???pagination.result.count???
???pagination.result.page???
1
Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer. , Levin M ., Cell. April 15, 2021;
GiTx1(β/κ-theraphotoxin-Gi1a), a novel toxin from the venom of Brazilian tarantula Grammostola iheringi (Mygalomorphae, Theraphosidae): Isolation, structural assessments and activity on voltage-gated ion channels. , Montandon GG., Biochimie. September 1, 2020; 176 138-149.
Design and Synthesis of Novel Positive Allosteric Modulators of α7 Nicotinic Acetylcholine Receptors with the Ability To Rescue Auditory Gating Deficit in Mice. , Li Y., J Med Chem. January 10, 2019; 62 (1): 159-173.
Kcnh1 voltage-gated potassium channels are essential for early zebrafish development. , Stengel R., J Biol Chem. October 12, 2012; 287 (42): 35565-35575.
Sig1R protein regulates hERG channel expression through a post-translational mechanism in leukemic cells. , Crottès D., J Biol Chem. August 12, 2011; 286 (32): 27947-58.
Ginsenoside Rg(3) decelerates hERG K(+) channel deactivation through Ser631 residue interaction. , Choi SH., Eur J Pharmacol. August 1, 2011; 663 (1-3): 59-67.
Differential effects of Kv11.1 activators on Kv11.1a, Kv11.1b and Kv11.1a/Kv11.1b channels. , Larsen AP., Br J Pharmacol. October 1, 2010; 161 (3): 614-28.
Tel1/ ETV6 specifies blood stem cells through the agency of VEGF signaling. , Ciau-Uitz A ., Dev Cell. April 20, 2010; 18 (4): 569-78.
Synthesis, structural activity-relationships, and biological evaluation of novel amide-based allosteric binding site antagonists in NR1A/ NR2B N-methyl-D-aspartate receptors. , Mosley CA., Bioorg Med Chem. September 1, 2009; 17 (17): 6463-80.
C101, a novel 4-amino-piperidine derivative selectively blocks N-type calcium channels. , Zhang S., Eur J Pharmacol. June 10, 2008; 587 (1-3): 42-7.
An extracellular Cu2+ binding site in the voltage sensor of BK and Shaker potassium channels. , Ma Z., J Gen Physiol. May 1, 2008; 131 (5): 483-502.
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.
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.
The antidepressant drug fluoxetine is an inhibitor of human ether-a- go-go-related gene ( HERG) potassium channels. , Thomas D., J Pharmacol Exp Ther. February 1, 2002; 300 (2): 543-8.
[Cardiotoxicity of lindane, a gamma isomer of hexachlorocyclohexane]. , Sauviat MP., J Soc Biol. January 1, 2002; 196 (4): 339-48.
Effects of gallium and mercury ions on transport systems. , Moschèn., J Dent Res. August 1, 2001; 80 (8): 1753-7.
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.
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.
Functional analysis of a mouse brain Elk-type K+ channel. , Trudeau MC., J Neurosci. April 15, 1999; 19 (8): 2906-18.
Identification of two nervous system-specific members of the erg potassium channel gene family. , Shi W., J Neurosci. December 15, 1997; 17 (24): 9423-32.
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.
Tissue and species distribution of mRNA for the IKr-like K+ channel, erg. , Wymore RS., Circ Res. February 1, 1997; 80 (2): 261-8.
Potassium currents expressed from Drosophila and mouse eag cDNAs in Xenopus oocytes. , Robertson GA., Neuropharmacology. January 1, 1996; 35 (7): 841-50.