Papers associated with oocyte (and ikzf1)

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	Enhanced Membrane Incorporation of H289Y Mutant GluK1 Receptors from the Audiogenic Seizure-Prone GASH/Sal Model: Functional and Morphological Impacts on Xenopus Oocytes., Díaz-Rodríguez SM., Int J Mol Sci. November 28, 2023; 24 (23):
	Verapamil inhibits Kir2.3 channels by binding to the pore and interfering with PIP2 binding., Xynogalos P., Naunyn Schmiedebergs Arch Pharmacol. April 1, 2023; 396 (4): 659-667.
	Nocturnal Atrial Fibrillation Caused by Mutation in KCND2, Encoding Pore-Forming (α) Subunit of the Cardiac Kv4.2 Potassium Channel., Drabkin M., Circ Genom Precis Med. November 1, 2018; 11 (11): e002293.
	Dual Mechanism for Inhibition of Inwardly Rectifying Kir2.x Channels by Quinidine Involving Direct Pore Block and PIP2-interference., Koepple C., J Pharmacol Exp Ther. May 1, 2017; 361 (2): 209-218.
	Inhibition of Cardiac Kir Current (IK1) by Protein Kinase C Critically Depends on PKCβ and Kir2.2., Scherer D., PLoS One. May 23, 2016; 11 (5): e0156181.
	Class III antiarrhythmic drug dronedarone inhibits cardiac inwardly rectifying Kir2.1 channels through binding at residue E224., Xynogalos P., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2014; 387 (12): 1153-61.
	Regulation of cardiac inwardly rectifying potassium current IK1 and Kir2.x channels by endothelin-1., Kiesecker C., J Mol Med (Berl). January 1, 2006; 84 (1): 46-56.

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