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Moreover, emerging technologies such as targeted protein/RNA degradation methods (e.g., LYTAC, ATTEC), as well as novel approaches targeting cell substructures (exosomes, lysosomes), nuclear export pathways, the cell membrane, and RNA molecules, offer promising opportunities for advancing medicinal chemistry

Additionally, Se treatment (100 nmol/L) was shown to inhibit glucose-induced expression of adhesion molecules in the human umbilical vein endothelial cells (Zheng et al., 2008)

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