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Chen-Xi Yang

Showing results (31-40 of 88) with videos related to

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Experimental and Therapeutic Medicine|January 26, 2024
Somatic <i>GATA4</i> mutation contributes to tetralogy of FallotPradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, et al.
European Journal of Medical Genetics|December 21, 2019
Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathyRuo-Min Di, Chen-Xi Yang, Cui-Mei Zhao, et al.
Journal of Cardiovascular Translational Research|December 12, 2018
Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated CardiomyopathyYing-Jia Xu, Zhang-Sheng Wang, Chen-Xi Yang, et al.
Science Advances|June 11, 2020
Monocyte-derived multipotent cell delivered programmed therapeutics to reverse idiopathic pulmonary fibrosisXin Chang, Lei Xing, Yi Wang, et al.
American Journal of Translational Research|April 15, 2022
SOX7 loss-of-function variation as a cause of familial congenital heart diseaseRi-Tai Huang, Yu-Han Guo, Chen-Xi Yang, et al.
Diagnostics (Basel, Switzerland)|January 21, 2023
Identification of <i>BMP10</i> as a Novel Gene Contributing to Dilated CardiomyopathyJia-Ning Gu, Chen-Xi Yang, Yuan-Yuan Ding, et al.
World Journal of Pediatrics : WJP|March 17, 2018
Establishment of age- and gender-specific pediatric reference intervals for liver function tests in healthy Han childrenXin Li, Di Wang, Chun Yang, et al.
Scientific Reports|December 15, 2020
Gene expression network analysis provides potential targets against SARS-CoV-2Ana I Hernández Cordero, Xuan Li, Chen Xi Yang, et al.
Human Genetics|February 19, 2021
Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19Ana I Hernández Cordero, Xuan Li, Stephen Milne, et al.
Journal of the American Heart Association|November 8, 2022
KLF13 Loss-of-Function Mutations Underlying Familial Dilated CardiomyopathyYu-Han Guo, Jun Wang, Xiao-Juan Guo, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Experimental and Therapeutic Medicine|January 26, 2024
Somatic <i>GATA4</i> mutation contributes to tetralogy of FallotPradhan Abhinav, Yan-Jie Li, Ri-Tai Huang, et al.
European Journal of Medical Genetics|December 21, 2019
Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathyRuo-Min Di, Chen-Xi Yang, Cui-Mei Zhao, et al.
Journal of Cardiovascular Translational Research|December 12, 2018
Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated CardiomyopathyYing-Jia Xu, Zhang-Sheng Wang, Chen-Xi Yang, et al.
Science Advances|June 11, 2020
Monocyte-derived multipotent cell delivered programmed therapeutics to reverse idiopathic pulmonary fibrosisXin Chang, Lei Xing, Yi Wang, et al.
American Journal of Translational Research|April 15, 2022
SOX7 loss-of-function variation as a cause of familial congenital heart diseaseRi-Tai Huang, Yu-Han Guo, Chen-Xi Yang, et al.
Diagnostics (Basel, Switzerland)|January 21, 2023
Identification of <i>BMP10</i> as a Novel Gene Contributing to Dilated CardiomyopathyJia-Ning Gu, Chen-Xi Yang, Yuan-Yuan Ding, et al.
World Journal of Pediatrics : WJP|March 17, 2018
Establishment of age- and gender-specific pediatric reference intervals for liver function tests in healthy Han childrenXin Li, Di Wang, Chun Yang, et al.
Scientific Reports|December 15, 2020
Gene expression network analysis provides potential targets against SARS-CoV-2Ana I Hernández Cordero, Xuan Li, Chen Xi Yang, et al.
Human Genetics|February 19, 2021
Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19Ana I Hernández Cordero, Xuan Li, Stephen Milne, et al.
Journal of the American Heart Association|November 8, 2022
KLF13 Loss-of-Function Mutations Underlying Familial Dilated CardiomyopathyYu-Han Guo, Jun Wang, Xiao-Juan Guo, et al.
Pageof 9