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Items: 1 to 20 of 436

1.

Selectivity filter gating in large-conductance Ca(2+)-activated K+ channels.

Thompson J, Begenisich T.

J Gen Physiol. 2012 Mar;139(3):235-44. doi: 10.1085/jgp.201110748.

2.

State-dependent block of BK channels by synthesized shaker ball peptides.

Li W, Aldrich RW.

J Gen Physiol. 2006 Oct;128(4):423-41. Epub 2006 Sep 11.

3.

Functional identification of ion binding sites at the internal end of the pore in Shaker K+ channels.

Thompson J, Begenisich T.

J Physiol. 2003 May 15;549(Pt 1):107-20. Epub 2003 Mar 28.

4.

Unique inner pore properties of BK channels revealed by quaternary ammonium block.

Li W, Aldrich RW.

J Gen Physiol. 2004 Jul;124(1):43-57. Epub 2004 Jun 14.

5.

State-independent block of BK channels by an intracellular quaternary ammonium.

Wilkens CM, Aldrich RW.

J Gen Physiol. 2006 Sep;128(3):347-64.

6.

Evidence for a deep pore activation gate in small conductance Ca2+-activated K+ channels.

Bruening-Wright A, Lee WS, Adelman JP, Maylie J.

J Gen Physiol. 2007 Dec;130(6):601-10. Epub 2007 Nov 12.

8.
9.

Localization of the activation gate for small conductance Ca2+-activated K+ channels.

Bruening-Wright A, Schumacher MA, Adelman JP, Maylie J.

J Neurosci. 2002 Aug 1;22(15):6499-506.

10.

Relationship between pore occupancy and gating in BK potassium channels.

Piskorowski RA, Aldrich RW.

J Gen Physiol. 2006 May;127(5):557-76.

11.

Mechanistic details of BK channel inhibition by the intermediate conductance, Ca2+-activated K channel.

Thompson J, Begenisich T.

Channels (Austin). 2009 May-Jun;3(3):194-204. Epub 2009 May 18.

12.

Block of mouse Slo1 and Slo3 K+ channels by CTX, IbTX, TEA, 4-AP and quinidine.

Tang QY, Zhang Z, Xia XM, Lingle CJ.

Channels (Austin). 2010 Jan-Feb;4(1):22-41. Epub 2010 Jan 2.

13.

Ca2+-activated K channels in parotid acinar cells: The functional basis for the hyperpolarized activation of BK channels.

Romanenko VG, Thompson J, Begenisich T.

Channels (Austin). 2010 Jul-Aug;4(4):278-88. Epub 2010 Jul 28.

14.

Role of charged residues in the S1-S4 voltage sensor of BK channels.

Ma Z, Lou XJ, Horrigan FT.

J Gen Physiol. 2006 Mar;127(3):309-28.

15.

Lack of negative slope in I-V plots for BK channels at positive potentials in the absence of intracellular blockers.

Geng Y, Wang X, Magleby KL.

J Gen Physiol. 2013 Apr;141(4):493-7. doi: 10.1085/jgp.201210955.

17.

Stereospecific binding of a disordered peptide segment mediates BK channel inactivation.

Gonzalez-Perez V, Zeng XH, Henzler-Wildman K, Lingle CJ.

Nature. 2012 May 3;485(7396):133-6. doi: 10.1038/nature10994. Erratum in: Nature. 2012 Sep 27;489(7417):590.

18.

Modulation of BK channel gating by the ß2 subunit involves both membrane-spanning and cytoplasmic domains of Slo1.

Lee US, Shi J, Cui J.

J Neurosci. 2010 Dec 1;30(48):16170-9. doi: 10.1523/JNEUROSCI.2323-10.2010.

19.
20.

1-[1-Hexyl-6-(methyloxy)-1H-indazol-3-yl]-2-methyl-1-propanone, a potent and highly selective small molecule blocker of the large-conductance voltage-gated and calcium-dependent K+ channel.

Zeng H, Gordon E, Lin Z, Lozinskaya IM, Willette RN, Xu X.

J Pharmacol Exp Ther. 2008 Oct;327(1):168-77. doi: 10.1124/jpet.108.139733. Epub 2008 Jun 30.

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