P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanism

2014
Written by Stellate Comms

Wissing ER, Boyer JG, Kwong JQ, Sargent MA, Karch J, McNally EM, Otsu K, Molkentin JD (2014) Human Molecular Genetics

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Physiological and pathological roles of the mitochondrial permeability transition pore in the heart
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Enhanced Ca²⁺ influx from STIM1-Orai1 induces muscle pathology in mouse models of muscular dystrophy