BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 27221044)

  • 1. Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family.
    Xu DL; Tian HL; Cai WL; Zheng J; Gao M; Zhang MX; Zheng ZT; Lu QH
    Mol Med Rep; 2016 Jul; 14(1):649-54. PubMed ID: 27221044
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis.
    Liu Y; Niu W; Wu Z; Su X; Chen Q; Lu L; Jin W
    PLoS One; 2012; 7(2):e31406. PubMed ID: 22363637
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lack of MEF2A mutations in coronary artery disease.
    Weng L; Kavaslar N; Ustaszewska A; Doelle H; Schackwitz W; Hébert S; Cohen JC; McPherson R; Pennacchio LA
    J Clin Invest; 2005 Apr; 115(4):1016-20. PubMed ID: 15841183
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.
    Dai DP; Zhou XY; Xiao Y; Xu F; Sun FC; Ji FS; Zhang ZX; Hu JH; Guo J; Zheng JD; Dong JM; Zhu WG; Shen Y; Qian YJ; He Q; Cai JP
    Eur J Clin Invest; 2010 Aug; 40(8):669-77. PubMed ID: 20546016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of MEF2A mutations in a Chinese population with premature coronary artery disease.
    Dai Y; Zhang S; Wu W
    Genet Test Mol Biomarkers; 2013 Apr; 17(4):352-5. PubMed ID: 23461724
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lack of Association between the MEF2A Gene and Coronary Artery Disease in Iranian Families.
    Inanloo Rahatloo K; Davaran S; Elahi E
    Iran J Basic Med Sci; 2013 Aug; 16(8):950-4. PubMed ID: 24106602
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation of MEF2A in an inherited disorder with features of coronary artery disease.
    Wang L; Fan C; Topol SE; Topol EJ; Wang Q
    Science; 2003 Nov; 302(5650):1578-81. PubMed ID: 14645853
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transcription factor MEF2A mutations in patients with coronary artery disease.
    Bhagavatula MR; Fan C; Shen GQ; Cassano J; Plow EF; Topol EJ; Wang Q
    Hum Mol Genet; 2004 Dec; 13(24):3181-8. PubMed ID: 15496429
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.
    Li J; Chen HX; Yang JG; Li W; Du R; Tian L
    Genet Mol Res; 2014 Oct; 13(4):8396-402. PubMed ID: 25366733
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease.
    Guella I; Rimoldi V; Asselta R; Ardissino D; Francolini M; Martinelli N; Girelli D; Peyvandi F; Tubaro M; Merlini PA; Mannucci PM; Duga S
    Circ Cardiovasc Genet; 2009 Apr; 2(2):165-72. PubMed ID: 20031581
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MEF2A sequence variants and coronary artery disease: a change of heart?
    Altshuler D; Hirschhorn JN
    J Clin Invest; 2005 Apr; 115(4):831-3. PubMed ID: 15841171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.
    Han Y; Yang Y; Zhang X; Yan C; Xi S; Kang J
    Clin Chem Lab Med; 2007; 45(8):987-92. PubMed ID: 17579569
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of MEF2A gene 3'UTR mutations with coronary artery disease.
    Huang XC; Wang W
    Genet Mol Res; 2015 Sep; 14(3):11073-8. PubMed ID: 26400337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of association between the MEF2A gene and myocardial infarction.
    Lieb W; Mayer B; König IR; Borwitzky I; Götz A; Kain S; Hengstenberg C; Linsel-Nitschke P; Fischer M; Döring A; Wichmann HE; Meitinger T; Kreutz R; Ziegler A; Schunkert H; Erdmann J
    Circulation; 2008 Jan; 117(2):185-91. PubMed ID: 18086930
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].
    Li J; Yang JG; Li W; Du R; Gui L; Tian L; Guo QH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):265-8. PubMed ID: 16767660
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assessment of MEF2A mutations in myocardial infarction in Japanese patients.
    Kajimoto K; Shioji K; Tago N; Tomoike H; Nonogi H; Goto Y; Iwai N
    Circ J; 2005 Oct; 69(10):1192-5. PubMed ID: 16195615
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exon 11 deletion in the myocyte enhancer factor (MEF)2A and early onset coronary artery disease gene in a Sicilian family.
    Maiolino G; Colonna S; Zanchetta M; Pedon L; Seccia TM; Cesari M; Vigili de Kreutzenberg S; Avogaro A; Rossi GP
    Eur J Cardiovasc Prev Rehabil; 2011 Aug; 18(4):557-60. PubMed ID: 21450604
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Systematic analysis of variants related to familial hypercholesterolemia in families with premature myocardial infarction.
    Brænne I; Kleinecke M; Reiz B; Graf E; Strom T; Wieland T; Fischer M; Kessler T; Hengstenberg C; Meitinger T; Erdmann J; Schunkert H
    Eur J Hum Genet; 2016 Feb; 24(2):191-7. PubMed ID: 26036859
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Study of transcription factor MEF2A gene polymorphisms in patients with coronary artery disease.
    Muhammad Sulaiman K
    Cell Mol Biol (Noisy-le-grand); 2024 Jan; 70(1):80-86. PubMed ID: 38372109
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.
    Mehvari S; Karimian Fathi N; Saki S; Asadnezhad M; Arzhangi S; Ghodratpour F; Mohseni M; Zare Ashrafi F; Sadeghian S; Boroumand M; Shokohizadeh F; Rostami E; Boroumand R; Najafipour R; Malekzadeh R; Riazalhosseini Y; Akbari M; Lathrop M; Najmabadi H; Hosseini K; Kahrizi K
    Clin Genet; 2024 Jun; 105(6):611-619. PubMed ID: 38308583
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.