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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.
A quantitative hypermorphic CNGC allele confers ectopic calcium flux and impairs cellular development. , Chiasson DM., Elife. September 21, 2017; 6
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.
Global absolute quantification reveals tight regulation of protein expression in single Xenopus eggs. , Smits AH., Nucleic Acids Res. September 1, 2014; 42 (15): 9880-91.
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.
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.
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.
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 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.
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.
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.
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.
Molecular mapping of a site for Cd2+-induced modification of human ether-à- go-go-related gene ( hERG) channel activation. , Fernandez D., J Physiol. September 15, 2005; 567 (Pt 3): 737-55.
Go G-proteins mediate rapid heterologous desensitization of G-protein coupled receptors in Xenopus oocytes. , Van-Ham II., J Cell Physiol. August 1, 2005; 204 (2): 455-62.
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.
Response to lysophosphatidic acid in Xenopus oocytes and its rapid desensitization: the role of Gq and Go G-protein families. , Van-Ham II., J Cell Physiol. July 1, 2004; 200 (1): 125-33.
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.
Open channel block by KCB-328 [1-(2-amino-4-methanesulfonamidophenoxy)-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane hydrochloride] of the heterologously expressed human ether-a- go-go-related gene K+ channels. , Park JB ., J Pharmacol Exp Ther. July 1, 2002; 302 (1): 314-9.
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.
Antiarrhythmic drug carvedilol inhibits HERG potassium channels. , Karle CA., Cardiovasc Res. February 1, 2001; 49 (2): 361-70.
Inhibition of human ether à go-go potassium channels by Ca(2+)/calmodulin. , Schönherr R., EMBO J. July 3, 2000; 19 (13): 3263-71.
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.