(1997). Human Cytochrome P450 Enzymes: A Status Report Summarizing Their Reactions, Substrates, Inducers, and Inhibitors. Drug Metabolism Reviews: Vol. 29, No. 1-2, pp. 413-580.
Drug Metabolism Reviews Template
Write in a clean editor, then format for Drug Metabolism Reviews in one click — DocuGuru applies the official Taylor & Francis template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the Drug Metabolism Reviews format
Drug Metabolism Reviews is a peer-reviewed journal published by Taylor & Francis, covering Pharmacogenetics and Drug Metabolism, Drug Transport and Resistance Mechanisms, Drug-Induced Hepatotoxicity and Protection.
| Publisher | Taylor & Francis |
|---|---|
| Reference style | Author–year (Chicago, T&F) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Drug Metabolism Reviews 12 (3): 45–58.
Formats any DOI in Drug Metabolism Reviews style. No sign-up. |
| Publishes research in | Pharmacogenetics and Drug Metabolism Drug Transport and Resistance Mechanisms Drug-Induced Hepatotoxicity and Protection Computational Drug Discovery Methods Carcinogens and Genotoxicity Assessment |
| ISSN | 0360-2532 |
| Citation impact (2-yr) | 4.42 |
| h-index | 145 |
| i10-index | 1,065 |
| Total citations | 89,596 |
| Top institutions publishing here | National Institutes of Health |
| Journal website | www.informapharmascience.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Drug Metabolism Reviews per year
Citation impact of Drug Metabolism Reviews by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in Drug Metabolism Reviews
Since eukaryotic cells constantly encounter various environmental insults, they have evolved defense mechanisms to cope with toxicant- and carcinogen-induced oxidative stress or electrophiles. One of the most important cellular defense mechanisms against oxidative stress or electrophiles is mediated by the transcription factor Nrf2. Under the basal condition, Nrf2-dependent transcription is repressed by a negative regulator…
Hepatotoxicity is a serious problem during drug development and for the use of many established drugs. For example, acetaminophen overdose is currently the most frequent cause of acute liver failure in the United States and Great Britain. Evaluation of the mechanisms of drug-induced liver injury indicates that mitochondria are critical targets for drug toxicity, either…
Highly reactive oxygen species that are formed during normal metabolism and under conditions of oxidative stress are able to oxidize proteins or convert lipid and carbohydrate derivatives to compounds that react with functional groups on proteins. Among other changes, these ROS-mediated reactions lead to the formation of protein carbonyl derivatives, which serves as a marker…
Pharmacogenetics is the study of how interindividual variations in the DNA sequence of specific genes affect drug response. This article highlights current pharmacogenetic knowledge on important human drug-metabolizing cytochrome P450s (CYPs) to understand the large interindividual variability in drug clearance and responses in clinical practice. The human CYP superfamily contains 57 functional genes and 58…