Papers associated with kcnd2

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	Diminished Kv4.2/3 but not KChIP2 levels reduce the cardiac transient outward K+ current in spontaneously hypertensive rats., Goltz D, Schultz JH, Stucke C, Wagner M, Bassalaý P, Schwoerer AP, Ehmke H, Volk T., Cardiovasc Res. April 1, 2007; 74 (1): 85-95.
	Effects and mechanism of Chinese tarantula toxins on the Kv2.1 potassium channels., Yuan C, Yang S, Liao Z, Liang S., Biochem Biophys Res Commun. January 19, 2007; 352 (3): 799-804.
	A dipeptidyl aminopeptidase-like protein remodels gating charge dynamics in Kv4.2 channels., Dougherty K, Covarrubias M., J Gen Physiol. December 1, 2006; 128 (6): 745-53.
	1,4-Diazabicyclo[2.2.2]octane derivatives: a novel class of voltage-gated potassium channel blockers., Gordon E, Cohen JL, Engel R, Abbott GW., Mol Pharmacol. March 1, 2006; 69 (3): 718-26.
	ERK/MAPK regulates the Kv4.2 potassium channel by direct phosphorylation of the pore-forming subunit., Schrader LA, Birnbaum SG, Nadin BM, Ren Y, Bui D, Anderson AE, Sweatt JD., Am J Physiol Cell Physiol. March 1, 2006; 290 (3): C852-61.
	Multiprotein assembly of Kv4.2, KChIP3 and DPP10 produces ternary channel complexes with ISA-like properties., Jerng HH, Kunjilwar K, Pfaffinger PJ., J Physiol. November 1, 2005; 568 (Pt 3): 767-88.
	A single residue in the S6 transmembrane domain governs the differential flecainide sensitivity of voltage-gated potassium channels., Herrera D, Mamarbachi A, Simoes M, Parent L, Sauvé R, Wang Z, Nattel S., Mol Pharmacol. August 1, 2005; 68 (2): 305-16.
	Functionally active t1-t1 interfaces revealed by the accessibility of intracellular thiolate groups in kv4 channels., Wang G, Shahidullah M, Rocha CA, Strang C, Pfaffinger PJ, Covarrubias M., J Gen Physiol. July 1, 2005; 126 (1): 55-69.
	Modulation of Kv4.2 channel expression and gating by dipeptidyl peptidase 10 (DPP10)., Jerng HH, Qian Y, Pfaffinger PJ., Biophys J. October 1, 2004; 87 (4): 2380-96.
	Calcium-calmodulin-dependent kinase II modulates Kv4.2 channel expression and upregulates neuronal A-type potassium currents., Varga AW, Yuan LL, Anderson AE, Schrader LA, Wu GY, Gatchel JR, Johnston D, Sweatt JD., J Neurosci. April 7, 2004; 24 (14): 3643-54.
	Ito channels are octomeric complexes with four subunits of each Kv4.2 and K+ channel-interacting protein 2., Kim LA, Furst J, Butler MH, Xu S, Grigorieff N, Goldstein SA., J Biol Chem. February 13, 2004; 279 (7): 5549-54.
	PKA modulation of Kv4.2-encoded A-type potassium channels requires formation of a supramolecular complex., Schrader LA, Anderson AE, Mayne A, Pfaffinger PJ, Sweatt JD., J Neurosci. December 1, 2002; 22 (23): 10123-33.
	A role for frequenin, a Ca2+-binding protein, as a regulator of Kv4 K+-currents., Nakamura TY, Pountney DJ, Ozaita A, Nandi S, Ueda S, Rudy B, Coetzee WA., Proc Natl Acad Sci U S A. October 23, 2001; 98 (22): 12808-13.
	Different effects of the Ca(2+)-binding protein, KChIP1, on two Kv4 subfamily members, Kv4.1 and Kv4.2., Nakamura TY, Nandi S, Pountney DJ, Artman M, Rudy B, Coetzee WA., FEBS Lett. June 22, 2001; 499 (3): 205-9.
	minK-related peptide 1 associates with Kv4.2 and modulates its gating function: potential role as beta subunit of cardiac transient outward channel?, Zhang M, Jiang M, Tseng GN., Circ Res. May 25, 2001; 88 (10): 1012-9.
	Nicotine is a potent blocker of the cardiac A-type K(+) channels. Effects on cloned Kv4.3 channels and native transient outward current., Wang H, Shi H, Zhang L, Pourrier M, Yang B, Nattel S, Wang Z., Circulation. September 5, 2000; 102 (10): 1165-71.
	[The expression of arrhythmic related genes on Xenopus oocytes for evaluation of class III antiarrhythmic drugs from ocean active material]., Xu DH, Xu SB., Yi Chuan Xue Bao. January 1, 2000; 27 (3): 195-201.
	Effect of Cd2+ on Kv4.2 and Kv1.4 expressed in Xenopus oocytes and on the transient outward currents in rat and rabbit ventricular myocytes., Wickenden AD, Tsushima RG, Losito VA, Kaprielian R, Backx PH., Cell Physiol Biochem. January 1, 1999; 9 (1): 11-28.
	Unexpected and differential effects of Cl- channel blockers on the Kv4.3 and Kv4.2 K+ channels. Implications for the study of the I(to2) current., Wang HS, Dixon JE, McKinnon D., Circ Res. November 1, 1997; 81 (5): 711-8.
	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.
	Heteropodatoxins: peptides isolated from spider venom that block Kv4.2 potassium channels., Sanguinetti MC, Johnson JH, Hammerland LG, Kelbaugh PR, Volkmann RA, Saccomano NA, Mueller AL., Mol Pharmacol. March 1, 1997; 51 (3): 491-8.
	Reverse use dependence of Kv4.2 blockade by 4-aminopyridine., Tseng GN, Jiang M, Yao JA., J Pharmacol Exp Ther. November 1, 1996; 279 (2): 865-76.

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