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Localization of receptor site on insect sodium channel for depressant β-toxin BmK IT2. , He H , Liu Z, Dong B, Zhang J, Shu X, Zhou J, Ji Y., PLoS One. January 7, 2011; 6 (1): e14510.
Design of a specific activator for skeletal muscle sodium channels uncovers channel architecture. , Cohen L, Ilan N, Gur M, Stühmer W, Gordon D, Gurevitz M., J Biol Chem. October 5, 2007; 282 (40): 29424-30.
A tryptophan residue (W736) in the amino-terminus of the P-segment of domain II is involved in pore formation in Na(v)1.4 voltage-gated sodium channels. , Carbonneau E, Vijayaragavan K, Chahine M., Pflugers Arch. October 1, 2002; 445 (1): 18-24.
Slow inactivation does not block the aqueous accessibility to the outer pore of voltage-gated Na channels. , Struyk AF, Cannon SC., J Gen Physiol. October 1, 2002; 120 (4): 509-16.
Architecture of Ca(2+) channel pore-lining segments revealed by covalent modification of substituted cysteines. , Koch SE, Bodi I, Schwartz A, Varadi G., J Biol Chem. November 3, 2000; 275 (44): 34493-500.
A new beta subtype-specific interaction in alpha1A subunit controls P/Q-type Ca2+ channel activation. , Walker D, Bichet D, Geib S, Mori E, Cornet V, Snutch TP, Mori Y, De Waard M., J Biol Chem. April 30, 1999; 274 (18): 12383-90.
A single serine residue confers tetrodotoxin insensitivity on the rat sensory- neuron-specific sodium channel SNS. , Sivilotti L, Okuse K, Akopian AN, Moss S, Wood JN., FEBS Lett. June 2, 1997; 409 (1): 49-52.
Molecular determinants of beta 1 subunit-induced gating modulation in voltage-dependent Na+ channels. , Makita N, Bennett PB, George AL., J Neurosci. November 15, 1996; 16 (22): 7117-27.
Quantity, bundle types, and distribution of hair cells in the sacculus of Xenopus laevis during development. , Díaz ME, Varela-Ramírez A, Serrano EE ., Hear Res. November 1, 1995; 91 (1-2): 33-42.
Glutamate substitution in repeat IV alters divalent and monovalent cation permeation in the heart Ca2+ channel. , Parent L, Gopalakrishnan M., Biophys J. November 1, 1995; 69 (5): 1801-13.
Single amino acid substitutions within the ion permeation pathway alter single-channel conductance of the human L-type cardiac Ca2+ channel. , Yatani A, Bahinski A, Mikala G, Yamamoto S, Schwartz A., Circ Res. August 1, 1994; 75 (2): 315-23.
Evidence that the S6 segment of the Shaker voltage-gated K+ channel comprises part of the pore. , Lopez GA, Jan YN, Jan LY., Nature. January 13, 1994; 367 (6459): 179-82.
Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action. , Tang S, Yatani A, Bahinski A, Mori Y, Schwartz A., Neuron. December 1, 1993; 11 (6): 1013-21.
Role of H5 domain in determining pore diameter and ion permeation through cyclic nucleotide-gated channels. , Goulding EH, Tibbs GR, Liu D, Siegelbaum SA., Nature. July 1, 1993; 364 (6432): 61-4.
Structural determinants of ion selectivity in brain calcium channel. , Kim MS , Morii T, Sun LX, Imoto K, Mori Y., FEBS Lett. March 1, 1993; 318 (2): 145-8.
Chimeric study of sodium channels from rat skeletal and cardiac muscle. , Chen LQ, Chahine M, Kallen RG, Barchi RL, Horn R., FEBS Lett. September 14, 1992; 309 (3): 253-7.
Mapping the site of block by tetrodotoxin and saxitoxin of sodium channel II. , Terlau H, Heinemann SH, Stühmer W, Pusch M, Conti F, Imoto K, Numa S., FEBS Lett. November 18, 1991; 293 (1-2): 93-6.