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1.
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2021/11
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Article
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Direct evidence of edge-to-face CH/π interaction for PAR-1 thrombin receptor activation Bioorganic & Medicinal Chemistry 51,pp.116498 (Collaboration)
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2.
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2021/04
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Article
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ERα-agonist and ERβ-antagonist bifunctional next-generation bisphenols with no halogens: BPAP, BPB, and BPZ Toxicology Letters 345,pp.24-33 (Collaboration)
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3.
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2021/02
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Article
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Bisphenol-C is the strongest bifunctional ERα-agonist and ERβ-antagonist due to magnified halogen bonding PLoS ONE 16(2),pp.e0246583 (Collaboration)
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4.
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2020/02
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Article
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Evaluation of the influence of halogenation on the binding of bisphenol A to the estrogen-related receptor γ Chemical Research in Toxicology 33(4),pp.889-902 (Collaboration)
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5.
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2019/12
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Article
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Bisphenol AF: Halogen bonding is a major driving force for the dual ERα-agonist and ERβ-antagonist activities Bioorganic & Medicinal Chemistry 28(3),pp.115274 (Collaboration)
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6.
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2019/07
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Article
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Discovery of novel oestrogen receptor α agonists and antagonists by screening a revisited privileged structure moiety for nuclear receptors. Scientific reports 9(1),pp.9954 (Collaboration)
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7.
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2019/06
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Article
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Receptor-binding affinities of bisphenol A and its next-generation analogs for human nuclear receptors. Toxicology and applied pharmacology 377,pp.114610 (Collaboration)
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8.
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2019/03
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Other
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Evaluation of the binding ability of an orphan nuclear receptor nurr1 to synthetic peptides. Peptide Science 2018 2018,pp.133 (Collaboration)
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9.
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2018/03
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Other
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Homodimer function of human nuclear receptor ERRγ evidenced using α-helix peptides in the dimer interface. Peptide Science 2017 pp.190-191 (Collaboration)
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10.
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2018/03
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Other
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Mutual co-work between nuclear receptor ERα and ERRα requires their homodimerization. Peptide Science 2017 pp.198-199 (Collaboration)
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11.
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2018/03
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Other
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Phe2715.39 of thrombin receptor PAR-1 is a specific target of Phe-2-phenyl group of its tethered ligand. Peptide Science 2017 pp.94-95 (Collaboration)
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12.
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2017/10
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Article
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Design and synthesis of benzoacridines as estrogenic and anti-estrogenic agents. Bioorganic & medicinal chemistry 25(20),pp.5216-5237 (Collaboration)
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13.
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2017/08
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Article
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α-Helix-peptides composing the human nuclear receptor ERRγ competitively provoke inhibition of functional homomeric dimerization. — Bisphenol A receptor ERRγ physiologically functions as homodimer. Biomedical Advances pp.ep-20178-10 (Collaboration)
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14.
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2017/03
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Other
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Docking simulation to elucidated the labeled cysteine residue of the nociception receptor ORL1 using a Cys(Npys)-containing peptide ligand. Peptide Science 2016 pp.87-88 (Collaboration)
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15.
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2016/11
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Article
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Specific affinity-labeling of the nociceptin ORL1 receptor using a thiol-activated Cys(Npys)-containing peptide ligand. Biopolymers: Peptide Science 106(4),pp.460-469 (Collaboration)
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16.
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2016/11
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Article
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α-Helix-peptides comprising the human nuclear receptor ERRγ competitively provoke inhibition of functional homomeric dimerization. Biopolymers: Peptide Science 106(4),pp.547-554 (Collaboration)
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17.
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2016/03
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Other
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Comparative analysis of the ligand binding domain secondary structures of human nuclear receptors. Peptide Science 2015 pp.337-338 (Collaboration)
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18.
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2016/03
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Other
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Comprehensive structural analysis of the nociception ORL1 receptor by means of virtual and experimental Ala-scanning combinated methods. Peptide Science 2015 pp.149-150 (Collaboration)
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19.
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2016/03
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Other
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Do the estrogen receptors function as a homodimer? Experimental validation of homodimerization by inhibitory peptides. Peptide Science 2015 pp.335-336 (Collaboration)
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20.
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2016/03
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Other
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Expression analysis of neuropeptide pdf mRNA in the hypoactive and hyperactive fruit flies Drosophila melanogaster. Peptide Science 2015 pp.317-318 (Collaboration)
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21.
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2016/03
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Other
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Functional role of the Phe-Phe stacking microswitch in the ORL1 nociceptin receptor activation. Peptide Science 2015 pp.147-148 (Collaboration)
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22.
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2016/03
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Other
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ORL1 nociceptin receptor response of opioid peptides derived from proenkephalin precursor protein. Peptide Science 2015 pp.181-182 (Collaboration)
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23.
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2016/03
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Other
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Protein constitutive peptide fragments to inhibit protein-protein interaction: Inhibitory peptides as molecular probe for clarification of human nuclear receptor activation mechanism. Peptide Science 2015 pp.319-320 (Collaboration)
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24.
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2015/03
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Other
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A novel method to identify and quantify the coactivator proteins that couple with human nuclear receptor: The use of interacting interface α-helix peptide for quantitative inhibition. Peptide Science 2014 pp.349-350 (Collaboration)
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25.
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2015/03
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Other
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Bisphenol A-induced substantial peak decay of Drosophila circadian neuropeptide hugin mRNA expression. Peptide Science 2014 pp.41-42 (Collaboration)
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26.
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2015/03
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Other
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GPCR functional role of Phe-269 and Phe-221 in the molecular switching of ORL1 nociceptin receptor activation. Peptide Science 2014 pp.203-204 (Collaboration)
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27.
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2015/03
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Other
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Structural and molecular evolutionary analysis of the ligand-binding domain of forty-eight human nuclear receptors. Peptide Science 2014 pp.347-348 (Collaboration)
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28.
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2015/03
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Other
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The molecular switching of ORL1 nociceptin receptor in activation/ inactivation. Peptide Science 2014 pp.201-202 (Collaboration)
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29.
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2014/06
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Article
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A characteristic back support structure in the bisphenol A-binding pocket in the human nuclear receptor ERRγ. PloS one 9(6),pp.e101252 (Collaboration)
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30.
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2014/03
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Other
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Bisphenol A- induced epigenetic mutations in circadian pacemaker neuropeptide mRNAs of hyperactive Drosophila fruit flies. Peptide Science 2013 pp.457-458 (Collaboration)
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31.
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2014/03
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Other
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Constitutive α-helix-peptides required for functional dimerization of estrogen-related receptor γ (ERRγ). Peptide Science 2013 pp.429-430 (Collaboration)
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32.
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2014/03
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Other
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Expression and mutation analyses of brain neuropeptide genes of endocrine-disrupting bisphenol A-exposed hypoactive mouse. Peptide Science 2013 pp.453-454 (Collaboration)
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33.
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2014/03
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Other
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Influence analysis of the circadian evening pacemaker neuropeptide hugγ gene in the bisphenol A-exposed fruit fly Drosophila brain. Peptide Science 2013 pp.455-456 (Collaboration)
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34.
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2014/03
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Other
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Three-dimensional docking modeling to human nuclear receptors for exploration of bisphenol-A targeting receptors. Peptide Science 2013 pp.459-460 (Collaboration)
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35.
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2013/03
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Other
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Bisphenol-binding pocket of constitutively active nuclear receptor CAR: Docking modeling for close-packing. Peptide Science 2012 pp.401-402 (Collaboration)
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36.
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2013/03
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Other
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The impact of bisphenol A-feeding on the Drosophila neuropeptide PDF mRNA structure. Peptide Science 2012 pp.75-76 (Collaboration)
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37.
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2012/04
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Article
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Fine spatial assembly for construction of the phenol-binding pocket to capture bisphenol A in the human nuclear receptor estrogen-related receptor γ. Journal of biochemistry 151(4),pp.403-415 (Collaboration)
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38.
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2010/09
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Article
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Bisphenol AF is a full agonist for the estrogen receptor ERalpha but a highly specific antagonist for ERbeta. Environmental health perspectives 118(9),pp.1267-1272 (Collaboration)
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39.
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2010/08
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Article
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Distinction of the binding modes for human nuclear receptor ERRgamma between bisphenol A and 4-hydroxytamoxifen. Journal of biochemistry 148(2),pp.247-254 (Collaboration)
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40.
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2010/03
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Other
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Functional role of the C-terminal helix 12 peptide in the receptor activation mechanism of estrogen-related receptor γ (ERRγ). Peptide Science 2009 pp.435-436 (Collaboration)
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41.
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2009/07
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Article
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Placenta expressing the greatest quantity of bisphenol A receptor ERR{gamma} among the human reproductive tissues: Predominant expression of type-1 ERRgamma isoform. Journal of biochemistry 146(1),pp.113-122 (Collaboration)
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42.
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2009/03
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Other
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Bisphenol A-specific nuclear receptor ERRγ: Structure-function analysis of the two novel isoforms lacking vital peptide fragment in the ligand binding domain. Peptide Science 2008 pp.517-518 (Collaboration)
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43.
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2009/03
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Other
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Induced-fit type ligand binding guided by free-rotatory Leu residue present in the 7th α-helix peptide in the estrogen-related receptor γ (ERRγ). Peptide Science 2008 pp.521-522 (Collaboration)
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44.
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2008/08
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Article
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ERRgamma tethers strongly bisphenol A and 4-alpha-cumylphenol in an induced-fit manner. Biochemical and biophysical research communications 373(3),pp.408-413 (Collaboration)
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45.
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2008/03
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Other
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The conformation change-sensing antibodies for retinoid-related orphan receptor family. Peptide Science 2007 pp.491-492 (Collaboration)
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46.
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2008/01
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Article
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Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma. Environmental health perspectives 116(1),pp.32-38 (Collaboration)
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47.
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2007/12
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Article
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Receptor binding characteristics of the endocrine disruptor bisphenol A for the human nuclear estrogen-related receptor gamma. Chief and corroborative hydrogen bonds of the bisphenol A phenol-hydroxyl group with Arg316 and Glu275 residues. The FEBS journal 274(24),pp.6340-6351 (Collaboration)
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48.
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2007/10
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Article
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Structural evidence for endocrine disruptor bisphenol A binding to human nuclear receptor ERR gamma. Journal of biochemistry 142(4),pp.517-524 (Collaboration)
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49.
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2007/03
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Other
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Conformation change of α-helix peptide for sensing of deactivation of nuclear receptor: Immunoassay using polyclonal antibody specific for the C-terminal α-helix 12 of estrogen-related receptor γ (ERRγ). Peptide Science 2006 pp.176 (Collaboration)
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50.
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2006/12
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Article
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Endocrine disruptor bisphenol A strongly binds to human estrogen-related receptor gamma (ERRgamma) with high constitutive activity. Toxicology letters 167(2),pp.95-105 (Collaboration)
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51.
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2005/03
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Other
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Structural characteristics of Drosophila estrogen-related receptor ligand binding domain to capture the peptide and non-peptide ligands. Peptide Science 2004 pp.303-304 (Collaboration)
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52.
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2003/10
|
Article
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Molecular cloning and circadian expression profile of insect neuropeptide PDF in black blowfly, Phormia regina. Letter in Peptide Science 10,pp.419-430 (Collaboration)
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