Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 34 Records) |
Query Trace: MEF2A[original query] |
---|
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 |
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 |
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 |
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 |
[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 |
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 |
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 |
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 |
Polymorphism in postinsulin receptor signaling pathway is not associated with polycystic ovary syndrome. Fertility and sterility 2008 Dec 90 (6): 2298-303. Jones Michelle R, Wilson Scott G, Mullin Ben H, Mead Robert, Dudbridge Frank, Watts Gerald F, Stuckey Bronwyn G |
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 |
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 |
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 |
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 |
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 |
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 |
Hemodynamic fluid shear stress response genes and carotid intima-media thickness: a candidate gene association analysis in the cardiovascular health study. International journal of molecular epidemiology and genetics 2012 3 (2): 174-8. Suchy-Dicey Astrid M, Enquobahrie Daniel A, Heckbert Susan R, Rotter Jerome I, Psaty Bruce M, McKnight Barba |
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 |
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 |
Association of MEF2A gene polymorphisms with coronary artery disease. Iranian Red Crescent medical journal 2014 Aug 16 (8): e13533. Foroughmand Ali Mohammad, Shahbazi Zahra, Galehdari Hamid, Purmahdi Borujeni Mahdi, Dinarvand Parvane, Golabgirkhademi Khadi |
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 |
Linkage and whole genome sequencing identify a locus on 6q25-26 for formal thought disorder and implicate MEF2A regulation. Schizophrenia research 2015 Sep . Thygesen Johan Hilge, Zambach Sine Katharina, Ingason Andrés, Lundin Pär, Hansen Thomas, Berlatan Marcelo, Rosengren Anders, Bjerre Ditte, Ferrero-Miliani Laura, Rasmussen Henrik Berg, Parnas Josef, Werge Thom |
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 |
Variants in MEF2A gene in relation with coronary artery disease in Saudi population. 3 Biotech 2018 Jul 8 (7): 289. Zargar Seema, Aljafari Abdulaziz A, Wani Tanveer |
Mapping genetic variants for cranial vault shape in humans.
PloS one 2018 13 (4): e0196148. Roosenboom Jasmien, Lee Myoung Keun, Hecht Jacqueline T, Heike Carrie L, Wehby George L, Christensen Kaare, Feingold Eleanor, Marazita Mary L, Maga A Murat, Shaffer John R, Weinberg Seth |
Germline but not somatic de novo mutations are common in human congenital diaphragmatic hernia. Birth defects research 2018 3 110 (7): 610-617. Matsunami Nori, Shanmugam Hari, Baird Lisa, Stevens Jeff, Byrne Janice L, Barnhart Douglas C, Rau Carrie, Feldkamp Marcia L, Yoder Bradley A, Leppert Mark F, Yost H Joseph, Brunelli Lu |
Functional SNPs in the Human Autoimmunity-Associated Locus 17q12-21. Genes 2019 1 10 (2): . Ustiugova Alina S, Korneev Kirill V, Kuprash Dmitry V, Afanasyeva And Marina |
Rare genetic variants in patients with cervical artery dissection. European stroke journal 2020 1 4 (4): 355-362. Traenka Christopher, Kloss Manja, Strom Tim, Lyrer Philippe, Brandt Tobias, Bonati Leo H, Grond-Ginsbach Caspar, Engelter Stef |
Genomic Mutation Profile of Primary Gastrointestinal Diffuse Large B-Cell Lymphoma. Frontiers in oncology 2021 3 11 622648. Li Peifeng, Chai Jia, Chen Zi, Liu Yang, Wei Jie, Liu Yixiong, Zhao Danhui, Ma Jing, Wang Kaijing, Li Xia, Shao Yang, Gong Li, Zhang Wei, Guo Shuangping, Yan Qingguo, Li Mingyang, Fan Linni, Wang Z |
Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy. Clinical chemistry and laboratory medicine 2021 2 59 (5): 955-963. Qiao Qi, Zhao Cui-Mei, Yang Chen-Xi, Gu Jia-Ning, Guo Yu-Han, Zhang Min, Li Ruo-Gu, Qiu Xing-Biao, Xu Ying-Jia, Yang Yi-Qi |
Effect of MEF2A and SLC22A3-LPAL2-LPA gene polymorphisms on warfarin sensitivity and responsiveness in Jordanian cardiovascular patients. PloS one 2023 11 18 (11): e0294226. Laith N Al-Eitan, Ayah Y Almasri, Adan H Alnaamneh, Ahmad Mihy |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: