Comparison of the susceptibility of wild-type and CYP2E1 knockout mice to the hepatotoxic and pneumotoxic effects of styrene and styrene oxide
Author:
Publisher
Elsevier BV
Subject
Toxicology,General Medicine
Reference20 articles.
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2. Comparison of mouse strains for susceptibility to styrene-induced hepatotoxicity and pneumotoxicity;Carlson;J. Toxicol. Environ. Health Part A,1997
3. Effects of inducers and inhibitors on the microsomal metabolism of styrene to styrene oxide in mice;Carlson;J. Toxicol. Environ. Health Part A,1997
4. In vitro metabolism of styrene to styrene oxide in liver and lung of CYP2E1 knockout mice;Carlson;J. Toxicol. Environ. Health,2003
5. A comprehensive evaluation of the potential health risks associated with occupational and environmental exposure to styrene;Cohen;J. Toxicol. Environ. Health Part B,2002
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2. Lung disease associated with occupational styrene exposure;American Journal of Industrial Medicine;2018-06-13
3. Assessing molecular initiating events (MIEs), key events (KEs) and modulating factors (MFs) for styrene responses in mouse lungs using whole genome gene expression profiling following 1-day and multi-week exposures;Toxicology and Applied Pharmacology;2017-11
4. Editor’s Highlight: Complete Attenuation of Mouse Lung Cell Proliferation and Tumorigenicity in CYP2F2 Knockout and CYP2F1 Humanized Mice Exposed to Inhaled Styrene for up to 2 Years Supports a Lack of Human Relevance;Toxicological Sciences;2017-07-13
5. Risk assessments for chronic exposure of children and prospective parents to ethylbenzene (CAS No. 100-41-4);Critical Reviews in Toxicology;2015-05-21
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