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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 21, 2019
Polo-like Kinase 1 Inhibition as a Therapeutic Approach to Selectively Target BRCA1-Deficient Cancer Cells by Synthetic Lethality InductionSofía Carbajosa, María Florencia Pansa, Natalia S Paviolo, et al.Nature Cell Biology|January 27, 2004
A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathwayTewis Bouwmeester, Angela Bauch, Heinz Ruffner, et al.Nature|October 4, 2011
Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemiaMark A Dawson, Rab K Prinjha, Antje Dittmann, et al.Science Translational Medicine|May 1, 2020
CDK12 inhibition reduces abnormalities in cells from patients with myotonic dystrophy and in a mouse modelAmi Ketley, Marzena Wojciechowska, Sonja Ghidelli-Disse, et al.Plos One|March 3, 2016
Biochemical Screening of Five Protein Kinases from Plasmodium falciparum against 14,000 Cell-Active CompoundsGregory J Crowther, Heidi K Hillesland, Katelyn R Keyloun, et al.Nature|January 24, 2006
Proteome survey reveals modularity of the yeast cell machineryAnne-Claude Gavin, Patrick Aloy, Paola Grandi, et al.Nature|July 31, 2012
A selective jumonji H3K27 demethylase inhibitor modulates the proinflammatory macrophage responseLaurens Kruidenier, Chun-wa Chung, Zhongjun Cheng, et al.Science (New York, N.Y.)|June 17, 2017
Click chemistry enables preclinical evaluation of targeted epigenetic therapiesDean S Tyler, Johanna Vappiani, Tatiana Cañeque, et al.Journal of Medicinal Chemistry|January 16, 2016
Cell Penetrant Inhibitors of the KDM4 and KDM5 Families of Histone Lysine Demethylases. 2. Pyrido[3,4-d]pyrimidin-4(3H)-one DerivativesSusan M Westaway, Alex G S Preston, Michael D Barker, et al.Nature Structural & Molecular Biology|June 14, 2016
Functional interdependence of BRD4 and DOT1L in MLL leukemiaOmer Gilan, Enid Y N Lam, Isabelle Becher, et al.Pageof 8