Results 131 to 140 of about 8,876 (157)

Integrative Single-Cell and Bulk Transcriptomic Analysis Identifies Macrophage-Related Gene Signatures Predictive of Hepatocellular Carcinoma in Cirrhosis. [PDF]

Genes (Basel)
Zhang Z, Zeng C, Yong X, Zhou W, Xie Y, Shu J.   +5 more
europepmc   +1 more source

Distinct Single-Cell Expression Pattern of the Soluble Epoxide Hydrolase and Cytochrome p450 Epoxygenases in Human and Mouse Small Intestinal Epithelia. [PDF]

J Histochem Cytochem
Sun L, Tang A, Liao J, Yang GY.
europepmc   +1 more source

Nutrient environment improves drug metabolic activity in human iPSC-derived hepatocytes and HepG2. [PDF]

Arch Toxicol
Pozo Garcia V, Çobanoğlu TS, Hammer HS, Carlota R, Holm K, Verfaillie C, Poetz O, Jennings P, Moco S.   +8 more
europepmc   +1 more source

Transcription factors of the Nuclear Factor I (NFI) family control hepatocyte differentiation and cytochrome P450 activity in human liver.

Pharmacol Res
Klein K, Burk O, Tremmel R, Buettner FA, Kaestle L, Schroth W, Muerdter TE, Eccles D, Schmidt AC, Nieß H, Zanger UM, Schwab M, Lauschke VM.   +12 more
europepmc   +1 more source

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Interplay of UDP-Glucuronosyltransferase and CYP2C8 for CYP2C8 Mediated Drug Oxidation and Its Impact on Drug–Drug Interaction Produced by Standardized CYP2C8 Inhibitors, Clopidogrel and Gemfibrozil

Clinical Pharmacokinetics, 2023
Early investigations into drug-drug interactions (DDIs) involving cytochrome P450 2C8 (CYP2C8) have highlighted the complexity of interactions between CYP2C8 substrate drugs, including montelukast, desloratadine, pioglitazone, repaglinide, and cerivastatin (the latter two being OATP1B1 substrates), and standardized CYP2C8 inhibitors such as clopidogrel
Katsumi Iga, Akiko Kiriyama
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CYP2C8 polymorphism among the Portuguese

Clinical Chemistry and Laboratory Medicine (CCLM), 2006
AbstractCytochrome P450 2C8 (CYP2C8) is a polymorphic phase I drug-metabolising enzyme involved in the metabolism of a wide variety of xenobiotics, as well as a proposed player in the regulation of vascular tone. Polymorphisms in this gene may have an impact on the metabolism of therapeutic drugs such as paclitaxel and verapamil. In this report we have
Isa, Cavaco, Rita, Piedade, J Pedro, Gil, Vera, Ribeiro   +3 more
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Evaluation of CYP2C8 Inhibition In Vitro: Utility of Montelukast as a Selective CYP2C8 Probe Substrate

Drug Metabolism and Disposition, 2011
Understanding the potential for cytochrome P450 (P450)-mediated drug-drug interactions is a critical step in the drug discovery process. Although in vitro studies with CYP3A4, CYP2C9, and CYP2C19 have suggested the presence of multiple binding regions within the P450 active site based on probe substrate-dependent inhibition profiles, similar studies ...
Brooke M, VandenBrink, Robert S, Foti, Dan A, Rock, Larry C, Wienkers, Jan L, Wahlstrom   +4 more
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GENETIC POLYMORPHISMS OF CYP2C8 IN JAPANESE POPULATION

Drug Metabolism and Disposition, 2003
CYP2C8 plays important roles in metabolizing therapeutic drugs and endogenous compounds. Although genetic polymorphisms of CYP2C8 were reported, there is little information on CYP2C8 polymorphisms in the Japanese population. In the present study, we screened for previously described polymorphisms in the coding region of this gene using polymerase chain
Miki, Nakajima, Yuto, Fujiki, Kumiko, Noda, Hiroki, Ohtsuka, Hisashi, Ohkuni, Satoru, Kyo, Masaki, Inoue, Yukio, Kuroiwa, Tsuyoshi, Yokoi   +8 more
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In Silico Prediction of CYP2C8 Inhibition with Machine-Learning Methods

Chemical Research in Toxicology, 2021
Cytochrome P450 2C8 (CYP2C8) is a major drug-metabolizing enzyme in humans and is responsible for the metabolism of ∼5% drugs in clinical use. Thus, inhibition of CYP2C8, which causes potential adverse drug events, cannot be neglected. The in vitro drug interaction studies guidelines for industry issued by the FDA also point out that it needs to be ...
Xiaoxiao Zhang, Piaopiao Zhao, Zhiyuan Wang, Xuan Xu, Guixia Liu, Yun Tang, Weihua Li   +6 more
openaire   +2 more sources