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Sglt2 inhibitor counteracts nlrp3 inflammasome via tubular metabolite itaconate in fibrosis kidney

Gaucher disease A primary, autosomal recessive lysosomal storage disease caused by mutations in the GBA1 gene, which encodes -glucocerebrosidase (GCase)

by aiding in the repair and regeneration of damaged tendons, BPC-157 could potentially help reduce recovery time and improve outcomes following an injury