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Atomic structure of progesterone complexed with its receptor.
Williams SP, Sigler PB. Williams SP, et al. Nature. 1998 May 28;393(6683):392-6. doi: 10.1038/30775. Nature. 1998. PMID: 9620806
The human nuclear xenobiotic receptor PXR: structural determinants of directed promiscuity.
Watkins RE, Wisely GB, Moore LB, Collins JL, Lambert MH, Williams SP, Willson TM, Kliewer SA, Redinbo MR. Watkins RE, et al. Among authors: williams sp. Science. 2001 Jun 22;292(5525):2329-33. doi: 10.1126/science.1060762. Epub 2001 Jun 14. Science. 2001. PMID: 11408620
Rational design of orally-active, pyrrolidine-based progesterone receptor partial agonists.
Thompson SK, Washburn DG, Frazee JS, Madauss KP, Hoang TH, Lapinski L, Grygielko ET, Glace LE, Trizna W, Williams SP, Duraiswami C, Bray JD, Laping NJ. Thompson SK, et al. Among authors: williams sp. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4777-80. doi: 10.1016/j.bmcl.2009.06.055. Epub 2009 Jun 17. Bioorg Med Chem Lett. 2009. PMID: 19595590
The evolution of progesterone receptor ligands.
Madauss KP, Stewart EL, Williams SP. Madauss KP, et al. Among authors: williams sp. Med Res Rev. 2007 May;27(3):374-400. doi: 10.1002/med.20083. Med Res Rev. 2007. PMID: 17013809 Review.
A structural and in vitro characterization of asoprisnil: a selective progesterone receptor modulator.
Madauss KP, Grygielko ET, Deng SJ, Sulpizio AC, Stanley TB, Wu C, Short SA, Thompson SK, Stewart EL, Laping NJ, Williams SP, Bray JD. Madauss KP, et al. Among authors: williams sp. Mol Endocrinol. 2007 May;21(5):1066-81. doi: 10.1210/me.2006-0524. Epub 2007 Mar 13. Mol Endocrinol. 2007. PMID: 17356170
Structure of Rev-erbalpha bound to N-CoR reveals a unique mechanism of nuclear receptor-co-repressor interaction.
Phelan CA, Gampe RT Jr, Lambert MH, Parks DJ, Montana V, Bynum J, Broderick TM, Hu X, Williams SP, Nolte RT, Lazar MA. Phelan CA, et al. Among authors: williams sp. Nat Struct Mol Biol. 2010 Jul;17(7):808-14. doi: 10.1038/nsmb.1860. Epub 2010 Jun 27. Nat Struct Mol Biol. 2010. PMID: 20581824 Free PMC article.
A human fatty acid synthase inhibitor binds β-ketoacyl reductase in the keto-substrate site.
Hardwicke MA, Rendina AR, Williams SP, Moore ML, Wang L, Krueger JA, Plant RN, Totoritis RD, Zhang G, Briand J, Burkhart WA, Brown KK, Parrish CA. Hardwicke MA, et al. Among authors: williams sp. Nat Chem Biol. 2014 Sep;10(9):774-9. doi: 10.1038/nchembio.1603. Epub 2014 Aug 3. Nat Chem Biol. 2014. PMID: 25086508
A ligand-mediated hydrogen bond network required for the activation of the mineralocorticoid receptor.
Bledsoe RK, Madauss KP, Holt JA, Apolito CJ, Lambert MH, Pearce KH, Stanley TB, Stewart EL, Trump RP, Willson TM, Williams SP. Bledsoe RK, et al. Among authors: williams sp. J Biol Chem. 2005 Sep 2;280(35):31283-93. doi: 10.1074/jbc.M504098200. Epub 2005 Jun 20. J Biol Chem. 2005. PMID: 15967794
Progesterone receptor ligand binding pocket flexibility: crystal structures of the norethindrone and mometasone furoate complexes.
Madauss KP, Deng SJ, Austin RJ, Lambert MH, McLay I, Pritchard J, Short SA, Stewart EL, Uings IJ, Williams SP. Madauss KP, et al. Among authors: williams sp. J Med Chem. 2004 Jun 17;47(13):3381-7. doi: 10.1021/jm030640n. J Med Chem. 2004. PMID: 15189034
The first X-ray crystal structure of the glucocorticoid receptor bound to a non-steroidal agonist.
Madauss KP, Bledsoe RK, Mclay I, Stewart EL, Uings IJ, Weingarten G, Williams SP. Madauss KP, et al. Among authors: williams sp. Bioorg Med Chem Lett. 2008 Dec 1;18(23):6097-9. doi: 10.1016/j.bmcl.2008.10.021. Epub 2008 Oct 8. Bioorg Med Chem Lett. 2008. PMID: 18952422
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