Liu X - Search Results

1

The N-terminal activation function AF-1 domain of ERα interacts directly with the C-terminal AF-2-holding ligand-binding domain to recruit the coactivator proteins.

Liu X, Matsuyama Y, Sugiyama M, Suyama K, Nose T, Shimohigashi M, Shimohigashi Y. Liu X, et al. PLoS One. 2024 Oct 21;19(10):e0312276. doi: 10.1371/journal.pone.0312276. eCollection 2024. PLoS One. 2024. PMID: 39432505 Free PMC article.

2

Bisphenol AF is a full agonist for the estrogen receptor ERalpha but a highly specific antagonist for ERbeta.

Matsushima A, Liu X, Okada H, Shimohigashi M, Shimohigashi Y. Matsushima A, et al. Among authors: liu x. Environ Health Perspect. 2010 Sep;118(9):1267-72. doi: 10.1289/ehp.0901819. Epub 2010 Apr 28. Environ Health Perspect. 2010. PMID: 20427257 Free PMC article.

3

A characteristic back support structure in the bisphenol A-binding pocket in the human nuclear receptor ERRγ.

Liu X, Matsushima A, Shimohigashi M, Shimohigashi Y. Liu X, et al. PLoS One. 2014 Jun 30;9(6):e101252. doi: 10.1371/journal.pone.0101252. eCollection 2014. PLoS One. 2014. PMID: 24978476 Free PMC article.

4

Bisphenol AF: Halogen bonding effect is a major driving force for the dual ERα-agonist and ERβ-antagonist activities.

Liu X, Suyama K, Shiki J, Torikai K, Nose T, Shimohigashi M, Shimohigashi Y. Liu X, et al. Bioorg Med Chem. 2020 Feb 1;28(3):115274. doi: 10.1016/j.bmc.2019.115274. Epub 2019 Dec 18. Bioorg Med Chem. 2020. PMID: 31879182

5

Bisphenol-C is the strongest bifunctional ERα-agonist and ERβ-antagonist due to magnified halogen bonding.

Liu X, Suyama K, Nose T, Shimohigashi M, Shimohigashi Y. Liu X, et al. PLoS One. 2021 Feb 9;16(2):e0246583. doi: 10.1371/journal.pone.0246583. eCollection 2021. PLoS One. 2021. PMID: 33561155 Free PMC article.

6

ERα-agonist and ERβ-antagonist bifunctional next-generation bisphenols with no halogens: BPAP, BPB, and BPZ.

Liu X, Matsuyama Y, Shimohigashi M, Shimohigashi Y. Liu X, et al. Toxicol Lett. 2021 Jul 1;345:24-33. doi: 10.1016/j.toxlet.2021.04.001. Epub 2021 Apr 12. Toxicol Lett. 2021. PMID: 33857583

7

Endocrine disruptor bisphenol A strongly binds to human estrogen-related receptor gamma (ERRgamma) with high constitutive activity.

Takayanagi S, Tokunaga T, Liu X, Okada H, Matsushima A, Shimohigashi Y. Takayanagi S, et al. Among authors: liu x. Toxicol Lett. 2006 Dec 1;167(2):95-105. doi: 10.1016/j.toxlet.2006.08.012. Epub 2006 Sep 3. Toxicol Lett. 2006. PMID: 17049190

8

ERRgamma tethers strongly bisphenol A and 4-alpha-cumylphenol in an induced-fit manner.

Matsushima A, Teramoto T, Okada H, Liu X, Tokunaga T, Kakuta Y, Shimohigashi Y. Matsushima A, et al. Among authors: liu x. Biochem Biophys Res Commun. 2008 Aug 29;373(3):408-13. doi: 10.1016/j.bbrc.2008.06.050. Epub 2008 Jun 26. Biochem Biophys Res Commun. 2008. PMID: 18582436

9

Placenta expressing the greatest quantity of bisphenol A receptor ERR{gamma} among the human reproductive tissues: Predominant expression of type-1 ERRgamma isoform.

Takeda Y, Liu X, Sumiyoshi M, Matsushima A, Shimohigashi M, Shimohigashi Y. Takeda Y, et al. Among authors: liu x. J Biochem. 2009 Jul;146(1):113-22. doi: 10.1093/jb/mvp049. Epub 2009 Mar 20. J Biochem. 2009. PMID: 19304792

10

Distinction of the binding modes for human nuclear receptor ERRgamma between bisphenol A and 4-hydroxytamoxifen.

Liu X, Matsushima A, Okada H, Shimohigashi Y. Liu X, et al. J Biochem. 2010 Aug;148(2):247-54. doi: 10.1093/jb/mvq056. Epub 2010 Jun 11. J Biochem. 2010. PMID: 20542892

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