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Inhibition of human ether-a- go-go-related gene K+ channel and IKr of guinea pig cardiomyocytes by antipsychotic drug trifluoperazine. , Choi SY., J Pharmacol Exp Ther. May 1, 2005; 313 (2): 888-95.
Class Ia anti-arrhythmic drug ajmaline blocks HERG potassium channels: mode of action. , Kiesecker C., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2004; 370 (6): 423-35.
Block of wild-type and inactivation-deficient human ether-a- go-go-related gene K+ channels by halofantrine. , Sánchez-Chapula JA., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2004; 370 (6): 484-91.
Direct block of hERG potassium channels by the protein kinase C inhibitor bisindolylmaleimide I (GF109203X). , Thomas D., Cardiovasc Res. December 1, 2004; 64 (3): 467-76.
Activation of cardiac human ether-a- go-go related gene potassium currents is regulated by alpha(1A)-adrenoceptors. , Thomas D., J Mol Med (Berl). December 1, 2004; 82 (12): 826-37.
Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome. , Zehelein J., Biochim Biophys Acta. November 5, 2004; 1690 (3): 185-92.
Activation properties of Kv4.3 channels: time, voltage and [K+]o dependence. , Wang S., J Physiol. June 15, 2004; 557 (Pt 3): 705-17.
Inhibition of human ether-a- go-go-related gene potassium channels by alpha 1-adrenoceptor antagonists prazosin, doxazosin, and terazosin. , Thomas D., Naunyn Schmiedebergs Arch Pharmacol. May 1, 2004; 369 (5): 462-72.
Block of HERG human K(+) channel and IKr of guinea pig cardiomyocytes by chlorpromazine. , Lee SY., J Cardiovasc Pharmacol. May 1, 2004; 43 (5): 706-14.
Physicochemical features of the HERG channel drug binding site. , Fernandez D., J Biol Chem. March 12, 2004; 279 (11): 10120-7.
Drug binding to aromatic residues in the HERG channel pore cavity as possible explanation for acquired Long QT syndrome by antiparkinsonian drug budipine. , Scholz EP., Naunyn Schmiedebergs Arch Pharmacol. November 1, 2003; 368 (5): 404-14.
Acute effects of dronedarone on both components of the cardiac delayed rectifier K+ current, HERG and KvLQT1/ minK potassium channels. , Thomas D., Br J Pharmacol. November 1, 2003; 140 (5): 996-1002.
The antipsychotic drug chlorpromazine inhibits HERG potassium channels. , Thomas D., Br J Pharmacol. June 1, 2003; 139 (3): 567-74.
Cloning and functional characterization of the smooth muscle ether-a- go-go-related gene K+ channel. Potential role of a conserved amino acid substitution in the S4 region. , Shoeb F., J Biol Chem. January 24, 2003; 278 (4): 2503-14.
Inhibitory effect of the class III antiarrhythmic drug nifekalant on HERG channels: mode of action. , Kushida S., Eur J Pharmacol. December 13, 2002; 457 (1): 19-27.
Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à- go-go-Related Gene. , Roti EC., J Biol Chem. December 6, 2002; 277 (49): 47779-85.
Fenamate-induced enhancement of heterologously expressed HERG currents in Xenopus oocytes. , Malykhina AP., Eur J Pharmacol. October 11, 2002; 452 (3): 269-77.
KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current. , Angelo K., Biophys J. October 1, 2002; 83 (4): 1997-2006.
[Evaluation of pro-arrhythmic risk of drugs due to QT interval prolongation by the HERG expression system]. , Chachin M., Nihon Yakurigaku Zasshi. June 1, 2002; 119 (6): 345-51.
Histidines 578 and 587 in the S5-S6 linker of the human Ether-a-gogo Related Gene-1 K+ channels confer sensitivity to reactive oxygen species. , Pannaccione A., J Biol Chem. March 15, 2002; 277 (11): 8912-9.
[Cardiotoxicity of lindane, a gamma isomer of hexachlorocyclohexane]. , Sauviat MP., J Soc Biol. January 1, 2002; 196 (4): 339-48.
Inhibition of cardiac potassium currents by pentobarbital. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.
Characterization of a novel Kv1.5 channel blocker in Xenopus oocytes, CHO cells, human and rat cardiomyocytes. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. November 1, 2001; 364 (5): 472-8.
Molecular cloning and expression of cERG, the ether à go-go-related gene from canine myocardium. , Zehelein J., Pflugers Arch. May 1, 2001; 442 (2): 188-91.
High-affinity blockade of human ether-a- go-go-related gene human cardiac potassium channels by the novel antiarrhythmic drug BRL-32872. , Thomas D., J Pharmacol Exp Ther. May 1, 2001; 297 (2): 753-61.
Blocking effects of the antiarrhythmic drug propafenone on the HERG potassium channel. , Mergenthaler J., Naunyn Schmiedebergs Arch Pharmacol. April 1, 2001; 363 (4): 472-80.
Short- and long-term effects of amiodarone on the two components of cardiac delayed rectifier K(+) current. , Kamiya K., Circulation. March 6, 2001; 103 (9): 1317-24.
Inhibitory effects of berberine on IK1, IK, and HERG channels of cardiac myocytes. , Li BX., Acta Pharmacol Sin. February 1, 2001; 22 (2): 125-31.
Antiarrhythmic drug carvedilol inhibits HERG potassium channels. , Karle CA., Cardiovasc Res. February 1, 2001; 49 (2): 361-70.
Inhibition of IKs channels by HMR 1556. , Gögelein H., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2000; 362 (6): 480-8.
Preclinical pharmacology of desloratadine, a selective and nonsedating histamine H1 receptor antagonist. 2nd communication: lack of central nervous system and cardiovascular effects. , Kreutner W., Arzneimittelforschung. May 1, 2000; 50 (5): 441-8.
KChAP as a chaperone for specific K(+) channels. , Kuryshev YA., Am J Physiol Cell Physiol. May 1, 2000; 278 (5): C931-41.
The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family. , St-Pierre J., Can J Cardiol. March 1, 2000; 16 (3): 307-12.
Norpropoxyphene-induced cardiotoxicity is associated with changes in ion-selectivity and gating of HERG currents. , Ulens C., Cardiovasc Res. December 1, 1999; 44 (3): 568-78.
Mechanism for the effects of extracellular acidification on HERG-channel function. , Jiang M., Am J Physiol. October 1, 1999; 277 (4): H1283-92.
Pathways of HERG inactivation. , Kiehn J., Am J Physiol. July 1, 1999; 277 (1): H199-210.
Functional analysis of a mouse brain Elk-type K+ channel. , Trudeau MC., J Neurosci. April 15, 1999; 19 (8): 2906-18.
HERG potassium channel activation is shifted by phorbol esters via protein kinase A-dependent pathways. , Kiehn J., J Biol Chem. September 25, 1998; 273 (39): 25285-91.
Differential effects of bupivacaine on cardiac K channels: role of channel inactivation and subunit composition in drug-channel interaction. , Lipka LJ., J Cardiovasc Electrophysiol. July 1, 1998; 9 (7): 727-42.
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., 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., J Physiol. March 15, 1998; 507 ( Pt 3) (Pt 3): 631-8.
herg encodes a K+ current highly conserved in tumors of different histogenesis: a selective advantage for cancer cells? , Bianchi L., Cancer Res. February 15, 1998; 58 (4): 815-22.
Blockade of HERG channels by the class III antiarrhythmic azimilide: mode of action. , Busch AE., Br J Pharmacol. January 1, 1998; 123 (1): 23-30.
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., 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., Circ Res. November 1, 1997; 81 (5): 719-26.
Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart. , Jiang M., J Biol Chem. September 26, 1997; 272 (39): 24109-12.
Interactions of the nonsedating antihistamine loratadine with a Kv1.5-type potassium channel cloned from human heart. , Lacerda AE., Mol Pharmacol. August 1, 1997; 52 (2): 314-22.
A minK- HERG complex regulates the cardiac potassium current I(Kr). , McDonald TV., Nature. July 17, 1997; 388 (6639): 289-92.
A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes. , Wang S., J Physiol. July 1, 1997; 502 ( Pt 1) 45-60.
Suppression of mammalian K+ channel family by ebastine. , Ko CM ., J Pharmacol Exp Ther. April 1, 1997; 281 (1): 233-44.