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Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
To further elucidate the mechanism of action, TUNEL analysis of tumor tissue sections was performed via IF double-staining, which revealed increased activation of tumor apoptosis in the Psa-AR-treated group (Fig
Fe-S cluster coordination by Grx2 also requires 2GSH molecules which are required to stabilize the Grx2 dimer2Fe2S cluster assembly (Berndt et al., 2013)
doi: 10.1002/pca.2808 104
