E Megan Flynn
Affiliations: | Early Discovery Biochemistry | Genentech, Inc., San Francisco, CA, United States |
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Publications
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Miller GM, Flynn EM, Tom J, et al. (2022) Trifluoroacetyl Lysine as a Bromodomain Binding Mimic of Lysine Acetylation. Acs Chemical Biology |
Wang S, Tsui V, Crawford TD, et al. (2018) GNE-371, a Potent and Selective Chemical Probe for the Second Bromodomains of Human Transcription-Initiation-Factor TFIID Subunit 1 and Transcription-Initiation-Factor TFIID Subunit 1-like. Journal of Medicinal Chemistry |
Raisner R, Kharbanda S, Jin L, et al. (2018) Enhancer Activity Requires CBP/P300 Bromodomain-Dependent Histone H3K27 Acetylation. Cell Reports. 24: 1722-1729 |
Oppikofer M, Sagolla M, Haley B, et al. (2017) Non-canonical reader modules of BAZ1A promote recovery from DNA damage. Nature Communications. 8: 862 |
Crawford TD, Audia JE, Bellon S, et al. (2017) GNE-886: A Potent and Selective Inhibitor of the Cat Eye Syndrome Chromosome Region Candidate 2 Bromodomain (CECR2). Acs Medicinal Chemistry Letters. 8: 737-741 |
Crawford TD, Vartanian S, Côté A, et al. (2017) Inhibition of bromodomain-containing protein 9 for the prevention of epigenetically-defined drug resistance. Bioorganic & Medicinal Chemistry Letters |
Crawford TD, Tsui V, Flynn EM, et al. (2016) Diving into the water: Inducible binding conformations for BRD4, TAF1(2), BRD9, and CECR2 bromodomains. Journal of Medicinal Chemistry |
Vinogradova M, Gehling VS, Gustafson A, et al. (2016) An inhibitor of KDM5 demethylases reduces survival of drug-tolerant cancer cells. Nature Chemical Biology |
Taylor AM, Côté A, Hewitt MC, et al. (2016) Fragment-Based Discovery of a Selective and Cell-Active Benzodiazepinone CBP/EP300 Bromodomain Inhibitor (CPI-637). Acs Medicinal Chemistry Letters. 7: 531-536 |
Flynn EM, Huang OW, Poy F, et al. (2015) A Subset of Human Bromodomains Recognizes Butyryllysine and Crotonyllysine Histone Peptide Modifications. Structure (London, England : 1993) |