Papers associated with Xenopus anatomical entity (and kcnd3)

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	β Subunits Functionally Differentiate Human Kv4.3 Potassium Channel Splice Variants., Abbott GW., Front Physiol. January 1, 2017; 8 66.
	Genome evolution in the allotetraploid frog Xenopus laevis., Session AM., Nature. October 20, 2016; 538 (7625): 336-343.
	Diminished Kv4.2/3 but not KChIP2 levels reduce the cardiac transient outward K+ current in spontaneously hypertensive rats., Goltz D., Cardiovasc Res. April 1, 2007; 74 (1): 85-95.
	Structural basis for modulation of Kv4 K+ channels by auxiliary KChIP subunits., Wang H., Nat Neurosci. January 1, 2007; 10 (1): 32-9.
	Regulation of Kv4.3 closed state inactivation and recovery by extracellular potassium and intracellular KChIP2b., Amadi CC., Channels (Austin). January 1, 2007; 1 (4): 305-14.
	Functionally active t1-t1 interfaces revealed by the accessibility of intracellular thiolate groups in kv4 channels., Wang G., J Gen Physiol. July 1, 2005; 126 (1): 55-69.
	Expression of voltage-dependent potassium channels in the developing visual system of Xenopus laevis., Pollock NS., J Comp Neurol. October 28, 2002; 452 (4): 381-91.
	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, expression and CNS distribution of Kv4.3, an A-type K+ channel alpha subunit., Tsaur ML., FEBS Lett. January 3, 1997; 400 (2): 215-20.

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