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Circulation Research|July 17, 2013
Phospholamban knockout breaks arrhythmogenic Ca²⁺ waves and suppresses catecholaminergic polymorphic ventricular tachycardia in miceYunlong Bai, Peter P Jones, Jiqing Guo, et al.
Journal of Cellular Physiology|May 27, 2022
A gain-of-function mutation in the ITPR1 gating domain causes male infertility in miceBo Sun, Mingke Ni, Shanshan Tian, et al.
Circulation. Arrhythmia and Electrophysiology|September 21, 2021
Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations: Clinical Phenotypes and In Vitro CharacterizationYanhui Li, Jinhong Wei, Wenting Guo, et al.
Circulation. Genomic and Precision Medicine|December 24, 2021
Provocation Testing and Therapeutic Response in a Newly Described Channelopathy: RyR2 Calcium Release Deficiency SyndromeJulian O M Ormerod, Elizabeth Ormondroyd, Yanhui Li, et al.
Communications Biology|March 2, 2022
Subcellular localization of hippocampal ryanodine receptor 2 and its role in neuronal excitability and memoryFlorian Hiess, Jinjing Yao, Zhenpeng Song, et al.
Circulation Research|June 16, 2023
Increased Ca<sup>2+</sup> Transient Underlies RyR2-Related Left Ventricular NoncompactionMingke Ni, Yanhui Li, Jinhong Wei, et al.
Cell Reports|September 23, 2020
Limiting RyR2 Open Time Prevents Alzheimer's Disease-Related Neuronal Hyperactivity and Memory Loss but Not β-Amyloid AccumulationJinjing Yao, Bo Sun, Adam Institoris, et al.
European Journal of Human Genetics : EJHG|June 22, 2018
De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel functionMatthis Synofzik, Katherine L Helbig, Florian Harmuth, et al.
Journal of Molecular and Cellular Cardiology|February 26, 2018
Pathogenic mechanism of a catecholaminergic polymorphic ventricular tachycardia causing-mutation in cardiac calcium release channel RyR2Jing Xiong, Xijun Liu, Yunyun Gong, et al.
The Journal of Clinical Investigation|December 15, 2023
Foxp3-mediated blockage of ryanodine receptor 2 underlies contact-based suppression by regulatory T cellsXiaobo Wang, Shuang Geng, Junchen Meng, et al.
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