Papers associated with cranial nerve (and kcnq1)

Limit to papers also referencing gene:
Show all cranial nerve papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	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.
	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.
	Discovery of a novel activator of KCNQ1-KCNE1 K channel complexes., Mruk K., PLoS One. January 1, 2009; 4 (1): e4236.
	Bimodal effects of the Kv7 channel activator retigabine on vascular K+ currents., Yeung S., Br J Pharmacol. September 1, 2008; 155 (1): 62-72.
	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.
	KCNE1 constrains the voltage sensor of Kv7.1 K+ channels., Shamgar L., PLoS One. April 9, 2008; 3 (4): e1943.
	KCNQ1 and KCNE1 K+ channel components are involved in early left-right patterning in Xenopus laevis embryos., Morokuma J., Cell Physiol Biochem. January 1, 2008; 21 (5-6): 357-72.
	hKCNE4 inhibits the hKCNQ1 potassium current without affecting the activation kinetics., Grunnet M., Biochem Biophys Res Commun. March 25, 2005; 328 (4): 1146-53.
	Mutation of colocalized residues of the pore helix and transmembrane segments S5 and S6 disrupt deactivation and modify inactivation of KCNQ1 K+ channels., Seebohm G., J Physiol. March 1, 2005; 563 (Pt 2): 359-68.
	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.
	Effective long-term control of cardiac events with beta-blockers in a family with a common LQT1 mutation., Wedekind H., Clin Genet. March 1, 2004; 65 (3): 233-41.
	Pharmacological activation of normal and arrhythmia-associated mutant KCNQ1 potassium channels., Seebohm G., Circ Res. November 14, 2003; 93 (10): 941-7.
	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.
	Functional coupling between heterologously expressed dopamine D(2) receptors and KCNQ channels., Ljungstrom T., Pflugers Arch. September 1, 2003; 446 (6): 684-94.
	Pore- and state-dependent cadmium block of I(Ks) channels formed with MinK-55C and wild-type KCNQ1 subunits., Chen H., Biophys J. June 1, 2003; 84 (6): 3679-89.
	C-terminal interaction of KCNQ2 and KCNQ3 K+ channels., Maljevic S., J Physiol. April 15, 2003; 548 (Pt 2): 353-60.
	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.
	C-terminal domains implicated in the functional surface expression of potassium channels., Jenke M., EMBO J. February 3, 2003; 22 (3): 395-403.
	Regulation of KCNE1-dependent K(+) current by the serum and glucocorticoid-inducible kinase (SGK) isoforms., Embark HM., Pflugers Arch. February 1, 2003; 445 (5): 601-6.
	A carboxy-terminal domain determines the subunit specificity of KCNQ K+ channel assembly., Schwake M., EMBO Rep. January 1, 2003; 4 (1): 76-81.
	Modulation of homomeric and heteromeric KCNQ1 channels by external acidification., Peretz A., J Physiol. December 15, 2002; 545 (3): 751-66.

???pagination.result.page??? 1