???pagination.result.count???
???pagination.result.page???
1
Dual Mechanism for Inhibition of Inwardly Rectifying Kir2.x Channels by Quinidine Involving Direct Pore Block and PIP2-interference. , Koepple C., J Pharmacol Exp Ther. May 1, 2017; 361 (2): 209-218.
Pregnenolone sulfate potentiates the inwardly rectifying K channel Kir2.3. , Kobayashi T., PLoS One. July 21, 2009; 4 (7): e6311.
Molecular basis for genistein-induced inhibition of Kir2.3 currents. , Zhao Z., Pflugers Arch. May 1, 2008; 456 (2): 413-23.
Arachidonic acid activates Kir2.3 channels by enhancing channel-phosphatidyl-inositol 4,5-bisphosphate interactions. , Wang C ., Mol Pharmacol. April 1, 2008; 73 (4): 1185-94.
Comparison of cloned Kir2 channels with native inward rectifier K+ channels from guinea-pig cardiomyocytes. , Liu GX ., J Physiol. April 1, 2001; 532 (Pt 1): 115-26.
Suppression of Kir2.3 activity by protein kinase C phosphorylation of the channel protein at threonine 53. , Zhu G., J Biol Chem. April 23, 1999; 274 (17): 11643-6.
Molecular and functional heterogeneity of inward rectifier potassium channels in brain and heart. , Kurachi Y., J Card Fail. December 1, 1996; 2 (4 Suppl): S59-62.
Susceptibility of cloned K+ channels to reactive oxygen species. , Duprat F., Proc Natl Acad Sci U S A. December 5, 1995; 92 (25): 11796-800.
Identification and molecular localization of a pH-sensing domain for the inward rectifier potassium channel HIR. , Coulter KL., Neuron. November 1, 1995; 15 (5): 1157-68.
Cloning, localization, and functional expression of a human brain inward rectifier potassium channel (hIRK1). , Tang W., Recept Channels. January 1, 1995; 3 (3): 175-83.
Cloning a novel human brain inward rectifier potassium channel and its functional expression in Xenopus oocytes. , Tang W., FEBS Lett. July 18, 1994; 348 (3): 239-43.
Primary structure and characterization of a small-conductance inwardly rectifying potassium channel from human hippocampus. , Périer F., Proc Natl Acad Sci U S A. June 21, 1994; 91 (13): 6240-4.