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Primary carnitine deficiency (PCD) is an autosomal recessive disorder of mitochondrial -oxidation resulting from defective carnitine transport and is one of the rare treatable etiologies of metabolic cardiomyopathies
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B12 protects your brain cells in the same way it helps protect nerve cells, by protecting their myelin sheaths
Clinical trials conducted in the early 2000s showed modest results, and the compound failed to demonstrate sufficient efficacy to support regulatory approval as a weight-loss medicine
Quantitative proteomics identifies NCOA4 as the cargo receptor mediating ferritinophagy
Radevski, F., Peraic, P., Maek, T., Starevi, K., Krezic, I., Pavlov, K., Drmic, D., Kralj, T., Seiwerth, S., Sikiric, P., & Kokot, A
