Decoding the role of S5, the fifth transmembrane segment in the type 1 ryanodine receptor (RyR1) channel (IMAGE)
Caption
S5 mutations disrupt RyR1 channel function, influencing both channel activity and gating mechanisms. This impacts the release of calcium and affects muscle contractions, leading to severe muscle diseases such as malignant hyperthermia and central core disease.
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Associate Professor Takashi Murayama from Juntendo University, Japan and Associate Professor Haruo Ogawa from Kyoto University, Japan
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