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XB--1010661
Papers associated with kcna1 (and Disease Ontology)
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Selective block of human Kv1.1 channels and an epilepsy-associated gain-of-function mutation by AETX-K peptide., Zhao R, Qasim A, Sophanpanichkul P, Dai H, Nayak M, Sher I, Chill J, Goldstein SAN., FASEB J. January 1, 2024; 38 (1): e23381.  |
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A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel., Zhao J, Petitjean D, Haddad GA, Batulan Z, Blunck R., Int J Mol Sci. October 14, 2020; 21 (20):  |
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Electromechanical coupling of the Kv1.1 voltage-gated K+ channel is fine-tuned by the simplest amino acid residue in the S4-S5 linker., Hasan S, Megaro A, Cenciarini M, Coretti L, Botti FM, Imbrici P, Steinbusch HWM, Hunter T, Hunter G, Pessia M, D'Adamo MC., Pflugers Arch. July 1, 2020; 472 (7): 899-909. |
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Isoform-Selective KCNA1 Potassium Channel Openers Built from Glycine., Manville RW, Abbott GW., J Pharmacol Exp Ther. June 1, 2020; 373 (3): 391-401. |
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Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures., Ishida S, Sakamoto Y, Nishio T, Baulac S, Kuwamura M, Ohno Y, Takizawa A, Kaneko S, Serikawa T, Mashimo T., Dev Biol. January 30, 2012; 1435 154-66. |
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Episodic ataxia type 1 mutations affect fast inactivation of K+ channels by a reduction in either subunit surface expression or affinity for inactivation domain., Imbrici P, D'Adamo MC, Grottesi A, Biscarini A, Pessia M., Am J Physiol Cell Physiol. June 1, 2011; 300 (6): C1314-22. |
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Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia., Chen H, von Hehn C, Kaczmarek LK, Ment LR, Pober BR, Hisama FM., Neurogenetics. April 1, 2007; 8 (2): 131-5.  |
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A truncated Kv1.1 protein in the brain of the megencephaly mouse: expression and interaction., Persson AS, Klement G, Almgren M, Sahlholm K, Nilsson J, Petersson S, Arhem P, Schalling M, Lavebratt C., BMC Neurosci. November 23, 2005; 6 65.  |
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