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Basic Research in Cardiology|December 25, 2023
Striated preferentially expressed gene deficiency leads to mitochondrial dysfunction in developing cardiomyocytesGu Li, He Huang, Yanshuang Wu, et al.
International Journal of Medical Sciences|February 27, 2016
Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial FibrillationZhan-Cheng Wang, Wen-Hui Ji, Chang-Wu Ruan, et al.
Pediatric Cardiology|November 9, 2014
A novel NKX2.6 mutation associated with congenital ventricular septal defectJuan Wang, Jian-Hui Mao, Ke-Ke Ding, et al.
Frontiers in Cellular and Infection Microbiology|March 26, 2021
Microbiota in Gut, Oral Cavity, and Mitral Valves Are Associated With Rheumatic Heart DiseaseXue-Rui Shi, Bo-Yan Chen, Wen-Zhen Lin, et al.
International Heart Journal|July 11, 2017
Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated CardiomyopathyJia-Hong Xu, Jian-Yun Gu, Yu-Han Guo, et al.
European Journal of Medical Genetics|September 8, 2014
Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart diseaseLan Zhao, Shi-Hong Ni, Xing-Yuan Liu, et al.
International Journal of Medical Sciences|May 30, 2017
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosusRi-Tai Huang, Juan Wang, Song Xue, et al.
European Journal of Medical Genetics|December 10, 2017
A novel NR2F2 loss-of-function mutation predisposes to congenital heart defectXiao-Hui Qiao, Qian Wang, Juan Wang, et al.
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