HuGE Literature Finder
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MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations. BMC cardiovascular disorders 2022 6 22 (1): 278. Lin Li-Rong, Hu Xue-Qun, Lu Li-Hong, Dai Jia-Zhen, Lin Ning-Ning, Wang Re-Hua, Xie Zhang-Xin, Chen Xue-M |
Association of NFKB1, NKX2-5, GATA4 and RANKL Gene Polymorphisms with Sporadic Congenital Heart Disease in Greek Patients. Balkan journal of medical genetics : BJMG 2021 8 24 (1): 15-20. Aidinidou L, Chatzikyriakidou A, Giannopoulos A, Karpa V, Tzimou I, Aidinidou E, Fidani |
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 |
ISL1 loss-of-function variation causes familial atrial fibrillation. European journal of medical genetics 2020 8 63 (11): 104029. Wu Shao-Hui, Wang Xin-Hua, Xu Ying-Jia, Gu Jia-Ning, Yang Chen-Xi, Qiao Qi, Guo Xiao-Juan, Guo Yu-Han, Qiu Xing-Biao, Jiang Wei-Feng, Yang Yi-Qi |
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
[Mutations in the GATA4 gen in patients with non-syndromic congenital heart disease]. Investigación clínica 2014 Sep 55 (3): 207-16. Orjuela Quintero Diana Carolina, Núñez Federico, Caicedo Víctor, Pachón Sonia, Salazar Salazar Marle |
Promoter methylation of GATA4, WIF1, NTRK1 and other selected tumour suppressor genes in ovarian cancer. Folia biologica 2013 6 59 (2): 87-92. Chmela?ová M, Dvo?áková E, Špa?ek J, Laco J, Mžik M, Pali?ka |
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