We are improving our search experience. To check which content you have full access to, or for advanced search, go back to the old search.

Search

Please fill in this field.
Filters applied:

Search Results

Showing 1-20 of 104 results
  1. Human variability in isoform-specific UDP-glucuronosyltransferases: markers of acute and chronic exposure, polymorphisms and uncertainty factors

    UDP-glucuronosyltransferases (UGTs) are involved in phase II conjugation reactions of xenobiotics and differences in their isoform activities result...

    E. E. J. Kasteel, K. Darney, ... L. S. Lautz in Archives of Toxicology
    Article Open access 15 May 2020
  2. Enzyme Kinetics of Uridine Diphosphate Glucuronosyltransferases (UGTs)

    Glucuronidation, catalyzed by uridine diphosphate glucuronosyltransferases (UGTs), is an important process for the metabolism and clearance of many...
    ** Zhou, Upendra A. Argikar, John O. Miners in Enzyme Kinetics in Drug Metabolism
    Protocol 2021
  3. Pharmacogenomics and Pediatrics

    Catherine M. Sherwin in The ADME Encyclopedia
    Reference work entry 2022
  4. Human Family 1–4 cytochrome P450 enzymes involved in the metabolic activation of xenobiotic and physiological chemicals: an update

    This is an overview of the metabolic activation of drugs, natural products, physiological compounds, and general chemicals by the catalytic activity...

    Slobodan P. Rendic, F. Peter Guengerich in Archives of Toxicology
    Article 18 January 2021
  5. Predicting the presence and mechanism of busulfan drug-drug interactions in hematopoietic stem cell transplantation using pharmacokinetic interaction network–based molecular structure similarity and network pharmacology

    Purpose

    This study aimed to predict the presence and mechanism of busulfan drug-drug interactions (DDIs) in hematopoietic stem cell transplantation...

    Chenxia Hao, **aoqin Ma, ... Wanhua Yang in European Journal of Clinical Pharmacology
    Article 11 November 2020
  6. 3,3′-Diindolylmethane and indole-3-carbinol: potential therapeutic molecules for cancer chemoprevention and treatment via regulating cellular signaling pathways

    Dietary compounds in cancer prevention have gained significant consideration as a viable method. Indole-3-carbinol (I3C) and 3,3′-diindolylmethane...

    Octavio Daniel Reyes-Hernández, Gabriela Figueroa-González, ... Javad Sharifi-Rad in Cancer Cell International
    Article Open access 26 August 2023
  7. Extracellular Vesicles as Potential Therapeutic Targets and Biomarkers for Liver Disease

    The accumulated evidence indicates that extracellular vesicles (EVs) play a critical role in the organs of multicellular organisms (Raposo and Stahl,...
    Chapter 2021
  8. Pharmacogenomics in and Its Influence on Pharmacokinetics

    CYP1A2 is involved to a major extent in the metabolism of several drugs (imipramine, clozapine, fluvoxamine, olanzapine, theophylline, acetaminophen,...
    Guy Montay, Jochen Maas, Roland Wesch in Drug Discovery and Evaluation: Methods in Clinical Pharmacology
    Reference work entry 2020
  9. Potent aneugenicity of 1-methylpyrene in human cells dependent on metabolic activation by endogenous enzymes

    1-Methylpyrene (1-MP) is a common environmental pollutant and animal carcinogen. After sequential activation by cytochromes P450 and...

    Zihuan Li, Hang Yu, ... Yungang Liu in Archives of Toxicology
    Article 15 October 2020
  10. Enzyme Polymorphisms Affecting Xenobiotic Toxicity

    Individual differences resulting from enzyme polymorphisms in gene structure and tissue-specific expression can have a significant impact to the...
    Chapter 2020
  11. Cardiovascular Pharmacogenomics: An Update on Clinical Studies of Antithrombotic Drugs in Brazilian Patients

    Anticoagulant and antiplatelet drugs effectively prevent thrombotic events in patients with cardiovascular diseases, ischemic stroke, peripheral...

    Thiago Dominguez Crespo Hirata, Carolina Dagli-Hernandez, ... Rosario Dominguez Crespo Hirata in Molecular Diagnosis & Therapy
    Article 06 August 2021
  12. Xenobiotica-metabolizing enzyme induction potential of chemicals in animal studies: NanoString nCounter gene expression and peptide group-specific immunoaffinity as accelerated and economical substitutions for enzyme activity determinations?

    Xenobiotica-metabolizing enzyme (XME) induction is a relevant biological/biochemical process vital to understanding the toxicological profile of...

    Brandy Riffle, Franz Oesch, ... Robert Landsiedel in Archives of Toxicology
    Article 25 May 2020
  13. Pharmacogenomics of Alzheimer’s Disease: Novel Strategies for Drug Utilization and Development

    Alzheimer’s disease (AD) is a priority health problem in developed countries with a high cost to society. Approximately 20% of direct costs are...
    Ramón Cacabelos, Vinogran Naidoo, ... Juan C. Carril in Pharmacogenomics in Drug Discovery and Development
    Protocol 2022
  14. Catechol-O-Methyltransferase and UDP-Glucuronosyltransferases in the Metabolism of Baicalein in Different Species

    Background

    Baicalein is the major bioactive flavonoid in some herb medicines and dietary plants; however, the detailed metabolism pathway of its major...

    Ruiya Zhang, Yonglei Cui, ... Zhonghui Yu in European Journal of Drug Metabolism and Pharmacokinetics
    Article 23 May 2017
  15. Drug Metabolism

    Living systems have developed elimination mechanisms to dispose waste products and to protect themselves from exposure to potentially harmful...
    Alan Talevi, Carolina Leticia Bellera in ADME Processes in Pharmaceutical Sciences
    Chapter 2018
  16. Advanced In Vitro HepaRG Culture Systems for Xenobiotic Metabolism and Toxicity Characterization

    Several HepaRG three-dimensional (3D) in vitro model systems have been developed to improve the predictability of xenobiotic metabolism and toxicity....

    Muhammad Nadeem Ashraf, Muhammad Waheed Asghar, ... Tony K. L. Kiang in European Journal of Drug Metabolism and Pharmacokinetics
    Article 10 December 2018
  17. The Fusarium metabolite culmorin suppresses the in vitro glucuronidation of deoxynivalenol

    Glucuronidation is a major phase II conjugation pathway in mammals, playing an important role in the detoxification and biotransformation of...

    Lydia Woelflingseder, Benedikt Warth, ... Doris Marko in Archives of Toxicology
    Article Open access 02 May 2019
  18. Co-treatment of Tuberculosis and HIV: Pharmacologic Considerations

    Having HIV and TB worsens the impact of both. The treatment of HIV-TB coinfection is beset by challenges, including drug-drug-interactions,...
    Ethel D. Weld, Alice K. Pau, ... Kelly E. Dooley in HIV and Tuberculosis
    Chapter 2019
  19. Relation of Transcriptional Factors to the Expression and Activity of Cytochrome P450 and UDP-Glucuronosyltransferases 1A in Human Liver: Co-Expression Network Analysis

    Cytochrome P450 (CYPs) and UDP-glucuronosyltransferases (UGTs) play important roles in the metabolism of exogenous and endogenous compounds. The gene...

    Shilong Zhong, Weichao Han, ... Lan Tang in The AAPS Journal
    Article 28 September 2016
  20. Pharmacogenomics in and its Influence on Pharmacokinetics

    CYP1A2 is involved to a major extent in the metabolism of several drugs (imipramine, clozapine, fluvoxamine, olanzapine, theophylline, acetaminophen,...
    Guy Montay, Jochen Maas, Roland Wesch in Drug Discovery and Evaluation: Methods in Clinical Pharmacology
    Living reference work entry 2018
Did you find what you were looking for? Share feedback.