These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
263 related articles for article (PubMed ID: 19219384)
21. The KCNE2 potassium channel β subunit is required for normal lung function and resilience to ischemia and reperfusion injury. Zhou L; Köhncke C; Hu Z; Roepke TK; Abbott GW FASEB J; 2019 Sep; 33(9):9762-9774. PubMed ID: 31162977 [TBL] [Abstract][Full Text] [Related]
22. An LQTS6 MiRP1 mutation suppresses pacemaker current and is associated with sinus bradycardia. Nawathe PA; Kryukova Y; Oren RV; Milanesi R; Clancy CE; Lu JT; Moss AJ; Difrancesco D; Robinson RB J Cardiovasc Electrophysiol; 2013 Sep; 24(9):1021-7. PubMed ID: 23631727 [TBL] [Abstract][Full Text] [Related]
23. Comparison of the endogenous IK currents in rat hippocampal neurons and cloned Kv2.1 channels in CHO cells. Liu M; Gong B; Qi Z Cell Biol Int; 2008 Dec; 32(12):1514-20. PubMed ID: 18801450 [TBL] [Abstract][Full Text] [Related]
24. A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization. Thiffault I; Speca DJ; Austin DC; Cobb MM; Eum KS; Safina NP; Grote L; Farrow EG; Miller N; Soden S; Kingsmore SF; Trimmer JS; Saunders CJ; Sack JT J Gen Physiol; 2015 Nov; 146(5):399-410. PubMed ID: 26503721 [TBL] [Abstract][Full Text] [Related]
25. A comparison of currents carried by HERG, with and without coexpression of MiRP1, and the native rapid delayed rectifier current. Is MiRP1 the missing link? Weerapura M; Nattel S; Chartier D; Caballero R; Hébert TE J Physiol; 2002 Apr; 540(Pt 1):15-27. PubMed ID: 11927665 [TBL] [Abstract][Full Text] [Related]
26. Functional modulation of the transient outward current Ito by KCNE beta-subunits and regional distribution in human non-failing and failing hearts. Radicke S; Cotella D; Graf EM; Banse U; Jost N; Varró A; Tseng GN; Ravens U; Wettwer E Cardiovasc Res; 2006 Sep; 71(4):695-703. PubMed ID: 16876774 [TBL] [Abstract][Full Text] [Related]
27. Characterization of the heteromeric potassium channel formed by kv2.1 and the retinal subunit kv8.2 in Xenopus oocytes. Czirják G; Tóth ZE; Enyedi P J Neurophysiol; 2007 Sep; 98(3):1213-22. PubMed ID: 17652418 [TBL] [Abstract][Full Text] [Related]
28. Novel KCNE3 mutation reduces repolarizing potassium current and associated with long QT syndrome. Ohno S; Toyoda F; Zankov DP; Yoshida H; Makiyama T; Tsuji K; Honda T; Obayashi K; Ueyama H; Shimizu W; Miyamoto Y; Kamakura S; Matsuura H; Kita T; Horie M Hum Mutat; 2009 Apr; 30(4):557-63. PubMed ID: 19306396 [TBL] [Abstract][Full Text] [Related]
29. KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel. Tinel N; Diochot S; Borsotto M; Lazdunski M; Barhanin J EMBO J; 2000 Dec; 19(23):6326-30. PubMed ID: 11101505 [TBL] [Abstract][Full Text] [Related]
30. Open form of syntaxin-1A is a more potent inhibitor than wild-type syntaxin-1A of Kv2.1 channels. Leung YM; Kang Y; Xia F; Sheu L; Gao X; Xie H; Tsushima RG; Gaisano HY Biochem J; 2005 Apr; 387(Pt 1):195-202. PubMed ID: 15518587 [TBL] [Abstract][Full Text] [Related]
31. The role of S4 charges in voltage-dependent and voltage-independent KCNQ1 potassium channel complexes. Panaghie G; Abbott GW J Gen Physiol; 2007 Feb; 129(2):121-33. PubMed ID: 17227916 [TBL] [Abstract][Full Text] [Related]
33. Rb+ efflux through functional activation of cardiac KCNQ1/minK channels by the benzodiazepine R-L3 (L-364,373). Jow F; Tseng E; Maddox T; Shen R; Kowal D; Dunlop J; Mekonnen B; Wang K Assay Drug Dev Technol; 2006 Aug; 4(4):443-50. PubMed ID: 16945016 [TBL] [Abstract][Full Text] [Related]
34. Expression of multiple KCNE genes in human heart may enable variable modulation of I(Ks). Lundquist AL; Manderfield LJ; Vanoye CG; Rogers CS; Donahue BS; Chang PA; Drinkwater DC; Murray KT; George AL J Mol Cell Cardiol; 2005 Feb; 38(2):277-87. PubMed ID: 15698834 [TBL] [Abstract][Full Text] [Related]
35. The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome. Eldstrom J; Fedida D Expert Rev Mol Med; 2011 Dec; 13():e38. PubMed ID: 22166675 [TBL] [Abstract][Full Text] [Related]
36. Single-channel characteristics of wild-type IKs channels and channels formed with two minK mutants that cause long QT syndrome. Sesti F; Goldstein SA J Gen Physiol; 1998 Dec; 112(6):651-63. PubMed ID: 9834138 [TBL] [Abstract][Full Text] [Related]
37. Transcripts of Kv7.1 and MinK channels and slow delayed rectifier K Abramochkin DV; Hassinen M; Vornanen M Pflugers Arch; 2018 Dec; 470(12):1753-1764. PubMed ID: 30116893 [TBL] [Abstract][Full Text] [Related]
38. Salidroside modulates repolarization through stimulating Kv2.1 in rats. Zhang Y; Li R; Jiang H; Hou Y; Zhang Y; Meng X; Wang X Eur J Pharmacol; 2024 Aug; 977():176741. PubMed ID: 38880221 [TBL] [Abstract][Full Text] [Related]
39. Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations. Möller L; Regnier G; Labro AJ; Blunck R; Snyders DJ Proc Natl Acad Sci U S A; 2020 Apr; 117(17):9365-9376. PubMed ID: 32284408 [TBL] [Abstract][Full Text] [Related]
40. Interdomain cytoplasmic interactions govern the intracellular trafficking, gating, and modulation of the Kv2.1 channel. Mohapatra DP; Siino DF; Trimmer JS J Neurosci; 2008 May; 28(19):4982-94. PubMed ID: 18463252 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]