Total calcium content of both human and porcine MHS skeletal muscle is significantly less than normal. This data is consistent with the concept that some organelle (prob-ably the sarcoplasmic reticulum, the mitochondrion or even the sarcolemma) within the MHS muscle stores less than normal amounts of calcium. The large variability between muscle specimens rules out measurement of total calcium content of skeletal muscle as a routine diagnostic test for malignant hyperthermia susceptibility. Malignant hyperthermic susceptible (MHS) muscle has been postulated to be less capable than normal of storing calcium within some organelle or membrane. The defective organelle might be the sarcoplasmic reticulum (SR) (Britt et al., 1973; Kalow et al., 1...
Previous studies have demonstrated a defect associated with the calcium release mechanism of sarcopl...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
The hypothesis that intracellular Ca2+ is elevated in dystrophic (mdx) skeletal muscle due to increa...
Malignant hyperthermia (MH) is a pharmacogenetic disease of humans and various animal species that p...
Malignant hyperthermia (MH) is a pharmacogenetic disease of humans and various animal species that p...
Inward Ca transport and spontaneous Ca release activities were compared among sarcoplasmic reticul...
Single sarcoplasmic reticulum (SR) Ca2+ release channels were reconstituted from normal and malignan...
Malignant hyperthermia (MH) is a potentially lethal pharmacogenetic disorder. Numerous mutations of ...
AbstractCalcium pulse additions to isolated SR membranes can cause a reversible efflux of calcium. T...
AbstractCalcium-induced calcium release and halothane-induced calcium release from pig sarcoplasmic ...
In malignant hyperthermia (MH), mutations in RyR1 underlie direct activation of the channel by volat...
Item does not contain fulltextChanges in intracellular Ca2+-concentration play an important role in ...
Malignant hyperthermia (MH) is a potentially fatal pharmacogenetic disorder of skeletal muscle that ...
AbstractMalignant hyperthermia occurs in man and pigs as a hereditary disorder notably as a complica...
The neuroleptic malignant syndrome (NMS) is an uncommon but serious adverse effect of antipsychotic ...
Previous studies have demonstrated a defect associated with the calcium release mechanism of sarcopl...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
The hypothesis that intracellular Ca2+ is elevated in dystrophic (mdx) skeletal muscle due to increa...
Malignant hyperthermia (MH) is a pharmacogenetic disease of humans and various animal species that p...
Malignant hyperthermia (MH) is a pharmacogenetic disease of humans and various animal species that p...
Inward Ca transport and spontaneous Ca release activities were compared among sarcoplasmic reticul...
Single sarcoplasmic reticulum (SR) Ca2+ release channels were reconstituted from normal and malignan...
Malignant hyperthermia (MH) is a potentially lethal pharmacogenetic disorder. Numerous mutations of ...
AbstractCalcium pulse additions to isolated SR membranes can cause a reversible efflux of calcium. T...
AbstractCalcium-induced calcium release and halothane-induced calcium release from pig sarcoplasmic ...
In malignant hyperthermia (MH), mutations in RyR1 underlie direct activation of the channel by volat...
Item does not contain fulltextChanges in intracellular Ca2+-concentration play an important role in ...
Malignant hyperthermia (MH) is a potentially fatal pharmacogenetic disorder of skeletal muscle that ...
AbstractMalignant hyperthermia occurs in man and pigs as a hereditary disorder notably as a complica...
The neuroleptic malignant syndrome (NMS) is an uncommon but serious adverse effect of antipsychotic ...
Previous studies have demonstrated a defect associated with the calcium release mechanism of sarcopl...
The ReJI29 murine model of muscular dystrophy was employed to investigate the properties of skeletal...
The hypothesis that intracellular Ca2+ is elevated in dystrophic (mdx) skeletal muscle due to increa...