AbstractThe occupancy of high-affinity ryanodine-binding sites of isolated heavy sarcoplasmic reticulum vesicles occurring in concentrated salt solutions affects ATP-dependent calcium accumulation and caffeine-induced calcium release. The initial suppression of calcium uptake is followed by a marked uptake activation resulting in a reduction of the final calcium level in the medium. Simultaneously, caffeine-induced calcium release is blocked. The dependence of inhibition of calcium uptake and caffeine-induced calcium release observed in assay media containing physiological concentrations of magnesium and ATP on the concentration of ryanodine corresponds to the drug's effectiveness in living muscles
Sarcoplasmic reticulum vesicles isolated from fast-twitch frog skeletal muscle presented two classes...
The sarcoplasmic reticulum (SR) of skeletal muscle is an intracellular membraneous network that, thr...
son. Metabolic end products inhibit sarcoplasmic reticulum Ca2 ’ release and [3H]ryanodine binding. ...
AbstractThe occupancy of high-affinity ryanodine-binding sites of isolated heavy sarcoplasmic reticu...
The effect of ATP on the calcium release channel in heavy sarcoplasmic reticulum vesicles modulated ...
Heavy sarcoplasmic reticulum vesicles isolated from rabbit skeletal muscle were reacted in high ioni...
The inhibition by ryanodine of caffeine induced calcium release from actively loaded heavy sarcoplas...
The effect of the plant alkaloid ryanodine on the skeletal muscle sarcoplasmic reticulum Ca2+ releas...
Heavy sarcoplasmic reticulum vesicles were reacted with ryanodine in 0.6 M KCl 0.3 M sucrose at pH 6...
AbstractAt micromolar concentrations, ryanodine interacts with the dihydropyridine receptor of rabbi...
Sarcoplasmic reticulum vesicles isolated from fast-twitch frog skeletal muscle presented two classes...
AbstractA heavy skeletal muscle sarcoplasmic reticulum (SR) fraction was actively loaded stepwise wi...
The effects of the ionophore, X537A, and caffeine on ATP-dependent calcium transport by fragmented s...
AbstractThe efflux of 45Ca2+ from preloaded intracellular stores of saponin-permeabilised human uter...
The effects of ionic composition and strength on rabbit skeletal muscle Ca2+ release channel (ryanod...
Sarcoplasmic reticulum vesicles isolated from fast-twitch frog skeletal muscle presented two classes...
The sarcoplasmic reticulum (SR) of skeletal muscle is an intracellular membraneous network that, thr...
son. Metabolic end products inhibit sarcoplasmic reticulum Ca2 ’ release and [3H]ryanodine binding. ...
AbstractThe occupancy of high-affinity ryanodine-binding sites of isolated heavy sarcoplasmic reticu...
The effect of ATP on the calcium release channel in heavy sarcoplasmic reticulum vesicles modulated ...
Heavy sarcoplasmic reticulum vesicles isolated from rabbit skeletal muscle were reacted in high ioni...
The inhibition by ryanodine of caffeine induced calcium release from actively loaded heavy sarcoplas...
The effect of the plant alkaloid ryanodine on the skeletal muscle sarcoplasmic reticulum Ca2+ releas...
Heavy sarcoplasmic reticulum vesicles were reacted with ryanodine in 0.6 M KCl 0.3 M sucrose at pH 6...
AbstractAt micromolar concentrations, ryanodine interacts with the dihydropyridine receptor of rabbi...
Sarcoplasmic reticulum vesicles isolated from fast-twitch frog skeletal muscle presented two classes...
AbstractA heavy skeletal muscle sarcoplasmic reticulum (SR) fraction was actively loaded stepwise wi...
The effects of the ionophore, X537A, and caffeine on ATP-dependent calcium transport by fragmented s...
AbstractThe efflux of 45Ca2+ from preloaded intracellular stores of saponin-permeabilised human uter...
The effects of ionic composition and strength on rabbit skeletal muscle Ca2+ release channel (ryanod...
Sarcoplasmic reticulum vesicles isolated from fast-twitch frog skeletal muscle presented two classes...
The sarcoplasmic reticulum (SR) of skeletal muscle is an intracellular membraneous network that, thr...
son. Metabolic end products inhibit sarcoplasmic reticulum Ca2 ’ release and [3H]ryanodine binding. ...