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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.
The RCK2 domain uses a coordination site present in Kir channels to confer sodium sensitivity to Slo2.2 channels. , Zhang Z ., J Neurosci. June 2, 2010; 30 (22): 7554-62.
Synthesis and characterisation of NS13558: a new important tool for addressing KCa1.1 channel function ex vivo. , Bentzen BH., Naunyn Schmiedebergs Arch Pharmacol. March 1, 2010; 381 (3): 271-83.
Channel beta2-4 subunits fail to substitute for beta1 in sensitizing BK channels to lithocholate. , Bukiya AN., Biochem Biophys Res Commun. December 18, 2009; 390 (3): 995-1000.
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.
Differential expression of BK channel isoforms and beta-subunits in rat neuro-vascular tissues. , Poulsen AN., Biochim Biophys Acta. February 1, 2009; 1788 (2): 380-9.
Ethanol modulates BKCa channels by acting as an adjuvant of calcium. , Liu J ., Mol Pharmacol. September 1, 2008; 74 (3): 628-40.
Mg2+ enhances voltage sensor/gate coupling in BK channels. , Horrigan FT., J Gen Physiol. January 1, 2008; 131 (1): 13-32.
The small molecule NS11021 is a potent and specific activator of Ca2+-activated big-conductance K+ channels. , Bentzen BH., Mol Pharmacol. October 1, 2007; 72 (4): 1033-44.
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.
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.
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 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.
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.