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Together, these foundational studies elucidated NRF2-ARE-induced genes involved in glutathione production and activity

N-methylated glutathione analogues demonstrate a 16.1-fold increase in oral bioavailability compared to native GSH

A study on genetic linkages between aberrant lipid metabolism and PD directly demonstrates that glucocerebrosidase and sphingomyelin phosphodiesterase 1 mutations enhance PD risk in humans, and that galactosylceramide beta hydrolase function loss increases -synuclein aggregation and accumulation in experimental murine models

ANDREW GALLIMORE: No

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