Cytochrome P450s and other enzymes in drug metabolism and toxicity
By F. Guengerich. AAPS Journal, 2006
617 citations recorded by the source corpus.
Subfields: Oncology, Pharmacology
View Paper: https://www.semanticscholar.org/paper/5669c60dedd2e81aa1bc9d8e37dc4075c0359135
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- Garima Sharma
- C. Doss
- Sang-Soo Lee
- C. Chakraborty
- M. Santacroce
- G. Crescenzo
- E. Casalino
- O. Lai
Citations in the corpus
- Aflatoxins in aquatic species: metabolism, toxicity and perspectives (2008, background): “Once formed inside the cell, the exo-epoxide is sufficiently stable to migrate from the endoplasmic reticulum to the nucleus where it binds covalently to genetic material, inducing structural modifications and a spectrum of DNA lesions (Bailey et al. 1996; Guengerich 2006).”
- Therapeutic miRNA and siRNA: Moving from Bench to Clinic as Next Generation Medicine (2017, background): “Drug-metabolizing enzymes, such as cytochrome P450 (CYP or P450) isoforms, play crucial roles in drug metabolism.(71) Drug transporters, including ABC and SLC transporters, also play key roles in drug absorption, distribution, and excretion.”