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Summary Anatomy Item Literature (3673) Expression Attributions Wiki
XB-ANAT-490

Papers associated with tail (and kcnc3)

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A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy., Muona M., Nat Genet. January 1, 2015; 47 (1): 39-46.      

Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)., Figueroa KP., PLoS One. March 29, 2011; 6 (3): e17811.      

Binding site of a novel Kv1.5 blocker: a "foot in the door" against atrial fibrillation., Decher N., Mol Pharmacol. October 1, 2006; 70 (4): 1204-11.

Novel, potent inhibitors of human Kv1.5 K+ channels and ultrarapidly activating delayed rectifier potassium current., Lagrutta A., J Pharmacol Exp Ther. June 1, 2006; 317 (3): 1054-63.

Deranged Kv channel regulation in fibroblasts from mice lacking the serum and glucocorticoid inducible kinase SGK1., Shumilina E., J Cell Physiol. July 1, 2005; 204 (1): 87-98.

Role of transmembrane segment S5 on gating of voltage-dependent K+ channels., Shieh CC., J Gen Physiol. June 1, 1997; 109 (6): 767-78.                

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

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