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A domain peptide of the cardiac ryanodine receptor regulates channel sensitivity to luminal Ca²⁺ via cytoplasmic Ca²⁺ sites

Calmodulin inhibition of human RyR2 channels requires phosphorylation of RyR2-S2808 or RyR2-S2814

Cardiac calcium release channel (ryanodine receptor 2) regulation by halogenated anesthetics

Coupled calcium release channels and their regulation by luminal and cytosolic ions

Effects of calmodulin on the function of cardiac and skeletal ryanodine receptors

  • Creator: Oo, Ye Wint
  • Resource Type: thesis
  • Date: 2016

Luminal Ca²⁺ activation of cardiac ryanodine receptors by luminal and cytoplasmic domains

Luminal Ca²⁺-regulated Mg²⁺ inhibition of skeletal RyRs reconstituted as isolated channels or coupled clusters

Mechanisms of SR calcium release in healthy and failing human hearts

Phenytoin Reduces Activity of Cardiac Ryanodine Receptor 2; A Potential Mechanism for Its Cardioprotective Action

Regulation of RyR Channel Gating by Ca²⁺, Mg²⁺ and ATP

Regulation of the RyR channel gating by Ca²⁺ and Mg²⁺

Ryanodine receptor modification and regulation by intracellular Ca²⁺ and Mg²⁺ in healthy and failing human hearts

RYR2 channel inhibition is the principal mechanism of flecainide action in CPVT

The emerging role of calmodulin regulation of RyR2 in controlling heart rhythm, the progression of heart failure and the antiarrhythmic action of dantrolene

The ryanodine receptor pore blocker neomycin also inhibits channel activity via a previously undescribed high-affinity Ca²⁺ binding site

Three independent mechanisms contribute to tetracaine inhibition of cardiac calcium release channels

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