Epigenetic protein families: a new frontier for drug discovery
By C. Arrowsmith, C. Bountra, Paul V. Fish, Kevin Lee, M. Schapira. Nature reviews. Drug discovery, 2012
1,283 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/fd3346db3efdf967ef263b7d902523d5edecb53e
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Citations in the corpus
- YTH Domain: A Family of N6-methyladenosine (m6A) Readers (2018, background): “In the epigenetic field, the structural information of known mediators or readers of histone acetyllysine and methyllysine has been used to guide the design and development of chemical probes [69].”
- Single-cell RNA-seq and computational analysis using temporal mixture modelling resolves Th1/Tfh fate bifurcation in malaria (2017, background): “Given the enthusiasm surrounding the therapeutic tractability of histone binding domains by chemical inhibitors (7), it is worth noting that our results suggest that targeting this particular bromodomain-containing epigenetic reader may not be desirable, at least in subsets of CD (or CLL or MS) pati”
- Epigenetic Determinants of Cancer. (2016, background): “The clinical successes with current epigenetic drugs have led to a big increase in interest from the pharmaceutical industry in developing compounds that will target epigenetic abnormalities in cancers (Kelly et al. 2010; Dawson et al. 2011; Arrowsmith et al. 2012).”
- Histone Modifications and Cancer. (2016, background): “…tools that can be used are the recently described selective, cell-active inhibitors of EZH2, DOT1L, SMYD2, G9a/GLP1, PRMT3, JMJD3, LSD1, BET (BRD2-4), L3MBTL1, L3MBTL3, CBP/EP300, PCAF, and BAZ bromodomains (Arrowsmith et al. 2012; Muller and Brown 2012; James et al. 2013; Gallenkamp et al. 2014).”
- The world of protein acetylation. (2016, background): “So far, 17–22 ‘classical’ KATs have been identified in the human genome [14,15,167,186].”