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Summary Expression Phenotypes Gene Literature (63) GO Terms (4) Nucleotides (53) Proteins (34) Interactants (60) Wiki
XB-GENEPAGE-991577

Papers associated with kcna3



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A four-disulphide-bridged toxin, with high affinity towards voltage-gated K+ channels, isolated from Heterometrus spinnifer (Scorpionidae) venom., Lebrun B, Romi-Lebrun R, Martin-Eauclaire MF, Yasuda A, Ishiguro M, Oyama Y, Pongs O, Nakajima T., Biochem J. November 15, 1997; 328 ( Pt 1) 321-7.

Purification, characterization, and synthesis of three novel toxins from the Chinese scorpion Buthus martensi, which act on K+ channels., Romi-Lebrun R, Lebrun B, Martin-Eauclaire MF, Ishiguro M, Escoubas P, Wu FQ, Hisada M, Pongs O, Nakajima T., Biochemistry. November 4, 1997; 36 (44): 13473-82.

Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channels., Kharrat R, Mansuelle P, Sampieri F, Crest M, Oughideni R, Van Rietschoten J, Martin-Eauclaire MF, Rochat H, El Ayeb M., FEBS Lett. April 14, 1997; 406 (3): 284-90.

A potassium-channel toxin from the sea anemone Bunodosoma granulifera, an inhibitor for Kv1 channels. Revision of the amino acid sequence, disulfide-bridge assignment, chemical synthesis, and biological activity., Cotton J, Crest M, Bouet F, Alessandri N, Gola M, Forest E, Karlsson E, Castañeda O, Harvey AL, Vita C, Ménez A., Eur J Biochem. February 15, 1997; 244 (1): 192-202.

Voltage-gated K+ channels contain multiple intersubunit association sites., Tu L, Santarelli V, Sheng Z, Skach W, Pain D, Deutsch C., J Biol Chem. August 2, 1996; 271 (31): 18904-11.

Molecular cloning of a glibenclamide-sensitive, voltage-gated potassium channel expressed in rabbit kidney., Yao X, Chang AY, Boulpaep EL, Segal AS, Desir GV., J Clin Invest. June 1, 1996; 97 (11): 2525-33.

Susceptibility of cloned K+ channels to reactive oxygen species., Duprat F, Guillemare E, Romey G, Fink M, Lesage F, Lazdunski M, Honore E., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.

Stable expression of human Kv1.3 potassium channels resets the resting membrane potential of cultured mammalian cells., Defarias FP, Stevens SP, Leonard RJ., Recept Channels. January 1, 1995; 3 (4): 273-81.

Truncated K+ channel DNA sequences specifically suppress lymphocyte K+ channel gene expression., Tu L, Santarelli V, Deutsch C., Biophys J. January 1, 1995; 68 (1): 147-56.

The P-region and S6 of Kv3.1 contribute to the formation of the ion conduction pathway., Aiyar J, Nguyen AN, Chandy KG, Grissmer S., Biophys J. December 1, 1994; 67 (6): 2261-4.

Injection of a K+ channel (Kv1.3) cRNA in fertilized eggs leads to functional expression in cultured myotomal muscle cells from Xenopus embryos., Honoré E, Guillemare E, Lesage F, Barhanin J, Lazdunski M., FEBS Lett. July 18, 1994; 348 (3): 259-62.

Chemical synthesis and structure-function studies of margatoxin, a potent inhibitor of voltage-dependent potassium channel in human T lymphocytes., Bednarek MA, Bugianesi RM, Leonard RJ, Felix JP., Biochem Biophys Res Commun. January 28, 1994; 198 (2): 619-25.

Full-length and truncated Kv1.3 K+ channels are modulated by 5-HT1c receptor activation and independently by PKC., Aiyar J, Grissmer S, Chandy KG., Am J Physiol. December 1, 1993; 265 (6 Pt 1): C1571-8.

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