These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
246 related articles for article (PubMed ID: 7854352)
1. A third transactivation function (AF3) of human progesterone receptors located in the unique N-terminal segment of the B-isoform. Sartorius CA; Melville MY; Hovland AR; Tung L; Takimoto GS; Horwitz KB Mol Endocrinol; 1994 Oct; 8(10):1347-60. PubMed ID: 7854352 [TBL] [Abstract][Full Text] [Related]
2. Antagonist-occupied human progesterone B-receptors activate transcription without binding to progesterone response elements and are dominantly inhibited by A-receptors. Tung L; Mohamed MK; Hoeffler JP; Takimoto GS; Horwitz KB Mol Endocrinol; 1993 Oct; 7(10):1256-65. PubMed ID: 8123133 [TBL] [Abstract][Full Text] [Related]
3. Role of phosphorylation on DNA binding and transcriptional functions of human progesterone receptors. Takimoto GS; Hovland AR; Tasset DM; Melville MY; Tung L; Horwitz KB J Biol Chem; 1996 Jun; 271(23):13308-16. PubMed ID: 8662865 [TBL] [Abstract][Full Text] [Related]
4. Functional properties of the N-terminal region of progesterone receptors and their mechanistic relationship to structure. Takimoto GS; Tung L; Abdel-Hafiz H; Abel MG; Sartorius CA; Richer JK; Jacobsen BM; Bain DL; Horwitz KB J Steroid Biochem Mol Biol; 2003 Jun; 85(2-5):209-19. PubMed ID: 12943706 [TBL] [Abstract][Full Text] [Related]
5. Differential regulation of human progesterone receptor A and B form-mediated trans-activation by phosphorylation. Kazmi SM; Visconti V; Plante RK; Ishaque A; Lau C Endocrinology; 1993 Sep; 133(3):1230-8. PubMed ID: 8365365 [TBL] [Abstract][Full Text] [Related]
6. Antagonist-occupied human progesterone receptors bound to DNA are functionally switched to transcriptional agonists by cAMP. Sartorius CA; Tung L; Takimoto GS; Horwitz KB J Biol Chem; 1993 May; 268(13):9262-6. PubMed ID: 8387487 [TBL] [Abstract][Full Text] [Related]
7. An N-terminal inhibitory function, IF, suppresses transcription by the A-isoform but not the B-isoform of human progesterone receptors. Hovland AR; Powell RL; Takimoto GS; Tung L; Horwitz KB J Biol Chem; 1998 Mar; 273(10):5455-60. PubMed ID: 9488667 [TBL] [Abstract][Full Text] [Related]
8. Progesterone receptors (PR)-B and -A regulate transcription by different mechanisms: AF-3 exerts regulatory control over coactivator binding to PR-B. Tung L; Abdel-Hafiz H; Shen T; Harvell DM; Nitao LK; Richer JK; Sartorius CA; Takimoto GS; Horwitz KB Mol Endocrinol; 2006 Nov; 20(11):2656-70. PubMed ID: 16762974 [TBL] [Abstract][Full Text] [Related]
9. Mapping the unique activation function 3 in the progesterone B-receptor upstream segment. Two LXXLL motifs and a tryptophan residue are required for activity. Tung L; Shen T; Abel MG; Powell RL; Takimoto GS; Sartorius CA; Horwitz KB J Biol Chem; 2001 Oct; 276(43):39843-51. PubMed ID: 11546784 [TBL] [Abstract][Full Text] [Related]
10. Effects of hormone and cellular modulators of protein phosphorylation on transcriptional activity, DNA binding, and phosphorylation of human progesterone receptors. Beck CA; Weigel NL; Edwards DP Mol Endocrinol; 1992 Apr; 6(4):607-20. PubMed ID: 1316549 [TBL] [Abstract][Full Text] [Related]
11. New T47D breast cancer cell lines for the independent study of progesterone B- and A-receptors: only antiprogestin-occupied B-receptors are switched to transcriptional agonists by cAMP. Sartorius CA; Groshong SD; Miller LA; Powell RL; Tung L; Takimoto GS; Horwitz KB Cancer Res; 1994 Jul; 54(14):3868-77. PubMed ID: 8033109 [TBL] [Abstract][Full Text] [Related]
12. Selective down-regulation of progesterone receptor isoform B in poorly differentiated human endometrial cancer cells: implications for unopposed estrogen action. Kumar NS; Richer J; Owen G; Litman E; Horwitz KB; Leslie KK Cancer Res; 1998 May; 58(9):1860-5. PubMed ID: 9581825 [TBL] [Abstract][Full Text] [Related]
13. Agonist and antagonists induce homodimerization and mixed ligand heterodimerization of human progesterone receptors in vivo by a mammalian two-hybrid assay. Leonhardt SA; Altmann M; Edwards DP Mol Endocrinol; 1998 Dec; 12(12):1914-30. PubMed ID: 9849965 [TBL] [Abstract][Full Text] [Related]
14. The progesterone antagonist RU486 acquires agonist activity upon stimulation of cAMP signaling pathways. Beck CA; Weigel NL; Moyer ML; Nordeen SK; Edwards DP Proc Natl Acad Sci U S A; 1993 May; 90(10):4441-5. PubMed ID: 8389450 [TBL] [Abstract][Full Text] [Related]
15. Ligand-activated progesterone receptor isoform hPR-A is a stronger transactivator than hPR-B for the expression of IGFBP-1 (insulin-like growth factor binding protein-1) in human endometrial stromal cells. Gao J; Mazella J; Tang M; Tseng L Mol Endocrinol; 2000 Dec; 14(12):1954-61. PubMed ID: 11117526 [TBL] [Abstract][Full Text] [Related]
16. The opposing transcriptional activities of the two isoforms of the human progesterone receptor are due to differential cofactor binding. Giangrande PH; Kimbrel EA; Edwards DP; McDonnell DP Mol Cell Biol; 2000 May; 20(9):3102-15. PubMed ID: 10757795 [TBL] [Abstract][Full Text] [Related]
17. Human progesterone receptor A form is a cell- and promoter-specific repressor of human progesterone receptor B function. Vegeto E; Shahbaz MM; Wen DX; Goldman ME; O'Malley BW; McDonnell DP Mol Endocrinol; 1993 Oct; 7(10):1244-55. PubMed ID: 8264658 [TBL] [Abstract][Full Text] [Related]
18. Ligand-dependent cross-talk between steroid and thyroid hormone receptors. Evidence for common transcriptional coactivator(s). Zhang X; Jeyakumar M; Bagchi MK J Biol Chem; 1996 Jun; 271(25):14825-33. PubMed ID: 8662980 [TBL] [Abstract][Full Text] [Related]
19. Progesterone receptor activates its promoter activity in human endometrial stromal cells. Tang M; Mazella J; Gao J; Tseng L Mol Cell Endocrinol; 2002 Jun; 192(1-2):45-53. PubMed ID: 12088866 [TBL] [Abstract][Full Text] [Related]
20. The phosphoenolpyruvate carboxykinase gene glucocorticoid response unit: identification of the functional domains of accessory factors HNF3 beta (hepatic nuclear factor-3 beta) and HNF4 and the necessity of proper alignment of their cognate binding sites. Wang JC; Strömstedt PE; Sugiyama T; Granner DK Mol Endocrinol; 1999 Apr; 13(4):604-18. PubMed ID: 10194766 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]