Papers associated with anatomical group (and kcnh2)

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	Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer., Levin M., Cell. April 15, 2021;
	hERG Channel Inhibitory Daphnane Diterpenoid Orthoesters and Polycephalones A and B with Unprecedented Skeletons from Gnidia polycephala., De Mieri M., J Nat Prod. July 24, 2015; 78 (7): 1697-707.
	hERGAPDbase: a database documenting hERG channel inhibitory potentials and APD-prolongation activities of chemical compounds., Hishigaki H., Database (Oxford). May 17, 2011; 2011 bar017.
	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.
	The effects of quinidine and its chiral isolates on erg-1sm potassium current and correlation with gastrointestinal augmentation., Cvetanovic I., Am J Ther. January 1, 2007; 14 (3): 269-76.
	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.
	Effect of beta-adrenoceptor blockers on human ether-a-go-go-related gene (HERG) potassium channels., Dupuis DS., Basic Clin Pharmacol Toxicol. February 1, 2005; 96 (2): 123-30.
	Molecular basis of slow activation of the human ether-a-go-go related gene potassium channel., Subbiah RN., J Physiol. July 15, 2004; 558 (Pt 2): 417-31.
	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.
	Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels., Chen J., Proc Natl Acad Sci U S A. September 17, 2002; 99 (19): 12461-6.
	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.
	Testosterone-mediated modulation of HERG blockade by proarrhythmic agents., Shuba YM., Biochem Pharmacol. July 1, 2001; 62 (1): 41-9.
	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.
	Trapping of a methanesulfonanilide by closure of the HERG potassium channel activation gate., Mitcheson JS., J Gen Physiol. March 1, 2000; 115 (3): 229-40.
	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.
	Potassium currents expressed from Drosophila and mouse eag cDNAs in Xenopus oocytes., Robertson GA., Neuropharmacology. January 1, 1996; 35 (7): 841-50.

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