Large effects from small exposures. III. Endocrine mechanisms mediating effects of bisphenol A at levels of human exposure.
By W. Welshons, Susan C. Nagel, F. V. vom Saal. Endocrinology, 2006
1,021 citations recorded by the source corpus.
Subfields: Health, Toxicology and Mutagenesis, Pollution
View Paper: https://www.semanticscholar.org/paper/1a7f8708a3e5fef35f3e4b2850358ad558cdf780
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Citations in the corpus
- In vivo effects of bisphenol A in laboratory rodent studies. (2007, background): “However, effects of BPA mediated by binding to androen and thyroid hormone receptors appear to require higher oses than those required to elicit estrogenic or antiestrogenic esponses [7].”
- Endocrine disrupting chemicals: exposure, effects on human health, mechanism of action, models for testing and strategies for prevention (2019, background): “Why some EDCs produce non-traditional dose-response curves is not understood [216].”
- In vitro molecular mechanisms of bisphenol A action. (2007, neutral): “, that BPA is a SERM [4].”
- Urinary, Circulating, and Tissue Biomonitoring Studies Indicate Widespread Exposure to Bisphenol A (2010, neutral): “It is also found in papers and in implanted medical devices and other medical equipment (Welshons et al. 2006).”
- Chapel Hill bisphenol A expert panel consensus statement: integration of mechanisms, effects in animals and potential to impact human health at current levels of exposure. (2007, background): “While BPA was initially considered to be a “weak” estrogen based on a lower affinity for estrogen receptor alpha relative to estradiol [18], research shows that BPA is equipotent with estradiol in its ability activate responses via recently discovered estrogen receptors associated with the cell memb”
- Endocrine-disrupting chemicals and public health protection: a statement of principles from The Endocrine Society. (2012, background): “BPA also produces significant effects in the adult, with some of the effects being mediated by the ER (57) and others by ER (58).”
- Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses. (2012, neutral): “In the multitude of chemicals that have never been tested at low doses, or in the development of new chemicals, to determine whether a chemical has low-dose effects in laboratory animals, we suggest setting the NOAEL or LOAEL from traditional toxicological studies as the highest dose in experiments ”
- Human exposure to bisphenol A (BPA). (2007, background): “[6] Welshons WV, Nagel SC, vom Saal FS.”