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AI-enabled in silico approaches, in tandem with high-throughput target binding assays (e.g., small-molecule microarrays) and phenotypic screens (perhaps using cAMP+ as a readout), may further uncover some of these incredibly useful molecules
The present study observed reduced expression of 25-hydroxylase enzymes and 1--hydroxylase, vitamin D receptor, and increased expression of the 24-hydroxylase enzyme in the livers of HFD-fed mice
Round, P., Priestley, A
TEM analysis revealed mean particle sizes of 8.06 nm for ASC.QDS, 7.13 nm for BER.QDS, and 5.12 nm for GLU.QDS, with varying morphologies and aggregation patterns
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