B. Astroff

发表

A nonlethal young domesticated ferret (Mustela putorius furo) model for studying pandemic influenza virus A/California/04/2009 (H1N1).

J. Lednicky, C. Croutch, Sara B Hamilton, 2010, Comparative medicine.

6-Methyl-1,3,8-trichlorodibenzofuran (MCDF) as a 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonist in C57BL/6 mice.

S. Safe, D. Davis, L. Biegel, 1989, Toxicology.

6-substituted-1,3,8-trichlorodibenzofurans as 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonists in the rat: structure activity relationships.

S. Safe, B. Astroff, 1989, Toxicology.

Mechanism of action of 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonists: characterization of 6-[125I]methyl-8-iodo-1,3-dichlorodibenzofuran-Ah receptor complexes.

J. Piskorska-Pliszczynska, S. Safe, T. Zacharewski, 1991, Archives of biochemistry and biophysics.

Partial antagonism of 2,3,7,8-tetrachlorodibenzo-p-dioxin-mediated induction of aryl hydrocarbon hydroxylase by 6-methyl-1,3,8-trichlorodibenzofuran: mechanistic studies.

S. Safe, T. Zacharewski, M. Harris, 1989, Molecular pharmacology.

Pharmacokinetics of doxorubicin loaded and glutaraldehyde treated erythrocytes in healthy and lymphoma bearing dogs.

M. Tonetti, L. Rowe, W. Satterfield, 1992, Advances in experimental medicine and biology.

2,3,7,8-Tetrachlorodibenzo-p-dioxin inhibition of 17 beta-estradiol-induced increases in rat uterine epidermal growth factor receptor binding activity and gene expression.

S. Safe, B. Astroff, C. Rowlands, 1990, Molecular and cellular endocrinology.

Construction and characterization of adriamycin‐loaded canine red blood cells as a potential slow delivery system

M. Tonetti, U. Benatti, A. Flora, 1990, Biotechnology and applied biochemistry.

Inhibition of the 17 beta-estradiol-induced and constitutive expression of the cellular protooncogene c-fos by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in the female rat uterus.

S. Safe, B. Eldridge, B. Astroff, 1991, Toxicology letters.

2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) and related compounds as antioestrogens: characterization and mechanism of action.

M. Romkes, S. Safe, T. Zacharewski, 1991, Pharmacology & toxicology.

6-Methyl-1,3,8-trichlorodibenzofuran as a 2,3,7,8-tetrachlorodibenzo-p-dioxin antagonist: inhibition of the induction of rat cytochrome P-450 isozymes and related monooxygenase activities.

M. P. Arlotto, S. Safe, T. Zacharewski, 1988, Molecular pharmacology.

2,3,7,8-Tetrachlorodibenzo-p-dioxin as an antiestrogen: effect on rat uterine peroxidase activity.

S. Safe, B. Astroff, 1990, Biochemical pharmacology.

6-Alkyl-1,3,8-trichlorodibenzofurans as antiestrogens in female Sprague-Dawley rats.

S. Safe, B. Astroff, 1991, Toxicology.

2,3,7,8-Tetrachlorodibenzo-p-dioxin inhibition of 17β-estradiol-induced increases in rat uterine epidermal growth factor receptor binding activity and gene expression

S. Safe, B. Astroff, C. Rowlands, 1990, Molecular and Cellular Endocrinology.

Comparative antiestrogenic activities of 2,3,7,8-tetrachlorodibenzo-p-dioxin and 6-methyl-1,3,8-trichlorodibenzofuran in the female rat.

S. Safe, B. Astroff, 1988, Toxicology and applied pharmacology.

Mechanism of action of 2,3,7,8-tcdd and 6-methyl-1,3,8-trichlorodibenzofuran (MCDF) as antiestrogens in the female rat

M. Romkes, S. Safe, B. Astroff, 1989 .