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

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

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

showed that 92.3% and 72.2% participants on liraglutide 3.0 mg achieved remission of prediabetes by 6 and 12 months, respectively 68 and Ruseva et al

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Neuroendocrine signaling balance studies