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International Journal of Molecular Medicine|April 23, 2013
Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillationRuo-Gu Li, Qian Wang, Ying-Jia Xu, et al.Molecular and Cellular Biochemistry|June 2, 2023
Epigallocatechin-3-gallate restores mitochondrial homeostasis impairment by inhibiting HDAC1-mediated NRF1 histone deacetylation in cardiac hypertrophyGu Li, Bo Pan, Lifei Liu, et al.Organic Letters|April 1, 2025
Unveiling the Biosynthesis of Sphaerols A-E: Catalyzed by Two Uncommon Diterpene Synthases AsSS and CvSSGui-Hu Lu, Zhe-Hui Hu, Ping-Ping Wu, et al.Journal of Ethnopharmacology|April 18, 2008
Traditional Chinese drug ShuXueTong facilitates angiogenesis during wound healing following traumatic brain injuryXiaoying Jin, Gang Shen, Feng Gao, et al.Genes & Diseases|September 26, 2022
Intranuclear cardiac troponin I plays a functional role in regulating <i>Atp2a2</i> expression in cardiomyocytesQian Lu, Bo Pan, Haobo Bai, et al.Clinics (Sao Paulo, Brazil)|January 30, 2014
PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillationXing-Biao Qiu, Ying-Jia Xu, Ruo-Gu Li, et al.Clinics (Sao Paulo, Brazil)|June 20, 2013
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillationWen-Hui Xie, Cheng Chang, Ying-Jia Xu, et al.Heart Rhythm|January 11, 2021
Connexin45 (GJC1) loss-of-function mutation contributes to familial atrial fibrillation and conduction diseaseRuo-Gu Li, Ying-Jia Xu, Willy G Ye, et al.International Journal of Molecular Medicine|November 24, 2012
A novel GATA5 loss-of-function mutation underlies lone atrial fibrillationXin-Hua Wang, Cong-Xin Huang, Qian Wang, et al.JCI Insight|June 28, 2022
Dynamin-2 reduction rescues the skeletal myopathy of a SPEG-deficient mouse modelQifei Li, Jasmine Lin, Jeffrey J Widrick, et al.Pageof 22