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Items: 1 to 20 of 99

1.

Nuclear entry of activated MAPK is restricted in primary ovarian and mammary epithelial cells.

Smith ER, Cai KQ, Smedberg JL, Ribeiro MM, Rula ME, Slater C, Godwin AK, Xu XX.

PLoS One. 2010 Feb 18;5(2):e9295. doi: 10.1371/journal.pone.0009295.

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Bacterial heat shock protein-60 increases epithelial cell proliferation through the ERK1/2 MAP kinases.

Zhang L, Pelech SL, Mayrand D, Grenier D, Heino J, Uitto VJ.

Exp Cell Res. 2001 May 15;266(1):11-20.

PMID:
11339820
7.

Nuclear extracellular signal-regulated kinase 1 and 2 translocation is mediated by casein kinase 2 and accelerated by autophosphorylation.

Plotnikov A, Chuderland D, Karamansha Y, Livnah O, Seger R.

Mol Cell Biol. 2011 Sep;31(17):3515-30. doi: 10.1128/MCB.05424-11. Epub 2011 Jul 5.

8.

ERK1/2 regulates ANG II-dependent cell proliferation via cytoplasmic activation of RSK2 and nuclear activation of elk1.

Godeny MD, Sayeski PP.

Am J Physiol Cell Physiol. 2006 Dec;291(6):C1308-17. Epub 2006 May 24.

9.

Dissecting the transcriptional networks underlying breast cancer: NR4A1 reduces the migration of normal and breast cancer cell lines.

Alexopoulou AN, Leao M, Caballero OL, Da Silva L, Reid L, Lakhani SR, Simpson AJ, Marshall JF, Neville AM, Jat PS.

Breast Cancer Res. 2010;12(4):R51. doi: 10.1186/bcr2610. Epub 2010 Jul 19.

11.

Nuclear import of factors involved in signaling is inhibited in C3H/10T1/2 cells treated with tetradecylthioacetic acid.

Bjørndal B, Helleland C, Bøe SO, Gudbrandsen OA, Kalland KH, Bohov P, Berge RK, Lillehaug JR.

J Lipid Res. 2002 Oct;43(10):1630-40.

12.

PEA-15 is inhibited by adenovirus E1A and plays a role in ERK nuclear export and Ras-induced senescence.

Gaumont-Leclerc MF, Mukhopadhyay UK, Goumard S, Ferbeyre G.

J Biol Chem. 2004 Nov 5;279(45):46802-9. Epub 2004 Aug 25.

13.

Mouse tissues that undergo neoplastic progression after K-Ras activation are distinguished by nuclear translocation of phospho-Erk1/2 and robust tumor suppressor responses.

Parikh N, Shuck RL, Nguyen TA, Herron A, Donehower LA.

Mol Cancer Res. 2012 Jun;10(6):845-55. doi: 10.1158/1541-7786.MCR-12-0089. Epub 2012 Apr 24.

15.

Mitogenic signalling by B2 bradykinin receptor in epithelial breast cells.

Greco S, Muscella A, Elia MG, Romano S, Storelli C, Marsigliante S.

J Cell Physiol. 2004 Oct;201(1):84-96.

PMID:
15281091
17.

The nuclear import of oncoprotein hepatitis B X-interacting protein depends on interacting with c-Fos and phosphorylation of both proteins in breast cancer cells.

Zhang Y, Zhao Y, Li H, Li Y, Cai X, Shen Y, Shi H, Li L, Liu Q, Zhang X, Ye L.

J Biol Chem. 2013 Jun 28;288(26):18961-74. doi: 10.1074/jbc.M113.458638. Epub 2013 May 10.

18.

TRAPPC4-ERK2 interaction activates ERK1/2, modulates its nuclear localization and regulates proliferation and apoptosis of colorectal cancer cells.

Zhao SL, Hong J, Xie ZQ, Tang JT, Su WY, Du W, Chen YX, Lu R, Sun DF, Fang JY.

PLoS One. 2011;6(8):e23262. doi: 10.1371/journal.pone.0023262. Epub 2011 Aug 3.

19.

Human biliverdin reductase is an ERK activator; hBVR is an ERK nuclear transporter and is required for MAPK signaling.

Lerner-Marmarosh N, Miralem T, Gibbs PE, Maines MD.

Proc Natl Acad Sci U S A. 2008 May 13;105(19):6870-5. doi: 10.1073/pnas.0800750105. Epub 2008 May 7.

20.

Nec-1 enhances shikonin-induced apoptosis in leukemia cells by inhibition of RIP-1 and ERK1/2.

Han W, Xie J, Fang Y, Wang Z, Pan H.

Int J Mol Sci. 2012;13(6):7212-25. doi: 10.3390/ijms13067212. Epub 2012 Jun 12.

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