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

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

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

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

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

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

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

gan Liu, Yingjie, Wei, Jinhong, Wong King Yuen, Siobhan M., Sun, Bo, Tang, Yijun, Wang, Ruiwu, Van Petegem, Filip, Chen, S. R. Wayne
Cyhoeddwyd yn 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

gan Chen, Wenqian, Koop, Andrea, Liu, Yingjie, Guo, Wenting, Wei, Jinhong, Wang, Ruiwu, MacLennan, David H., Dirksen, Robert T., Chen, Sui Rong Wayne
Cyhoeddwyd yn 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

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

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

gan 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
Cyhoeddwyd yn J Biol Chem (2016)

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

gan 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
Cyhoeddwyd yn Biosci Rep (2021)

Infanticide vs. inherited cardiac arrhythmias

gan 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
Cyhoeddwyd yn Europace (2020)