Rachel M. Sammons
Affiliations: | 2011-2018 | Chemical Biology and Medicinal Chemistry | University of Texas at Austin, Austin, Texas, U.S.A. |
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| Sammons RM, Bohanon AL, Kowtha A, et al. (2022) High-Throughput Assay for Identifying Diverse Antagonists of the Binding Interaction between the ACE2 Receptor and the Dynamic Spike Proteins of SARS-CoV-2. Acs Infectious Diseases. 8: 2259-2270 |
| Gagliardi M, Pitner MK, Park J, et al. (2020) Differential functions of ERK1 and ERK2 in lung metastasis processes in triple-negative breast cancer. Scientific Reports. 10: 8537 |
| Semba T, Sammons R, Wang X, et al. (2020) JNK Signaling in Stem Cell Self-Renewal and Differentiation. International Journal of Molecular Sciences. 21 |
| Kaoud TS, Johnson WH, Ebelt ND, et al. (2019) Modulating multi-functional ERK complexes by covalent targeting of a recruitment site in vivo. Nature Communications. 10: 5232 |
| Sammons RM, Ghose R, Tsai KY, et al. (2019) Targeting ERK beyond the boundaries of the kinase active site in melanoma. Molecular Carcinogenesis |
| Sammons RM, Perry NA, Li Y, et al. (2019) A Novel Class of Common Docking Domain Inhibitors That Prevent ERK2 Activation and Substrate Phosphorylation. Acs Chemical Biology |
| Kaoud TS, Johnson WH, Ebelt ND, et al. (2019) Abstract 3872: Targeting multi-functional ERK-protein complexesin vivo Cancer Research. 79: 3872-3872 |
| Kaoud TS, Johnson WH, Ebelt ND, et al. (2016) Abstract 3771: Discovery of a covalent inhibitor of ERK docking-interactions that inhibits A375 melanoma cells proliferation Cancer Research. 76: 3771-3771 |
| Pitner MK, Saso H, Larson R, et al. (2016) Abstract 1624: Silencing of ERK2 reverses EMT and suppresses the CSC phenotype, inhibiting lung metastasis in triple-negative breast cancer Cancer Research. 76: 1624-1624 |
| Sammons RM, Kaoud TS, Devkota AK, et al. (2015) Abstract 3648: A high-throughput fluorescence anisotropy screening for discovery of inhibitors that target the D-recruitment site of ERK in vitro and in cells Cancer Research. 75: 3648-3648 |