Papers associated with heart (and kcnj5)

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	A revised mechanism of action of hyperaldosteronism-linked mutations in cytosolic domains of GIRK4 (KCNJ5)., Shalomov B., J Physiol. March 1, 2022; 600 (6): 1419-1437.
	Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation., Yamada N., Circulation. April 30, 2019; 139 (18): 2157-2169.
	Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K+ Channel) Channel Function., Kuß J., Circ Genom Precis Med. January 1, 2019; 12 (1): e002238.
	Cardiac arrhythmia induced by genetic silencing of 'funny' (f) channels is rescued by GIRK4 inactivation., Mesirca P., Nat Commun. August 21, 2014; 5 4664.
	A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1., Kokunai Y., Neurology. March 25, 2014; 82 (12): 1058-64.
	Crystal structure of the mammalian GIRK2 K+ channel and gating regulation by G proteins, PIP2, and sodium., Whorton MR., Cell. September 30, 2011; 147 (1): 199-208.
	Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants., Kobayashi T., PLoS One. January 1, 2011; 6 (12): e28208.
	Characterizations of a loss-of-function mutation in the Kir3.4 channel subunit., Calloe K., Biochem Biophys Res Commun. December 28, 2007; 364 (4): 889-95.
	Inhibition by cocaine of G protein-activated inwardly rectifying K+ channels expressed in Xenopus oocytes., Kobayashi T., Toxicol In Vitro. June 1, 2007; 21 (4): 656-64.
	Mutation of critical GIRK subunit residues disrupts N- and C-termini association and channel function., Sarac R., J Neurosci. February 16, 2005; 25 (7): 1836-46.
	G-protein mediated gating of inward-rectifier K+ channels., Mark MD., Eur J Biochem. October 1, 2000; 267 (19): 5830-6.
	Heterologous facilitation of G protein-activated K(+) channels by beta-adrenergic stimulation via cAMP-dependent protein kinase., Müllner C., J Gen Physiol. May 1, 2000; 115 (5): 547-58.
	Probing the G-protein regulation of GIRK1 and GIRK4, the two subunits of the KACh channel, using functional homomeric mutants., Vivaudou M., J Biol Chem. December 12, 1997; 272 (50): 31553-60.
	Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K+ channel subunit., Chan KW., Proc Natl Acad Sci U S A. November 26, 1996; 93 (24): 14193-8.
	Specificity of coupling of muscarinic receptor isoforms to a novel chick inward-rectifying acetylcholine-sensitive K+ channel., Gadbut AP., J Biol Chem. March 15, 1996; 271 (11): 6398-402.
	Localization and interaction of epitope-tagged GIRK1 and CIR inward rectifier K+ channel subunits., Kennedy ME., Neuropharmacology. January 1, 1996; 35 (7): 831-9.

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