Bisphenol-A glucuronidation in human liver and breast: identification of UDP-glucuronosyltransferases (UGTs) and influence of genetic polymorphisms
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Title
Bisphenol-A glucuronidation in human liver and breast: identification of UDP-glucuronosyltransferases (UGTs) and influence of genetic polymorphisms
Authors
Keywords
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Journal
XENOBIOTICA
Volume 47, Issue 1, Pages 1-10
Publisher
Informa UK Limited
Online
2016-03-22
DOI
10.3109/00498254.2016.1156784
References
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- Individual Variability in the Detoxification of Carcinogenic Arylhydroxylamines in Human Breast
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- The association between TA-repeat polymorphism in the promoter region of UGT1A1 and breast cancer risk: a meta-analysis
- (2010) Lei Yao et al. BREAST CANCER RESEARCH AND TREATMENT
- Species difference of metabolic clearance of bisphenol A using cryopreserved hepatocytes from rats, monkeys and humans
- (2010) Hideo Kurebayashi et al. TOXICOLOGY LETTERS
- Genetic polymorphisms in phase I and phase II enzymes and breast cancer risk associated with menopausal hormone therapy in postmenopausal women
- (2009) BREAST CANCER RESEARCH AND TREATMENT
- Interindividual variability in hepatic drug glucuronidation: studies into the role of age, sex, enzyme inducers, and genetic polymorphism using the human liver bank as a model system
- (2009) Michael H. Court DRUG METABOLISM REVIEWS
- Human UDP-glucuronosyltransferase UGT2A2: cDNA construction, expression, and functional characterization in comparison with UGT2A1 and UGT2A3
- (2009) Nina Sneitz et al. Pharmacogenetics and Genomics
- Human UDP-glucuronosyltransferase isoforms involved in bisphenol A glucuronidation
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