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Journal Abstract Search

133 related items for PubMed ID: 11042095

  • 1. Metabolism and disposition of bisphenol A in female rats.
    Snyder RW, Maness SC, Gaido KW, Welsch F, Sumner SC, Fennell TR.
    Toxicol Appl Pharmacol; 2000 Nov 01; 168(3):225-34. PubMed ID: 11042095
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  • 2. Disposition of low doses of 14C-bisphenol A in male, female, pregnant, fetal, and neonatal rats.
    Kurebayashi H, Nagatsuka S, Nemoto H, Noguchi H, Ohno Y.
    Arch Toxicol; 2005 May 01; 79(5):243-52. PubMed ID: 15902421
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  • 3. Disposition of a low dose of 14C-bisphenol A in male rats and its main biliary excretion as BPA glucuronide.
    Kurebayashi H, Betsui H, Ohno Y.
    Toxicol Sci; 2003 May 01; 73(1):17-25. PubMed ID: 12700409
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  • 4. Age and dose dependency of the pharmacokinetics and metabolism of bisphenol A in neonatal sprague-dawley rats following oral administration.
    Domoradzki JY, Thornton CM, Pottenger LH, Hansen SC, Card TL, Markham DA, Dryzga MD, Shiotsuka RN, Waechter JM.
    Toxicol Sci; 2004 Feb 01; 77(2):230-42. PubMed ID: 14691203
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  • 6. Metabolism and pharmacokinetics of bisphenol A (BPA) and the embryo-fetal distribution of BPA and BPA-monoglucuronide in CD Sprague-Dawley rats at three gestational stages.
    Domoradzki JY, Pottenger LH, Thornton CM, Hansen SC, Card TL, Markham DA, Dryzga MD, Shiotsuka RN, Waechter JM.
    Toxicol Sci; 2003 Nov 01; 76(1):21-34. PubMed ID: 12915710
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  • 12. Species difference of metabolic clearance of bisphenol A using cryopreserved hepatocytes from rats, monkeys and humans.
    Kurebayashi H, Okudaira K, Ohno Y.
    Toxicol Lett; 2010 Oct 05; 198(2):210-5. PubMed ID: 20599483
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  • 13. Bisphenol a glucuronide, a major metabolite in rat bile after liver perfusion.
    Inoue H, Yokota H, Makino T, Yuasa A, Kato S.
    Drug Metab Dispos; 2001 Aug 05; 29(8):1084-7. PubMed ID: 11454725
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  • 17. Excretion of bisphenol A into rat milk.
    Okabayashi K, Watanabe T.
    Toxicol Mech Methods; 2010 Mar 05; 20(3):133-6. PubMed ID: 20163291
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  • 18. The relative bioavailability and metabolism of bisphenol A in rats is dependent upon the route of administration.
    Pottenger LH, Domoradzki JY, Markham DA, Hansen SC, Cagen SZ, Waechter JM.
    Toxicol Sci; 2000 Mar 05; 54(1):3-18. PubMed ID: 10746927
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  • 19. Evaluation of oral and intravenous route pharmacokinetics, plasma protein binding, and uterine tissue dose metrics of bisphenol A: a physiologically based pharmacokinetic approach.
    Teeguarden JG, Waechter JM, Clewell HJ, Covington TR, Barton HA.
    Toxicol Sci; 2005 Jun 05; 85(2):823-38. PubMed ID: 15746009
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