Papers associated with right (and kcnj2)

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	Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer., Levin M., Cell. April 15, 2021;
	Identification of a unique endoplasmic retention motif in the Xenopus GIRK5 channel and its contribution to oocyte maturation., Rangel-Garcia CI., FEBS Open Bio. April 1, 2021; 11 (4): 1093-1108.
	Andersen-Tawil Syndrome Is Associated With Impaired PIP2 Regulation of the Potassium Channel Kir2.1., Handklo-Jamal R., Front Pharmacol. April 7, 2020; 11 672.
	Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome., Adams DS., J Physiol. June 15, 2016; 594 (12): 3245-70.
	Conformational changes underlying pore dilation in the cytoplasmic domain of mammalian inward rectifier K+ channels., Inanobe A., PLoS One. January 1, 2013; 8 (11): e79844.
	Inhibition of G protein-activated inwardly rectifying K+ channels by different classes of antidepressants., Kobayashi T., PLoS One. January 1, 2011; 6 (12): e28208.
	Structural changes in the cytoplasmic pore of the Kir1.1 channel during pHi-gating probed by FRET., Lee JR., J Biomed Sci. March 6, 2009; 16 29.
	Functional roles of charged amino acid residues on the wall of the cytoplasmic pore of Kir2.1., Fujiwara Y., J Gen Physiol. April 1, 2006; 127 (4): 401-19.
	Electrostatics in the cytoplasmic pore produce intrinsic inward rectification in kir2.1 channels., Yeh SH., J Gen Physiol. December 1, 2005; 126 (6): 551-62.
	Long polyamines act as cofactors in PIP2 activation of inward rectifier potassium (Kir2.1) channels., Xie LH., J Gen Physiol. December 1, 2005; 126 (6): 541-9.
	Evidence for sequential ion-binding loci along the inner pore of the IRK1 inward-rectifier K+ channel., Shin HG., J Gen Physiol. August 1, 2005; 126 (2): 123-35.
	Carboxy-terminal determinants of conductance in inward-rectifier K channels., Zhang YY., J Gen Physiol. December 1, 2004; 124 (6): 729-39.
	Molecular basis of inward rectification: polyamine interaction sites located by combined channel and ligand mutagenesis., Kurata HT., J Gen Physiol. November 1, 2004; 124 (5): 541-54.
	Mechanism of inward rectification in Kir channels., John SA., J Gen Physiol. May 1, 2004; 123 (5): 623-5.
	Regulation of Kir channels by intracellular pH and extracellular K(+): mechanisms of coupling., Dahlmann A., J Gen Physiol. April 1, 2004; 123 (4): 441-54.
	Ser165 in the second transmembrane region of the Kir2.1 channel determines its susceptibility to blockade by intracellular Mg2+., Fujiwara Y., J Gen Physiol. November 1, 2002; 120 (5): 677-93.
	Spermine block of the strong inward rectifier potassium channel Kir2.1: dual roles of surface charge screening and pore block., Xie LH., J Gen Physiol. July 1, 2002; 120 (1): 53-66.
	Mutations within the P-loop of Kir6.2 modulate the intraburst kinetics of the ATP-sensitive potassium channel., Proks P., J Gen Physiol. October 1, 2001; 118 (4): 341-53.
	Tyrosine decaging leads to substantial membrane trafficking during modulation of an inward rectifier potassium channel., Tong Y., J Gen Physiol. February 1, 2001; 117 (2): 103-18.
	Mechanism of IRK1 channel block by intracellular polyamines., Guo D., J Gen Physiol. June 1, 2000; 115 (6): 799-814.
	Novel gating mechanism of polyamine block in the strong inward rectifier K channel Kir2.1., Lee JK, Lee JK., J Gen Physiol. April 1, 1999; 113 (4): 555-64.
	Block of the Kir2.1 channel pore by alkylamine analogues of endogenous polyamines., Pearson WL., J Gen Physiol. September 1, 1998; 112 (3): 351-63.
	A conserved arginine residue in the pore region of an inward rectifier K channel (IRK1) as an external barrier for cationic blockers., Sabirov RZ., J Gen Physiol. December 1, 1997; 110 (6): 665-77.

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