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The clustering of the R-domain and Lasso motif also provides a plausible explanation for the inhibitory role of S251 phosphorylation, which is poised to disrupt the R-domain interaction network by charge repulsion (IFwide inhibitedFig
In Vitro and in Vivo Interactions of Bisphenol A and Its Metabolite, Bisphenol A Glucuronide, with Estrogen Receptors Alpha and Beta. Chemical Research in Toxicology, vol
10.1124/mol.52.6.1113 36
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