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Experimental and Therapeutic Medicine
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January 26, 2024
Somatic <i>GATA4</i> mutation contributes to tetralogy of Fallot
Pradhan 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 cardiomyopathy
Ruo-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 Cardiomyopathy
Ying-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 fibrosis
Xin 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 disease
Ri-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 Cardiomyopathy
Jia-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 children
Xin Li, Di Wang, Chun Yang, et al.
Scientific Reports
|
December 15, 2020
Gene expression network analysis provides potential targets against SARS-CoV-2
Ana 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-19
Ana 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 Cardiomyopathy
Yu-Han Guo, Jun Wang, Xiao-Juan Guo, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 88) with videos related to
Sort By:
Page
of 9
Experimental and Therapeutic Medicine
|
January 26, 2024
Somatic <i>GATA4</i> mutation contributes to tetralogy of Fallot
Pradhan 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 cardiomyopathy
Ruo-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 Cardiomyopathy
Ying-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 fibrosis
Xin 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 disease
Ri-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 Cardiomyopathy
Jia-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 children
Xin Li, Di Wang, Chun Yang, et al.
Scientific Reports
|
December 15, 2020
Gene expression network analysis provides potential targets against SARS-CoV-2
Ana 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-19
Ana 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 Cardiomyopathy
Yu-Han Guo, Jun Wang, Xiao-Juan Guo, et al.
Page
of 9