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FDA drug approval is a full review process involving Phase IIII clinical trials, demonstrated safety and efficacy in humans, and post-market surveillance obligations

Proanthocyanidins purified from fruit pericarp of Clausena lansium (Lour.) Skeels as efficient tyrosinase inhibitors: structure evaluation, inhibitory activity and molecular mechanism

The PCA was conducted using the FactoMineR package (52) in R, with the first five principal components capturing the primary sources of variation in the data

Injections were administered intraperitoneally once per day, the first application was given 30 min after ligature placement, while the final application 24 h before the tissue harvest

cDNA Cloning of the Developmentally Regulated Lamin Liii of Xenopus-Laevis