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Inhibition of estrogen-induced progesterone receptor in MCF-7 human breast cancer cells by aryl hydrocarbon (Ah) receptor agonists.
Harper N, Wang X, Liu H, Safe S. Harper N, et al. Mol Cell Endocrinol. 1994 Aug;104(1):47-55. doi: 10.1016/0303-7207(94)90050-7. Mol Cell Endocrinol. 1994. PMID: 7821706
For a series of halogenated aromatics including 2,3,7,8- and 1,2,7,8-tetrachlorodibenzofuran, 1,3,7,8-TCDD and 6-methyl-1,3,8-trichlorodibenzofuran, their rank order potency for inhibiting E2-induced PR binding paralleled their rank order …
For a series of halogenated aromatics including 2,3,7,8- and 1,2,7,8-tetrachlorodibenzofuran, 1,3, …
Characterization of the molecular and structural properties of the transformed and nuclear aryl hydrocarbon (Ah) receptor complexes by proteolytic digestion.
Santostefano M, Safe S. Santostefano M, et al. Chem Biol Interact. 1996 May 6;100(3):221-40. doi: 10.1016/0009-2797(96)03701-5. Chem Biol Interact. 1996. PMID: 8653805
The results showed that for several different AhR ligands including 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 2,3,7,8-tetrachlorodibenzofuran, 1,2,7,8-tetrachlorodibenzofuran and alpha-naphthoflavone, the pattern of degrad …
The results showed that for several different AhR ligands including 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 2,3,7,8-tet …