|
XB-GENEPAGE-952636
Papers associated with kcnh3
???pagination.result.count???
???pagination.result.page??? 1
| Sort Newest To Oldest | Sort Oldest To Newest |
Loss-of-function variant in KCNH3 is associated with global developmental delay, autistic behavior, insomnia, and nocturnal seizures., Bauer CK, Kortüm F, Möllring A, Grinstein L, Denecke J, Alawi M, Bähring R, Harms FL., Seizure. March 20, 2025; 129 14-21.  |
|
External pH modulates EAG superfamily K+ channels through EAG-specific acidic residues in the voltage sensor., Kazmierczak M, Zhang X, Chen B, Mulkey DK, Shi Y, Wagner PG, Pivaroff-Ward K, Sassic JK, Bayliss DA, Jegla T., J Gen Physiol. June 1, 2013; 141 (6): 721-35.  |
|
Deletion of the potassium channel Kv12.2 causes hippocampal hyperexcitability and epilepsy., Zhang X, Bertaso F, Yoo JW, Baumgärtel K, Clancy SM, Lee V, Cienfuegos C, Wilmot C, Avis J, Hunyh T, Daguia C, Schmedt C, Noebels J, Jegla T., Nat Neurosci. September 1, 2010; 13 (9): 1056-8.  |
|
KCNE1 and KCNE3 beta-subunits regulate membrane surface expression of Kv12.2 K(+) channels in vitro and form a tripartite complex in vivo., Clancy SM, Chen B, Bertaso F, Mamet J, Jegla T., PLoS One. July 22, 2009; 4 (7): e6330.  |
|
Effect of S5P alpha-helix charge mutants on inactivation of hERG K+ channels., Clarke CE, Hill AP, Zhao J, Kondo M, Subbiah RN, Campbell TJ, Vandenberg JI., J Physiol. June 1, 2006; 573 (Pt 2): 291-304. |
|
Distribution and functional properties of human KCNH8 (Elk1) potassium channels., Zou A, Lin Z, Humble M, Creech CD, Wagoner PK, Krafte D, Jegla TJ, Wickenden AD., Am J Physiol Cell Physiol. December 1, 2003; 285 (6): C1356-66. |
???pagination.result.page??? 1