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XB-GENEPAGE-1013571
Papers associated with kcnh5
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Exome sequencing reveals new causal mutations in children with epileptic encephalopathies., Veeramah KR, Johnstone L, Karafet TM, Wolf D, Sprissler R, Salogiannis J, Barth-Maron A, Greenberg ME, Stuhlmann T, Weinert S, Jentsch TJ, Pazzi M, Restifo LL, Talwar D, Erickson RP, Hammer MF., Epilepsia. July 1, 2013; 54 (7): 1270-81. |
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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.  |
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Kcnh1 voltage-gated potassium channels are essential for early zebrafish development., Stengel R, Rivera-Milla E, Sahoo N, Ebert C, Bollig F, Heinemann SH, Schönherr R, Englert C., J Biol Chem. October 12, 2012; 287 (42): 35565-35575.  |
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Divalent cations slow activation of EAG family K+ channels through direct binding to S4., Zhang X, Bursulaya B, Lee CC, Lee CC, Chen B, Pivaroff K, Jegla T., Biophys J. July 8, 2009; 97 (1): 110-20. |
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Functional distinction of human EAG1 and EAG2 potassium channels., Schönherr R, Gessner G, Löber K, Heinemann SH., FEBS Lett. March 13, 2002; 514 (2-3): 204-8. |
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Cloning of components of a novel subthreshold-activating K(+) channel with a unique pattern of expression in the cerebral cortex., Saganich MJ, Vega-Saenz de Miera E, Nadal MS, Baker H, Coetzee WA, Rudy B., J Neurosci. December 15, 1999; 19 (24): 10789-802. |
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