BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 20031581)

  • 1. 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]  

  • 2. CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.
    Hsu LA; Chang CJ; Teng MS; Semon Wu ; Hu CF; Chang WY; Ko YL
    Clin Appl Thromb Hemost; 2010 Jun; 16(3):301-5. PubMed ID: 19153100
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. MEF2A sequence variants in Turkish population.
    Gulec S; Ruchan Akar A; Akar N
    Clin Appl Thromb Hemost; 2008 Oct; 14(4):465-7. PubMed ID: 18160598
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction.
    González P; García-Castro M; Reguero JR; Batalla A; Ordóñez AG; Palop RL; Lozano I; Montes M; Alvarez V; Coto E
    J Med Genet; 2006 Feb; 43(2):167-9. PubMed ID: 15958500
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MEF2A gene and susceptibility to coronary artery disease in the Chinese people.
    Yuan H; Lü HW; Hu J; Chen SH; Yang GP; Huang ZJ
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2006 Aug; 31(4):453-7. PubMed ID: 16951497
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coronary artery disease and the MEF2A transcription factor.
    Olson EN
    Sci Aging Knowledge Environ; 2003 Dec; 2003(48):pe33. PubMed ID: 14657507
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based study.
    Horan PG; Allen AR; Hughes AE; Patterson CC; Spence M; McGlinchey PG; Belton C; Jardine TC; McKeown PP
    BMC Med Genet; 2006 Jul; 7():65. PubMed ID: 16872533
    [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. 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; 16(8):887-99. PubMed ID: 17324965
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Miscues on the "lack of MEF2A mutations" in coronary artery disease.
    Wang Q; Rao S; Topol EJ
    J Clin Invest; 2005 Jun; 115(6):1399-400; author reply 1400-1. PubMed ID: 15931371
    [No Abstract]   [Full Text] [Related]  

  • 15. Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms.
    González P; Alvarez V; Menéndez M; Lahoz CH; Martínez C; Corao AI; Calatayud MT; Peña J; García-Castro M; Coto E
    Neurosci Lett; 2007 Jan; 411(1):47-51. PubMed ID: 17112666
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. The common Y402H variant in complement factor H gene is not associated with susceptibility to myocardial infarction and its related risk factors.
    Stark K; Neureuther K; Sedlacek K; Hengstenberg W; Fischer M; Baessler A; Wiedmann S; Jeron A; Holmer S; Erdmann J; Schunkert H; Hengstenberg C
    Clin Sci (Lond); 2007 Aug; 113(4):213-8. PubMed ID: 17472578
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.