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      High-throughput screening to identify inhibitors of lysine demethylases.

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          Abstract

          Lysine demethylases (KDMs) are epigenetic regulators whose dysfunction is implicated in the pathology of many human diseases including various types of cancer, inflammation and X-linked intellectual disability. Particular demethylases have been identified as promising therapeutic targets, and tremendous efforts are being devoted toward developing suitable small-molecule inhibitors for clinical and research use. Several High-throughput screening strategies have been developed to screen for small-molecule inhibitors of KDMs, each with advantages and disadvantages in terms of time, cost, effort, reliability and sensitivity. In this Special Report, we review and evaluate the High-throughput screening methods utilized for discovery of novel small-molecule KDM inhibitors.

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          Author and article information

          Journal
          Epigenomics
          Epigenomics
          Future Medicine Ltd
          1750-192X
          1750-192X
          2015
          : 7
          : 1
          Affiliations
          [1 ] Department of Pathology, Yale School of Medicine, New Haven, 310 Cedar St., BML348C, PO Box 208023, New Haven, CT 06520, USA.
          Article
          NIHMS667145
          10.2217/epi.14.63
          4356004
          25687466
          e5a05660-6f01-46c5-9e76-34cf05a4e170
          History

          small-molecule inhibitor,High-throughput screening,JmjC,KDM,LSD1,lysine demethylase

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