Hasil Pencarian - Yi-Qing Yang

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  1. 1
    Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions

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

    Diterbitkan 2022-03-01
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  2. 2
    Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation

    Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation oleh Jian-Yun Gu, Jia-Hong Xu, Hong Yu, Yi-Qing Yang

    Diterbitkan 2012-12-01
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  3. 3
    Polyethyleneimine Addition for Control of Dissolved and Colloidal Substances: Effects on Wet-End Chemistry

    Polyethyleneimine Addition for Control of Dissolved and Colloidal Substances: Effects on Wet-End Chemistry oleh Chun-jian Wang, Chen Chen, Hao Ren, Yi-qing Yang, Hong-qi Dai

    Diterbitkan 2016-09-01
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  4. 4
    GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

    GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot oleh Dong Wei, Han Bao, Xing-Yuan Liu, Ning Zhou, Qian Wang, Ruo-Gu Li, Ying-Jia Xu, Yi-Qing Yang

    Diterbitkan 2013-01-01
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  5. 5
    Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

    Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation oleh Wen-Hui Xie, Cheng Chang, Ying-Jia Xu, Ruo-Gu Li, Xin-Kai Qu, Wei-Yi Fang, Xu Liu, Yi-Qing Yang

    Diterbitkan 2013-06-01
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  6. 6
    PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation

    PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation oleh Xing-Biao Qiu, Ying-Jia Xu, Ruo-Gu Li, Lei Xu, Xu Liu, Wei-Yi Fang, Yi-Qing Yang, Xin-Kai Qu

    Diterbitkan 2014-01-01
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  7. 7
    A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve

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

    Diterbitkan 2020-11-01
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  8. 8
    Identification of <i>SOX18</i> as a New Gene Predisposing to Congenital Heart Disease

    Identification of <i>SOX18</i> as a New Gene Predisposing to Congenital Heart Disease oleh Hong-Yu Shi, Meng-Shi Xie, Chen-Xi Yang, Ri-Tai Huang, Song Xue, Xing-Yuan Liu, Ying-Jia Xu, Yi-Qing Yang

    Diterbitkan 2022-08-01
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  9. 9
    Identification of <i>BMP10</i> as a Novel Gene Contributing to Dilated Cardiomyopathy

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

    Diterbitkan 2023-01-01
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  10. 10
    PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

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

    Diterbitkan 2015-01-01
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  11. 11
    m6A demethylase ALKBH5 attenuates doxorubicin-induced cardiotoxicity via posttranscriptional stabilization of Rasal3

    m6A demethylase ALKBH5 attenuates doxorubicin-induced cardiotoxicity via posttranscriptional stabilization of Rasal3 oleh Ri-Feng Gao, Kun Yang, Ya-Nan Qu, Xiang Wei, Jia-Ran Shi, Chun-Yu Lv, Yong-Chao Zhao, Xiao-Lei Sun, Ying-Jia Xu, Yi-Qing Yang

    Diterbitkan 2023-03-01
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  12. 12
    KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy

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

    Diterbitkan 2022-11-01
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  13. 13
    Discovery of <i>GJC1</i> (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias

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

    Diterbitkan 2023-02-01
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  14. 14
    A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis

    A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis oleh Yu-Min Sun, Jun Wang, Xing-Biao Qiu, Fang Yuan, Ruo-Gu Li, Ying-Jia Xu, Xin-Kai Qu, Hong-Yu Shi, Xu-Min Hou, Ri-Tai Huang, Song Xue, Yi-Qing Yang

    Diterbitkan 2016-04-01
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  15. 15
    Discovery of <i>TBX20</i> as a Novel Gene Underlying Atrial Fibrillation

    Discovery of <i>TBX20</i> as a Novel Gene Underlying Atrial Fibrillation oleh Ning Li, Yan-Jie Li, Xiao-Juan Guo, Shao-Hui Wu, Wei-Feng Jiang, Dao-Liang Zhang, Kun-Wei Wang, Li Li, Yu-Min Sun, Ying-Jia Xu, Yi-Qing Yang, Xing-Biao Qiu

    Diterbitkan 2023-08-01
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  16. 16
    PRRX1 Loss‐of‐Function Mutations Underlying Familial Atrial Fibrillation

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

    Diterbitkan 2021-12-01
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