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Description
Design and Synthesis of Irreversible Analogues of Bardoxolone Methyl for the Identification of Pharmacologically Relevant Targets and Interaction Sites
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These computational and structural approaches exemplify a design-driven paradigm, where antigen selection, epitope accessibility, and linker positioning are optimized specifically for infectious microenvironments, rather than relying on empirical oncology-focused strategies
Larger high-quality studies are needed
2019 Sep 16;11(9):2232
