메뉴 건너뛰기




Volumn 96, Issue 3, 2005, Pages 405-407

Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation

Author keywords

[No Author keywords available]

Indexed keywords

VOLTAGE GATED POTASSIUM CHANNEL;

EID: 23044467182     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjcard.2005.03.086     Document Type: Article
Times cited : (67)

References (20)
  • 1
    • 0043169377 scopus 로고    scopus 로고
    • Gene polymorphisms and cardiac arrhythmias
    • M. Firouzi, W.A. Groenewegen Gene polymorphisms and cardiac arrhythmias Europace 5 2003 235 242
    • (2003) Europace , vol.5 , pp. 235-242
    • Firouzi, M.1    Groenewegen, W.A.2
  • 3
    • 0037127028 scopus 로고    scopus 로고
    • Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel
    • S.O. Marx, J. Kurokawa, S. Reiken, H. Motoike, J. D'Armiento, A.R. Marks, R.S. Kass Requirement of a macromolecular signaling complex for beta adrenergic receptor modulation of the KCNQ1-KCNE1 potassium channel Science 295 2002 496 499
    • (2002) Science , vol.295 , pp. 496-499
    • Marx, S.O.1    Kurokawa, J.2    Reiken, S.3    Motoike, H.4    D'Armiento, J.5    Marks, A.R.6    Kass, R.S.7
  • 7
    • 0008530413 scopus 로고    scopus 로고
    • Potassium channel subunits encoded by the KCNE gene family: Physiology and pathophysiology of the MinK-related peptides (MiRPs)
    • G.W. Abbott, S.A. Goldstein Potassium channel subunits encoded by the KCNE gene family physiology and pathophysiology of the MinK-related peptides (MiRPs) Mol Interv 1 2001 95 107
    • (2001) Mol Interv , vol.1 , pp. 95-107
    • Abbott, G.W.1    Goldstein, S.A.2
  • 10
    • 0035951404 scopus 로고    scopus 로고
    • MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis
    • G.W. Abbott, M.H. Butler, S. Bendahhur, M.C. Dalakas, L.J. Ptacek, S.A.N. Goldstein MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis Cell 104 2001 217 231
    • (2001) Cell , vol.104 , pp. 217-231
    • Abbott, G.W.1    Butler, M.H.2    Bendahhur, S.3    Dalakas, M.C.4    Ptacek, L.J.5    Goldstein, S.A.N.6
  • 11
    • 0141430108 scopus 로고    scopus 로고
    • Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis
    • D. Sternberg, N. Tabti, E. Fournier, B. Hainque, B. Fontaine Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis Neurology 61 2003 857 859
    • (2003) Neurology , vol.61 , pp. 857-859
    • Sternberg, D.1    Tabti, N.2    Fournier, E.3    Hainque, B.4    Fontaine, B.5
  • 12
    • 0029952101 scopus 로고    scopus 로고
    • K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
    • J. Barhanin, F. Lesage, E. Guillemare, M. Fink, M. Lazdunski, G. Romey K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current Nature 384 1996 78 80
    • (1996) Nature , vol.384 , pp. 78-80
    • Barhanin, J.1    Lesage, F.2    Guillemare, E.3    Fink, M.4    Lazdunski, M.5    Romey, G.6
  • 13
    • 0033568148 scopus 로고    scopus 로고
    • KCNE1-like gene is deleted in AMME contiguous gene syndrome: Identification and characterization of the human and mouse homologs
    • M. Piccini, F. Vitelli, M. Seri, L.J. Galietta, O. Moran, A. Bulfone, S. Banfi, B. Pober, A. Renieri KCNE1-like gene is deleted in AMME contiguous gene syndrome identification and characterization of the human and mouse homologs Genomics 60 1999 251 257
    • (1999) Genomics , vol.60 , pp. 251-257
    • Piccini, M.1    Vitelli, F.2    Seri, M.3    Galietta, L.J.4    Moran, O.5    Bulfone, A.6    Banfi, S.7    Pober, B.8    Renieri, A.9
  • 15
    • 0036735143 scopus 로고    scopus 로고
    • Association of the human minK gene 38G allele with atrial fibrillation: Evidence of possible genetic control on the pathogenesis of atrial fibrillation
    • L.P. Lai, M.J. Su, H.M. Yeh, J.L. Lin, F.T. Chiang, J.J. Hwang, K.L. Hsu, C.D. Tseng, W.P. Lien, Y.Z. Tseng, S.K. Huang Association of the human minK gene 38G allele with atrial fibrillation evidence of possible genetic control on the pathogenesis of atrial fibrillation Am Heart J 144 2002 485 490
    • (2002) Am Heart J , vol.144 , pp. 485-490
    • Lai, L.P.1    Su, M.J.2    Yeh, H.M.3    Lin, J.L.4    Chiang, F.T.5    Hwang, J.J.6    Hsu, K.L.7    Tseng, C.D.8    Lien, W.P.9    Tseng, Y.Z.10    Huang, S.K.11
  • 17
    • 3142726476 scopus 로고    scopus 로고
    • Prolonged signal-averaged P wave duration after elective cardioversion increases the risk of recurrent atrial fibrillation
    • U. Dixen, C. Joens, J. Parner, V. Rasmussen, S.M. Pehrson, G.B. Jensen Prolonged signal-averaged P wave duration after elective cardioversion increases the risk of recurrent atrial fibrillation Scand Cardiovasc J 38 2004 147 151
    • (2004) Scand Cardiovasc J , vol.38 , pp. 147-151
    • Dixen, U.1    Joens, C.2    Parner, J.3    Rasmussen, V.4    Pehrson, S.M.5    Jensen, G.B.6
  • 20
    • 0345735752 scopus 로고    scopus 로고
    • Sex-specific increase in the prevalence of atrial fibrillation (the Copenhagen City Heart Study)
    • J. Friberg, H. Scharling, N. Gadsboll, G.B. Jensen Sex-specific increase in the prevalence of atrial fibrillation (the Copenhagen City Heart Study) Am J Cardiol 92 2003 1419 1423
    • (2003) Am J Cardiol , vol.92 , pp. 1419-1423
    • Friberg, J.1    Scharling, H.2    Gadsboll, N.3    Jensen, G.B.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.