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Peroxisome Proliferator-Activated Receptor γ Is a Target for Halogenated Analogs of Bisphenol A

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Academic year: 2021

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Figure

Figure 1. Chemical structures of BPA, TBBPA, and TCBPA.
Figure 2. Results of luciferase assays showing dose–response curves for BPA and its halogenated  analogs (TBBPA and/or TCBPA; A–G), and lower brominated analogs (monoBBPA, diBBPA, and  triBBPA; D–F), as well as MEHP, PFOA, and PFOS (G), in HGELN‑ERα (A,D),
Figure 3. Competitive inhibition of [ 3 H]‑rosiglita‑
Figure 5. Effect of halogenated BPAs on activation of human, zebrafish, and Xenopus PPARγ

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