Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions von Guo, Yu-Han, Yang, Yi-Qing

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GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve von Li, Ruo-Gu, Xu, Ying-Jia, Wang, Juan, Liu, Xing-Yuan, Yuan, Fang, Huang, Ri-Tai, Xue, Song, Li, Li, Liu, Hua, Li, Yan-Jie, Qu, Xin-Kai, Shi, Hong-Yu, Zhang, Min, Qiu, Xing-Biao, Yang, Yi-Qing

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SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension von Wang, Tian-Ming, Wang, Shan-Shan, Xu, Ying-Jia, Zhao, Cui-Mei, Qiao, Xiao-Hui, Yang, Chen-Xi, Liu, Xing-Yuan, Yang, Yi-Qing

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GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve von Xu, Ying-Jia, Di, Ruo-Min, Qiao, Qi, Li, Xiu-Mei, Huang, Ri-Tai, Xue, Song, Liu, Xing-Yuan, Wang, Juan, Yang, Yi-Qing

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Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction disease von Li, Ruo-Gu, Xu, Ying-Jia, Ye, Willy G., Li, Yan-Jie, Chen, Honghong, Qiu, Xing-Biao, Yang, Yi-Qing, Bai, Donglin

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A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation von Mechakra, Asma, Footz, Tim, Walter, Michael, Aránega, Amelia, Hernández-Torres, Francisco, Morel, Elodie, Millat, Gilles, Yang, Yi-Qing, Chahine, Mohamed, Chevalier, Philippe, Christé, Georges

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MiR‐22 restrains proliferation of rheumatoid arthritis by targeting IL6R and may be concerned with the suppression of NF‐κB pathway von Yang, Qing‐Yi, Yang, Kai‐Peng, Li, Zhi‐Zhou

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A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block von Zhang, Yan, Sun, Yu-Min, Xu, Ying-Jia, Zhao, Cui-Mei, Yuan, Fang, Guo, Xiao-Juan, Guo, Yu-Han, Yang, Chen-Xi, Gu, Jia-Ning, Qiao, Qi, Wang, Jun, Yang, Yi-Qing

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GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot von Yang, Yi-Qing, Gharibeh, Lara, Li, Ruo-Gu, Xin, Yuan-Feng, Wang, Juan, Liu, Zhong-Min, Qiu, Xing-Biao, Xu, Ying-Jia, Xu, Lei, Qu, Xin-Kai, Liu, Xu, Fang, Wei-Yi, Huang, Ri-Tai, Xue, Song, Nemer, Georges

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ISL1 loss-of-function mutation contributes to congenital heart defects von Ma, Lan, Wang, Juan, Li, Li, Qiao, Qi, Di, Ruo-Min, Li, Xiu-Mei, Xu, Ying-Jia, Zhang, Min, Li, Ruo-Gu, Qiu, Xing-Biao, Li, Xun, Yang, Yi-Qing

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KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy von Guo, Yu-Han, Wang, Jun, Guo, Xiao-Juan, Gao, Ri-Feng, Yang, Chen-Xi, Li, Li, Sun, Yu-Min, Qiu, Xing-Biao, Xu, Ying-Jia, Yang, Yi-Qing

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A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve von Qu, Xin-Kai, MD, Qiu, Xing-Biao, MD, Yuan, Fang, MD, Wang, Juan, MD, Zhao, Cui-Mei, MD, Liu, Xing-Yuan, MD, Zhang, Xian-Ling, MD, Li, Ruo-Gu, MD, Xu, Ying-Jia, MD, Hou, Xu-Min, MD, Fang, Wei-Yi, MD, Liu, Xu, MD, Yang, Yi-Qing, MD

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PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation von Guo, Xiao-Juan, Qiu, Xing-Biao, Wang, Jun, Guo, Yu-Han, Yang, Chen-Xi, Li, Li, Gao, Ri-Feng, Ke, Zun-Ping, Di, Ruo-Min, Sun, Yu-Min, Xu, Ying-Jia, Yang, Yi-Qing

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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome von Zhao, Cui-Mei, Peng, Lu-Ying, Li, Li, Liu, Xing-Yuan, Wang, Juan, Zhang, Xian-Ling, Yuan, Fang, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing

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Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias von Li, Yan-Jie, Wang, Juan, Ye, Willy G, Liu, Xing-Yuan, Li, Li, Qiu, Xing-Biao, Chen, Honghong, Xu, Ying-Jia, Yang, Yi-Qing, Bai, Donglin, Huang, Ri-Tai

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Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy von 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-Qing

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CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy von Qiu, Xing-Biao, Qu, Xin-Kai, Li, Ruo-Gu, Liu, Hua, Xu, Ying-Jia, Zhang, Min, Shi, Hong-Yu, Hou, Xu-Min, Liu, Xu, Yuan, Fang, Sun, Yu-Min, Wang, Jun, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

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Upregulation of wild-type p53 by small molecule-induced elevation of NQO1 in non-small cell lung cancer cells von Yu, Hong, Gao, Hong-ying, Guo, Hua, Wang, Gui-zhen, Yang, Yi-qing, Hu, Qian, Liang, Li-jun, Zhao, Qun, Xie, Da-wei, Rao, Yu, Zhou, Guang-biao

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Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication von Sun, Yiguo, Yang, Yi-Qing, Gong, Xiang-Qun, Wang, Xin-Hua, Li, Ruo-Gu, Tan, Hong-Wei, Liu, Xu, Fang, Wei-Yi, Bai, Donglin

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Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy von Gu, Jia-Ning, Yang, Chen-Xi, Ding, Yuan-Yuan, Qiao, Qi, Di, Ruo-Min, Sun, Yu-Min, Wang, Jun, Yang, Ling, Xu, Ying-Jia, Yang, Yi-Qing

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