Papers associated with right (and kcnh2)

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	Bioelectric signaling: Reprogrammable circuits underlying embryogenesis, regeneration, and cancer., Levin M., Cell. April 15, 2021;
	External Cd2+ and protons activate the hyperpolarization-gated K+ channel KAT1 at the voltage sensor., Zhou Y., J Gen Physiol. January 4, 2021; 153 (1):
	Regulation of Eag1 gating by its intracellular domains., Whicher JR., Elife. September 6, 2019; 8
	The molecular determinants of R-roscovitine block of hERG channels., Cernuda B., PLoS One. September 3, 2019; 14 (9): e0217733.
	Fluorescent analogues of BeKm-1 with high and specific activity against the hERG channel., Vasseur L., Toxicon X. February 23, 2019; 2 100010.
	Facilitation of IKr current by some hERG channel blockers suppresses early afterdepolarizations., Furutani K., J Gen Physiol. February 4, 2019; 151 (2): 214-230.
	Extracellular protons accelerate hERG channel deactivation by destabilizing voltage sensor relaxation., Shi YP., J Gen Physiol. February 4, 2019; 151 (2): 231-246.
	Functional characterization of Kv11.1 (hERG) potassium channels split in the voltage-sensing domain., de la Peña P., Pflugers Arch. July 1, 2018; 470 (7): 1069-1085.
	Probing the molecular basis of hERG drug block with unnatural amino acids., Macdonald LC., Sci Rep. January 10, 2018; 8 (1): 289.
	Regulation of human cardiac potassium channels by full-length KCNE3 and KCNE4., Abbott GW., Sci Rep. December 6, 2016; 6 38412.
	Molecular Cloning and Functional Expression of the Equine K+ Channel KV11.1 (Ether à Go-Go-Related/KCNH2 Gene) and the Regulatory Subunit KCNE2 from Equine Myocardium., Pedersen PJ., PLoS One. September 4, 2015; 10 (9): e0138320.
	Voltage-dependent gating of KCNH potassium channels lacking a covalent link between voltage-sensing and pore domains., Lörinczi É., Nat Commun. March 30, 2015; 6 6672.
	High incidence of functional ion-channel abnormalities in a consecutive Long QT cohort with novel missense genetic variants of unknown significance., Steffensen AB., Sci Rep. January 12, 2015; 5 10009.
	Xenopus borealis as an alternative source of oocytes for biophysical and pharmacological studies of neuronal ion channels., Cristofori-Armstrong B., Sci Rep. January 12, 2015; 5 14763.
	Up-regulation of hERG K⁺ channels by B-RAF., Pakladok T., PLoS One. January 1, 2014; 9 (1): e87457.
	The Eag domain regulates the voltage-dependent inactivation of rat Eag1 K+ channels., Lin TF., PLoS One. January 1, 2014; 9 (10): e110423.
	C-terminal β9-strand of the cyclic nucleotide-binding homology domain stabilizes activated states of Kv11.1 channels., Ng CA., PLoS One. October 4, 2013; 8 (10): e77032.
	Functional interactions of voltage sensor charges with an S2 hydrophobic plug in hERG channels., Cheng YM., J Gen Physiol. September 1, 2013; 142 (3): 289-303.
	VEGFA-dependent and -independent pathways synergise to drive Scl expression and initiate programming of the blood stem cell lineage in Xenopus., Ciau-Uitz A., Development. June 1, 2013; 140 (12): 2632-42.
	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.
	Modification of hERG1 channel gating by Cd2+., Abbruzzese J., J Gen Physiol. August 1, 2010; 136 (2): 203-24.
	Tel1/ETV6 specifies blood stem cells through the agency of VEGF signaling., Ciau-Uitz A., Dev Cell. April 20, 2010; 18 (4): 569-78.
	Inhibition of the human ether-a-go-go-related gene (HERG) K+ channels by Lindera erythrocarpa., Hong HK., J Korean Med Sci. December 1, 2009; 24 (6): 1089-98.
	Two separate interfaces between the voltage sensor and pore are required for the function of voltage-dependent K(+) channels., Lee SY., PLoS Biol. March 3, 2009; 7 (3): e47.
	Discovery of a novel activator of KCNQ1-KCNE1 K channel complexes., Mruk K., PLoS One. January 1, 2009; 4 (1): e4236.
	Characterization of hERG1a and hERG1b potassium channels-a possible role for hERG1b in the I (Kr) current., Larsen AP., Pflugers Arch. September 1, 2008; 456 (6): 1137-48.
	Activation of ERG2 potassium channels by the diphenylurea NS1643., Elmedyb P., Neuropharmacology. August 1, 2007; 53 (2): 283-94.
	Upregulation of KCNE1 induces QT interval prolongation in patients with chronic heart failure., Watanabe E., Circ J. April 1, 2007; 71 (4): 471-8.
	Chemical modification of the human ether-a-go-go-related gene (HERG) K+ current by the amino-group reagent trinitrobenzene sulfonic acid., Jo SH., Arch Pharm Res. April 1, 2006; 29 (4): 310-7.
	Salt bridges and gating in the COOH-terminal region of HCN2 and CNGA1 channels., Craven KB., J Gen Physiol. December 1, 2004; 124 (6): 663-77.
	Negative charges in the transmembrane domains of the HERG K channel are involved in the activation- and deactivation-gating processes., Liu J., J Gen Physiol. June 1, 2003; 121 (6): 599-614.
	Structural and functional role of the extracellular s5-p linker in the HERG potassium channel., Liu J., J Gen Physiol. November 1, 2002; 120 (5): 723-37.
	Fast and slow voltage sensor movements in HERG potassium channels., Smith PL., J Gen Physiol. March 1, 2002; 119 (3): 275-93.
	Inhibition of IKs channels by HMR 1556., Gögelein H., Naunyn Schmiedebergs Arch Pharmacol. December 1, 2000; 362 (6): 480-8.
	MinK subdomains that mediate modulation of and association with KvLQT1., Tapper AR., J Gen Physiol. September 1, 2000; 116 (3): 379-90.
	Dynamic control of deactivation gating by a soluble amino-terminal domain in HERG K(+) channels., Wang J., J Gen Physiol. June 1, 2000; 115 (6): 749-58.
	Blockade of HERG channels expressed in Xenopus laevis oocytes by external divalent cations., Ho WK., Biophys J. April 1, 1999; 76 (4): 1959-71.

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