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Scientific Reports|October 2, 2015
Stable expression and functional characterisation of the diamondback moth ryanodine receptor G4946E variant conferring resistance to diamide insecticidesBartlomiej J Troczka, Alan J Williams, Martin S Williamson, et al.
Journal of Cell Science|September 10, 2016
Calsequestrin interacts directly with the cardiac ryanodine receptor luminal domainAhmed Handhle, Chloe E Ormonde, N Lowri Thomas, et al.
Molecular Biology of the Cell|March 30, 2004
Ryanodine receptor regulation by intramolecular interaction between cytoplasmic and transmembrane domainsChristopher H George, Hala Jundi, N Lowri Thomas, et al.
Biophysical Journal|February 17, 2009
Changes in negative charge at the luminal mouth of the pore alter ion handling and gating in the cardiac ryanodine-receptorFiona C Mead-Savery, Ruiwu Wang, Bhavna Tanna-Topan, et al.
The Journal of General Physiology|August 30, 2012
The contribution of hydrophobic residues in the pore-forming region of the ryanodine receptor channel to block by large tetraalkylammonium cations and Shaker B inactivation peptidesSammy A Mason, Cedric Viero, Joanne Euden, et al.
The Journal of Biological Chemistry|October 15, 2003
Residue Gln4863 within a predicted transmembrane sequence of the Ca2+ release channel (ryanodine receptor) is critical for ryanodine interactionRuiwu Wang, Lin Zhang, Jeff Bolstad, et al.
Molecular Pharmacology|June 16, 2005
The Gln4863Ala mutation within a putative, pore-lining trans-membrane helix of the cardiac ryanodine receptor channel alters both the kinetics of ryanoid interaction and the subsequent fractional conductanceKishani M Ranatunga, Tracy M Moreno-King, Bhavna Tanna, et al.
Circulation Research|February 5, 2015
The mechanism of flecainide action in CPVT does not involve a direct effect on RyR2Mark L Bannister, N Lowri Thomas, Markus B Sikkel, et al.
Journal of Molecular Biology|April 10, 2009
CLIC2-RyR1 interaction and structural characterization by cryo-electron microscopyXing Meng, Guoliang Wang, Cedric Viero, et al.
Cardiovascular Research|January 22, 2013
Flecainide reduces Ca(2+) spark and wave frequency via inhibition of the sarcolemmal sodium currentMarkus B Sikkel, Thomas P Collins, Christina Rowlands, et al.
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