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Calcium-activated potassium channels expressed from cloned complementary DNAs. , Adelman JP, Shen KZ, Kavanaugh MP, Warren RA, Wu YN, Lagrutta A, Bond CT, North RA., Neuron. August 1, 1992; 9 (2): 209-16.
Reconstitution of expressed KCa channels from Xenopus oocytes to lipid bilayers. , Pérez G, Lagrutta A, Adelman JP, Toro L., Biophys J. April 1, 1994; 66 (4): 1022-7.
Opening of large-conductance calcium-activated potassium channels by the substituted benzimidazolone NS004. , McKay MC, Dworetzky SI, Meanwell NA, Olesen SP, Reinhart PH, Levitan IB, Adelman JP, Gribkoff VK., J Neurophysiol. May 1, 1994; 71 (5): 1873-82.
Cloned Ca(2+)-dependent K+ channel modulated by a functionally associated protein kinase. , Esguerra M, Wang J , Foster CD, Adelman JP, North RA, Levitan IB., Nature. June 16, 1994; 369 (6481): 563-5.
A calcium switch for the functional coupling between alpha (hslo) and beta subunits (KV,Ca beta) of maxi K channels. , Meera P, Wallner M, Jiang Z , Toro L., FEBS Lett. March 11, 1996; 382 (1-2): 84-8.
A cysteine-rich domain defined by a novel exon in a slo variant in rat adrenal chromaffin cells and PC12 cells. , Saito M, Nelson C, Salkoff L, Lingle CJ., J Biol Chem. May 2, 1997; 272 (18): 11710-7.
Voltage-controlled gating in a large conductance Ca2+-sensitive K+channel (hslo). , Stefani E, Ottolia M, Noceti F, Olcese R, Wallner M, Latorre R, Toro L., Proc Natl Acad Sci U S A. May 13, 1997; 94 (10): 5427-31.
dSLo interacting protein 1, a novel protein that interacts with large-conductance calcium-activated potassium channels. , Xia Xm, Hirschberg B, Smolik S, Forte M, Adelman JP., J Neurosci. April 1, 1998; 18 (7): 2360-9.
Control of alternative splicing of potassium channels by stress hormones. , Xie J, McCobb DP., Science. April 17, 1998; 280 (5362): 443-6.
Role of the S4 segment in a voltage-dependent calcium-sensitive potassium (hSlo) channel. , Díaz L, Meera P, Amigo J, Stefani E, Alvarez O, Toro L, Latorre R., J Biol Chem. December 4, 1998; 273 (49): 32430-6.
Molecular basis of fast inactivation in voltage and Ca2+-activated K+ channels: a transmembrane beta-subunit homolog. , Wallner M, Meera P, Toro L., Proc Natl Acad Sci U S A. March 30, 1999; 96 (7): 4137-42.
Transplantable sites confer calcium sensitivity to BK channels. , Schreiber M, Yuan A, Salkoff L., Nat Neurosci. May 1, 1999; 2 (5): 416-21.
Molecular basis for the inactivation of Ca2+- and voltage-dependent BK channels in adrenal chromaffin cells and rat insulinoma tumor cells. , Xia XM, Ding JP, Lingle CJ., J Neurosci. July 1, 1999; 19 (13): 5255-64.
MEK and Cdc2 kinase are sequentially required for Golgi disassembly in MDCK cells by the mitotic Xenopus extracts. , Kano F, Takenaka K, Yamamoto A, Nagayama K, Nishida E , Murata M., J Cell Biol. April 17, 2000; 149 (2): 357-68.
A neuronal beta subunit ( KCNMB4) makes the large conductance, voltage- and Ca2+-activated K+ channel resistant to charybdotoxin and iberiotoxin. , Meera P, Wallner M, Toro L., Proc Natl Acad Sci U S A. May 9, 2000; 97 (10): 5562-7.
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, Ding JP, Zeng XH, Duan KL, Lingle CJ., J Neurosci. July 1, 2000; 20 (13): 4890-903.
Gating properties conferred on BK channels by the beta3b auxiliary subunit in the absence of its NH(2)- and COOH termini. , Zeng XH, Ding JP, Xia XM, Lingle CJ., 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, Zeng XH, Ding JP, Xia XM., J Gen Physiol. June 1, 2001; 117 (6): 583-606.
Allosteric regulation of BK channel gating by Ca(2+) and Mg(2+) through a nonselective, low affinity divalent cation site. , Zhang X, Solaro CR, Lingle CJ., J Gen Physiol. November 1, 2001; 118 (5): 607-36.
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, Magleby KL., J Gen Physiol. December 1, 2001; 118 (6): 711-34.
SLO-1 potassium channels control quantal content of neurotransmitter release at the C. elegans neuromuscular junction. , Wang ZW, Saifee O, Nonet ML, Salkoff L., Neuron. December 6, 2001; 32 (5): 867-81.
Consequences of the stoichiometry of Slo1 alpha and auxiliary beta subunits on functional properties of large-conductance Ca2+-activated K+ channels. , Wang YW, Ding JP, Xia XM, Lingle CJ., J Neurosci. March 1, 2002; 22 (5): 1550-61.
Steady-state and closed-state inactivation properties of inactivating BK channels. , Ding JP, Lingle CJ., Biophys J. May 1, 2002; 82 (5): 2448-65.
Elimination of the BK(Ca) channel's high-affinity Ca(2+) sensitivity. , Bao L, Rapin AM, Holmstrand EC, Cox DH., J Gen Physiol. August 1, 2002; 120 (2): 173-89.
Coupling between voltage sensor activation, Ca2+ binding and channel opening in large conductance (BK) potassium channels. , Horrigan FT, Aldrich RW., J Gen Physiol. September 1, 2002; 120 (3): 267-305.
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, Nimigean CM, Niu X, Moss BL, Magleby KL., J Gen Physiol. December 1, 2002; 120 (6): 829-43.
Inactivation of BK channels by the NH2 terminus of the beta2 auxiliary subunit: an essential role of a terminal peptide segment of three hydrophobic residues. , Xia XM, Ding JP, Lingle CJ., J Gen Physiol. February 1, 2003; 121 (2): 125-48.
The sodium-activated potassium channel is encoded by a member of the Slo gene family. , Yuan A, Santi CM, Wei A, Wang ZW, Pollak K, Nonet M, Kaczmarek L, Crowder CM, Salkoff L., Neuron. March 6, 2003; 37 (5): 765-73.
Distinct regions of the slo subunit determine differential BKCa channel responses to ethanol. , Liu P, Liu J , Huang W, Li MD, Dopico AM., Alcohol Clin Exp Res. October 1, 2003; 27 (10): 1640-4.
Selective regulation of xSlo splice variants during Xenopus embryogenesis. , Kukuljan M , Taylor A, Chouinard H, Olguin P, Rojas CV, Ribera AB ., J Neurophysiol. November 1, 2003; 90 (5): 3352-60.
Functional effects of auxiliary beta4-subunit on rat large-conductance Ca(2+)-activated K(+) channel. , Ha TS, Heo MS, Park CS., Biophys J. May 1, 2004; 86 (5): 2871-82.
Ligand-dependent activation of Slo family channels is defined by interchangeable cytosolic domains. , Xia XM, Zhang X, Lingle CJ., J Neurosci. June 16, 2004; 24 (24): 5585-91.
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, Olcese R, Toro L, Stefani E., 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, Sigg D, Ciani S, Toro L, Stefani E, Olcese R., J Gen Physiol. August 1, 2004; 124 (2): 173-84.
BmBKTx1, a novel Ca2+-activated K+ channel blocker purified from the Asian scorpion Buthus martensi Karsch. , Xu CQ, Brône B, Wicher D, Bozkurt O, Lu WY, Huys I, Han YH, Tytgat J, Van Kerkhove E, Chi CW., J Biol Chem. August 13, 2004; 279 (33): 34562-9.
Divalent cation sensitivity of BK channel activation supports the existence of three distinct binding sites. , Zeng XH, Xia XM, Lingle CJ., J Gen Physiol. March 1, 2005; 125 (3): 273-86.
Tertiapin-Q blocks recombinant and native large conductance K+ channels in a use-dependent manner. , Kanjhan R, Coulson EJ, Adams DJ, Bellingham MC., J Pharmacol Exp Ther. September 1, 2005; 314 (3): 1353-61.
CaM kinase II phosphorylation of slo Thr107 regulates activity and ethanol responses of BK channels. , Liu J , Asuncion-Chin M, Liu P, Dopico AM., Nat Neurosci. January 1, 2006; 9 (1): 41-9.
Direct observation of a preinactivated, open state in BK channels with beta2 subunits. , Benzinger GR, Xia XM, Lingle CJ., J Gen Physiol. February 1, 2006; 127 (2): 119-31.
Opposite regulation of Slick and Slack K+ channels by neuromodulators. , Santi CM, Ferreira G, Yang B, Gazula VR, Butler A, Wei A, Kaczmarek LK, Salkoff L., J Neurosci. May 10, 2006; 26 (19): 5059-68.
Slo3 K+ channels: voltage and pH dependence of macroscopic currents. , Zhang X, Zeng X, Lingle CJ., J Gen Physiol. September 1, 2006; 128 (3): 317-36.
pH-regulated Slo3 K+ channels: properties of unitary currents. , Zhang X, Zeng X, Xia XM, Lingle CJ., J Gen Physiol. September 1, 2006; 128 (3): 301-15.
Interaction sites between the Slo1 pore and the NH2 terminus of the beta2 subunit, probed with a three-residue sensor. , Li H, Yao J, Tong X, Guo Z, Wu Y, Sun L, Pan N, Wu H, Xu T, Ding J., J Biol Chem. June 15, 2007; 282 (24): 17720-8.
Characterization of voltage-and Ca2+-activated K+ channels in rat dorsal root ganglion neurons. , Li W , Gao SB, Lv CX, Wu Y, Guo ZH, Ding JP, Xu T., J Cell Physiol. August 1, 2007; 212 (2): 348-57.
Presynaptic Ca2+/calmodulin-dependent protein kinase II modulates neurotransmitter release by activating BK channels at Caenorhabditis elegans neuromuscular junction. , Liu Q, Chen B, Ge Q, Wang ZW., J Neurosci. September 26, 2007; 27 (39): 10404-13.
The small molecule NS11021 is a potent and specific activator of Ca2+-activated big-conductance K+ channels. , Bentzen BH, Nardi A, Calloe K, Madsen LS, Olesen SP, Grunnet M., Mol Pharmacol. October 1, 2007; 72 (4): 1033-44.
Mg2+ enhances voltage sensor/gate coupling in BK channels. , Horrigan FT, Ma Z., J Gen Physiol. January 1, 2008; 131 (1): 13-32.
The sodium-activated potassium channel Slack is modulated by hypercapnia and acidosis. , Ruffin VA, Gu XQ, Zhou D, Douglas RM, Sun X, Trouth CO, Haddad GG., Neuroscience. January 24, 2008; 151 (2): 410-8.
Species-specific Differences among KCNMB3 BK beta3 auxiliary subunits: some beta3 N-terminal variants may be primate-specific subunits. , Zeng X, Xia XM, Lingle CJ., J Gen Physiol. July 1, 2008; 132 (1): 115-29.
Ethanol modulates BKCa channels by acting as an adjuvant of calcium. , Liu J , Vaithianathan T, Manivannan K, Parrill A, Dopico AM., Mol Pharmacol. September 1, 2008; 74 (3): 628-40.