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Items: 1 to 20 of 25

1.

The regulation of reproductive neuroendocrine function by insulin and insulin-like growth factor-1 (IGF-1).

Wolfe A, Divall S, Wu S.

Front Neuroendocrinol. 2014 Oct;35(4):558-72. doi: 10.1016/j.yfrne.2014.05.007. Epub 2014 Jun 12. Review.

2.

Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders.

Valor LM, Viosca J, Lopez-Atalaya JP, Barco A.

Curr Pharm Des. 2013;19(28):5051-64. Review.

3.

Insulin-like growth factor 1 mediates negative feedback to somatotroph GH expression via POU1F1/CREB binding protein interactions.

Romero CJ, Pine-Twaddell E, Sima DI, Miller RS, He L, Wondisford F, Radovick S.

Mol Cell Biol. 2012 Nov;32(21):4258-69. doi: 10.1128/MCB.00171-12. Epub 2012 Aug 13.

4.

CREB binding protein (CBP) activation is required for luteinizing hormone beta expression and normal fertility in mice.

Miller RS, Wolfe A, He L, Radovick S, Wondisford FE.

Mol Cell Biol. 2012 Jul;32(13):2349-58. doi: 10.1128/MCB.00394-12. Epub 2012 Apr 16.

5.

Disrupting the CH1 domain structure in the acetyltransferases CBP and p300 results in lean mice with increased metabolic control.

Bedford DC, Kasper LH, Wang R, Chang Y, Green DR, Brindle PK.

Cell Metab. 2011 Aug 3;14(2):219-30. doi: 10.1016/j.cmet.2011.06.010.

6.

Extracellular signal-regulated kinase 1/2-mediated phosphorylation of p300 enhances myosin heavy chain I/beta gene expression via acetylation of nuclear factor of activated T cells c1.

Meissner JD, Freund R, Krone D, Umeda PK, Chang KC, Gros G, Scheibe RJ.

Nucleic Acids Res. 2011 Aug;39(14):5907-25. doi: 10.1093/nar/gkr162. Epub 2011 Apr 15.

7.

Arsenite suppression of involucrin transcription through AP1 promoter sites in cultured human keratinocytes.

Sinitsyna NN, Reznikova TV, Qin Q, Song H, Phillips MA, Rice RH.

Toxicol Appl Pharmacol. 2010 Mar 15;243(3):275-82. doi: 10.1016/j.taap.2009.12.006. Epub 2009 Dec 16.

8.

SUMOylation regulates the nuclear mobility of CREB binding protein and its association with nuclear bodies in live cells.

Ryan CM, Kindle KB, Collins HM, Heery DM.

Biochem Biophys Res Commun. 2010 Jan 1;391(1):1136-41. doi: 10.1016/j.bbrc.2009.12.040. Epub 2009 Dec 16.

9.

Purification and characterization of recombinant CH3 domain fragment of the CREB-binding protein.

Drendall CI, Pham QH, Dietze EC.

Protein Expr Purif. 2010 Apr;70(2):196-205. doi: 10.1016/j.pep.2009.12.003. Epub 2009 Dec 6.

10.

A Pit-1 threonine 220 phosphomimic reduces binding to monomeric DNA sites to inhibit Ras and estrogen stimulation of the prolactin gene promoter.

Jean A, Gutierrez-Hartmann A, Duval DL.

Mol Endocrinol. 2010 Jan;24(1):91-103. doi: 10.1210/me.2009-0279. Epub 2009 Nov 3.

11.

The 26-amino acid beta-motif of the Pit-1beta transcription factor is a dominant and independent repressor domain.

Jonsen MD, Duval DL, Gutierrez-Hartmann A.

Mol Endocrinol. 2009 Sep;23(9):1371-84. doi: 10.1210/me.2008-0137. Epub 2009 Jun 25.

12.

Activator protein-1 has an essential role in pancreatic cancer cells and is regulated by a novel Akt-mediated mechanism.

Shin S, Asano T, Yao Y, Zhang R, Claret FX, Korc M, Sabapathy K, Menter DG, Abbruzzese JL, Reddy SAG.

Mol Cancer Res. 2009 May;7(5):745-754. doi: 10.1158/1541-7786.MCR-08-0462. Epub 2009 May 12.

13.

Organochlorine-mediated potentiation of the general coactivator p300 through p38 mitogen-activated protein kinase.

Bratton MR, Frigo DE, Vigh-Conrad KA, Fan D, Wadsworth S, McLachlan JA, Burow ME.

Carcinogenesis. 2009 Jan;30(1):106-13. doi: 10.1093/carcin/bgn213. Epub 2008 Sep 12.

14.

Extracellular signals regulate rapid coactivator recruitment at AP-1 sites by altered phosphorylation of both CREB binding protein and c-jun.

Tsai LN, Ku TK, Salib NK, Crowe DL.

Mol Cell Biol. 2008 Jul;28(13):4240-50. doi: 10.1128/MCB.01489-07. Epub 2008 Apr 28.

15.

FSH signaling pathways in immature granulosa cells that regulate target gene expression: branching out from protein kinase A.

Hunzicker-Dunn M, Maizels ET.

Cell Signal. 2006 Sep;18(9):1351-9. Epub 2006 Apr 17. Review.

16.

SUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx.

Kuo HY, Chang CC, Jeng JC, Hu HM, Lin DY, Maul GG, Kwok RP, Shih HM.

Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):16973-8. Epub 2005 Nov 15.

17.

Two transactivation mechanisms cooperate for the bulk of HIF-1-responsive gene expression.

Kasper LH, Boussouar F, Boyd K, Xu W, Biesen M, Rehg J, Baudino TA, Cleveland JL, Brindle PK.

EMBO J. 2005 Nov 16;24(22):3846-58. Epub 2005 Oct 20.

18.

HATs and HDACs in neurodegeneration: a tale of disconcerted acetylation homeostasis.

Saha RN, Pahan K.

Cell Death Differ. 2006 Apr;13(4):539-50. Review.

19.
20.

Regulating histone acetyltransferases and deacetylases.

Legube G, Trouche D.

EMBO Rep. 2003 Oct;4(10):944-7. Review.

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