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Regulation of ryanodine receptors by calsequestrin: effect of high luminal Ca²⁺ and phosphorylation

Protein interactions involving the γ2 large cytoplasmic loop of GABAA receptors modulate conductance

SR Ca²⁺ store refill-a key factor in cardiac pacemaking

Extraction of sub-microscopic Ca fluxes from blurred and noisy fluorescent indicator images with a detailed model fitting approach

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

Ca²⁺ stores regulate ryanodine receptor Ca²⁺ release channels via luminal and cytosolic Ca²⁺ sites

Disulfonic stilbene permeation and block of the anion channel from the sarcoplasmic reticulum of rabbit skeletal muscle

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

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

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

Ca²⁺ stores regulate ryanodine receptor Ca²⁺ release channels via luminal and cytosolic Ca²⁺ sites

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

Luminal Mg²⁺, a key factor controlling RYR2-mediated Ca²⁺ release: cytoplasmic and luminal regulation modeled in a tetrameric channel

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

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

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

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

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

Beta-adrenergic stimulation increases RyR2 activity via intracellular Ca²⁺ and Mg²⁺ regulation

A bivalent remipede toxin promotes calcium release via ryanodine receptor activation

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