Papers associated with oocyte (and kcnq1)

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	In silico re-engineering of a neurotransmitter to activate KCNQ potassium channels in an isoform-specific manner., Manville RW., Commun Biol. January 1, 2019; 2 401.
	Direct neurotransmitter activation of voltage-gated potassium channels., Manville RW., Nat Commun. May 10, 2018; 9 (1): 1847.
	PIP2 mediates functional coupling and pharmacology of neuronal KCNQ channels., Kim RY., Proc Natl Acad Sci U S A. November 7, 2017; 114 (45): E9702-E9711.
	Insulin treatment augments KCNQ1/KCNE1 currents but not KCNQ1 currents, which is associated with an increase in KCNE1 expression., Wu M., Biochem Biophys Res Commun. November 4, 2017; 493 (1): 409-415.
	Ginseng gintonin activates the human cardiac delayed rectifier K+ channel: involvement of Ca2+/calmodulin binding sites., Choi SH., Mol Cells. September 1, 2014; 37 (9): 656-63.
	Domain-domain interactions determine the gating, permeation, pharmacology, and subunit modulation of the IKs ion channel., Zaydman MA., Elife. March 12, 2014; 3 e03606.
	Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1., Aidery P., Gene. December 10, 2012; 511 (1): 26-33.
	AMP-activated protein kinase in BK-channel regulation and protection against hearing loss following acoustic overstimulation., Föller M., FASEB J. October 1, 2012; 26 (10): 4243-53.
	KCNQ1 subdomains involved in KCNE modulation revealed by an invertebrate KCNQ1 orthologue., Nakajo K., J Gen Physiol. November 1, 2011; 138 (5): 521-35.
	Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability., Aidery P., Biochim Biophys Acta. April 1, 2011; 1812 (4): 488-94.
	Functional delivery of a membrane protein into oocyte membranes using bicelles., Kang C., Biochemistry. February 2, 2010; 49 (4): 653-5.
	Selective interaction of syntaxin 1A with KCNQ2: possible implications for specific modulation of presynaptic activity., Regev N., PLoS One. August 13, 2009; 4 (8): e6586.
	The G314S KCNQ1 mutation exerts a dominant-negative effect on expression of KCNQ1 channels in oocytes., Li W., Biochem Biophys Res Commun. May 29, 2009; 383 (2): 206-9.
	Modulation of potassium channel function confers a hyperproliferative invasive phenotype on embryonic stem cells., Morokuma J., Proc Natl Acad Sci U S A. October 28, 2008; 105 (43): 16608-13.
	KCNQ1 and KCNE1 in the IKs channel complex make state-dependent contacts in their extracellular domains., Xu X., J Gen Physiol. June 1, 2008; 131 (6): 589-603.
	S1 constrains S4 in the voltage sensor domain of Kv7.1 K+ channels., Haitin Y., PLoS One. April 9, 2008; 3 (4): e1935.
	The KCNE1 beta-subunit exerts a transient effect on the KCNQ1 K+ channel., Poulsen AN., Biochem Biophys Res Commun. November 9, 2007; 363 (1): 133-9.
	KCNE1 and KCNE3 stabilize and/or slow voltage sensing S4 segment of KCNQ1 channel., Nakajo K., J Gen Physiol. September 1, 2007; 130 (3): 269-81.
	Secondary structure of a KCNE cytoplasmic domain., Rocheleau JM., J Gen Physiol. December 1, 2006; 128 (6): 721-9.
	Functional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytes., Strutz-Seebohm N., Cell Physiol Biochem. January 1, 2006; 18 (1-3): 57-66.
	KCNE3 truncation mutants reveal a bipartite modulation of KCNQ1 K+ channels., Gage SD., J Gen Physiol. December 1, 2004; 124 (6): 759-71.
	Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome., Zehelein J., Biochim Biophys Acta. November 5, 2004; 1690 (3): 185-92.
	External barium affects the gating of KCNQ1 potassium channels and produces a pore block via two discrete sites., Gibor G., J Gen Physiol. July 1, 2004; 124 (1): 83-102.
	Characterization of a novel Long QT syndrome mutation G52R-KCNE1 in a Chinese family., Ma L., Cardiovasc Res. September 1, 2003; 59 (3): 612-9.
	RNA interference reveals that endogenous Xenopus MinK-related peptides govern mammalian K+ channel function in oocyte expression studies., Anantharam A., J Biol Chem. April 4, 2003; 278 (14): 11739-45.

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