Sign in to add mentor
Russell Stephen Drago grad student 1972 UIUC
 (Time Correlation Function Analysis of Raman Lineshapes.)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
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
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
Hsu MH, Baer BR, Rettie AE, et al. (2017) The Crystal Structure of Cytochrome P450 4B1 (CYP4B1) Monoxygenase Complexed with Octane Discloses Several Structural Adaptations for ω-Hydroxylation. The Journal of Biological Chemistry
Butler CR, Ogilvie K, Martinez-Alsina L, et al. (2016) Aminomethyl-Derived Beta Secretase (BACE1) Inhibitors: Engaging Gly230 without an Anilide Functionality. Journal of Medicinal Chemistry
Savas U, Wei S, Hsu MH, et al. (2016) 20-Hydroxyeicosatetraenoic Acid (HETE) Dependent Hypertension in Human Cytochrome P450 (CYP) 4A11 Transgenic Mice: Normalization of Blood Pressure by Sodium Restriction, Hydrochlorothiazide, or Blockade of the Type 1 Angiotensin II Receptor. The Journal of Biological Chemistry
Brodney MA, Beck EM, Butler CR, et al. (2015) Utilizing structures of CYP2D6 and BACE1 complexes to reduce risk of drug-drug interactions with a novel series of centrally efficacious BACE1 inhibitors. Journal of Medicinal Chemistry. 58: 3223-52
See more...