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This protein, which is mainly expressed in the liver, is an inhibitor of LPL, endothelial lipase, and hepatic lipase

Similarly, one general approach, called multisubstrate adduct, can be applied in DNMTi design, in which the two substrates SAM and cytosine analog are combined into one single molecule

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Based on this public health concern, we reasoned that Gsts might participate in the detoxification of foreign substances, which could ultimately contribute to the antifungal drug resistance mechanism

[DOI] [PMC free article] [PubMed] [Google Scholar] 43.Segal L.N., Alekseyenko A.V., Clemente J.C., Kulkarni R., Wu B., Gao Z., Chen H., Berger K.I., Goldring R.M., Rom W.N., et al