A Poland

Pharmacokinetics of [125I]-2-iodo-3,7,8-trichlorodibenzo-p-dioxin in mice: analysis with a physiological modeling approach.

D J Paustenbach, M E Andersen, H W Leung, 1990, Toxicology and applied pharmacology.

An improved assay of 7-ethoxycoumarin O-deethylase activity: induction of hepatic enzyme activity in C57BL/6J and DBA/2J mice by phenobarbital, 3-methylcholanthrene and 2,3,7,8-tetrachlorodibenzo-p-dioxin.

A Poland, W F Greenlee, A. Poland, 1978, The Journal of pharmacology and experimental therapeutics.

A competitive binding assay for 2,3,7,8-tetrachlorodibenzo-p-dioxin and related ligands of the Ah receptor.

C. Bradfield, A Poland, A. Poland, 1988, Molecular pharmacology.

Stereospecific, high affinity binding of 2,3,7,8-tetrachlorodibenzo-p-dioxin by hepatic cytosol. Evidence that the binding species is receptor for induction of aryl hydrocarbon hydroxylase.

E. Glover, A Poland, A. Poland, 1976, The Journal of biological chemistry.

2,3,7,8-tetrachlorodibenzo-p-dioxin and related halogenated aromatic hydrocarbons: examination of the mechanism of toxicity.

A Poland, A. Poland, J C Knutson, 1982, Annual review of pharmacology and toxicology.

Strong evidence from studies with brachymorphic mice and pentachlorophenol that 1'-sulfoöxysafrole is the major ultimate electrophilic and carcinogenic metabolite of 1'-hydroxysafrole in mouse liver.

E C Miller, J A Miller, J. Miller, 1983, Cancer research.

Chlorinated biphenyl induction of aryl hydrocarbon hydroxylase activity: a study of the structure-activity relationship.

E. Glover, A Poland, A. Poland, 1977, Molecular pharmacology.