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ICA-105574 interacts with a common binding site to elicit opposite effects on inactivation gating of EAG and ERG potassium channels. , Garg V., Mol Pharmacol. April 1, 2013; 83 (4): 805-13.
Blocking of the human ether-à- go-go-related gene channel by imatinib mesylate. , Dong Q., Biol Pharm Bull. January 1, 2013; 36 (2): 268-75.
A natural point mutation changes both target selectivity and mechanism of action of sea anemone toxins. , Peigneur S., FASEB J. December 1, 2012; 26 (12): 5141-51.
Tuning of EAG K(+) channel inactivation: molecular determinants of amplification by mutations and a small molecule. , Garg V., J Gen Physiol. September 1, 2012; 140 (3): 307-24.
Molecular determinants for activation of human ether-à- go-go-related gene 1 potassium channels by 3-nitro-n-(4-phenoxyphenyl) benzamide. , Garg V., Mol Pharmacol. October 1, 2011; 80 (4): 630-7.
Split-inteins for simultaneous, site-specific conjugation of quantum dots to multiple protein targets in vivo. , Charalambous A., J Nanobiotechnology. September 15, 2011; 9 37.
Effects of the histamine H(1) receptor antagonist hydroxyzine on hERG K(+) channels and cardiac action potential duration. , Lee BH., Acta Pharmacol Sin. September 1, 2011; 32 (9): 1128-37.
Block of the human ether-a- go-go-related gene ( hERG) K+ channel by the antidepressant desipramine. , Hong HK., Biochem Biophys Res Commun. April 9, 2010; 394 (3): 536-41.
Block effect of capsaicin on hERG potassium currents is enhanced by S6 mutation at Y652. , Xing J., Eur J Pharmacol. March 25, 2010; 630 (1-3): 1-9.
Block of HERG k channel by classic histamine h(1) receptor antagonist chlorpheniramine. , Hong HK., Korean J Physiol Pharmacol. June 1, 2009; 13 (3): 215-20.
Protriptyline block of the human ether-à- go-go-related gene ( HERG) K+ channel. , Jo SH., Life Sci. January 30, 2008; 82 (5-6): 331-40.
In vitro modulation of HERG channels by organochlorine solvent trichlormethane as potential explanation for proarrhythmic effects of chloroform. , Scholz EP., Toxicol Lett. August 20, 2006; 165 (2): 156-66.
Blockade of HERG human K+ channels and IKr of guinea-pig cardiomyocytes by the antipsychotic drug clozapine. , Lee SY., Br J Pharmacol. June 1, 2006; 148 (4): 499-509.
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.
An atlas of differential gene expression during early Xenopus embryogenesis. , Pollet N ., Mech Dev. March 1, 2005; 122 (3): 365-439.
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.
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.
Voltage-dependent profile of human ether-a- go-go-related gene channel block is influenced by a single residue in the S6 transmembrane domain. , Sănchez-Chapula JA., Mol Pharmacol. May 1, 2003; 63 (5): 1051-8.
Molecular determinants of voltage-dependent human ether-a- go-go related gene ( HERG) K+ channel block. , Sánchez-Chapula JA., J Biol Chem. June 28, 2002; 277 (26): 23587-95.
Inhibition of cardiac potassium currents by pentobarbital. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.
Molecular determinants of inactivation and dofetilide block in ether a- go-go ( EAG) channels and EAG-related K(+) channels. , Ficker E., Mol Pharmacol. December 1, 2001; 60 (6): 1343-8.
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.
Blockade of the HERG human cardiac K(+) channel by the antidepressant drug amitriptyline. , Jo SH., Br J Pharmacol. April 1, 2000; 129 (7): 1474-80.
The organization of mesodermal pattern in Xenopus laevis: experiments using a Xenopus mesoderm-inducing factor. , Cooke J., Development. December 1, 1987; 101 (4): 893-908.