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Domain-domain interactions determine the gating, permeation, pharmacology, and subunit modulation of the IKs ion channel. , Zaydman MA., Elife. March 12, 2014; 3 e03606.
Hydrophobic interactions between the voltage sensor and pore mediate inactivation in Kv11.1 channels. , Perry MD ., J Gen Physiol. September 1, 2013; 142 (3): 275-88.
Molecular coupling in the human ether-a- go-go-related gene-1 ( hERG1) K+ channel inactivation pathway. , Ferrer T., J Biol Chem. November 11, 2011; 286 (45): 39091-9.
A molecular switch between the outer and the inner vestibules of the voltage-gated Na+ channel. , Zarrabi T., J Biol Chem. December 10, 2010; 285 (50): 39458-70.
Overlapping binding sites of structurally different antiarrhythmics flecainide and propafenone in the subunit interface of potassium channel Kv2.1. , Madeja M., J Biol Chem. October 29, 2010; 285 (44): 33898-905.
The molecular basis for the actions of KVbeta1.2 on the opening and closing of the KV1.2 delayed rectifier channel. , Peters CJ., Channels (Austin). January 1, 2009; 3 (5): 314-22.
KCNQ1 and KCNE1 in the IKs channel complex make state-dependent contacts in their extracellular domains. , Xu X., J Gen Physiol. June 1, 2008; 131 (6): 589-603.
Intrinsic electrostatic potential in the BK channel pore: role in determining single channel conductance and block. , Carvacho I., J Gen Physiol. February 1, 2008; 131 (2): 147-61.
KCNE1 and KCNE3 stabilize and/or slow voltage sensing S4 segment of KCNQ1 channel. , Nakajo K., J Gen Physiol. September 1, 2007; 130 (3): 269-81.
The role of S4 charges in voltage-dependent and voltage-independent KCNQ1 potassium channel complexes. , Panaghie G., J Gen Physiol. February 1, 2007; 129 (2): 121-33.
Access of quaternary ammonium blockers to the internal pore of cyclic nucleotide-gated channels: implications for the location of the gate. , Contreras JE., J Gen Physiol. May 1, 2006; 127 (5): 481-94.
Expression and function of native potassium channel [K(V)alpha1] subunits in terminal arterioles of rabbit. , Cheong A., J Physiol. August 1, 2001; 534 (Pt 3): 691-700.
Cloning and expression of three K+ channel cDNAs from Xenopus muscle. , Fry M., Brain Res Mol Brain Res. June 20, 2001; 90 (2): 135-48.
Inhibition of the K+ channel kv1.4 by acidosis: protonation of an extracellular histidine slows the recovery from N-type inactivation. , Claydon TW., J Physiol. July 15, 2000; 526 Pt 2 253-64.
Regulation of Shaker-type potassium channels by hypoxia. Oxygen-sensitive K+ channels in PC12 cells. , Conforti L., Adv Exp Med Biol. January 1, 2000; 475 265-74.
Distribution in rat brain of binding sites of kaliotoxin, a blocker of Kv1.1 and Kv1.3 alpha-subunits. , Mourre C., J Pharmacol Exp Ther. December 1, 1999; 291 (3): 943-52.
Differential sensitivity of voltage-gated potassium channels Kv1.5 and Kv1.2 to acidic pH and molecular identification of pH sensor. , Steidl JV., Mol Pharmacol. May 1, 1999; 55 (5): 812-20.
Specific block of cloned Herg channels by clofilium and its tertiary analog LY97241. , Suessbrich H., FEBS Lett. September 8, 1997; 414 (2): 435-8.
Xenopus spinal neurons express Kv2 potassium channel transcripts during embryonic development. , Burger C., J Neurosci. February 15, 1996; 16 (4): 1412-21.
Susceptibility of cloned K+ channels to reactive oxygen species. , Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.
Cloning and expression of a Kv1.2 class delayed rectifier K+ channel from canine colonic smooth muscle. , Hart PJ., Proc Natl Acad Sci U S A. October 15, 1993; 90 (20): 9659-63.