Papers associated with artery (and gnao1)

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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.
	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.
	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.
	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.
	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.
	Inhibition of human ether à go-go potassium channels by Ca(2+)/calmodulin., Schönherr R., EMBO J. July 3, 2000; 19 (13): 3263-71.

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