Kv7.1 in atrial fibrillation

Heart Rhythm

Volumn 6, Issue 8, 2009, Pages 1154-1155

  Seebohm, Guiscard ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; POTASSIUM CHANNEL KCNQ1;

EDITORIAL; GENE MUTATION; GENETIC ASSOCIATION; HEART ATRIUM FIBRILLATION; HUMAN; P WAVE; PATHOGENESIS; PRIORITY JOURNAL; QT INTERVAL;

ATRIAL FIBRILLATION; HUMANS; KCNQ1 POTASSIUM CHANNEL; MUTATION; RISK FACTORS; TANDEM REPEAT SEQUENCES;

EID: 67650753492     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2009.05.004     Document Type: Editorial

References (24)

1. Go A.S., Hylek E.M., Phillips K.A., et al. Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study. JAMA 285 (2001) 2370-2375
2. Wang T.J., Larson M.G., Levy D., et al. Temporal relations of atrial fibrillation and congestive heart failure and their joint influence on mortality: the Framingham Heart Study. Circulation 107 (2003) 2920-2925
3. Fox C.S., Parise H., D'Agostino Sr. R.B., et al. Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring. JAMA 291 (2004) 2851-2855
4. Ellinor P.T., Yoerger D.M., Ruskin J.N., and MacRae C.A. Familial aggregation in lone atrial fibrillation. Hum Genet 118 (2005) 179-184
5. Arnar D.O., Thorvaldsson S., Manolio T.A., et al. Familial aggregation of atrial fibrillation in Iceland. Eur Heart J 27 (2006) 708-712
6. Brugada R., Tapscott T., Czernuszewicz G.Z., et al. Identification of a genetic locus for familial atrial fibrillation. N Engl J Med 336 (1997) 905-911
7. Kr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG). Eur Heart J 29 (2008) 907-914
8. Xia M., Jin Q., Bendahhou S., et al. A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation. Biochem Biophys Res Commun 332 (2005) 1012-1019
9. Olson T.M., Alekseev A.E., Liu X.K., et al. Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation. Hum Mol Genet 15 (2006) 2185-2191
10. Yang Y., Xia M., Jin Q., et al. Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation. Am J Hum Genet 75 (2004) 899-905
11. Chen Y.H., Xu S.J., Bendahhou S., et al. KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science 299 (2003) 251-254
12. Barhanin J., Lesage F., Guillemare E., et al. K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current. Nature 384 (1996) 78-80
13. Sanguinetti M.C., Curran M.E., Zou A., et al. Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel. Nature 384 (1996) 80-83
14. Hong K., Piper D.R., Diaz-Valdecantos A., et al. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res 68 (2005) 433-440
15. Ks channels. J Physiol 586 Pt 17 (2008) 4179-4191
16. Lundby A., Ravn L.S., Svendsen J.H., Olesen S.P., and Schmitt N. KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval. Heart Rhythm 4 (2007) 1532-1541
17. Das S., Makino S., Melman Y.F., et al. Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation. Heart Rhythm 6 (2009) 1146-1153
18. Abbott G.W., Xu X., and Roepke T.K. Impact of ancillary subunits on ventricular repolarization. J Electrocardiol 40 (2007) S42-S46
19. + channel complexes. Proc Natl Acad Sci U S A 105 (2008) 1478-1482
20. Bendahhou S., Marionneau C., Haurogne K., et al. In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart. Cardiovasc Res 67 (2005) 529-538
21. Tseng G.N. The phenotype of a KCNQ1 mutation depends on its KCNE partners: is the cardiac slow delayed rectifier (IKs) channel more than a KCNQ1/KCNE1 complex?. Heart Rhythm 4 (2007) 1542-1543
22. Ks secondary to a mutation in KCNE5 associated with atrial fibrillation. Heart Rhythm 5 (2008) 427-435
23. Ks transgenic mouse. J Physiol 586 (2008) 627-637
24. Smith J.A., Vanoye C.G., George Jr. A.L., et al. Structural models for the KCNQ1 voltage-gated potassium channel. Biochemistry 46 (2007) 14141-14152