Simone Brixius-Anderko

Affiliations: 
2017- Medicinal Chemistry University of Michigan, Ann Arbor, Ann Arbor, MI 
Google:
"Simone Brixius-Anderko"
Mean distance: (not calculated yet)
 
BETA: Related publications

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.

Loomis CL, Brixius-Anderko S, Scott EE. (2022) Redox partner adrenodoxin alters cytochrome P450 11B1 ligand binding and inhibition. Journal of Inorganic Biochemistry. 235: 111934
Brixius-Anderko S, Scott EE. (2021) Aldosterone Synthase Structure With Cushing Disease Drug LCI699 Highlights Avenues for Selective CYP11B Drug Design. Hypertension (Dallas, Tex. : 1979). HYPERTENSIONAHA12117
Brixius-Anderko S, Scott EE. (2021) Structural and functional insights into aldosterone synthase interaction with its redox partner protein adrenodoxin. The Journal of Biological Chemistry. 100794
Wróbel TM, Rogova O, Andersen KL, et al. (2020) Discovery of Novel Non-Steroidal Cytochrome P450 17A1 Inhibitors as Potential Prostate Cancer Agents. International Journal of Molecular Sciences. 21
König L, Szczesny S, Brixius-Anderko S, et al. (2020) Mixed-culture fermentation for enhanced C21-hydroxylation of glucocorticoids. Journal of Biotechnology
Brixius-Anderko S, Scott EE. (2020) Abstract MP11: Aldosterone Synthase Structure With Cushing’s Disease Drug Osilodrostat Provides Clues For Treatment Of Primary Aldosteronism Hypertension. 76
Brixius-Anderko S, Scott E. (2020) Structural and Functional Insights into Aldosterone Synthase Interaction with Ligands and Redox Partner Proteins for Enhanced Treatment of Hypertension The Faseb Journal. 34: 1-1
Brixius-Anderko S, Scott EE. (2018) Structure of human cortisol-producing cytochrome P450 11B1 bound to the breast cancer drug fadrozole provides insights for drug design. The Journal of Biological Chemistry
Malikova J, Brixius-Anderko S, Udhane SS, et al. (2017) CYP17A1 inhibitor abiraterone, an anti-prostate cancer drug, also inhibits the 21-hydroxylase activity of CYP21A2. The Journal of Steroid Biochemistry and Molecular Biology
Schiffer L, Müller AR, Hobler A, et al. (2016) Biotransformation of the mineralocorticoid receptor antagonists spironolactone and canrenone by human CYP11B1 and CYP11B2: Characterization of the products and their influence on mineralocorticoid receptor transactivation. The Journal of Steroid Biochemistry and Molecular Biology. 163: 68-76
See more...