270 related articles for article (PubMed ID: 11468227)
1. Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.
Larsen LA; Andersen PS; Kanters J; Svendsen IH; Jacobsen JR; Vuust J; Wettrell G; Tranebjaerg L; Bathen J; Christiansen M
Clin Chem; 2001 Aug; 47(8):1390-5. PubMed ID: 11468227
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
Liu W; Yang J; Hu D; Kang C; Li C; Zhang S; Li P; Chen Z; Qin X; Ying K; Li Y; Li Y; Li Z; Cheng X; Li L; Qi Y; Chen S; Wang Q
Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
[TBL] [Abstract][Full Text] [Related]
4. Identical twins with long QT syndrome associated with a missense mutation in the S4 region of the HERG.
Hayashi K; Shimizu M; Ino H; Okeie K; Yamaguchi M; Yasuda T; Fujino N; Fujii H; Fujita S; Mabuchi H
Jpn Heart J; 2000 May; 41(3):399-404. PubMed ID: 10987356
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels.
Anson BD; Ackerman MJ; Tester DJ; Will ML; Delisle BP; Anderson CL; January CT
Am J Physiol Heart Circ Physiol; 2004 Jun; 286(6):H2434-41. PubMed ID: 14975928
[TBL] [Abstract][Full Text] [Related]
7. Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.
Chen J; Zou A; Splawski I; Keating MT; Sanguinetti MC
J Biol Chem; 1999 Apr; 274(15):10113-8. PubMed ID: 10187793
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency.
Paulussen A; Raes A; Matthijs G; Snyders DJ; Cohen N; Aerssens J
J Biol Chem; 2002 Dec; 277(50):48610-6. PubMed ID: 12354768
[TBL] [Abstract][Full Text] [Related]
9. Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome.
Itoh T; Tanaka T; Nagai R; Kamiya T; Sawayama T; Nakayama T; Tomoike H; Sakurada H; Yazaki Y; Nakamura Y
Hum Genet; 1998 Apr; 102(4):435-9. PubMed ID: 9600240
[TBL] [Abstract][Full Text] [Related]
10. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
Jongbloed RJ; Wilde AA; Geelen JL; Doevendans P; Schaap C; Van Langen I; van Tintelen JP; Cobben JM; Beaufort-Krol GC; Geraedts JP; Smeets HJ
Hum Mutat; 1999; 13(4):301-10. PubMed ID: 10220144
[TBL] [Abstract][Full Text] [Related]
11. Local anaesthetic sensitivities of cloned HERG channels from human heart: comparison with HERG/MiRP1 and HERG/MiRP1 T8A.
Friederich P; Solth A; Schillemeit S; Isbrandt D
Br J Anaesth; 2004 Jan; 92(1):93-101. PubMed ID: 14665560
[TBL] [Abstract][Full Text] [Related]
12. Familial and acquired long qt syndrome and the cardiac rapid delayed rectifier potassium current.
Witchel HJ; Hancox JC
Clin Exp Pharmacol Physiol; 2000 Oct; 27(10):753-66. PubMed ID: 11022966
[TBL] [Abstract][Full Text] [Related]
13. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
Antzelevitch C
J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
[TBL] [Abstract][Full Text] [Related]
14. C-terminal HERG mutations: the role of hypokalemia and a KCNQ1-associated mutation in cardiac event occurrence.
Berthet M; Denjoy I; Donger C; Demay L; Hammoude H; Klug D; Schulze-Bahr E; Richard P; Funke H; Schwartz K; Coumel P; Hainque B; Guicheney P
Circulation; 1999 Mar; 99(11):1464-70. PubMed ID: 10086971
[TBL] [Abstract][Full Text] [Related]
15. 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; BarĂ³ I; Touboul P
Cardiovasc Res; 2001 May; 50(2):386-98. PubMed ID: 11334843
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Moss AJ; Zareba W; Kaufman ES; Gartman E; Peterson DR; Benhorin J; Towbin JA; Keating MT; Priori SG; Schwartz PJ; Vincent GM; Robinson JL; Andrews ML; Feng C; Hall WJ; Medina A; Zhang L; Wang Z
Circulation; 2002 Feb; 105(7):794-9. PubMed ID: 11854117
[TBL] [Abstract][Full Text] [Related]
18. Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.
Yoshida H; Horie M; Otani H; Kawashima T; Onishi Y; Sasayama S
Am J Med Genet; 2001 Feb; 98(4):348-52. PubMed ID: 11170080
[TBL] [Abstract][Full Text] [Related]
19. The antihistamine fexofenadine does not affect I(Kr) currents in a case report of drug-induced cardiac arrhythmia.
Scherer CR; Lerche C; Decher N; Dennis AT; Maier P; Ficker E; Busch AE; Wollnik B; Steinmeyer K
Br J Pharmacol; 2002 Nov; 137(6):892-900. PubMed ID: 12411421
[TBL] [Abstract][Full Text] [Related]
20. Analysis of the cyclic nucleotide binding domain of the HERG potassium channel and interactions with KCNE2.
Cui J; Kagan A; Qin D; Mathew J; Melman YF; McDonald TV
J Biol Chem; 2001 May; 276(20):17244-51. PubMed ID: 11278781
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]