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These studies indicate the potential of utilizing the de novo pathway, a less extensively studied pathway, as a therapeutic strategy for metabolic diseases Barth syndrome is a rare disease caused by mutations in the tafazzin gene encoding for cardiolipin (CL), a phospholipid specific for the mitochondria 303

Further studies of the mechanism proved that HKC simultaneously decreased the protein expression of pp38MAPK, p-Akt, TGF-1, and TNF-by inhibiting the p38MAPK and Akt signaling pathways in the kidney in a rat model of DN

Alterations in T and B cell function persist in convalescent COVID-19 patients