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Role of 5'TG3'-interacting factors (TGIFs) in Vorinostat (HDAC inhibitor)-mediated Corneal Fibrosis Inhibition

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At present, the common modification sites in marketed drugs include amino, carboxyl, sulfo, disulfide, glycosyl, and some specific positions of non-polar amino acids

Taken together, the metabolomic differences observed in the BPD group suggest decreased glutathione levels, and thereby suggesting persistent oxidative stress, in the airways of preterm-born children with a history of BPD