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.
252 related articles for article (PubMed ID: 11222472)
21. Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2. January CT; Gong Q; Zhou Z J Cardiovasc Electrophysiol; 2000 Dec; 11(12):1413-8. PubMed ID: 11196567 [TBL] [Abstract][Full Text] [Related]
22. Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2. Nakajima T; Furukawa T; Hirano Y; Tanaka T; Sakurada H; Takahashi T; Nagai R; Itoh T; Katayama Y; Nakamura Y; Hiraoka M Cardiovasc Res; 1999 Nov; 44(2):283-93. PubMed ID: 10690305 [TBL] [Abstract][Full Text] [Related]
23. Inhibition of cardiac delayed rectifier K+ current by overexpression of the long-QT syndrome HERG G628S mutation in transgenic mice. Babij P; Askew GR; Nieuwenhuijsen B; Su CM; Bridal TR; Jow B; Argentieri TM; Kulik J; DeGennaro LJ; Spinelli W; Colatsky TJ Circ Res; 1998 Sep; 83(6):668-78. PubMed ID: 9742063 [TBL] [Abstract][Full Text] [Related]
24. T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome. Kanters JK; Fanoe S; Larsen LA; Bloch Thomsen PE; Toft E; Christiansen M Heart Rhythm; 2004 Sep; 1(3):285-92. PubMed ID: 15851171 [TBL] [Abstract][Full Text] [Related]
25. Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates. Chevalier P; Rodriguez C; Bontemps L; Miquel M; Kirkorian G; Rousson R; Potet F; Schott JJ; Baró I; Touboul P Cardiovasc Res; 2001 May; 50(2):386-98. PubMed ID: 11334843 [TBL] [Abstract][Full Text] [Related]
26. The inherited long QT syndrome: from ion channel to bedside. Vincent GM; Timothy K; Fox J; Zhang L Cardiol Rev; 1999; 7(1):44-55. PubMed ID: 10348966 [TBL] [Abstract][Full Text] [Related]
27. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns. Piippo K; Laitinen P; Swan H; Toivonen L; Viitasalo M; Pasternack M; Paavonen K; Chapman H; Wann KT; Hirvelä E; Sajantila A; Kontula K J Am Coll Cardiol; 2000 Jun; 35(7):1919-25. PubMed ID: 10841244 [TBL] [Abstract][Full Text] [Related]
28. Cellular consequences of HERG mutations in the long QT syndrome: precursors to sudden cardiac death. Clancy CE; Rudy Y Cardiovasc Res; 2001 May; 50(2):301-13. PubMed ID: 11334834 [TBL] [Abstract][Full Text] [Related]
29. Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations. Lupoglazoff JM; Denjoy I; Villain E; Fressart V; Simon F; Bozio A; Berthet M; Benammar N; Hainque B; Guicheney P J Am Coll Cardiol; 2004 Mar; 43(5):826-30. PubMed ID: 14998624 [TBL] [Abstract][Full Text] [Related]
30. Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes. Yang P; Kanki H; Drolet B; Yang T; Wei J; Viswanathan PC; Hohnloser SH; Shimizu W; Schwartz PJ; Stanton M; Murray KT; Norris K; George AL; Roden DM Circulation; 2002 Apr; 105(16):1943-8. PubMed ID: 11997281 [TBL] [Abstract][Full Text] [Related]
32. A quantitative assessment of T-wave morphology in LQT1, LQT2, and healthy individuals based on Holter recording technology. Vaglio M; Couderc JP; McNitt S; Xia X; Moss AJ; Zareba W Heart Rhythm; 2008 Jan; 5(1):11-8. PubMed ID: 18180017 [TBL] [Abstract][Full Text] [Related]
33. Is restoration of intracellular trafficking clinically feasible in the long QT syndrome?: The example of HERG mutations. Kaufman ES; Ficker E J Cardiovasc Electrophysiol; 2003 Mar; 14(3):320-2. PubMed ID: 12716119 [No Abstract] [Full Text] [Related]
34. Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics. Isbrandt D; Friederich P; Solth A; Haverkamp W; Ebneth A; Borggrefe M; Funke H; Sauter K; Breithardt G; Pongs O; Schulze-Bahr E J Mol Med (Berl); 2002 Aug; 80(8):524-32. PubMed ID: 12185453 [TBL] [Abstract][Full Text] [Related]
35. Interaction with GM130 during HERG ion channel trafficking. Disruption by type 2 congenital long QT syndrome mutations. Human Ether-à-go-go-Related Gene. Roti EC; Myers CD; Ayers RA; Boatman DE; Delfosse SA; Chan EK; Ackerman MJ; January CT; Robertson GA J Biol Chem; 2002 Dec; 277(49):47779-85. PubMed ID: 12270925 [TBL] [Abstract][Full Text] [Related]
36. Novel mechanism of HERG current suppression in LQT2: shift in voltage dependence of HERG inactivation. Nakajima T; Furukawa T; Tanaka T; Katayama Y; Nagai R; Nakamura Y; Hiraoka M Circ Res; 1998 Aug; 83(4):415-22. PubMed ID: 9721698 [TBL] [Abstract][Full Text] [Related]
37. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Curran ME; Splawski I; Timothy KW; Vincent GM; Green ED; Keating MT Cell; 1995 Mar; 80(5):795-803. PubMed ID: 7889573 [TBL] [Abstract][Full Text] [Related]
38. Electrocardiographic prediction of abnormal genotype in congenital long QT syndrome: experience in 101 related family members. Kaufman ES; Priori SG; Napolitano C; Schwartz PJ; Iyengar S; Elston RC; Schnell AH; Gorodeski EZ; Rammohan G; Bahhur NO; Connuck D; Verrilli L; Rosenbaum DS; Brown AM J Cardiovasc Electrophysiol; 2001 Apr; 12(4):455-61. PubMed ID: 11332568 [TBL] [Abstract][Full Text] [Related]