@article{
 title = {Highly selective inhibition of histone demethylases by de novo macrocyclic peptides},
 type = {article},
 year = {2017},
 pages = {14773},
 volume = {8},
 websites = {http://www.ncbi.nlm.nih.gov/pubmed/28382930},
 month = {4},
 day = {6},
 city = {England},
 id = {327067fd-d8ec-346b-b5bd-33a1bd3bcb6c},
 created = {2017-06-08T08:32:32.618Z},
 file_attached = {false},
 profile_id = {64f7fb50-d000-335d-a02d-06c5f340a97a},
 last_modified = {2018-07-09T12:39:48.705Z},
 read = {false},
 starred = {false},
 authored = {true},
 confirmed = {true},
 hidden = {false},
 citation_key = {Kawamura2017},
 source_type = {JOUR},
 private_publication = {false},
 abstract = {JmjC histone demethylases (KDMs) are cancer targets due to their links to cell proliferation, but selective inhibition remains a challenge. Here the authors identify potent inhibitors of KDM4A-C—via in vitro selection from a vast library of cyclic peptides—that show selectivity over other KDMs.},
 bibtype = {article},
 author = {Kawamura, Akane and Münzel, Martin and Kojima, Tatsuya and Yapp, Clarence and Bhushan, Bhaskar and Goto, Yuki and Tumber, Anthony and Katoh, Takayuki and King, Oliver N.F. and Passioura, Toby and Walport, Louise J. and Hatch, Stephanie B. and Madden, Sarah and Müller, Susanne and Brennan, Paul E. and Chowdhury, Rasheduzzaman and Hopkinson, Richard J. and Suga, Hiroaki and Schofield, Christopher J.},
 doi = {10.1038/ncomms14773},
 journal = {Nature Communications}
}

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