Papers associated with brain (and kcna2)

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	Sites and Functional Consequence of Alkylphenol Anesthetic Binding to Kv1.2 Channels., Bu W., Mol Neurobiol. February 1, 2018; 55 (2): 1692-1702.
	Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies., Masnada S., Brain. September 1, 2017; 140 (9): 2337-2354.
	Conformational rearrangements in the transmembrane domain of CNGA1 channels revealed by single-molecule force spectroscopy., Maity S., Nat Commun. May 12, 2015; 6 7093.
	Molecular mechanism of allosteric modification of voltage-dependent sodium channels by local anesthetics., Arcisio-Miranda M., J Gen Physiol. November 1, 2010; 136 (5): 541-54.
	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.
	Induction of vertebrate regeneration by a transient sodium current., Tseng AS., J Neurosci. September 29, 2010; 30 (39): 13192-200.
	Hemitoxin, the first potassium channel toxin from the venom of the Iranian scorpion Hemiscorpius lepturus., Srairi-Abid N., FEBS J. September 1, 2008; 275 (18): 4641-50.
	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.
	A truncated Kv1.1 protein in the brain of the megencephaly mouse: expression and interaction., Persson AS., BMC Neurosci. November 23, 2005; 6 65.
	Synthesis and characterization of Pi4, a scorpion toxin from Pandinus imperator that acts on K+ channels., M'Barek S., Eur J Biochem. September 1, 2003; 270 (17): 3583-92.
	Characteristics of brain Kv1 channels tailored to mimic native counterparts by tandem linkage of alpha subunits: implications for K+ channelopathies., Akhtar S., J Biol Chem. May 10, 2002; 277 (19): 16376-82.
	Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2)., McCormack K., J Biol Chem. April 12, 2002; 277 (15): 13219-28.
	Chemical synthesis and characterization of Pi1, a scorpion toxin from Pandinus imperator active on K+ channels., Fajloun Z., Eur J Biochem. August 1, 2000; 267 (16): 5149-55.
	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.
	Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: purification, structure and action on potassium channels., Kharrat R., 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., Eur J Biochem. February 15, 1997; 244 (1): 192-202.
	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.
	Effects of the level of mRNA expression on biophysical properties, sensitivity to neurotoxins, and regulation of the brain delayed-rectifier K+ channels Kv1.2., Guillemare E., Biochemistry. December 15, 1992; 31 (49): 12463-8.

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