Papers associated with kcnh1

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	Blockade of HERG channels expressed in Xenopus oocytes by external H+., Jo SH, Youm JB, Kim I, Lee CO, Lee CO, Earm YE, Ho WK., Pflugers Arch. June 1, 1999; 438 (1): 23-9.
	Functional analysis of a mouse brain Elk-type K+ channel., Trudeau MC, Titus SA, Branchaw JL, Ganetzky B, Robertson GA., J Neurosci. April 15, 1999; 19 (8): 2906-18.
	Blockade of HERG channels expressed in Xenopus laevis oocytes by external divalent cations., Ho WK, Kim I, Lee CO, Lee CO, Youm JB, Lee SH, Earm YE., Biophys J. April 1, 1999; 76 (4): 1959-71.
	Cell cycle-related changes in the conducting properties of r-eag K+ channels., Pardo LA, Brüggemann A, Camacho J, Stühmer W., J Cell Biol. November 2, 1998; 143 (3): 767-75.
	Cloning of a mammalian elk potassium channel gene and EAG mRNA distribution in rat sympathetic ganglia., Shi W, Wang HS, Pan Z, Wymore RS, Cohen IS, McKinnon D, Dixon JE., J Physiol. September 15, 1998; 511 ( Pt 3) (Pt 3): 675-82.
	KCR1, a membrane protein that facilitates functional expression of non-inactivating K+ currents associates with rat EAG voltage-dependent K+ channels., Hoshi N, Takahashi H, Shahidullah M, Yokoyama S, Higashida H., J Biol Chem. September 4, 1998; 273 (36): 23080-5.
	Shaker and ether-à-go-go K+ channel subunits fail to coassemble in Xenopus oocytes., Tang CY, Schulteis CT, Jiménez RM, Papazian DM., Biophys J. September 1, 1998; 75 (3): 1263-70.
	A mutation in the pore region of HERG K+ channels expressed in Xenopus oocytes reduces rectification by shifting the voltage dependence of inactivation., Zou A, Xu QP, Sanguinetti MC., J Physiol. May 15, 1998; 509 ( Pt 1) 129-37.
	Voltage-dependent blockade of HERG channels expressed in Xenopus oocytes by external Ca2+ and Mg2+., Ho WK, Kim I, Lee CO, Lee CO, Earm YE., J Physiol. March 15, 1998; 507 ( Pt 3) (Pt 3): 631-8.
	Interaction of the K channel beta subunit, Hyperkinetic, with eag family members., Wilson GF, Wang Z, Chouinard SW, Griffith LC, Ganetzky B., J Biol Chem. March 13, 1998; 273 (11): 6389-94.
	herg encodes a K+ current highly conserved in tumors of different histogenesis: a selective advantage for cancer cells?, Bianchi L, Wible B, Arcangeli A, Taglialatela M, Morra F, Castaldo P, Crociani O, Rosati B, Faravelli L, Olivotto M, Wanke E., Cancer Res. February 15, 1998; 58 (4): 815-22.
	Influence of detergents on the function of cloned potassium channels., Höllerer-Beitz G, Heinemann SH., Recept Channels. January 1, 1998; 5 (2): 61-78.
	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, Trudeau MC, Newton KP, Beyer AK, Copeland NG, Gilbert DJ, Jenkins NA, Satler CA, Robertson GA., Circ Res. November 1, 1997; 81 (5): 870-8.
	Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241., Suessbrich H, Schönherr R, Heinemann SH, Lang F, Busch AE., FEBS Lett. September 8, 1997; 414 (2): 435-8.
	Amino terminal-dependent gating of the potassium channel rat eag is compensated by a mutation in the S4 segment., Terlau H, Heinemann SH, Stühmer W, Pongs O, Ludwig J., J Physiol. August 1, 1997; 502 ( Pt 3) 537-43.
	The inhibitory effect of the antipsychotic drug haloperidol on HERG potassium channels expressed in Xenopus oocytes., Suessbrich H, Schönherr R, Heinemann SH, Attali B, Lang F, Busch AE., Br J Pharmacol. March 1, 1997; 120 (5): 968-74.
	Mitosis-promoting factor-mediated suppression of a cloned delayed rectifier potassium channel expressed in Xenopus oocytes., Brüggemann A, Stühmer W, Pardo LA., Proc Natl Acad Sci U S A. January 21, 1997; 94 (2): 537-42.
	Molecular physiology and pharmacology of HERG. Single-channel currents and block by dofetilide., Kiehn J, Lacerda AE, Wible B, Brown AM., Circulation. November 15, 1996; 94 (10): 2572-9.
	Heteromultimeric interactions among K+ channel subunits from Shaker and eag families in Xenopus oocytes., Chen ML, Hoshi T, Wu CF., Neuron. September 1, 1996; 17 (3): 535-42.
	HERG, a primary human ventricular target of the nonsedating antihistamine terfenadine., Roy M, Dumaine R, Brown AM., Circulation. August 15, 1996; 94 (4): 817-23.
	Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel., Schönherr R, Heinemann SH., J Physiol. June 15, 1996; 493 ( Pt 3) 635-42.
	Extracellular Mg2+ regulates activation of rat eag potassium channel., Terlau H, Ludwig J, Steffan R, Pongs O, Stühmer W, Heinemann SH., Pflugers Arch. June 1, 1996; 432 (2): 301-12.
	Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole., Suessbrich H, Waldegger S, Lang F, Busch AE., FEBS Lett. April 29, 1996; 385 (1-2): 77-80.
	Potassium currents expressed from Drosophila and mouse eag cDNAs in Xenopus oocytes., Robertson GA, Warmke JM, Ganetzky B., Neuropharmacology. January 1, 1996; 35 (7): 841-50.
	Functional expression of a rat homologue of the voltage gated either á go-go potassium channel reveals differences in selectivity and activation kinetics between the Drosophila channel and its mammalian counterpart., Ludwig J, Terlau H, Wunder F, Brüggemann A, Pardo LA, Marquardt A, Stühmer W, Pongs O., EMBO J. October 3, 1994; 13 (19): 4451-8.
	Ether-à-go-go encodes a voltage-gated channel permeable to K+ and Ca2+ and modulated by cAMP., Brüggemann A, Pardo LA, Stühmer W, Pongs O., Nature. September 30, 1993; 365 (6445): 445-8.

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