Symport and antiport mechanisms of human glutamate transporters von Qiu, Biao, Boudker, Olga

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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 New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle von Wang, Zhi, Song, Hao-Ming, Wang, Fei, Zhao, Cui-Mei, Huang, Ri-Tai, Xue, Song, Li, Ruo-Gu, Qiu, Xing-Biao, Xu, Ying-Jia, Liu, Xing-Yuan, Yang, Yi-Qing

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Phylogeny and re‐circumscription of Cheniella (Leguminosae: Cercidoideae) based on plastome data and morphology, with description of three new species von Gu, Shi‐Ran, Zeng, Qiu‐Biao, Clark, Ruth, Jiang, Kai‐Wen, Pérez‐Escobar, Oscar Alejandro, Li, Shi‐Jin, Tan, Wei‐Ning, Xie, Zhi, Mattapha, Sawai, Shi, Miao‐Miao, Wang, Xiang‐Ping, Zhao, Zhong‐Tao, Antonelli, Alexandre, Tu, Tie‐Yao, Wen, Jun, Zhang, Dian‐Xiang

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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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A randomized comparison of two paclitaxel‐coated balloons for the treatment of in‐stent restenosis: The LONGTY ISR China randomized trial (LONGTY DCB vs. SeQuent Please DCB) von Hu, Po, Sun, Yong, Li, Chang‐Ling, Jin, Rui, Xie, Qiang, Jiang, Xue‐Jun, Wu, Lian‐Pin, Jiang, Jian‐Jun, Qiu, Xin‐Biao, Cao, Yu, Ji, Guang, Wang, Hua, Yao, Zhu‐Hua, Li, Bin, Xia, Yong, Wang, Jian‐An, Jiang, Jun

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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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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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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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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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Cryo-EM structures of excitatory amino acid transporter 3 visualize coupled substrate, sodium, and proton binding and transport von Qiu, Biao, Matthies, Doreen, Fortea, Eva, Yu, Zhiheng, Boudker, Olga

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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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MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy von Yuan, Fang, Qiu, Zhao-Hui, Wang, Xing-Hua, Sun, Yu-Min, Wang, Jun, Li, Ruo-Gu, Liu, Hua, Zhang, Min, Shi, Hong-Yu, Zhao, Liang, Jiang, Wei-Feng, Liu, Xu, Qiu, Xing-Biao, Qu, Xin-Kai, Yang, Yi-Qing

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TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy von Zhang, Xian-Ling, Qiu, Xing-Biao, Yuan, Fang, Wang, Juan, Zhao, Cui-Mei, Li, Ruo-Gu, Xu, Lei, Xu, Ying-Jia, Shi, Hong-Yu, Hou, Xu-Min, Qu, Xin-Kai, Xu, Ya-Wei, 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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NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve von Wang, Juan, Abhinav, Pradhan, Xu, Ying-Jia, Li, Ruo-Gu, Zhang, Min, Qiu, Xing-Biao, Di, Ruo-Min, Qiao, Qi, Li, Xiu-Mei, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

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Effect of precursor and preparation method on manganese based activated carbon sorbents for removing H2S from hot coal gas von Wang, Jiancheng, Qiu, Biao, Han, Lina, Feng, Gang, Hu, Yongfeng, Chang, Liping, Bao, Weiren

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ISL1 loss-of-function variation causes familial atrial fibrillation von 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-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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A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve von Jiang, Wei-Feng, Xu, Ying-Jia, Zhao, Cui-Mei, Wang, Xin-Hua, Qiu, Xing-Biao, Liu, Xu, Wu, Shao-Hui, Yang, Yi-Qing

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