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Journal Abstract Search

236 related items for PubMed ID: 26662381

  • 41. S38G single-nucleotide polymorphism at the KCNE1 locus is associated with heart failure.
    Fatini C, Sticchi E, Marcucci R, Verdiani V, Nozzoli C, Vassallo C, Emdin M, Abbate R, Gensini GF.
    Heart Rhythm; 2010 Mar; 7(3):363-7. PubMed ID: 20185111
    [Abstract] [Full Text] [Related]

  • 42. [Association between GIRK4 gene polymorphisms and insulin resistance in Xinjiang Uygur population].
    Li NF, Kang YA, Zhang DL, Wang HM, Zhang JH, Hu YR, Hong J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):715-9. PubMed ID: 23225057
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  • 44. Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.
    Yamaguchi Y, Mizumaki K, Hata Y, Inoue H.
    J Electrocardiol; 2016 Dec; 49(1):94-8. PubMed ID: 26520166
    [Abstract] [Full Text] [Related]

  • 45. [C825T polymorphism of G protein beta3 subunit gene and Uygur Hilit type of essential hypertension: a correlation study].
    Li XX, A-Yi-Gu-Li YN, Huang JJ, Zhang JP, Ka-Si-Mu-Jiang AX, Ku-Re-Xi YN.
    Zhongguo Zhong Xi Yi Jie He Za Zhi; 2014 Mar; 34(3):297-302. PubMed ID: 24758080
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  • 48. Fibrinogen gene polymorphism (Bbeta-148C/T) in Uygur patients with cerebral infarction.
    Guo X, Zhang D, Zhang X.
    Neurol Res; 2009 May; 31(4):381-4. PubMed ID: 19508823
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  • 49. Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.
    Andreasen L, Nielsen JB, Christophersen IE, Holst AG, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS.
    Can J Cardiol; 2013 Oct; 29(10):1234-40. PubMed ID: 24074973
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  • 50. [The prevalence and distributing feature of atrial fibrillation in Xinjiang Uygur Autonomous Region Kazaks adult population].
    Lu WH, Mu HY, Liu ZQ, Yang YC, He PY, Yan HY, Jia M, Gu L, Kong B, Shagen D.
    Zhonghua Nei Ke Za Zhi; 2012 Sep; 51(9):674-6. PubMed ID: 23158913
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  • 51. Association of AGTR1 and ACE2 gene polymorphisms with structural atrial fibrillation in a Chinese Han population.
    Feng W, Sun L, Qu XF.
    Pharmazie; 2017 Jan 10; 72(1):17-21. PubMed ID: 29441892
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  • 53. [Epidemiological survey of atrial fibrillation among Uygur and Han elderly people in Xinjiang Uygur autonomous region].
    Miao H, Hong Y, Kabinur K, Zou T, Palida A, Zhou X.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2015 Oct 10; 36(10):1065-8. PubMed ID: 26837345
    [Abstract] [Full Text] [Related]

  • 54. Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation.
    Ravn LS, Hofman-Bang J, Dixen U, Larsen SO, Jensen G, Haunsø S, Svendsen JH, Christiansen M.
    Am J Cardiol; 2005 Aug 01; 96(3):405-7. PubMed ID: 16054468
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  • 55. Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.
    Nielsen JB, Bentzen BH, Olesen MS, David JP, Olesen SP, Haunsø S, Svendsen JH, Schmitt N.
    Biomark Med; 2014 Aug 01; 8(4):557-70. PubMed ID: 24796621
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  • 56. KIR gene polymorphism study in the Uygur population in Xinjiang, China.
    Lin GY, Wang YB.
    Genet Mol Res; 2014 Mar 17; 13(1):1813-22. PubMed ID: 24668669
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  • 58. Association of the human minK gene 38G allele with atrial fibrillation: evidence of possible genetic control on the pathogenesis of atrial fibrillation.
    Lai LP, Su MJ, Yeh HM, Lin JL, Chiang FT, Hwang JJ, Hsu KL, Tseng CD, Lien WP, Tseng YZ, Huang SK.
    Am Heart J; 2002 Sep 17; 144(3):485-90. PubMed ID: 12228786
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  • 59. The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population.
    Liu X, Li Y, Zhang H, Ji Y, Zhao Z, Wang C.
    Mol Genet Genomic Med; 2019 Aug 17; 7(8):e835. PubMed ID: 31270966
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