Eric F. Johnson, Ph.D.
|Department of Molecular Medicine||Scripps Research Institute, La Jolla, La Jolla, CA, United States|
|1972||Chemistry||University of Illinois, Urbana-Champaign, Urbana-Champaign, IL|
Google:"Eric F. Johnson" OR "Eric Foster Johnson"
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|Kozono DE, Stinchcombe TE, Salama JK, et al. (2021) Veliparib in combination with carboplatin/paclitaxel-based chemoradiotherapy in patients with stage III non-small cell lung cancer. Lung Cancer (Amsterdam, Netherlands). 159: 56-65|
|Mastracchio A, Lai C, Torrent M, et al. (2020) Corrigendum to "Investigation of biaryl heterocycles as inhibitors of Wee1 kinase" [Bioorg. Med. Chem. Lett. 29 (2019) 1481-1486]. Bioorganic & Medicinal Chemistry Letters. 126895|
|Mastracchio A, Lai C, Torrent M, et al. (2019) Investigation of biaryl heterocycles as inhibitors of Wee1 kinase. Bioorganic & Medicinal Chemistry Letters|
|Hsu MH, Johnson EF. (2019) Active site differences between substrate-free and ritonavir-bound cytochrome P450 (CYP) 3A5 reveal plasticity differences between CYP3A5 and CYP3A4. The Journal of Biological Chemistry|
|Hopkins TA, Ainsworth WB, Ellis PA, et al. (2018) PARP1 trapping by PARP inhibitors drives cytotoxicity both in cancer cells and healthy bone marrow. Molecular Cancer Research : McR|
|Jennings GK, Hsu MH, Shock LS, et al. (2018) Non-covalent interactions dominate dynamic heme distortion in cytochrome P450 4B1. The Journal of Biological Chemistry|
|Burns AJ, Johnson E. (2018) The Evolving Cyberthreat to Privacy It Professional. 20: 64-72|
|Hsu MH, Savas U, Johnson EF. (2017) The X-ray Crystal Structure of the Human Monooxygenase Cytochrome P450 3A5-Ritonavir Complex Reveals Active Site Differences between P450s 3A4 and 3A5. Molecular Pharmacology|
|Liu R, Lyu X, Hsu MH, et al. (2017) Determinants of the Inhibition of DprE1 and CYP2C9 by Antitubercular Thiophenes. Angewandte Chemie (International Ed. in English)|
|Albertolle ME, Kim D, Nagy LD, et al. (2017) Heme-thiolate sulfenylation of human cytochrome P450 4A11 functions as a redox switch for catalytic inhibition. The Journal of Biological Chemistry|