RyR2 disease mutations at the C-terminal domain intersubunit interface alter closed-state stability and channel activation

von Guo, Wenting, Wei, Jinhong, Estillore, John Paul, Zhang, Lin, Wang, Ruiwu, Sun, Bo, Chen, S. R. Wayne
Veröffentlicht in J Biol Chem (2021)

Novel RyR2 Mutation (G3118R) Is Associated With Autosomal Recessive Ventricular Fibrillation and Sudden Death: Clinical, Functional, and Computational Analysis

von Shauer, Ayelet, Shor, Oded, Wei, Jinhong, Elitzur, Yair, Kucherenko, Nataly, Wang, Ruiwu, Chen, S. R. Wayne, Einav, Yulia, Luria, David
Veröffentlicht in J Am Heart Assoc (2021)

Establishment of a Prognostic Model for Hepatocellular Carcinoma Based on Endoplasmic Reticulum Stress-Related Gene Analysis

von Liu, Peng, Wei, Jinhong, Mao, Feiyu, Xin, Zechang, Duan, Heng, Du, Yan, Wang, Xiaodong, Li, Zhennan, Qian, Jianjun, Yao, Jie
Veröffentlicht in Front Oncol (2021)

CPVT-associated cardiac ryanodine receptor mutation G357S with reduced penetrance impairs Ca(2+) release termination and diminishes protein expression

von Liu, Yingjie, Wei, Jinhong, Wong King Yuen, Siobhan M., Sun, Bo, Tang, Yijun, Wang, Ruiwu, Van Petegem, Filip, Chen, S. R. Wayne
Veröffentlicht in PLoS One (2017)

Reduced threshold for store overload-induced Ca(2+) release is a common defect of RyR1 mutations associated with malignant hyperthermia and central core disease

von Chen, Wenqian, Koop, Andrea, Liu, Yingjie, Guo, Wenting, Wei, Jinhong, Wang, Ruiwu, MacLennan, David H., Dirksen, Robert T., Chen, Sui Rong Wayne
Veröffentlicht in Biochem J (2017)

The cardiac ryanodine receptor, but not sarcoplasmic reticulum Ca(2+)-ATPase, is a major determinant of Ca(2+) alternans in intact mouse hearts

von Sun, Bo, Wei, Jinhong, Zhong, Xiaowei, Guo, Wenting, Yao, Jinjing, Wang, Ruiwu, Vallmitjana, Alexander, Benitez, Raul, Hove-Madsen, Leif, Chen, S. R. Wayne
Veröffentlicht in J Biol Chem (2018)

Enhanced Cytosolic Ca(2+) Activation Underlies a Common Defect of Central Domain Cardiac Ryanodine Receptor Mutations Linked to Arrhythmias

von Xiao, Zhichao, Guo, Wenting, Sun, Bo, Hunt, Donald J., Wei, Jinhong, Liu, Yingjie, Wang, Yundi, Wang, Ruiwu, Jones, Peter P., Back, Thomas G., Chen, S. R. Wayne
Veröffentlicht in J Biol Chem (2016)

Identification of loss-of-function RyR2 mutations associated with idiopathic ventricular fibrillation and sudden death

von Zhong, Xiaowei, Guo, Wenting, Wei, Jinhong, Tang, Yijun, Liu, Yingjie, Zhang, Joe Z., Tan, Vern Hsen, Zhang, Lin, Wang, Ruiwu, Jones, Peter P., Napolitano, Carlo, Priori, Silvia G., Chen, S.R. Wayne
Veröffentlicht in Biosci Rep (2021)

Infanticide vs. inherited cardiac arrhythmias

von Brohus, Malene, Arsov, Todor, Wallace, David A, Jensen, Helene Halkjær, Nyegaard, Mette, Crotti, Lia, Adamski, Marcin, Zhang, Yafei, Field, Matt A, Athanasopoulos, Vicki, Baró, Isabelle, Ribeiro de Oliveira-Mendes, Bárbara B, Redon, Richard, Charpentier, Flavien, Raju, Hariharan, DiSilvestre, Deborah, Wei, Jinhong, Wang, Ruiwu, Rafehi, Haloom, Kaspi, Antony, Bahlo, Melanie, Dick, Ivy E, Chen, Sui Rong Wayne, Cook, Matthew C, Vinuesa, Carola G, Overgaard, Michael Toft, Schwartz, Peter J
Veröffentlicht in Europace (2020)