Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (109) GO Terms (4) Nucleotides (55) Proteins (30) Interactants (110) Wiki
XB--1010661

Papers associated with kcna1 (and OMIM)



Limit to papers also referencing gene:
Show all kcna1 papers

Results 1 - 4 of 4 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

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.


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.


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.


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.      

Page(s): 1