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Volumn 7, Issue 3, 2010, Pages 368-369

Association of a common KCNE1 variant with heart failure

Author keywords

[No Author keywords available]

Indexed keywords

G PROTEIN COUPLED RECEPTOR KINASE 5; GLYCINE; POTASSIUM CHANNEL KCNE1; SERINE;

EID: 76849101928     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2009.12.014     Document Type: Editorial
Times cited : (2)

References (12)
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  • 3
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    • Dorn, G.W.1    Cresci, S.2
  • 6
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    • S38G SNP at KCNE1 locus is associated with heart failure
    • Fatini C., Sticchi E., Marcucci R., et al. S38G SNP at KCNE1 locus is associated with heart failure. Heart Rhythm 7 (2010) 363-367
    • (2010) Heart Rhythm , vol.7 , pp. 363-367
    • Fatini, C.1    Sticchi, E.2    Marcucci, R.3
  • 7
    • 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
    • Lai L.P., Su M.J., Yeh H.M., et al. 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
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  • 8
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    • Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation
    • Fatini C., Sticchi E., Genuardi M., et al. Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation. Eur Heart J 27 (2006) 1712-1718
    • (2006) Eur Heart J , vol.27 , pp. 1712-1718
    • Fatini, C.1    Sticchi, E.2    Genuardi, M.3
  • 9
    • 33845503506 scopus 로고    scopus 로고
    • MinK gene polymorphism in the pathogenesis of lone atrial fibrillation
    • Prystupa A., Dzida G., Myslinski W., Malaj G., and Lorenc T. MinK gene polymorphism in the pathogenesis of lone atrial fibrillation. Kardiol Pol 64 (2006) 1205-1211
    • (2006) Kardiol Pol , vol.64 , pp. 1205-1211
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  • 10
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    • Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes
    • Herlyn H., Zechner U., Oswald F., et al. Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes. BMC Evol Biol 9 (2009) 188
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    • A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.