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S R Wayne Chen

Showing results (51-60 of 142) with videos related to

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The Biochemical Journal|October 31, 2007
Localization of PKA phosphorylation site, Ser(2030), in the three-dimensional structure of cardiac ryanodine receptorPeter P Jones, Xing Meng, Bailong Xiao, et al.
The Journal of Biological Chemistry|August 27, 2015
Arrhythmogenic Calmodulin Mutations Affect the Activation and Termination of Cardiac Ryanodine Receptor-mediated Ca2+ ReleaseMads T Søndergaard, Xixi Tian, Yingjie Liu, et al.
Neuroscience|May 10, 2023
A Gain-of-function Mutation in the Gating Domain of ITPR1 Impairs Motor Movement and Increases Thermal and Mechanical SensitivityJinjing Yao, Mingke Ni, Shanshan Tian, et al.
The FEBS Journal|November 26, 2019
Role of cardiac ryanodine receptor calmodulin-binding domains in mediating the action of arrhythmogenic calmodulin N-domain mutation N54IMads T Søndergaard, Yingjie Liu, Wenting Guo, et al.
The Biochemical Journal|February 23, 2007
K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 associationDonald J Hunt, Peter P Jones, Ruiwu Wang, et al.
Journal of Cell Science|April 30, 2010
Dynamic, inter-subunit interactions between the N-terminal and central mutation regions of cardiac ryanodine receptorZheng Liu, Ruiwu Wang, Xixi Tian, et al.
Journal of the American Heart Association|March 9, 2021
Novel RyR2 Mutation (G3118R) Is Associated With Autosomal Recessive Ventricular Fibrillation and Sudden Death: Clinical, Functional, and Computational AnalysisAyelet Shauer, Oded Shor, Jinhong Wei, et al.
Journal of Cell Science|July 23, 2013
Two potential calmodulin-binding sequences in the ryanodine receptor contribute to a mobile, intra-subunit calmodulin-binding domainXiaojun Huang, Ying Liu, Ruiwu Wang, et al.
Plos One|September 26, 2015
The H29D Mutation Does Not Enhance Cytosolic Ca2+ Activation of the Cardiac Ryanodine ReceptorZhichao Xiao, Wenting Guo, Siobhan M Wong King Yuen, et al.
Journal of Electrocardiology|September 21, 2016
A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardiaThomas M Roston, Wenting Guo, Andrew D Krahn, et al.
Pageof 15

Showing results (51-60 of 142) with videos related to

Sort By:
Pageof 15
The Biochemical Journal|October 31, 2007
Localization of PKA phosphorylation site, Ser(2030), in the three-dimensional structure of cardiac ryanodine receptorPeter P Jones, Xing Meng, Bailong Xiao, et al.
The Journal of Biological Chemistry|August 27, 2015
Arrhythmogenic Calmodulin Mutations Affect the Activation and Termination of Cardiac Ryanodine Receptor-mediated Ca2+ ReleaseMads T Søndergaard, Xixi Tian, Yingjie Liu, et al.
Neuroscience|May 10, 2023
A Gain-of-function Mutation in the Gating Domain of ITPR1 Impairs Motor Movement and Increases Thermal and Mechanical SensitivityJinjing Yao, Mingke Ni, Shanshan Tian, et al.
The FEBS Journal|November 26, 2019
Role of cardiac ryanodine receptor calmodulin-binding domains in mediating the action of arrhythmogenic calmodulin N-domain mutation N54IMads T Søndergaard, Yingjie Liu, Wenting Guo, et al.
The Biochemical Journal|February 23, 2007
K201 (JTV519) suppresses spontaneous Ca2+ release and [3H]ryanodine binding to RyR2 irrespective of FKBP12.6 associationDonald J Hunt, Peter P Jones, Ruiwu Wang, et al.
Journal of Cell Science|April 30, 2010
Dynamic, inter-subunit interactions between the N-terminal and central mutation regions of cardiac ryanodine receptorZheng Liu, Ruiwu Wang, Xixi Tian, et al.
Journal of the American Heart Association|March 9, 2021
Novel RyR2 Mutation (G3118R) Is Associated With Autosomal Recessive Ventricular Fibrillation and Sudden Death: Clinical, Functional, and Computational AnalysisAyelet Shauer, Oded Shor, Jinhong Wei, et al.
Journal of Cell Science|July 23, 2013
Two potential calmodulin-binding sequences in the ryanodine receptor contribute to a mobile, intra-subunit calmodulin-binding domainXiaojun Huang, Ying Liu, Ruiwu Wang, et al.
Plos One|September 26, 2015
The H29D Mutation Does Not Enhance Cytosolic Ca2+ Activation of the Cardiac Ryanodine ReceptorZhichao Xiao, Wenting Guo, Siobhan M Wong King Yuen, et al.
Journal of Electrocardiology|September 21, 2016
A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardiaThomas M Roston, Wenting Guo, Andrew D Krahn, et al.
Pageof 15