<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu J</submitter><funding>NIH Research</funding><funding>NCRR NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>NIH Training</funding><funding>Intramural EPA</funding><pagination>279-286</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8215780</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(3)</volume><pubmed_abstract>Individual differences in cytochrome P450 (CYP) enzymes contribute to responses to drugs and environmental chemicals. The expression of CYPs is influenced by sex, age, and ethnicity. Human CYP studies are often conducted with human liver microsomes and liver cells to evaluate chemical induction and drug interactions. However, the basal or constitutive expression of CYP transcripts and enzyme activities in the intact liver are also important in our understanding of individual variation in CYPs. This study utilised 100 human liver samples to profile the constitutive expression of CYP1A2, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, 3A4, and 4A11 enzyme activity and transcript levels. The mRNA expression of the CYPs and xenobiotic receptors &lt;i>AhR&lt;/i>, &lt;i>CAR&lt;/i>, and &lt;i>PXR&lt;/i> was examined &lt;i>via&lt;/i> qPC</pubmed_abstract><journal>Xenobiotica; the fate of foreign compounds in biological systems</journal><pubmed_title>Expression of cytochrome P450 isozyme transcripts and activities in human livers.</pubmed_title><pmcid>PMC8215780</pmcid><funding_grant_id>R01 DK081461</funding_grant_id><funding_grant_id>T32 ES007079</funding_grant_id><funding_grant_id>ES-09716</funding_grant_id><funding_grant_id>R01 ES013714</funding_grant_id><funding_grant_id>EPA999999</funding_grant_id><funding_grant_id>ES-009649</funding_grant_id><funding_grant_id>ES-07079</funding_grant_id><funding_grant_id>RR-021940</funding_grant_id><funding_grant_id>ES-013714</funding_grant_id><funding_grant_id>P20 RR021940</funding_grant_id><funding_grant_id>R01 ES009716</funding_grant_id><funding_grant_id>DK-081461</funding_grant_id><funding_grant_id>R01 ES009649</funding_grant_id><pubmed_authors>Lu YF</pubmed_authors><pubmed_authors>Klaassen CD</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Corton JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Expression of cytochrome P450 isozyme transcripts and activities in human livers.</name><description>Individual differences in cytochrome P450 (CYP) enzymes contribute to responses to drugs and environmental chemicals. The expression of CYPs is influenced by sex, age, and ethnicity. Human CYP studies are often conducted with human liver microsomes and liver cells to evaluate chemical induction and drug interactions. However, the basal or constitutive expression of CYP transcripts and enzyme activities in the intact liver are also important in our understanding of individual variation in CYPs. This study utilised 100 human liver samples to profile the constitutive expression of CYP1A2, 2B6, 2C8, 2C9, 2C19, 2D6, 2E1, 3A4, and 4A11 enzyme activity and transcript levels. The mRNA expression of the CYPs and xenobiotic receptors &lt;i>AhR&lt;/i>, &lt;i>CAR&lt;/i>, and &lt;i>PXR&lt;/i> was examined &lt;i>via&lt;/i> qPC</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2025-04-04T10:16:02.294Z</modification><creation>2025-04-04T10:16:02.294Z</creation></dates><accession>S-EPMC8215780</accession><cross_references><pubmed>33350342</pubmed><doi>10.1080/00498254.2020.1867929</doi></cross_references></HashMap>