These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 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. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 5.