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Es erffnet auch neue Forschungsrichtungen, Anti-Mutagenese, mitochondriale Biogenese, Langlebigkeit

Genetic Basis and Pathophysiology Most cases of MH are associated with mutations in the RYR1 gene , which encodes the ryanodine receptor type 1 (RyR1) calcium-release channel in skeletal muscle

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Effect of MEK inhibition with PD184352 + Ara-c on patterns of expression of apoptosis regulating proteins in acute myelogenous leukemia (AML) surivivor cells