Lu NZ, Wardell SE, Burnstein KL, Defranco D, Fuller PJ, Giguere V, Hochberg RB, McKay L, Renoir JM, Weigel NL, Wilson EM, McDonnell DP, Cidlowski JA (2006). „International Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: glucocorticoid, mineralocorticoid, progesterone, and androgen receptors”. Pharmacol Revl. 58 (4): 782—97. PMID17132855. doi:10.1124/pr.58.4.9. [Free full text]
Rhen T, Cidlowski JA (2005). „Antiinflammatory action of glucocorticoids--new mechanisms for old drugs”. N. Engl. J. Med. 353 (16): 1711—23. PMID16236742. doi:10.1056/NEJMra050541.
Hollenberg SM, Weinberger C, Ong ES, Cerelli G, Oro A, Lebo R, Thompson EB, Rosenfeld MG, Evans RM (1985). „Primary structure and expression of a functional human glucocorticoid receptor cDNA”. Nature. 318 (6047): 635—41. PMID2867473. doi:10.1038/318635a0.
Mendonca B, Leite M, de Castro M, Kino T, Elias L, Bachega T, Arnhold I, Chrousos G, Latronico A (2002). „Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene”. J Clin Endocrinol Metab. 87 (4): 1805—9. PMID11932321. doi:10.1210/jc.87.4.1805.
Kullmann M, Schneikert J, Moll J, Heck S, Zeiner M, Gehring U, Cato AC (1998). „RAP46 is a negative regulator of glucocorticoid receptor action and hormone-induced apoptosis”. J. Biol. Chem. 273 (23): 14620—5. PMID9603979. doi:10.1074/jbc.273.23.14620.
Boruk M, Savory JG, Haché RJ (1998). „AF-2-dependent potentiation of CCAAT enhancer binding protein beta-mediated transcriptional activation by glucocorticoid receptor”. Mol. Endocrinol. 12 (11): 1749—63. PMID9817600. doi:10.1210/me.12.11.1749.
Almlöf T, Wallberg AE, Gustafsson JA, Wright AP (1998). „Role of important hydrophobic amino acids in the interaction between the glucocorticoid receptor tau 1-core activation domain and target factors”. Biochemistry. 37 (26): 9586—94. PMID9649342. doi:10.1021/bi973029x.
Lin DY, Lai MZ, Ann DK, Shih HM (2003). „Promyelocytic leukemia protein (PML) functions as a glucocorticoid receptor co-activator by sequestering Daxx to the PML oncogenic domains (PODs) to enhance its transactivation potential”. J. Biol. Chem. 278 (18): 15958—65. PMID12595526. doi:10.1074/jbc.M300387200.
Jibard N, Meng X, Leclerc P, Rajkowski K, Fortin D, Schweizer-Groyer G, Catelli MG, Baulieu EE, Cadepond F (1999). „Delimitation of two regions in the 90-kDa heat shock protein (Hsp90) able to interact with the glucocorticosteroid receptor (GR)”. Exp. Cell Res. 247 (2): 461—74. PMID10066374. doi:10.1006/excr.1998.4375.
Kanelakis KC, Shewach DS, Pratt WB (2002). „Nucleotide binding states of hsp70 and hsp90 during sequential steps in the process of glucocorticoid receptor.hsp90 heterocomplex assembly”. J. Biol. Chem. 277 (37): 33698—703. PMID12093808. doi:10.1074/jbc.M204164200.
Hecht K, Carlstedt-Duke J, Stierna P, Gustafsson J, Brönnegârd M, Wikström AC (1997). „Evidence that the beta-isoform of the human glucocorticoid receptor does not act as a physiologically significant repressor”. J. Biol. Chem. 272 (42): 26659—64. PMID9334248. doi:10.1074/jbc.272.42.26659.
Stancato LF, Silverstein AM, Gitler C, Groner B, Pratt WB (1996). „Use of the thiol-specific derivatizing agent N-iodoacetyl-3-[125I]iodotyrosine to demonstrate conformational differences between the unbound and hsp90-bound glucocorticoid receptor hormone binding domain”. J. Biol. Chem. 271 (15): 8831—6. PMID8621522. doi:10.1074/jbc.271.15.8831.
Eggert M, Michel J, Schneider S, Bornfleth H, Baniahmad A, Fackelmayer FO, Schmidt S, Renkawitz R (1997). „The glucocorticoid receptor is associated with the RNA-binding nuclear matrix protein hnRNP U”. J. Biol. Chem. 272 (45): 28471—8. PMID9353307. doi:10.1074/jbc.272.45.28471.
Zilliacus J, Holter E, Wakui H, Tazawa H, Treuter E, Gustafsson JA (2001). „Regulation of glucocorticoid receptor activity by 14--3-3-dependent intracellular relocalization of the corepressor RIP140”. Mol. Endocrinol. 15 (4): 501—11. PMID11266503. doi:10.1210/me.15.4.501.
Subramaniam N, Treuter E, Okret S (1999). „Receptor interacting protein RIP140 inhibits both positive and negative gene regulation by glucocorticoids”. J. Biol. Chem. 274 (25): 18121—7. PMID10364267. doi:10.1074/jbc.274.25.18121.
Stevens A, Garside H, Berry A, Waters C, White A, Ray D (2003). „Dissociation of steroid receptor coactivator 1 and nuclear receptor corepressor recruitment to the human glucocorticoid receptor by modification of the ligand-receptor interface: the role of tyrosine 735”. Mol. Endocrinol. 17 (5): 845—59. PMID12569182. doi:10.1210/me.2002-0320.
Schulz M, Eggert M, Baniahmad A, Dostert A, Heinzel T, Renkawitz R (2002). „RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding”. J. Biol. Chem. 277 (29): 26238—43. PMID12011091. doi:10.1074/jbc.M203268200.
Kucera T, Waltner-Law M, Scott DK, Prasad R, Granner DK (2002). „A point mutation of the AF2 transactivation domain of the glucocorticoid receptor disrupts its interaction with steroid receptor coactivator 1”. J. Biol. Chem. 277 (29): 26098—102. PMID12118039. doi:10.1074/jbc.M204013200.
Bledsoe RK, Montana VG, Stanley TB, Delves CJ, Apolito CJ, McKee DD, Consler TG, Parks DJ, Stewart EL, Willson TM, Lambert MH, Moore JT, Pearce KH, Xu HE (2002). „Crystal structure of the glucocorticoid receptor ligand binding domain reveals a novel mode of receptor dimerization and coactivator recognition”. Cell. 110 (1): 93—105. PMID12151000. doi:10.1016/S0092-8674(02)00817-6.
Préfontaine GG, Walther R, Giffin W, Lemieux ME, Pope L, Haché RJ (1999). „Selective binding of steroid hormone receptors to octamer transcription factors determines transcriptional synergism at the mouse mammary tumor virus promoter”. J. Biol. Chem. UNITED STATES. 274 (38): 26713—9. ISSN0021-9258. PMID10480874. doi:10.1074/jbc.274.38.26713.
Rao MA, Cheng H, Quayle AN, Nishitani H, Nelson CC, Rennie PS (2002). „RanBPM, a nuclear protein that interacts with and regulates transcriptional activity of androgen receptor and glucocorticoid receptor”. J. Biol. Chem. United States. 277 (50): 48020—7. ISSN0021-9258. PMID12361945. doi:10.1074/jbc.M209741200.
Caldenhoven E, Liden J, Wissink S, Van de Stolpe A, Raaijmakers J, Koenderman L, Okret S, Gustafsson JA, Van der Saag PT (1995). „Negative cross-talk between RelA and the glucocorticoid receptor: a possible mechanism for the antiinflammatory action of glucocorticoids”. Mol. Endocrinol. 9 (4): 401—12. PMID7659084. doi:10.1210/me.9.4.401.
Li G, Wang S, Gelehrter TD (2003). „Identification of glucocorticoid receptor domains involved in transrepression of transforming growth factor-beta action”. J. Biol. Chem. 278 (43): 41779—88. PMID12902338. doi:10.1074/jbc.M305350200.
Zhang Z, Jones S, Hagood JS, Fuentes NL, Fuller GM (1997). „STAT3 acts as a co-activator of glucocorticoid receptor signaling”. J. Biol. Chem. 272 (49): 30607—10. PMID9388192. doi:10.1074/jbc.272.49.30607.
Stöcklin E, Wissler M, Gouilleux F, Groner B (1996). „Functional interactions between Stat5 and the glucocorticoid receptor”. Nature. 383 (6602): 726—8. PMID8878484. doi:10.1038/383726a0.
Makino Y, Yoshikawa N, Okamoto K, Hirota K, Yodoi J, Makino I, Tanaka H (1999). „Direct association with thioredoxin allows redox regulation of glucocorticoid receptor function”. J. Biol. Chem. 274 (5): 3182—8. PMID9915858. doi:10.1074/jbc.274.5.3182.
Wakui H, Wright AP, Gustafsson J, Zilliacus J (1997). „Interaction of the ligand-activated glucocorticoid receptor with the 14-3-3 eta protein”. J. Biol. Chem. 272 (13): 8153—6. PMID9079630. doi:10.1074/jbc.272.13.8153.
nih.gov
ncbi.nlm.nih.gov
Lu NZ, Wardell SE, Burnstein KL, Defranco D, Fuller PJ, Giguere V, Hochberg RB, McKay L, Renoir JM, Weigel NL, Wilson EM, McDonnell DP, Cidlowski JA (2006). „International Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: glucocorticoid, mineralocorticoid, progesterone, and androgen receptors”. Pharmacol Revl. 58 (4): 782—97. PMID17132855. doi:10.1124/pr.58.4.9. [Free full text]
Rhen T, Cidlowski JA (2005). „Antiinflammatory action of glucocorticoids--new mechanisms for old drugs”. N. Engl. J. Med. 353 (16): 1711—23. PMID16236742. doi:10.1056/NEJMra050541.
Hollenberg SM, Weinberger C, Ong ES, Cerelli G, Oro A, Lebo R, Thompson EB, Rosenfeld MG, Evans RM (1985). „Primary structure and expression of a functional human glucocorticoid receptor cDNA”. Nature. 318 (6047): 635—41. PMID2867473. doi:10.1038/318635a0.
Mendonca B, Leite M, de Castro M, Kino T, Elias L, Bachega T, Arnhold I, Chrousos G, Latronico A (2002). „Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene”. J Clin Endocrinol Metab. 87 (4): 1805—9. PMID11932321. doi:10.1210/jc.87.4.1805.
Kullmann M, Schneikert J, Moll J, Heck S, Zeiner M, Gehring U, Cato AC (1998). „RAP46 is a negative regulator of glucocorticoid receptor action and hormone-induced apoptosis”. J. Biol. Chem. 273 (23): 14620—5. PMID9603979. doi:10.1074/jbc.273.23.14620.
Boruk M, Savory JG, Haché RJ (1998). „AF-2-dependent potentiation of CCAAT enhancer binding protein beta-mediated transcriptional activation by glucocorticoid receptor”. Mol. Endocrinol. 12 (11): 1749—63. PMID9817600. doi:10.1210/me.12.11.1749.
Almlöf T, Wallberg AE, Gustafsson JA, Wright AP (1998). „Role of important hydrophobic amino acids in the interaction between the glucocorticoid receptor tau 1-core activation domain and target factors”. Biochemistry. 37 (26): 9586—94. PMID9649342. doi:10.1021/bi973029x.
Lin DY, Lai MZ, Ann DK, Shih HM (2003). „Promyelocytic leukemia protein (PML) functions as a glucocorticoid receptor co-activator by sequestering Daxx to the PML oncogenic domains (PODs) to enhance its transactivation potential”. J. Biol. Chem. 278 (18): 15958—65. PMID12595526. doi:10.1074/jbc.M300387200.
Jibard N, Meng X, Leclerc P, Rajkowski K, Fortin D, Schweizer-Groyer G, Catelli MG, Baulieu EE, Cadepond F (1999). „Delimitation of two regions in the 90-kDa heat shock protein (Hsp90) able to interact with the glucocorticosteroid receptor (GR)”. Exp. Cell Res. 247 (2): 461—74. PMID10066374. doi:10.1006/excr.1998.4375.
Kanelakis KC, Shewach DS, Pratt WB (2002). „Nucleotide binding states of hsp70 and hsp90 during sequential steps in the process of glucocorticoid receptor.hsp90 heterocomplex assembly”. J. Biol. Chem. 277 (37): 33698—703. PMID12093808. doi:10.1074/jbc.M204164200.
Hecht K, Carlstedt-Duke J, Stierna P, Gustafsson J, Brönnegârd M, Wikström AC (1997). „Evidence that the beta-isoform of the human glucocorticoid receptor does not act as a physiologically significant repressor”. J. Biol. Chem. 272 (42): 26659—64. PMID9334248. doi:10.1074/jbc.272.42.26659.
Stancato LF, Silverstein AM, Gitler C, Groner B, Pratt WB (1996). „Use of the thiol-specific derivatizing agent N-iodoacetyl-3-[125I]iodotyrosine to demonstrate conformational differences between the unbound and hsp90-bound glucocorticoid receptor hormone binding domain”. J. Biol. Chem. 271 (15): 8831—6. PMID8621522. doi:10.1074/jbc.271.15.8831.
Eggert M, Michel J, Schneider S, Bornfleth H, Baniahmad A, Fackelmayer FO, Schmidt S, Renkawitz R (1997). „The glucocorticoid receptor is associated with the RNA-binding nuclear matrix protein hnRNP U”. J. Biol. Chem. 272 (45): 28471—8. PMID9353307. doi:10.1074/jbc.272.45.28471.
Zilliacus J, Holter E, Wakui H, Tazawa H, Treuter E, Gustafsson JA (2001). „Regulation of glucocorticoid receptor activity by 14--3-3-dependent intracellular relocalization of the corepressor RIP140”. Mol. Endocrinol. 15 (4): 501—11. PMID11266503. doi:10.1210/me.15.4.501.
Subramaniam N, Treuter E, Okret S (1999). „Receptor interacting protein RIP140 inhibits both positive and negative gene regulation by glucocorticoids”. J. Biol. Chem. 274 (25): 18121—7. PMID10364267. doi:10.1074/jbc.274.25.18121.
Stevens A, Garside H, Berry A, Waters C, White A, Ray D (2003). „Dissociation of steroid receptor coactivator 1 and nuclear receptor corepressor recruitment to the human glucocorticoid receptor by modification of the ligand-receptor interface: the role of tyrosine 735”. Mol. Endocrinol. 17 (5): 845—59. PMID12569182. doi:10.1210/me.2002-0320.
Schulz M, Eggert M, Baniahmad A, Dostert A, Heinzel T, Renkawitz R (2002). „RU486-induced glucocorticoid receptor agonism is controlled by the receptor N terminus and by corepressor binding”. J. Biol. Chem. 277 (29): 26238—43. PMID12011091. doi:10.1074/jbc.M203268200.
Kucera T, Waltner-Law M, Scott DK, Prasad R, Granner DK (2002). „A point mutation of the AF2 transactivation domain of the glucocorticoid receptor disrupts its interaction with steroid receptor coactivator 1”. J. Biol. Chem. 277 (29): 26098—102. PMID12118039. doi:10.1074/jbc.M204013200.
Bledsoe RK, Montana VG, Stanley TB, Delves CJ, Apolito CJ, McKee DD, Consler TG, Parks DJ, Stewart EL, Willson TM, Lambert MH, Moore JT, Pearce KH, Xu HE (2002). „Crystal structure of the glucocorticoid receptor ligand binding domain reveals a novel mode of receptor dimerization and coactivator recognition”. Cell. 110 (1): 93—105. PMID12151000. doi:10.1016/S0092-8674(02)00817-6.
Rao MA, Cheng H, Quayle AN, Nishitani H, Nelson CC, Rennie PS (2002). „RanBPM, a nuclear protein that interacts with and regulates transcriptional activity of androgen receptor and glucocorticoid receptor”. J. Biol. Chem. United States. 277 (50): 48020—7. ISSN0021-9258. PMID12361945. doi:10.1074/jbc.M209741200.
Caldenhoven E, Liden J, Wissink S, Van de Stolpe A, Raaijmakers J, Koenderman L, Okret S, Gustafsson JA, Van der Saag PT (1995). „Negative cross-talk between RelA and the glucocorticoid receptor: a possible mechanism for the antiinflammatory action of glucocorticoids”. Mol. Endocrinol. 9 (4): 401—12. PMID7659084. doi:10.1210/me.9.4.401.
Li G, Wang S, Gelehrter TD (2003). „Identification of glucocorticoid receptor domains involved in transrepression of transforming growth factor-beta action”. J. Biol. Chem. 278 (43): 41779—88. PMID12902338. doi:10.1074/jbc.M305350200.
Zhang Z, Jones S, Hagood JS, Fuentes NL, Fuller GM (1997). „STAT3 acts as a co-activator of glucocorticoid receptor signaling”. J. Biol. Chem. 272 (49): 30607—10. PMID9388192. doi:10.1074/jbc.272.49.30607.
Stöcklin E, Wissler M, Gouilleux F, Groner B (1996). „Functional interactions between Stat5 and the glucocorticoid receptor”. Nature. 383 (6602): 726—8. PMID8878484. doi:10.1038/383726a0.
Makino Y, Yoshikawa N, Okamoto K, Hirota K, Yodoi J, Makino I, Tanaka H (1999). „Direct association with thioredoxin allows redox regulation of glucocorticoid receptor function”. J. Biol. Chem. 274 (5): 3182—8. PMID9915858. doi:10.1074/jbc.274.5.3182.
Wakui H, Wright AP, Gustafsson J, Zilliacus J (1997). „Interaction of the ligand-activated glucocorticoid receptor with the 14-3-3 eta protein”. J. Biol. Chem. 272 (13): 8153—6. PMID9079630. doi:10.1074/jbc.272.13.8153.
worldcat.org
Préfontaine GG, Walther R, Giffin W, Lemieux ME, Pope L, Haché RJ (1999). „Selective binding of steroid hormone receptors to octamer transcription factors determines transcriptional synergism at the mouse mammary tumor virus promoter”. J. Biol. Chem. UNITED STATES. 274 (38): 26713—9. ISSN0021-9258. PMID10480874. doi:10.1074/jbc.274.38.26713.
Rao MA, Cheng H, Quayle AN, Nishitani H, Nelson CC, Rennie PS (2002). „RanBPM, a nuclear protein that interacts with and regulates transcriptional activity of androgen receptor and glucocorticoid receptor”. J. Biol. Chem. United States. 277 (50): 48020—7. ISSN0021-9258. PMID12361945. doi:10.1074/jbc.M209741200.