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Biochemical evidence that the whole compartment activity behavior of GAPDH differs between the cytoplasm and nucleus. , Tang HS., PLoS One. January 1, 2023; 18 (8): e0290892.
Measuring Absolute RNA Copy Numbers at High Temporal Resolution Reveals Transcriptome Kinetics in Development. , Owens ND., Cell Rep. January 26, 2016; 14 (3): 632-47.
Concatenated hERG1 tetramers reveal stoichiometry of altered channel gating by RPR-260243. , Wu W., Mol Pharmacol. January 1, 2015; 87 (3): 401-9.
Concerted all-or-none subunit interactions mediate slow deactivation of human ether-à- go-go-related gene K+ channels. , Thomson SJ., J Biol Chem. August 22, 2014; 289 (34): 23428-36.
Effect of azelastine on cardiac repolarization of guinea-pig cardiomyocytes, hERG K⁺ channel, and human L-type and T-type Ca²⁺ channel. , Park MH., J Pharmacol Sci. September 20, 2013; 123 (1): 67-77.
Hydrophobic interactions between the voltage sensor and pore mediate inactivation in Kv11.1 channels. , Perry MD ., J Gen Physiol. September 1, 2013; 142 (3): 275-88.
Serotonin has early, cilia-independent roles in Xenopus left- right patterning. , Vandenberg LN., Dis Model Mech. January 1, 2013; 6 (1): 261-8.
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.
Molecular coupling in the human ether-a- go-go-related gene-1 ( hERG1) K+ channel inactivation pathway. , Ferrer T., J Biol Chem. November 11, 2011; 286 (45): 39091-9.
The amiodarone derivative KB130015 activates hERG1 potassium channels via a novel mechanism. , Gessner G., Eur J Pharmacol. April 25, 2010; 632 (1-3): 52-9.
Topological mapping of the asymmetric drug binding to the human ether-à- go-go-related gene product ( HERG) potassium channel by use of tandem dimers. , Myokai T., Mol Pharmacol. June 1, 2008; 73 (6): 1643-51.
Molecular interaction of droperidol with human ether-a- go-go-related gene channels: prolongation of action potential duration without inducing early afterdepolarization. , Schwoerer AP., Anesthesiology. May 1, 2007; 106 (5): 967-76.
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.
Activation of human ether-a- go-go-related gene potassium channels by the diphenylurea 1,3- bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643). , Hansen RS., Mol Pharmacol. January 1, 2006; 69 (1): 266-77.
Expression and functional characterization of the human ether-à- go-go-related gene ( HERG) K+ channel cardiac splice variant in Xenopus laevis oocytes. , Aydar E., J Membr Biol. January 1, 2006; 211 (2): 115-26.
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.
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.
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.
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.
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.
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.
KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current. , Angelo K., Biophys J. October 1, 2002; 83 (4): 1997-2006.
Inhibition of cardiac potassium currents by pentobarbital. , Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. January 1, 2002; 365 (1): 29-37.
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.
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.
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.
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.
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.
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.
Over-expression of GATA-6 in Xenopus embryos blocks differentiation of heart precursors. , Gove C., EMBO J. January 15, 1997; 16 (2): 355-68.
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.