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GAUCHER DISEASE Gaucher disease (GD) is a rare lysosomal disease caused by mutations in the GBA1 gene, which encodes for glucocerebrosidase, commonly abbreviated as GCase [5]

The pathway for the reduction of a protein disulfide by TRX entails nucleophilic attack by one of the active-site SH to form a protein-protein disulfide followed by intramolecular displacement of the reduced target proteins with concomitant formation of oxidized TRX

But it sits squarely at the intersection of fat loss and longevity science, which is why it belongs in the catalog

From Beverly Hills to Harvard, NAD+ has become a cornerstone of biohacking and regenerative medicine

Fecal microbiota transplantation (FMT) alleviates experimental colitis in mice by gut microbiota regulation