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Chen-Xi Yang

Showing results (21-30 of 88) with videos related to

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Diagnostics (Basel, Switzerland)|August 26, 2022
Identification of <i>SOX18</i> as a New Gene Predisposing to Congenital Heart DiseaseHong-Yu Shi, Meng-Shi Xie, Chen-Xi Yang, et al.
Diagnostics (Basel, Switzerland)|January 10, 2026
Discovery of <i>SOX5</i> as a New Causative Gene for Atrial FibrillationDao-Liang Zhang, Xing-Biao Qiu, Ning Li, et al.
Military Medical Research|May 1, 2026
Immune microenvironment dynamics in pregnant patients with concomitant autoimmune diseases: mechanisms, challenges, and clinical significanceZi-Jun Ma, Jun Chen, Chen-Xi Yang, et al.
American Journal of Translational Research|February 7, 2024
Discovery of <i>BMP10</i> as a new gene underpinning congenital heart defectsBin-Bin Dong, Yan-Jie Li, Xing-Yuan Liu, et al.
Genes|June 26, 2026
Rare Truncating <i>HAND2</i> Variants Predispose to Atrial FibrillationHong Zhang, Xiao-Qing Hu, Ning Li, et al.
International Heart Journal|May 6, 2021
SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial HypertensionTian-Ming Wang, Shan-Shan Wang, Ying-Jia Xu, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|March 12, 2026
[Comparative study on composition and content of β-(1→3)-D-glucan in different medicinal parts of Poria cocos]Chen-Xi Yang, Wei-Wei Wang, Wei-Hong Feng, et al.
Plos Computational Biology|April 3, 2026
Using cell-specific late-phase asthma mRNA biomarkers to repurpose drugs that concurrently reverse disease signatures across multiple immune cell-typesMingming Zhang, Young Woong Kim, Chen Xi Yang, et al.
Genes|April 3, 2021
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and CardiomyopathyNing Li, Ying-Jia Xu, Hong-Yu Shi, et al.
European Journal of Medical Genetics|April 1, 2021
SOX17 loss-of-function variation underlying familial congenital heart diseaseLan Zhao, Wei-Feng Jiang, Chen-Xi Yang, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
Diagnostics (Basel, Switzerland)|August 26, 2022
Identification of <i>SOX18</i> as a New Gene Predisposing to Congenital Heart DiseaseHong-Yu Shi, Meng-Shi Xie, Chen-Xi Yang, et al.
Diagnostics (Basel, Switzerland)|January 10, 2026
Discovery of <i>SOX5</i> as a New Causative Gene for Atrial FibrillationDao-Liang Zhang, Xing-Biao Qiu, Ning Li, et al.
Military Medical Research|May 1, 2026
Immune microenvironment dynamics in pregnant patients with concomitant autoimmune diseases: mechanisms, challenges, and clinical significanceZi-Jun Ma, Jun Chen, Chen-Xi Yang, et al.
American Journal of Translational Research|February 7, 2024
Discovery of <i>BMP10</i> as a new gene underpinning congenital heart defectsBin-Bin Dong, Yan-Jie Li, Xing-Yuan Liu, et al.
Genes|June 26, 2026
Rare Truncating <i>HAND2</i> Variants Predispose to Atrial FibrillationHong Zhang, Xiao-Qing Hu, Ning Li, et al.
International Heart Journal|May 6, 2021
SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial HypertensionTian-Ming Wang, Shan-Shan Wang, Ying-Jia Xu, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|March 12, 2026
[Comparative study on composition and content of β-(1→3)-D-glucan in different medicinal parts of Poria cocos]Chen-Xi Yang, Wei-Wei Wang, Wei-Hong Feng, et al.
Plos Computational Biology|April 3, 2026
Using cell-specific late-phase asthma mRNA biomarkers to repurpose drugs that concurrently reverse disease signatures across multiple immune cell-typesMingming Zhang, Young Woong Kim, Chen Xi Yang, et al.
Genes|April 3, 2021
KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and CardiomyopathyNing Li, Ying-Jia Xu, Hong-Yu Shi, et al.
European Journal of Medical Genetics|April 1, 2021
SOX17 loss-of-function variation underlying familial congenital heart diseaseLan Zhao, Wei-Feng Jiang, Chen-Xi Yang, et al.
Pageof 9