Similar articles for PMID: 29659837

Year	Number of Results
1999	1
2000	1
2001	1
2003	1
2004	7
2005	5
2006	4
2007	6
2008	6
2009	5
2010	7
2011	3
2012	7
2013	5
2014	10
2015	7
2016	5
2017	7
2018	6
2019	7
2020	11
2021	4
2022	5
2023	5
2024	0

1

Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growth.

Tajan M, Pernin-Grandjean J, Beton N, Gennero I, Capilla F, Neel BG, Araki T, Valet P, Tauber M, Salles JP, Yart A, Edouard T. Tajan M, et al. Hum Mol Genet. 2018 Jul 1;27(13):2276-2289. doi: 10.1093/hmg/ddy133. Hum Mol Genet. 2018. PMID: 29659837 Free PMC article.

2

Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature.

De Rocca Serra-Nédélec A, Edouard T, Tréguer K, Tajan M, Araki T, Dance M, Mus M, Montagner A, Tauber M, Salles JP, Valet P, Neel BG, Raynal P, Yart A. De Rocca Serra-Nédélec A, et al. Proc Natl Acad Sci U S A. 2012 Mar 13;109(11):4257-62. doi: 10.1073/pnas.1119803109. Epub 2012 Feb 27. Proc Natl Acad Sci U S A. 2012. PMID: 22371576 Free PMC article.

3

SHP2 regulates chondrocyte terminal differentiation, growth plate architecture and skeletal cell fates.

Bowen ME, Ayturk UM, Kurek KC, Yang W, Warman ML. Bowen ME, et al. PLoS Genet. 2014 May 29;10(5):e1004364. doi: 10.1371/journal.pgen.1004364. eCollection 2014. PLoS Genet. 2014. PMID: 24875294 Free PMC article.

4

Noonan and LEOPARD syndrome Shp2 variants induce heart displacement defects in zebrafish.

Bonetti M, Paardekooper Overman J, Tessadori F, Noël E, Bakkers J, den Hertog J. Bonetti M, et al. Development. 2014 May;141(9):1961-70. doi: 10.1242/dev.106310. Epub 2014 Apr 9. Development. 2014. PMID: 24718990 Free article.

5

Structural insights into Noonan/LEOPARD syndrome-related mutants of protein-tyrosine phosphatase SHP2 (PTPN11).

Qiu W, Wang X, Romanov V, Hutchinson A, Lin A, Ruzanov M, Battaile KP, Pai EF, Neel BG, Chirgadze NY. Qiu W, et al. BMC Struct Biol. 2014 Mar 14;14:10. doi: 10.1186/1472-6807-14-10. BMC Struct Biol. 2014. PMID: 24628801 Free PMC article.

6

SHP2 Regulates the Osteogenic Fate of Growth Plate Hypertrophic Chondrocytes.

Wang L, Huang J, Moore DC, Zuo C, Wu Q, Xie L, von der Mark K, Yuan X, Chen D, Warman ML, Ehrlich MG, Yang W. Wang L, et al. Sci Rep. 2017 Oct 5;7(1):12699. doi: 10.1038/s41598-017-12767-9. Sci Rep. 2017. PMID: 28983104 Free PMC article.

7

Role of ERK1/2 signaling in congenital valve malformations in Noonan syndrome.

Krenz M, Gulick J, Osinska HE, Colbert MC, Molkentin JD, Robbins J. Krenz M, et al. Proc Natl Acad Sci U S A. 2008 Dec 2;105(48):18930-5. doi: 10.1073/pnas.0806556105. Epub 2008 Nov 18. Proc Natl Acad Sci U S A. 2008. PMID: 19017799 Free PMC article.

8

Noonan syndrome mutation Q79R in Shp2 increases proliferation of valve primordia mesenchymal cells via extracellular signal-regulated kinase 1/2 signaling.

Krenz M, Yutzey KE, Robbins J. Krenz M, et al. Circ Res. 2005 Oct 14;97(8):813-20. doi: 10.1161/01.RES.0000186194.06514.b0. Epub 2005 Sep 15. Circ Res. 2005. PMID: 16166557 Free PMC article.

9

SHP2 sails from physiology to pathology.

Tajan M, de Rocca Serra A, Valet P, Edouard T, Yart A. Tajan M, et al. Eur J Med Genet. 2015 Oct;58(10):509-25. doi: 10.1016/j.ejmg.2015.08.005. Epub 2015 Sep 2. Eur J Med Genet. 2015. PMID: 26341048 Review.

10

Involvement of EphA2-mediated tyrosine phosphorylation of Shp2 in Shp2-regulated activation of extracellular signal-regulated kinase.

Miura K, Wakayama Y, Tanino M, Orba Y, Sawa H, Hatakeyama M, Tanaka S, Sabe H, Mochizuki N. Miura K, et al. Oncogene. 2013 Nov 7;32(45):5292-301. doi: 10.1038/onc.2012.571. Epub 2013 Jan 14. Oncogene. 2013. PMID: 23318428

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