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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes. , Neal SJ, Rajasekaran A, Jusić N, Taylor L , Read M, Alfandari D , Alfandari D , Pignoni F, Moody SA ., J Exp Zool B Mol Dev Evol. May 1, 2024; 342 (3): 212-240.
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.
Probing the interaction between KCNE2 and KCNQ1 in their transmembrane regions. , Liu XS, Zhang M, Jiang M, Wu DM, Tseng GN., J Membr Biol. April 1, 2007; 216 (2-3): 117-27.
Tight coupling of rubidium conductance and inactivation in human KCNQ1 potassium channels. , Seebohm G , Sanguinetti MC, Pusch M., J Physiol. October 15, 2003; 552 (Pt 2): 369-78.
KCNE5 induces time- and voltage-dependent modulation of the KCNQ1 current. , Angelo K, Jespersen T, Grunnet M, Nielsen MS, Klaerke DA, Olesen SP., Biophys J. October 1, 2002; 83 (4): 1997-2006.