???pagination.result.count???
???pagination.result.page???
1
Bioelectric signalling via potassium channels: a mechanism for craniofacial dysmorphogenesis in KCNJ2-associated Andersen-Tawil Syndrome. , Adams DS ., J Physiol. June 15, 2016; 594 (12): 3245-70.
Engineering of an artificial light-modulated potassium channel. , Caro LN., PLoS One. January 1, 2012; 7 (8): e43766.
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain. , Shimomura K., Neurology. September 25, 2007; 69 (13): 1342-9.
Functional effects of naturally occurring KCNJ11 mutations causing neonatal diabetes on cloned cardiac KATP channels. , Tammaro P., J Physiol. February 15, 2006; 571 (Pt 1): 3-14.
Determinant role of membrane helices in K ATP channel gating. , Wang R ., J Membr Biol. March 1, 2005; 204 (1): 1-10.
Structural basis for the interference between nicorandil and sulfonylurea action. , Reimann F., Diabetes. October 1, 2001; 50 (10): 2253-9.
Altered functional properties of KATP channel conferred by a novel splice variant of SUR1. , Sakura H., J Physiol. December 1, 1999; 521 Pt 2 337-50.