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ACS Chemical Biology, Vol. 5, No. 2. (19 February 2010), pp. 159-161, doi:10.1021/cb100029t Key: citeulike:6721831
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PMID: 20166761 In recent years in vivo chemical screening in zebrafish has emerged as a rapid and efficient method to identify lead compounds that modulate specific biological processes. By performing primary screening in vivo, the bioactivity, toxicity, and off-target side effects are determined from the onset of drug development. A recent study demonstrates that in vivo screening can be used successfully to perform structure−activity relationship (SAR) studies. This work validates the zebrafish as an effective model for not only drug discovery but also drug optimization.
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