期刊
NATURE CHEMICAL BIOLOGY
卷 14, 期 12, 页码 1068-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/s41589-018-0147-8
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Current drug discovery efforts focus on proteins because of their ability to form stable, structured pockets. A recent study demonstrates that targeting stable, structured bioactive RNA motifs, such as autocatalytic introns, may provide a novel method of expanding druggability and selectivity.
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