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Journal Abstract Search

145 related items for PubMed ID: 16563243

  • 1. [The association of single nucleotide polymorphism of slow delayed rectifier K+ channel genes with atrial fibrillation in Han nationality Chinese].
    Zeng ZY, Pu JL, Tan C, Teng SY, Chen JH, Su SY, Zhou XY, Zhang S, Li YS, Wang FZ, Gu DF.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2005 Nov; 33(11):987-91. PubMed ID: 16563243
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  • 2. The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population.
    Zeng Z, Tan C, Teng S, Chen J, Su S, Zhou X, Wang F, Zhang S, Gu D, Makielski JC, Pu J.
    Cardiology; 2007 Nov; 108(2):97-103. PubMed ID: 17016049
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  • 4. Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.
    Li L, Shen C, Yao Z, Liang J, Huang C.
    Genet Test Mol Biomarkers; 2015 Jul; 19(7):359-65. PubMed ID: 26066992
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  • 5. Correlation analysis between the delayed rectifier potassium channel KCNE1 (G38S) polymorphism and atrial fibrillation among the senior Uygur population in Xinjiang.
    Wugeti N, Yu-Jun G, Juan S, Mahemuti A.
    Genet Mol Res; 2015 Dec 07; 14(4):15906-12. PubMed ID: 26662381
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  • 6. Modulation of KCNQ1 current by atrial fibrillation-associated KCNE4 (145E/D) gene polymorphism.
    Ma KJ, Li N, Teng SY, Zhang YH, Sun Q, Gu DF, Pu JL.
    Chin Med J (Engl); 2007 Jan 20; 120(2):150-4. PubMed ID: 17335661
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  • 10. Selective targeting of gain-of-function KCNQ1 mutations predisposing to atrial fibrillation.
    Campbell CM, Campbell JD, Thompson CH, Galimberti ES, Darbar D, Vanoye CG, George AL.
    Circ Arrhythm Electrophysiol; 2013 Oct 20; 6(5):960-6. PubMed ID: 24006450
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  • 12. Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1.
    Chan PJ, Osteen JD, Xiong D, Bohnen MS, Doshi D, Sampson KJ, Marx SO, Karlin A, Kass RS.
    J Gen Physiol; 2012 Feb 20; 139(2):135-44. PubMed ID: 22250012
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  • 13. Association of KCNE1 genetic polymorphisms with atrial fibrillation in a Chinese Han population.
    Yao J, Ma YT, Xie X, Liu F, Chen BD.
    Genet Test Mol Biomarkers; 2012 Nov 20; 16(11):1343-6. PubMed ID: 23020083
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  • 15. Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.
    Chu HM, Feng MJ, Li YG, Zhang YX, Ma JF, He B, Yu YB, Liu J, Chen XM.
    ScientificWorldJournal; 2013 Nov 20; 2013():373454. PubMed ID: 23710137
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  • 16. [Association of rs1805127 polymorphism of KCNE1 gene with atrial fibrillation in Uigur population of Xinjiang].
    Yao J, Ma YT, Xie X, Liu F, Chen BD, An Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug 20; 28(4):436-40. PubMed ID: 21811988
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  • 17. Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?
    Otway R, Vandenberg JI, Guo G, Varghese A, Castro ML, Liu J, Zhao J, Bursill JA, Wyse KR, Crotty H, Baddeley O, Walker B, Kuchar D, Thorburn C, Fatkin D.
    J Am Coll Cardiol; 2007 Feb 06; 49(5):578-86. PubMed ID: 17276182
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  • 20. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels.
    Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M.
    Heart Rhythm; 2014 Jan 06; 11(1):67-75. PubMed ID: 24096004
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