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The Journal of Physiology|July 10, 2013
Cardiac calcium signalling pathologies associated with defective calmodulin regulation of type 2 ryanodine receptorJuan José Arnáiz-Cot, Brooke James Damon, Xiao-Hua Zhang, et al.
American Journal of Physiology. Cell Physiology|June 6, 2019
A central core disease mutation in the Ca<sup>2+</sup>-binding site of skeletal muscle ryanodine receptor impairs single-channel regulationVenkat R Chirasani, Le Xu, Hannah G Addis, et al.
The Journal of Biological Chemistry|May 23, 2015
Channel Gating Dependence on Pore Lining Helix Glycine Residues in Skeletal Muscle Ryanodine ReceptorYingwu Mei, Le Xu, David D Mowrey, et al.
Human Molecular Genetics|February 5, 2003
Clinical and functional effects of a deletion in a COOH-terminal lumenal loop of the skeletal muscle ryanodine receptorFrancesco Zorzato, Naohiro Yamaguchi, Le Xu, et al.
Human Molecular Genetics|August 31, 2006
Characterization of recessive RYR1 mutations in core myopathiesHaiyan Zhou, Naohiro Yamaguchi, Le Xu, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|November 8, 2003
Regulation of ion channel structure and function by reactive oxygen-nitrogen speciesSadis Matalon, Karin M Hardiman, Lucky Jain, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 8, 2011
Oxygen-coupled redox regulation of the skeletal muscle ryanodine receptor-Ca2+ release channel by NADPH oxidase 4Qi-An Sun, Douglas T Hess, Leonardo Nogueira, et al.
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