Papers associated with tail (and kcnma1)

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	BK channel inhibition by strong extracellular acidification., Zhou Y., Elife. July 2, 2018; 7
	Alcohol modulation of BK channel gating depends on β subunit composition., Kuntamallappanavar G., J Gen Physiol. November 1, 2016; 148 (5): 419-440.
	Paxilline inhibits BK channels by an almost exclusively closed-channel block mechanism., Zhou Y., J Gen Physiol. November 1, 2014; 144 (5): 415-40.
	Properties of Slo1 K+ channels with and without the gating ring., Budelli G., Proc Natl Acad Sci U S A. October 8, 2013; 110 (41): 16657-62.
	Distinct sensitivity of slo1 channel proteins to ethanol., Liu J., Mol Pharmacol. January 1, 2013; 83 (1): 235-44.
	Block of mouse Slo1 and Slo3 K+ channels by CTX, IbTX, TEA, 4-AP and quinidine., Tang QY., Channels (Austin). January 1, 2010; 4 (1): 22-41.
	Closed-channel block of BK potassium channels by bbTBA requires partial activation., Tang QY., J Gen Physiol. November 1, 2009; 134 (5): 409-36.
	Interactions between beta subunits of the KCNMB family and Slo3: beta4 selectively modulates Slo3 expression and function., Yang CT., PLoS One. July 3, 2009; 4 (7): e6135.
	{beta} subunit-specific modulations of BK channel function by a mutation associated with epilepsy and dyskinesia., Lee US., J Physiol. April 1, 2009; 587 (Pt 7): 1481-98.
	Ethanol modulates BKCa channels by acting as an adjuvant of calcium., Liu J., Mol Pharmacol. September 1, 2008; 74 (3): 628-40.
	Species-specific Differences among KCNMB3 BK beta3 auxiliary subunits: some beta3 N-terminal variants may be primate-specific subunits., Zeng X., J Gen Physiol. July 1, 2008; 132 (1): 115-29.
	Mg2+ enhances voltage sensor/gate coupling in BK channels., Horrigan FT., J Gen Physiol. January 1, 2008; 131 (1): 13-32.
	Slo3 K+ channels: voltage and pH dependence of macroscopic currents., Zhang X., J Gen Physiol. September 1, 2006; 128 (3): 317-36.
	pH-regulated Slo3 K+ channels: properties of unitary currents., Zhang X., J Gen Physiol. September 1, 2006; 128 (3): 301-15.
	Direct observation of a preinactivated, open state in BK channels with beta2 subunits., Benzinger GR., J Gen Physiol. February 1, 2006; 127 (2): 119-31.
	CaM kinase II phosphorylation of slo Thr107 regulates activity and ethanol responses of BK channels., Liu J., Nat Neurosci. January 1, 2006; 9 (1): 41-9.
	Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner., Kanjhan R., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.
	Divalent cation sensitivity of BK channel activation supports the existence of three distinct binding sites., Zeng XH., J Gen Physiol. March 1, 2005; 125 (3): 273-86.
	BmBKTx1, a novel Ca2+-activated K+ channel blocker purified from the Asian scorpion Buthus martensi Karsch., Xu CQ., J Biol Chem. August 13, 2004; 279 (33): 34562-9.
	Regulation of K+ flow by a ring of negative charges in the outer pore of BKCa channels. Part II: Neutralization of aspartate 292 reduces long channel openings and gating current slow component., Haug T., J Gen Physiol. August 1, 2004; 124 (2): 185-97.
	Regulation of K+ flow by a ring of negative charges in the outer pore of BKCa channels. Part I: Aspartate 292 modulates K+ conduction by external surface charge effect., Haug T., J Gen Physiol. August 1, 2004; 124 (2): 173-84.
	Functional effects of auxiliary beta4-subunit on rat large-conductance Ca(2+)-activated K(+) channel., Ha TS., Biophys J. May 1, 2004; 86 (5): 2871-82.
	Distinct regions of the slo subunit determine differential BKCa channel responses to ethanol., Liu P., Alcohol Clin Exp Res. October 1, 2003; 27 (10): 1640-4.
	Slo1 tail domains, but not the Ca2+ bowl, are required for the beta 1 subunit to increase the apparent Ca2+ sensitivity of BK channels., Qian X., J Gen Physiol. December 1, 2002; 120 (6): 829-43.
	Coupling between voltage sensor activation, Ca2+ binding and channel opening in large conductance (BK) potassium channels., Horrigan FT., J Gen Physiol. September 1, 2002; 120 (3): 267-305.
	Elimination of the BK(Ca) channel's high-affinity Ca(2+) sensitivity., Bao L., J Gen Physiol. August 1, 2002; 120 (2): 173-89.
	Gating and conductance properties of BK channels are modulated by the S9-S10 tail domain of the alpha subunit. A study of mSlo1 and mSlo3 wild-type and chimeric channels., Moss BL., J Gen Physiol. December 1, 2001; 118 (6): 711-34.
	Allosteric regulation of BK channel gating by Ca(2+) and Mg(2+) through a nonselective, low affinity divalent cation site., Zhang X., J Gen Physiol. November 1, 2001; 118 (5): 607-36.
	Gating properties conferred on BK channels by the beta3b auxiliary subunit in the absence of its NH(2)- and COOH termini., Zeng XH., J Gen Physiol. June 1, 2001; 117 (6): 607-28.
	Inactivation of BK channels mediated by the NH(2) terminus of the beta3b auxiliary subunit involves a two-step mechanism: possible separation of binding and blockade., Lingle CJ., J Gen Physiol. June 1, 2001; 117 (6): 583-606.
	Rectification and rapid activation at low Ca2+ of Ca2+-activated, voltage-dependent BK currents: consequences of rapid inactivation by a novel beta subunit., Xia XM., J Neurosci. July 1, 2000; 20 (13): 4890-903.
	Transplantable sites confer calcium sensitivity to BK channels., Schreiber M., Nat Neurosci. May 1, 1999; 2 (5): 416-21.

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