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Steady-state activation and modulation of the synaptic-type α1β2γ2L GABAA receptor by combinations of physiological and clinical ligands. , Germann AL, Pierce SR, Senneff TC, Burbridge AB, Steinbach JH, Akk G., Physiol Rep. September 1, 2019; 7 (18): e14230.
Tarantula toxins use common surfaces for interacting with Kv and ASIC ion channels. , Gupta K, Zamanian M, Bae C, Milescu M, Krepkiy D, Tilley DC, Sack JT, Yarov-Yarovoy V, Kim JI , Swartz KJ., Elife. January 6, 2015; 4 e06774.
Intrinsic versus extrinsic voltage sensitivity of blocker interaction with an ion channel pore. , Martínez-François JR, Lu Z., J Gen Physiol. February 1, 2010; 135 (2): 149-67.
Tarantula toxins interact with voltage sensors within lipid membranes. , Milescu M, Vobecky J, Roh SH, Kim SH, Jung HJ , Kim JI , Swartz KJ., J Gen Physiol. November 1, 2007; 130 (5): 497-511.
Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes. , Czirjak G, Toth ZE, Enyedi P., J Neurophysiol. September 1, 2007; 98 (3): 1213-22.
Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine. , Shin HG, Lu Z., J Gen Physiol. April 1, 2005; 125 (4): 413-26.
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.
Mechanism of IRK1 channel block by intracellular polyamines. , Guo D, Lu Z., J Gen Physiol. June 1, 2000; 115 (6): 799-814.
Mechanism of cGMP-gated channel block by intracellular polyamines. , Guo D, Lu Z., J Gen Physiol. June 1, 2000; 115 (6): 783-98.