172 related articles for article (PubMed ID: 16472284)
1. Functional significance of KCNH2 (HERG) K897T polymorphism for cardiac repolarization assessed by analysis of T-wave morphology.
Linna EH; Perkiömäki JS; Karsikas M; Seppänen T; Savolainen M; Kesäniemi YA; Mäkikallio T; Huikuri HV
Ann Noninvasive Electrocardiol; 2006 Jan; 11(1):57-62. PubMed ID: 16472284
[TBL] [Abstract][Full Text] [Related]
2. Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women.
Pietilä E; Fodstad H; Niskasaari E; Laitinen P PJ; Swan H; Savolainen M; Kesäniemi YA; Kontula K; Huikuri HV
J Am Coll Cardiol; 2002 Aug; 40(3):511-4. PubMed ID: 12142119
[TBL] [Abstract][Full Text] [Related]
3. Potassium channel KCNH2 K897T polymorphism and cardiac repolarization during exercise test: The Finnish Cardiovascular Study.
Koskela J; Laiho J; KäHönen M; Rontu R; Lehtinen R; Viik J; Niemi M; Niemelä K; Kööbi T; Turjanmaa V; Pörsti I; Lehtimäki T; Nieminen T
Scand J Clin Lab Invest; 2008; 68(1):31-8. PubMed ID: 17852802
[TBL] [Abstract][Full Text] [Related]
4. Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG).
Paavonen KJ; Chapman H; Laitinen PJ; Fodstad H; Piippo K; Swan H; Toivonen L; Viitasalo M; Kontula K; Pasternack M
Cardiovasc Res; 2003 Sep; 59(3):603-11. PubMed ID: 14499861
[TBL] [Abstract][Full Text] [Related]
5. A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization.
Bezzina CR; Verkerk AO; Busjahn A; Jeron A; Erdmann J; Koopmann TT; Bhuiyan ZA; Wilders R; Mannens MM; Tan HL; Luft FC; Schunkert H; Wilde AA
Cardiovasc Res; 2003 Jul; 59(1):27-36. PubMed ID: 12829173
[TBL] [Abstract][Full Text] [Related]
6. Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
Zhang X; Chen S; Zhang L; Liu M; Redfearn S; Bryant RM; Oberti C; Vincent GM; Wang QK
BMC Med Genet; 2008 Sep; 9():87. PubMed ID: 18808722
[TBL] [Abstract][Full Text] [Related]
7. Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
Gouas L; Nicaud V; Berthet M; Forhan A; Tiret L; Balkau B; Guicheney P;
Eur J Hum Genet; 2005 Nov; 13(11):1213-22. PubMed ID: 16132053
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Crotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL; Schwartz PJ
Circulation; 2005 Aug; 112(9):1251-8. PubMed ID: 16116052
[TBL] [Abstract][Full Text] [Related]
10. The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
Sinner MF; Pfeufer A; Akyol M; Beckmann BM; Hinterseer M; Wacker A; Perz S; Sauter W; Illig T; Näbauer M; Schmitt C; Wichmann HE; Schömig A; Steinbeck G; Meitinger T; Kääb S
Eur Heart J; 2008 Apr; 29(7):907-14. PubMed ID: 18222980
[TBL] [Abstract][Full Text] [Related]
11. Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2.
Cordeiro JM; Perez GJ; Schmitt N; Pfeiffer R; Nesterenko VV; Burashnikov E; Veltmann C; Borggrefe M; Wolpert C; Schimpf R; Antzelevitch C
Can J Physiol Pharmacol; 2010 Dec; 88(12):1181-90. PubMed ID: 21164565
[TBL] [Abstract][Full Text] [Related]
12. Relationship of common candidate gene variants to electrocardiographic T-wave peak to T-wave end interval and T-wave morphology parameters.
Porthan K; Marjamaa A; Viitasalo M; Väänänen H; Jula A; Toivonen L; Nieminen MS; Newton-Cheh C; Salomaa V; Kontula K; Oikarinen L
Heart Rhythm; 2010 Jul; 7(7):898-903. PubMed ID: 20215044
[TBL] [Abstract][Full Text] [Related]
13. Common candidate gene variants are associated with QT interval duration in the general population.
Marjamaa A; Newton-Cheh C; Porthan K; Reunanen A; Lahermo P; Väänänen H; Jula A; Karanko H; Swan H; Toivonen L; Nieminen MS; Viitasalo M; Peltonen L; Oikarinen L; Palotie A; Kontula K; Salomaa V
J Intern Med; 2009 Apr; 265(4):448-58. PubMed ID: 19019189
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Common genetic variation in KCNH2 is associated with QT interval duration: the Framingham Heart Study.
Newton-Cheh C; Guo CY; Larson MG; Musone SL; Surti A; Camargo AL; Drake JA; Benjamin EJ; Levy D; D'Agostino RB; Hirschhorn JN; O'donnell CJ
Circulation; 2007 Sep; 116(10):1128-36. PubMed ID: 17709632
[TBL] [Abstract][Full Text] [Related]
16. KCNH2 polymorphism and methadone dosage interact to enhance QT duration.
Hajj A; Ksouda K; Peoc'h K; Curis E; Messali A; Deveaux LL; Bloch V; Prince N; Mouly S; Scherrmann JM; Lépine JP; Laplanche JL; Drici MD; Vorspan F
Drug Alcohol Depend; 2014 Aug; 141():34-8. PubMed ID: 24875677
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study.
Raitakari OT; Blom-Nyholm J; Koskinen TA; Kähönen M; Viikari JS; Lehtimäki T
Ann Med; 2009; 41(2):144-51. PubMed ID: 18785031
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The functional HERG variant 897T is associated with Conn's adenoma.
Sarzani R; Pietrucci F; Corinaldesi C; Francioni M; Letizia C; D'Erasmo E; Dessì-Fulgheri P; Rappelli A
J Hypertens; 2006 Mar; 24(3):479-87. PubMed ID: 16467651
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
