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Journal Abstract Search

105 related items for PubMed ID: 21733517

  • 1. Fine mapping of chromosome 3q22.3 identifies two haplotype blocks in ESYT3 associated with coronary artery disease in female Han Chinese.
    Jiang F, Dong Y, Wu C, Yang X, Zhao L, Guo J, Li Y, Dong J, Zheng GY, Cao H, Jin L, Ren Y, Cheng W, Li W, Tian XL, Li X.
    Atherosclerosis; 2011 Oct; 218(2):397-403. PubMed ID: 21733517
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  • 3. Genomic risk variants at 1p13.3, 1q41, and 3q22.3 are associated with subsequent cardiovascular outcomes in healthy controls and in established coronary artery disease.
    Ellis KL, Frampton CM, Pilbrow AP, Troughton RW, Doughty RN, Whalley GA, Ellis CJ, Skelton L, Thomson J, Yandle TG, Richards AM, Cameron VA.
    Circ Cardiovasc Genet; 2011 Dec; 4(6):636-46. PubMed ID: 21984477
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  • 5. Gene polymorphisms associated with susceptibility to coronary artery disease in Han Chinese people.
    Liu YH, Zhou YW, Yang JA, Tu ZG, Ji SY, Huang ZY, Zhou ZJ.
    Genet Mol Res; 2014 Apr 08; 13(2):2619-27. PubMed ID: 24782050
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  • 6. Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.
    Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C.
    Hum Mol Genet; 2007 Apr 15; 16(8):887-99. PubMed ID: 17324965
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  • 12. Two- and three-locus haplotypes of the paraoxonase (PON1) gene are associated with coronary artery disease in Asian Indians.
    Ahmad I, Narang R, Venkatraman A, Das N.
    Gene; 2012 Sep 10; 506(1):242-7. PubMed ID: 22750797
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  • 14. Association of MEF2A gene 3'UTR mutations with coronary artery disease.
    Huang XC, Wang W.
    Genet Mol Res; 2015 Sep 21; 14(3):11073-8. PubMed ID: 26400337
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  • 16. A novel block at chromosome 12q24.1 is associated with coronary artery disease in Han Chinese populations.
    Jiang F, Yan H, Wu C, Song C, Zhao B, Li Y, Dong J, Zheng GY, Jin LJ, Li XQ, Li WY, Cai J, Yang XC, Tian XL.
    Pharmacogenet Genomics; 2016 Nov 21; 26(11):497-504. PubMed ID: 27602548
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  • 18. Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus.
    Zollbrecht C, Grassl M, Fenk S, Höcherl R, Hubauer U, Reinhard W, Esslinger UB, Ebert S, Langmann T, Stark K, Hengstenberg C.
    Atherosclerosis; 2013 Apr 21; 227(2):244-9. PubMed ID: 23375685
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