342 related articles for article (PubMed ID: 12185453)
1. 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]
2. 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]
3. Mutant MiRP1 subunits modulate HERG K+ channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6.
Lu Y; Mahaut-Smith MP; Huang CL; Vandenberg JI
J Physiol; 2003 Aug; 551(Pt 1):253-62. PubMed ID: 12923204
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel.
Huang FD; Chen J; Lin M; Keating MT; Sanguinetti MC
Circulation; 2001 Aug; 104(9):1071-5. PubMed ID: 11524404
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.
Abbott GW; Sesti F; Splawski I; Buck ME; Lehmann MH; Timothy KW; Keating MT; Goldstein SA
Cell; 1999 Apr; 97(2):175-87. PubMed ID: 10219239
[TBL] [Abstract][Full Text] [Related]
10. 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]
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. Characterization of a novel missense mutation in the pore of HERG in a patient with long QT syndrome.
Yoshida H; Horie M; Otani H; Takano M; Tsuji K; Kubota T; Fukunami M; Sasayama S
J Cardiovasc Electrophysiol; 1999 Sep; 10(9):1262-70. PubMed ID: 10517660
[TBL] [Abstract][Full Text] [Related]
13. The long QT syndromes: genetic basis and clinical implications.
Chiang CE; Roden DM
J Am Coll Cardiol; 2000 Jul; 36(1):1-12. PubMed ID: 10898405
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Inhibition of HERG potassium channel current by the class 1a antiarrhythmic agent disopyramide.
Paul AA; Witchel HJ; Hancox JC
Biochem Biophys Res Commun; 2001 Feb; 280(5):1243-50. PubMed ID: 11162661
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Identification of a COOH-terminal segment involved in maturation and stability of human ether-a-go-go-related gene potassium channels.
Akhavan A; Atanasiu R; Shrier A
J Biol Chem; 2003 Oct; 278(41):40105-12. PubMed ID: 12885765
[TBL] [Abstract][Full Text] [Related]
19. High affinity open channel block by dofetilide of HERG expressed in a human cell line.
Snyders DJ; Chaudhary A
Mol Pharmacol; 1996 Jun; 49(6):949-55. PubMed ID: 8649354
[TBL] [Abstract][Full Text] [Related]
20. Multiple different missense mutations in the pore region of HERG in patients with long QT syndrome.
Satler CA; Vesely MR; Duggal P; Ginsburg GS; Beggs AH
Hum Genet; 1998 Mar; 102(3):265-72. PubMed ID: 9544837
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
