HuGE Literature Finder
Records 1-23
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Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family.
Molecular medicine reports 2016 Jul 14 (1): 649-54. Xu Dong-Ling, Tian Hong-Liang, Cai Wei-Li, Zheng Jie, Gao Min, Zhang Ming-Xiang, Zheng Zhao-Tong, Lu Qing-H |
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Association of MEF2A gene 3'UTR mutations with coronary artery disease.
Genetics and molecular research : GMR 2015 14 (3): 11073-8. Huang X C, Wang |
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MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.
Genetics and molecular research : GMR 2014 13 (4): 8396-402. Li J, Chen H-X, Yang J-G, Li W, Du R, Tian |
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Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis.
PloS one 2012 7 (2): e31406. Liu Yan, Niu Wenquan, Wu Zhijun, Su Xiuxiu, Chen Qiujin, Lu Lin, Jin W |
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Exon 11 deletion in the myocyte enhancer factor (MEF)2A and early onset coronary artery disease gene in a Sicilian family.
European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology 2011 Aug 18 (4): 557-60. Maiolino Giuseppe, Colonna Stefania, Zanchetta Mario, Pedon Luigi, Seccia Teresa Maria, Cesari Maurizio, Vigili de Kreutzenberg Saula, Avogaro Angelo, Rossi Gian Pao |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.
European journal of clinical investigation 2010 Aug 40 (8): 669-77. Dai Da-Peng, Zhou Xiao-Yang, Xiao Yao, Xu Feng, Sun Fu-Cheng, Ji Fu-Sui, Zhang Zhi-Xin, Hu Ji-Hong, Guo Jian, Zheng Jun-De, Dong Jia-Mei, Zhu Wei-Guo, Shen Yan, Qian Yi-Jian, He Qing, Cai Jian-Pi |
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CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2010 Jun 16 (3): 301-5. Hsu Lung-An, Chang Chi-Jen, Teng Ming-Sheng, Semon Wu , Hu Chiao-Feng, Chang Wen-Ya, Ko Yu-L |
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Regulatory polymorphism in transcription factor KLF5 at the MEF2 element alters the response to angiotensin II and is associated with human hypertension.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010 Jun 24 (6): 1780-8. Oishi Yumiko, Manabe Ichiro, Imai Yasushi, Hara Kazuo, Horikoshi Momoko, Fujiu Katsuhito, Tanaka Toshihiro, Aizawa Tadanori, Kadowaki Takashi, Nagai Ryo |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease.
Circulation. Cardiovascular genetics 2009 Apr 2 (2): 165-72. Guella Ilaria, Rimoldi Valeria, Asselta Rosanna, Ardissino Diego, Francolini Maura, Martinelli Nicola, Girelli Domenico, Peyvandi Flora, Tubaro Marco, Merlini Pier Angelica, Mannucci Pier Mannuccio, Duga Stefa |
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Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy.
American journal of medical genetics. Part A 2009 Feb 149A (2): 286-9. Coto Eliecer, Castro Mónica G, Corao Ana I, Alonso-Montes Cristina, Reguero Julián R, Morís César, Alvarez Victor |
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MEF2A sequence variants in Turkish population.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008 Oct 14 (4): 465-7. Gulec Sukru, Ruchan Akar Ahmet, Akar Nej |
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Lack of association between the MEF2A gene and myocardial infarction.
Circulation 2008 Jan 117 (2): 185-91. Lieb Wolfgang, Mayer Björn, König Inke R, Borwitzky Iris, Götz Anika, Kain Silke, Hengstenberg Christian, Linsel-Nitschke Patrick, Fischer Marcus, Döring Angela, Wichmann H-Erich, Meitinger Thomas, Kreutz Reinhold, Ziegler Andreas, Schunkert Heribert, Erdmann Jeanet |
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Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2007 45 (8): 987-92. Han Yaling, Yang Yong, Zhang Xiaolin, Yan Chenghui, Xi Suya, Kang Ji |
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MEF2A gene and susceptibility to coronary artery disease in the Chinese people.
Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2006 Aug 31 (4): 453-7. Yuan Hong, Lü Hong-wei, Hu Jing, Chen Shu-hua, Yang Guo-ping, Huang Zhi-j |
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[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2006 Jun 23 (3): 265-8. Li Jing, Yang Jun-guo, Li Wei, Du Rong, Gui Le, Tian Li, Guo Qiu-h |
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The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction.
Journal of medical genetics 2006 Feb 43 (2): 167-9. González P, García-Castro M, Reguero J R, Batalla A, Ordóñez A G, Palop R L, Lozano I, Montes M, Alvarez V, Coto |
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Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based study.
BMC medical genetics 2006 7 (): 65. Horan Paul G, Allen Adrian R, Hughes Anne E, Patterson Chris C, Spence Mark, McGlinchey Paul G, Belton Christine, Jardine Tracy C L, McKeown Pascal |
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Assessment of MEF2A mutations in myocardial infarction in Japanese patients.
Circulation journal : official journal of the Japanese Circulation Society 2005 Oct 69 (10): 1192-5. Kajimoto Kazuaki, Shioji Keisuke, Tago Naomi, Tomoike Hitonobu, Nonogi Hiroshi, Goto Yoichi, Iwai Naoha |
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Lack of MEF2A mutations in coronary artery disease.
The Journal of clinical investigation 2005 Apr 115 (4): 1016-20. Weng Li, Kavaslar Nihan, Ustaszewska Anna, Doelle Heather, Schackwitz Wendy, Hébert Sybil, Cohen Jonathan C, McPherson Ruth, Pennacchio Len |
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MEF2A sequence variants and coronary artery disease: a change of heart?
The Journal of clinical investigation 2005 Apr 115 (4): 831-3. Altshuler David, Hirschhorn Joel |
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Transcription factor MEF2A mutations in patients with coronary artery disease.
Human molecular genetics 2004 Dec 13 (24): 3181-8. Bhagavatula M R Krishna, Fan Chun, Shen Gong-Qing, Cassano June, Plow Edward F, Topol Eric J, Wang Qi |
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- Page last updated:Jan 23, 2020
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