Papers associated with plasma membrane (and kcnh2)

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	APETx4, a Novel Sea Anemone Toxin and a Modulator of the Cancer-Relevant Potassium Channel KV10.1., Moreels L., Mar Drugs. September 13, 2017; 15 (9):
	High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance., Steffensen AB., Sci Rep. January 12, 2015; 5 10009.
	Xenopus borealis as an alternative source of oocytes for biophysical and pharmacological studies of neuronal ion channels., Cristofori-Armstrong B., Sci Rep. January 12, 2015; 5 14763.
	Up-regulation of hERG K⁺ channels by B-RAF., Pakladok T., PLoS One. January 1, 2014; 9 (1): e87457.
	Up-regulation of Kir2.1 (KCNJ2) by the serum & glucocorticoid inducible SGK3., Munoz C., Cell Physiol Biochem. January 1, 2014; 33 (2): 491-500.
	Coxsackievirus B3 modulates cardiac ion channels., Steinke K., FASEB J. October 1, 2013; 27 (10): 4108-21.
	Klotho sensitivity of the hERG channel., Munoz C., FEBS Lett. June 5, 2013; 587 (11): 1663-8.
	PIKfyve sensitivity of hERG channels., Pakladok T., Cell Physiol Biochem. January 1, 2013; 31 (6): 785-94.
	Kcnh1 voltage-gated potassium channels are essential for early zebrafish development., Stengel R., J Biol Chem. October 12, 2012; 287 (42): 35565-35575.
	Stimulation of HERG channel activity by β-catenin., Munoz C., PLoS One. January 1, 2012; 7 (8): e43353.
	A recombinant N-terminal domain fully restores deactivation gating in N-truncated and long QT syndrome mutant hERG potassium channels., Gustina AS., Proc Natl Acad Sci U S A. August 4, 2009; 106 (31): 13082-7.
	Differential modulation of cardiac potassium channels by Grb adaptor proteins., Ureche ON., Biochem Biophys Res Commun. June 19, 2009; 384 (1): 28-31.
	Probing the binding sites and mechanisms of action of two human ether-a-go-go-related gene channel activators, 1,3-bis-(2-hydroxy-5-trifluoromethyl-phenyl)-urea (NS1643) and 2-[2-(3,4-dichloro-phenyl)-2,3-dihydro-1H-isoindol-5-ylamino]-nicotinic acid (PD307243)., Xu X., Mol Pharmacol. June 1, 2008; 73 (6): 1709-21.
	Zebrafish model for human long QT syndrome., Arnaout R., Proc Natl Acad Sci U S A. July 3, 2007; 104 (27): 11316-21.
	Involvement of Golgin-160 in cell surface transport of renal ROMK channel: co-expression of Golgin-160 increases ROMK currents., Bundis F., Cell Physiol Biochem. January 1, 2006; 17 (1-2): 1-12.
	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.
	Upregulation of HERG channels by the serum and glucocorticoid inducible kinase isoform SGK3., Maier G., Cell Physiol Biochem. January 1, 2006; 18 (4-5): 177-86.
	Structural and functional role of the extracellular s5-p linker in the HERG potassium channel., Liu J., J Gen Physiol. November 1, 2002; 120 (5): 723-37.
	KCNE4 is an inhibitory subunit to the KCNQ1 channel., Grunnet M., J Physiol. July 1, 2002; 542 (Pt 1): 119-30.
	Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome., Ficker E., Am J Physiol Heart Circ Physiol. October 1, 2000; 279 (4): H1748-56.
	Novel mechanism associated with an inherited cardiac arrhythmia: defective protein trafficking by the mutant HERG (G601S) potassium channel., Furutani M., Circulation. May 4, 1999; 99 (17): 2290-4.

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