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Results: 1 to 20 of 105

Similar articles for PubMed (Select 18771283)

1.

Control of glucocorticoid and progesterone receptor subcellular localization by the ligand-binding domain is mediated by distinct interactions with tetratricopeptide repeat proteins.

Banerjee A, Periyasamy S, Wolf IM, Hinds TD Jr, Yong W, Shou W, Sanchez ER.

Biochemistry. 2008 Sep 30;47(39):10471-80. doi: 10.1021/bi8011862. Epub 2008 Sep 5.

4.

Protein phosphatase 5 is a major component of glucocorticoid receptor.hsp90 complexes with properties of an FK506-binding immunophilin.

Silverstein AM, Galigniana MD, Chen MS, Owens-Grillo JK, Chinkers M, Pratt WB.

J Biol Chem. 1997 Jun 27;272(26):16224-30.

5.

Analysis of FKBP51/FKBP52 chimeras and mutants for Hsp90 binding and association with progesterone receptor complexes.

Barent RL, Nair SC, Carr DC, Ruan Y, Rimerman RA, Fulton J, Zhang Y, Smith DF.

Mol Endocrinol. 1998 Mar;12(3):342-54.

PMID:
9514152
6.

The helix 1-3 loop in the glucocorticoid receptor LBD is a regulatory element for FKBP cochaperones.

Cluning C, Ward BK, Rea SL, Arulpragasam A, Fuller PJ, Ratajczak T.

Mol Endocrinol. 2013 Jul;27(7):1020-35. doi: 10.1210/me.2012-1023. Epub 2013 May 17.

PMID:
23686112
7.

C-terminal sequences outside the tetratricopeptide repeat domain of FKBP51 and FKBP52 cause differential binding to Hsp90.

Cheung-Flynn J, Roberts PJ, Riggs DL, Smith DF.

J Biol Chem. 2003 May 9;278(19):17388-94. Epub 2003 Feb 27.

8.

Targeted ablation reveals a novel role of FKBP52 in gene-specific regulation of glucocorticoid receptor transcriptional activity.

Wolf IM, Periyasamy S, Hinds T Jr, Yong W, Shou W, Sanchez ER.

J Steroid Biochem Mol Biol. 2009 Jan;113(1-2):36-45. doi: 10.1016/j.jsbmb.2008.11.006. Epub 2008 Nov 27.

10.

A new first step in activation of steroid receptors: hormone-induced switching of FKBP51 and FKBP52 immunophilins.

Davies TH, Ning YM, Sánchez ER.

J Biol Chem. 2002 Feb 15;277(7):4597-600. Epub 2001 Dec 20.

11.

Structure-function analysis of squirrel monkey FK506-binding protein 51, a potent inhibitor of glucocorticoid receptor activity.

Denny WB, Prapapanich V, Smith DF, Scammell JG.

Endocrinology. 2005 Jul;146(7):3194-201. Epub 2005 Mar 31.

PMID:
15802496
12.
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15.

Nuclear import of the glucocorticoid receptor-hsp90 complex through the nuclear pore complex is mediated by its interaction with Nup62 and importin beta.

Echeverría PC, Mazaira G, Erlejman A, Gomez-Sanchez C, Piwien Pilipuk G, Galigniana MD.

Mol Cell Biol. 2009 Sep;29(17):4788-97. doi: 10.1128/MCB.00649-09. Epub 2009 Jul 6.

16.

Interaction of the Hsp90 cochaperone cyclophilin 40 with Hsc70.

Carrello A, Allan RK, Morgan SL, Owen BA, Mok D, Ward BK, Minchin RF, Toft DO, Ratajczak T.

Cell Stress Chaperones. 2004 Summer;9(2):167-81.

19.

Binding of hsp90-associated immunophilins to cytoplasmic dynein: direct binding and in vivo evidence that the peptidylprolyl isomerase domain is a dynein interaction domain.

Galigniana MD, Harrell JM, Murphy PJ, Chinkers M, Radanyi C, Renoir JM, Zhang M, Pratt WB.

Biochemistry. 2002 Nov 19;41(46):13602-10.

PMID:
12427021
20.

NF-κB transcriptional activity is modulated by FK506-binding proteins FKBP51 and FKBP52: a role for peptidyl-prolyl isomerase activity.

Erlejman AG, De Leo SA, Mazaira GI, Molinari AM, Camisay MF, Fontana V, Cox MB, Piwien-Pilipuk G, Galigniana MD.

J Biol Chem. 2014 Sep 19;289(38):26263-76. doi: 10.1074/jbc.M114.582882. Epub 2014 Aug 7.

PMID:
25104352
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