Similar articles for PMID: 11751906

Year	Number of Results
1993	1
1994	4
1995	2
1996	3
1997	4
1998	6
1999	9
2000	22
2001	23
2002	23
2003	12
2004	12
2005	9
2006	4
2007	1
2008	2
2009	7
2010	6
2011	4
2012	3
2013	2
2014	2
2015	3
2016	1
2017	1
2018	1
2019	1
2021	5
2022	4
2024	0

1

The role of Hsp90N, a new member of the Hsp90 family, in signal transduction and neoplastic transformation.

Grammatikakis N, Vultur A, Ramana CV, Siganou A, Schweinfest CW, Watson DK, Raptis L. Grammatikakis N, et al. J Biol Chem. 2002 Mar 8;277(10):8312-20. doi: 10.1074/jbc.M109200200. Epub 2001 Dec 20. J Biol Chem. 2002. PMID: 11751906 Free article.

2

Hsp90/p50cdc37 is required for mixed-lineage kinase (MLK) 3 signaling.

Zhang H, Wu W, Du Y, Santos SJ, Conrad SE, Watson JT, Grammatikakis N, Gallo KA. Zhang H, et al. J Biol Chem. 2004 May 7;279(19):19457-63. doi: 10.1074/jbc.M311377200. Epub 2004 Mar 4. J Biol Chem. 2004. PMID: 15001580 Free article.

3

p50(cdc37) acting in concert with Hsp90 is required for Raf-1 function.

Grammatikakis N, Lin JH, Grammatikakis A, Tsichlis PN, Cochran BH. Grammatikakis N, et al. Mol Cell Biol. 1999 Mar;19(3):1661-72. doi: 10.1128/MCB.19.3.1661. Mol Cell Biol. 1999. PMID: 10022854 Free PMC article.

4

Specific association of a set of molecular chaperones including HSP90 and Cdc37 with MOK, a member of the mitogen-activated protein kinase superfamily.

Miyata Y, Ikawa Y, Shibuya M, Nishida E. Miyata Y, et al. J Biol Chem. 2001 Jun 15;276(24):21841-8. doi: 10.1074/jbc.M010944200. Epub 2001 Mar 16. J Biol Chem. 2001. PMID: 11278794 Free article.

5

p50(cdc37) binds directly to the catalytic domain of Raf as well as to a site on hsp90 that is topologically adjacent to the tetratricopeptide repeat binding site.

Silverstein AM, Grammatikakis N, Cochran BH, Chinkers M, Pratt WB. Silverstein AM, et al. J Biol Chem. 1998 Aug 7;273(32):20090-5. doi: 10.1074/jbc.273.32.20090. J Biol Chem. 1998. PMID: 9685350 Free article.

6

A Raf-1 mutant that dissociates MEK/extracellular signal-regulated kinase activation from malignant transformation and differentiation but not proliferation.

Dhillon AS, Meikle S, Peyssonnaux C, Grindlay J, Kaiser C, Steen H, Shaw PE, Mischak H, Eychène A, Kolch W. Dhillon AS, et al. Mol Cell Biol. 2003 Mar;23(6):1983-93. doi: 10.1128/MCB.23.6.1983-1993.2003. Mol Cell Biol. 2003. PMID: 12612072 Free PMC article.

7

Opposite role of Ras in tumor necrosis factor-alpha-induced cell cycle regulation: competition for Raf kinase.

Park SJ, Kim YY, Lim JY, Seo GJ, Kim J, Park SI, Park BJ. Park SJ, et al. Biochem Biophys Res Commun. 2001 Oct 12;287(5):1140-7. doi: 10.1006/bbrc.2001.5713. Biochem Biophys Res Commun. 2001. PMID: 11587542

8

Cholecystokinin stimulates extracellular signal-regulated kinase through activation of the epidermal growth factor receptor, Yes, and protein kinase C. Signal amplification at the level of Raf by activation of protein kinase Cepsilon.

Piiper A, Elez R, You SJ, Kronenberger B, Loitsch S, Roche S, Zeuzem S. Piiper A, et al. J Biol Chem. 2003 Feb 28;278(9):7065-72. doi: 10.1074/jbc.M211234200. Epub 2002 Dec 20. J Biol Chem. 2003. PMID: 12496267 Free article.

9

TC21 and Ras share indistinguishable transforming and differentiating activities.

Graham SM, Oldham SM, Martin CB, Drugan JK, Zohn IE, Campbell S, Der CJ. Graham SM, et al. Oncogene. 1999 Mar 25;18(12):2107-16. doi: 10.1038/sj.onc.1202517. Oncogene. 1999. PMID: 10321735

10

Activation of B-Raf kinase requires phosphorylation of the conserved residues Thr598 and Ser601.

Zhang BH, Guan KL. Zhang BH, et al. EMBO J. 2000 Oct 16;19(20):5429-39. doi: 10.1093/emboj/19.20.5429. EMBO J. 2000. PMID: 11032810 Free PMC article.

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