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Summary Anatomy Item Literature (2360) Expression Attributions Wiki

Papers associated with heart (and kcnd3)

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β Subunits Functionally Differentiate Human Kv4.3 Potassium Channel Splice Variants., Abbott GW., Front Physiol. February 8, 2017; 8 66.                  

Central role of PKCα in isoenzyme-selective regulation of cardiac transient outward current Ito and Kv4.3 channels., Scholz EP., J Mol Cell Cardiol. November 1, 2011; 51 (5): 722-9.

Extracellular potassium inhibits Kv7.1 potassium channels by stabilizing an inactivated state., Larsen AP., Biophys J. August 17, 2011; 101 (4): 818-27.

[Inhibition of Jingzhaotoxin-V on Kv4.3 channel]., Cai LJ., Sheng Li Xue Bao. June 25, 2010; 62 (3): 255-60.

Structural basis for modulation of Kv4 K+ channels by auxiliary KChIP subunits., Wang H., Nat Neurosci. January 1, 2007; 10 (1): 32-9.

KCNE3 is an inhibitory subunit of the Kv4.3 potassium channel., Lundby A., Biochem Biophys Res Commun. August 4, 2006; 346 (3): 958-67.

KChIP2b modulates the affinity and use-dependent block of Kv4.3 by nifedipine., Bett GC., Biochem Biophys Res Commun. February 24, 2006; 340 (4): 1167-77.

Heteropoda toxin 2 is a gating modifier toxin specific for voltage-gated K+ channels of the Kv4 family., Zarayskiy VV., Toxicon. March 15, 2005; 45 (4): 431-42.

Novel KChIP2 isoforms increase functional diversity of transient outward potassium currents., Decher N., J Physiol. June 15, 2004; 557 (Pt 3): 761-72.

Activation properties of Kv4.3 channels: time, voltage and [K+]o dependence., Wang S., J Physiol. June 15, 2004; 557 (Pt 3): 705-17.

Differential inhibition of transient outward currents of Kv1.4 and Kv4.3 by endothelin., Hagiwara K., Biochem Biophys Res Commun. October 17, 2003; 310 (2): 634-40.

Elucidating KChIP effects on Kv4.3 inactivation and recovery kinetics with a minimal KChIP2 isoform., Patel SP., J Physiol. November 15, 2002; 545 (1): 5-11.

Heterogeneous expression of KChIP2 isoforms in the ferret heart., Patel SP., J Physiol. March 15, 2002; 539 (Pt 3): 649-56.

Elimination of fast inactivation in Kv4 A-type potassium channels by an auxiliary subunit domain., Holmqvist MH., Proc Natl Acad Sci U S A. January 22, 2002; 99 (2): 1035-40.

Characterization of a novel Kv1.5 channel blocker in Xenopus oocytes, CHO cells, human and rat cardiomyocytes., Bachmann A., Naunyn Schmiedebergs Arch Pharmacol. November 1, 2001; 364 (5): 472-8.

Remodeling of Kv4.3 potassium channel gene expression under the control of sex hormones., Song M., J Biol Chem. August 24, 2001; 276 (34): 31883-90.

Regulation of KChIP2 potassium channel beta subunit gene expression underlies the gradient of transient outward current in canine and human ventricle., Rosati B., J Physiol. May 15, 2001; 533 (Pt 1): 119-25.

Cloning and expression of the human kv4.3 potassium channel., Dilks D., J Neurophysiol. April 1, 1999; 81 (4): 1974-7.

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., Circ Res. November 1, 1997; 81 (5): 711-8.

Suppression of slow delayed rectifier current by a truncated isoform of KvLQT1 cloned from normal human heart., Jiang M., J Biol Chem. September 26, 1997; 272 (39): 24109-12.

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