Papers associated with nerve (and kcnj2)

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	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.
	Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3., Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
	K+ binding in the G-loop and water cavity facilitates Ba2+ movement in the Kir2.1 channel., Chang HK., Biochim Biophys Acta. February 1, 2009; 1788 (2): 500-6.
	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.
	Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation., Davies NP., Neurology. October 11, 2005; 65 (7): 1083-9.
	Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine., Shin HG., J Gen Physiol. April 1, 2005; 125 (4): 413-26.
	Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification., Pegan S., Nat Neurosci. March 1, 2005; 8 (3): 279-87.
	A ring of negative charges in the intracellular vestibule of Kir2.1 channel modulates K+ permeation., Chang HK., Biophys J. January 1, 2005; 88 (1): 243-54.
	Carboxy-terminal determinants of conductance in inward-rectifier K channels., Zhang YY., J Gen Physiol. December 1, 2004; 124 (6): 729-39.
	Regulation of gating by negative charges in the cytoplasmic pore in the Kir2.1 channel., Xie LH., J Physiol. November 15, 2004; 561 (Pt 1): 159-68.
	Polymorphic ventricular tachycardia and KCNJ2 mutations., Chun TU., Heart Rhythm. July 1, 2004; 1 (2): 235-41.
	betaL-betaM loop in the C-terminal domain of G protein-activated inwardly rectifying K(+) channels is important for G(betagamma) subunit activation., Finley M., J Physiol. March 16, 2004; 555 (Pt 3): 643-57.
	The effects of spermine on the accessibility of residues in the M2 segment of Kir2.1 channels expressed in Xenopus oocytes., Chang HK., J Physiol. November 15, 2003; 553 (Pt 1): 101-12.
	Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components., Xie LH., J Physiol. July 1, 2003; 550 (Pt 1): 67-82.
	Contribution of cytosolic cysteine residues to the gating properties of the Kir2.1 inward rectifier., Garneau L., Biophys J. June 1, 2003; 84 (6): 3717-29.
	Mechanism of rectification in inward-rectifier K+ channels., Guo D., J Gen Physiol. April 1, 2003; 121 (4): 261-75.
	Inhibition of G protein-activated inwardly rectifying K+ channels by fluoxetine (Prozac)., Kobayashi T., Br J Pharmacol. March 1, 2003; 138 (6): 1119-28.
	Specificity of activation by phosphoinositides determines lipid regulation of Kir channels., Rohács T., Proc Natl Acad Sci U S A. January 21, 2003; 100 (2): 745-50.
	Conformational changes in Kir2.1 channels during NH4+-induced inactivation., Chang HK., J Biol Chem. January 10, 2003; 278 (2): 908-18.
	Identification of a site involved in the block by extracellular Mg(2+) and Ba(2+) as well as permeation of K(+) in the Kir2.1 K(+) channel., Murata Y., J Physiol. November 1, 2002; 544 (3): 665-77.
	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.
	Acute suppression of inwardly rectifying Kir2.1 channels by direct tyrosine kinase phosphorylation., Wischmeyer E., J Biol Chem. December 18, 1998; 273 (51): 34063-8.
	Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel., Kubo Y., Nature. August 26, 1993; 364 (6440): 802-6.

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