Papers associated with cardiovascular system (and kcnb1)

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	Overlapping binding sites of structurally different antiarrhythmics flecainide and propafenone in the subunit interface of potassium channel Kv2.1., Madeja M., J Biol Chem. October 29, 2010; 285 (44): 33898-905.
	Endogenous KCNE subunits govern Kv2.1 K+ channel activation kinetics in Xenopus oocyte studies., Gordon E., Biophys J. February 15, 2006; 90 (4): 1223-31.
	Analysis of voltage-gated potassium channel beta1 subunits in the porcine neonatal ductus arteriosus., Hayama E., Pediatr Res. February 1, 2006; 59 (2): 167-74.
	Kv2.1 channel activation and inactivation is influenced by physical interactions of both syntaxin 1A and the syntaxin 1A/soluble N-ethylmaleimide-sensitive factor-25 (t-SNARE) complex with the C terminus of the channel., Tsuk S., Mol Pharmacol. February 1, 2005; 67 (2): 480-8.
	Regulation of Shaker-type potassium channels by hypoxia. Oxygen-sensitive K+ channels in PC12 cells., Conforti L., Adv Exp Med Biol. January 1, 2000; 475 265-74.
	Heteromeric assembly of Kv2.1 with Kv9.3: effect on the state dependence of inactivation., Kerschensteiner D., Biophys J. July 1, 1999; 77 (1): 248-57.
	Kv2.1/Kv9.3, an ATP-dependent delayed-rectifier K+ channel in pulmonary artery myocytes., Patel AJ., Ann N Y Acad Sci. April 30, 1999; 868 438-41.
	Stable expression and characterization of the human brain potassium channel Kv2.1: blockade by antipsychotic agents., Wible B., Dev Biol. June 27, 1997; 761 (1): 42-50.
	Susceptibility of cloned K+ channels to reactive oxygen species., Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.

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