Compounding oxidation of the RyR1 and subsequent accumulation of cytosolic Ca 2+ due to both increased RyR1 leakage and impaired PMCA activity may be significant factors that underlie the onset and progression of pathology.
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Muscle-specific Ryanodine receptor 1 properties underlie limb-girdle muscular dystrophy 2B/R2 progression.
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The sentences
The mitochondrial Ca 2+ content in the BlaJ TA and psoas showed a trend towards an increase with age, but this was not significant.