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A PIP2 substitute mediates voltage sensor-pore coupling in KCNQ activation. , Liu Y ., Commun Biol. July 16, 2020; 3 (1): 385.
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.
KCNQ1, KCNE2, and Na+-coupled solute transporters form reciprocally regulating complexes that affect neuronal excitability. , Abbott GW., Sci Signal. March 4, 2014; 7 (315): ra22.
Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene. , Geng FS., Development. November 1, 2013; 140 (21): 4362-74.
Extracellular potassium inhibits Kv7.1 potassium channels by stabilizing an inactivated state. , Larsen AP., Biophys J. August 17, 2011; 101 (4): 818-27.
Ginsenoside Rg3 activates human KCNQ1 K+ channel currents through interacting with the K318 and V319 residues: a role of KCNE1 subunit. , Choi SH., Eur J Pharmacol. July 10, 2010; 637 (1-3): 138-47.
Counting membrane-embedded KCNE beta-subunits in functioning K+ channel complexes. , Morin TJ., Proc Natl Acad Sci U S A. February 5, 2008; 105 (5): 1478-82.
Ancillary subunits and stimulation frequency determine the potency of chromanol 293B block of the KCNQ1 potassium channel. , Bett GC., J Physiol. November 1, 2006; 576 (Pt 3): 755-67.
Xe991 reveals differences in K(+) channels regulating chloride secretion in murine airway and colonic epithelium. , MacVinish LJ., Mol Pharmacol. October 1, 2001; 60 (4): 753-60.
KCNQ4 channels expressed in mammalian cells: functional characteristics and pharmacology. , Søgaard R., Am J Physiol Cell Physiol. April 1, 2001; 280 (4): C859-66.