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Lysosomal storage disorders (LSDs) are a series of metabolic disorders that are mainly due to mutations in genes encoding proteolytic enzymes within lysosomes, resulting in the aggregation of relevant substrates and cell death (Zhao et al., 2003), Fabry disease (mutations in the -galactosidase A gene) (Suntjens et al., 2015), Pompe disease (mutations in the acid -glucosidase gene) (van Capelle et al., 2010), and -mannosidosis (mutations in the -mannosidosis gene) ( + into the lysosomes by the H + -ATPase pump
J Clin Endocrinol Metab 107:29732981 Berry MJ, Larsen PR (1992) The role of selenium in thyroid hormone action
In the scientific talk "Real-time monitoring of redox changes in cells with a microplate reader", Prof
A detoxifying antioxidant that fights free radicals to maintain youthful, healthy skin
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