Persistent, Low-Dose 2,3,7,8-Tetrachlorodibenzo-p-dioxin Exposure: Effect on Aryl Hydrocarbon Receptor Expression in a Dioxin-Resistance Model

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Toxicology and Applied Pharmacology, Vol. 175, Iss. 1, 2001-08 ,pp. : 43-53

Elsevier

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A Chimeric Aryl Hydrocarbon Receptor Knockout Mouse Model Indicates That Aryl Hydrocarbon Receptor Activation in Hematopoietic Cells Contributes to the Hepatic Lesions Induced by 2,3,7,8-Tetrachlorodibenzo-p-dioxin

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Toxicology and Applied Pharmacology, Vol. 158, Iss. 1, 1999-07 ,pp. : 33-40

Elsevier

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The Aryl Hydrocarbon Receptor Has a Role in the in Vivo Maturation of Murine Bone Marrow B Lymphocytes and Their Response to 2,3,7,8-Tetrachlorodibenzo-p-dioxin

By Thurmond T.S.   Staples J.E.   Silverstone A.E.   Gasiewicz T.A.  

Toxicology and Applied Pharmacology, Vol. 165, Iss. 3, 2000-06 ,pp. : 227-236

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Effect of 2,3,7,8-Tetrachlorodibenzo-p-dioxin on the Expression of Cytochrome P450 1A1, the Aryl Hydrocarbon Receptor, and the Aryl Hydrocarbon Receptor Nuclear Translocator in Rat Brain and Pituitary

By Huang P.   Rannug A.   Ahlbom E.   Hakansson H.   Ceccatelli S.  

Toxicology and Applied Pharmacology, Vol. 169, Iss. 2, 2000-12 ,pp. : 159-167

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Expression of the Aryl Hydrocarbon Receptor (AhR) and AhR Nuclear Translocator during Chick Cardiogenesis Is Consistent with 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Induced Heart Defects

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