (2): 727-35.
Differential effects of bupivacaine on cardiac K channels: role of channel inactivation and subunit composition in drug-channel interaction. , Lipka LJ, Jiang M, Tseng GN., J Cardiovasc Electrophysiol. July 1, 1998; 9 (7): 727-42.
Molecular basis for the lack of HERG K+ channel block-related cardiotoxicity by the H1 receptor blocker cetirizine compared with other second-generation antihistamines. , Taglialatela M, Pannaccione A, Castaldo P, Giorgio G, Zhou Z, January CT, Genovese A, Marone G, Annunziato L., Mol Pharmacol. July 1, 1998; 54 (1): 113-21.
A mutation in the pore region of HERG K+ channels expressed in Xenopus oocytes reduces rectification by shifting the voltage dependence of inactivation. , Zou A, Xu QP, Sanguinetti MC., J Physiol. May 15, 1998; 509 ( Pt 1) 129-37.
Effects of the chromanol 293B, a selective blocker of the slow, component of the delayed rectifier K+ current, on repolarization in human and guinea pig ventricular myocytes. , Bosch RF, Gaspo R, Busch AE, Lang HJ, Li GR, Nattel S., Cardiovasc Res. May 1, 1998; 38 (2): 441-50.
Voltage-dependent blockade of HERG channels expressed in Xenopus oocytes by external Ca2+ and Mg2+. , Ho WK, Kim I, Lee CO , Lee CO , Earm YE., J Physiol. March 15, 1998; 507 ( Pt 3) (Pt 3): 631-8.
Molecular determinants of dofetilide block of HERG K+ channels. , Ficker E, Jarolimek W, Kiehn J, Baumann A, Brown AM., Circ Res. February 23, 1998; 82 (3): 386-95.
herg encodes a K+ current highly conserved in tumors of different histogenesis: a selective advantage for cancer cells? , Bianchi L, Wible B, Arcangeli A, Taglialatela M, Morra F, Castaldo P, Crociani O, Rosati B, Faravelli L, Olivotto M, Wanke E., Cancer Res. February 15, 1998; 58 (4): 815-22.
Blockade of HERG channels by the class III antiarrhythmic azimilide: mode of action. , Busch AE, Eigenberger B, Jurkiewicz NK, Salata JJ, Pica A, Suessbrich H, Lang F ., Br J Pharmacol. January 1, 1998; 123 (1): 23-30.
Identification of two nervous system-specific members of the erg potassium channel gene family. , Shi W, Wymore RS, Wang HS, Pan Z, Cohen IS, McKinnon D, Dixon JE., J Neurosci. December 15, 1997; 17 (24): 9423-32.
Modulation of HERG affinity for E-4031 by [K+]o and C-type inactivation. , Wang S, Morales MJ, Liu S , Strauss HC, Rasmusson RL., FEBS Lett. November 3, 1997; 417 (1): 43-7.
Two isoforms of the mouse ether-a- go-go-related gene coassemble to form channels with properties similar to the rapidly activating component of the cardiac delayed rectifier K+ current. , London B, Trudeau MC, Newton KP, Beyer AK, Copeland NG, Gilbert DJ, Jenkins NA, Satler CA, Robertson GA., Circ Res. November 1, 1997; 81 (5): 870-8.
Electrophysiological characterization of an alternatively processed ERG K+ channel in mouse and human hearts. , Lees-Miller JP, Kondo C, Wang L, Duff HJ., Circ Res. November 1, 1997; 81 (5): 719-26.
Regulation of the human ether-a-gogo related gene ( HERG) K+ channels by reactive oxygen species. , Taglialatela M, Castaldo P, Iossa S, Pannaccione A, Fresi A, Ficker E, Annunziato L., Proc Natl Acad Sci U S A. October 14, 1997; 94 (21): 11698-703.
Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart. , Jiang M, Tseng-Crank J, Tseng GN., J Biol Chem. September 26, 1997; 272 (39): 24109-12.
Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241. , Suessbrich H, Schönherr R, Heinemann SH, Lang F , Busch AE., FEBS Lett. September 8, 1997; 414 (2): 435-8.
Amino terminal-dependent gating of the potassium channel rat eag is compensated by a mutation in the S4 segment. , Terlau H, Heinemann SH, Stühmer W, Pongs O, Ludwig J., J Physiol. August 1, 1997; 502 ( Pt 3) 537-43.
Interactions of the nonsedating antihistamine loratadine with a Kv1.5-type potassium channel cloned from human heart. , Lacerda AE, Roy ML, Lewis EW, Rampe D., Mol Pharmacol. August 1, 1997; 52 (2): 314-22.
A minK- HERG complex regulates the cardiac potassium current I(Kr). , McDonald TV, Yu Z, Ming Z, Palma E , Meyers MB, Wang KW, Goldstein SA, Fishman GI., Nature. July 17, 1997; 388 (6639): 289-92.
Comparative effects of loratadine and terfenadine on cardiac K+ channels. , Ducic I, Ko CM , Shuba Y, Morad M., J Cardiovasc Pharmacol. July 1, 1997; 30 (1): 42-54.
A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes. , Wang S, Liu S , Morales MJ, Strauss HC, Rasmusson RL., J Physiol. July 1, 1997; 502 ( Pt 1) 45-60.
Suppression of mammalian K+ channel family by ebastine. , Ko CM , Ducic I, Fan J, Shuba YM, Morad M., J Pharmacol Exp Ther. April 1, 1997; 281 (1): 233-44.
The inhibitory effect of the antipsychotic drug haloperidol on HERG potassium channels expressed in Xenopus oocytes. , Suessbrich H, Schönherr R, Heinemann SH, Attali B, Lang F , Busch AE., Br J Pharmacol. March 1, 1997; 120 (5): 968-74.
Single HERG delayed rectifier K+ channels expressed in Xenopus oocytes. , Zou A, Curran ME, Keating MT, Sanguinetti MC., Am J Physiol. March 1, 1997; 272 (3 Pt 2): H1309-14.
Tissue and species distribution of mRNA for the IKr-like K+ channel, erg. , Wymore RS, Gintant GA, Wymore RT, Dixon JE, McKinnon D, Cohen IS., Circ Res. February 1, 1997; 80 (2): 261-8.
Mechanism of action potential prolongation by RP 58866 and its active enantiomer, terikalant. Block of the rapidly activating delayed rectifier K+ current, IKr. , Jurkiewicz NK, Wang J , Fermini B, Sanguinetti MC, Salata JJ., Circulation. December 1, 1996; 94 (11): 2938-46.
Molecular physiology and pharmacology of HERG. Single-channel currents and block by dofetilide. , Kiehn J, Lacerda AE, Wible B, Brown AM., Circulation. November 15, 1996; 94 (10): 2572-9.
K(V)LQT1 and lsK ( minK) proteins associate to form the I(Ks) cardiac potassium current. , Barhanin J , Lesage F , Guillemare E, Fink M, Lazdunski M, Romey G., Nature. November 7, 1996; 384 (6604): 78-80.
Inhibition of IKs in guinea pig cardiac myocytes and guinea pig IsK channels by the chromanol 293B. , Busch AE, Suessbrich H, Waldegger S, Sailer E, Greger R, Lang H, Lang F , Gibson KJ, Maylie JG., Pflugers Arch. October 1, 1996; 432 (6): 1094-6.
HERG, a primary human ventricular target of the nonsedating antihistamine terfenadine. , Roy M, Dumaine R, Brown AM., Circulation. August 15, 1996; 94 (4): 817-23.
Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel. , Schönherr R, Heinemann SH., J Physiol. June 15, 1996; 493 ( Pt 3) 635-42.
High affinity open channel block by dofetilide of HERG expressed in a human cell line. , Snyders DJ, Chaudhary A., Mol Pharmacol. June 1, 1996; 49 (6): 949-55.
Fast inactivation causes rectification of the IKr channel. , Spector PS, Curran ME, Zou A, Keating MT, Sanguinetti MC., J Gen Physiol. May 1, 1996; 107 (5): 611-9.
Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole. , Suessbrich H, Waldegger S, Lang F , Busch AE., FEBS Lett. April 29, 1996; 385 (1-2): 77-80.
Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia. , Sanguinetti MC, Curran ME, Spector PS, Keating MT., Proc Natl Acad Sci U S A. March 5, 1996; 93 (5): 2208-12.
Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K+ channel. Open-channel block by methanesulfonanilides. , Spector PS, Curran ME, Keating MT, Sanguinetti MC., Circ Res. March 1, 1996; 78 (3): 499-503.
Potassium currents expressed from Drosophila and mouse eag cDNAs in Xenopus oocytes. , Robertson GA, Warmke JM, Ganetzky B., Neuropharmacology. January 1, 1996; 35 (7): 841-50.
Cloned human inward rectifier K+ channel as a target for class III methanesulfonanilides. , Kiehn J, Wible B, Ficker E, Taglialatela M, Brown AM., Circ Res. December 1, 1995; 77 (6): 1151-5.
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel. , Sanguinetti MC, Jiang C, Curran ME, Keating MT., Cell. April 21, 1995; 81 (2): 299-307.