A team-oriented and enthusiastic drug discovery biologist. Broad interests in multiple disease areas, with experience spanning oncology, immunology, liver disease, and infectious disease.
Nagarajan A, Amberg-Johnson K, Paull E, Huang K, Ghanakota P, Chandrasinghe A, et al. (2024). ChemRxiv. doi:10.26434/chemrxiv-2024-q2v3l (This is a preprint and in submission for peer-review.)
Igawa H, Konst ZA, Therrien E, Shelley M, Koldsø H, Bos PH, Negri A, Verras A, Guo J, Dahlgren MK, Levinson A, Parr BT, Kurhade SE, Latthe P, Shetty R, Santhanakrishnan S, Amberg-Johnson K, Futran AS, Atsriku C, Pelletier RD, Liu Z, Bell JA, Bhat S, Svensson M, Gerasyuto AI. (2024). J Med Chem. 2024 Dec 26;67(24):21811-21840. doi: 10.1021/acs.jmedchem.4c01405. Epub 2024 Dec 12. PMID: 39666597.
Futran AS, Lu T, Amberg-Johnson K, et al. (2024). iScience. 2024;27(5):109693. doi:10.1016/j.isci.2024.109693
Tang, Y., Meister, T. R., Walczak, M., Pulkoski-Gross, M. J., Hari, S. B., Sauer, R. T., Amberg-Johnson, K., & Yeh, E. (2019) PLoS biology, 17(2).
Amberg-Johnson, K., & Yeh, E. (2019). Antimicrob Agents Chemother. 2019 Jan 29; 63(2)
Foe, IT., Onguka, O., Amberg-Johnson, K., Garner, R., Amara, N., Beatty, W., Yeh, E., Bogyo, M., mSphere. (2018).
We report on a physics-based computationally driven lead identification approach that identified structurally unique imidazo pyrazoles as reversible and wild-type-sparing EGFR TKIs of classical mutations.
drug resistance computational prediction EGFR
Read MoreWe describe the discovery of potent and specific USP7 inhibitors exemplified by FX1-5303.
acute myeloid leukemia USP7 p53 mechanism-of-action
Read MoreWe report on a physics-based computationally driven lead identification approach that identified structurally unique imidazo pyrazoles as reversible and wild-type-sparing EGFR TKIs of classical mutations
non-small cell lung cancer EGFR drug discovery
Read More