Similar articles for PMID: 27034231

Year	Number of Results
1906	1
1983	1
1986	1
1994	1
1996	1
1997	4
1998	3
2000	3
2001	4
2003	2
2004	5
2005	3
2006	9
2007	4
2008	1
2009	4
2010	6
2011	4
2012	8
2013	6
2014	8
2015	6
2016	5
2017	5
2018	14
2019	4
2020	12
2021	10
2022	11
2023	6
2024	1

1

FGFR2c-mediated ERK-MAPK activity regulates coronal suture development.

Pfaff MJ, Xue K, Li L, Horowitz MC, Steinbacher DM, Eswarakumar JVP. Pfaff MJ, et al. Dev Biol. 2016 Jul 15;415(2):242-250. doi: 10.1016/j.ydbio.2016.03.026. Epub 2016 Mar 28. Dev Biol. 2016. PMID: 27034231 Free PMC article.

2

Overexpression of Fgfr2c causes craniofacial bone hypoplasia and ameliorates craniosynostosis in the Crouzon mouse.

Lee KKL, Peskett E, Quinn CM, Aiello R, Adeeva L, Moulding DA, Stanier P, Pauws E. Lee KKL, et al. Dis Model Mech. 2018 Nov 9;11(11):dmm035311. doi: 10.1242/dmm.035311. Dis Model Mech. 2018. PMID: 30266836 Free PMC article.

3

A model for the pharmacological treatment of crouzon syndrome.

Perlyn CA, Morriss-Kay G, Darvann T, Tenenbaum M, Ornitz DM. Perlyn CA, et al. Neurosurgery. 2006 Jul;59(1):210-5; discussion 210-5. doi: 10.1227/01.NEU.0000224323.53866.1E. Neurosurgery. 2006. PMID: 16823318 Free PMC article.

4

Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts.

Ang BU, Spivak RM, Nah HD, Kirschner RE. Ang BU, et al. J Craniofac Surg. 2010 Mar;21(2):462-7. doi: 10.1097/SCS.0b013e3181cfe9a0. J Craniofac Surg. 2010. PMID: 20489451

5

A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.

Eswarakumar VP, Horowitz MC, Locklin R, Morriss-Kay GM, Lonai P. Eswarakumar VP, et al. Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12555-60. doi: 10.1073/pnas.0405031101. Epub 2004 Aug 17. Proc Natl Acad Sci U S A. 2004. PMID: 15316116 Free PMC article.

6

Medical treatment of craniosynostosis: recombinant Noggin inhibits coronal suture closure in the rat craniosynostosis model.

Shen K, Krakora SM, Cunningham M, Singh M, Wang X, Hu FZ, Post JC, Ehrlich GD. Shen K, et al. Orthod Craniofac Res. 2009 Aug;12(3):254-62. doi: 10.1111/j.1601-6343.2009.01460.x. Orthod Craniofac Res. 2009. PMID: 19627528 Free PMC article.

7

Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.

Martínez-Abadías N, Motch SM, Pankratz TL, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT. Martínez-Abadías N, et al. Dev Dyn. 2013 Jan;242(1):80-94. doi: 10.1002/dvdy.23903. Epub 2012 Dec 5. Dev Dyn. 2013. PMID: 23172727 Free PMC article.

8

Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.

Liu J, Nam HK, Wang E, Hatch NE. Liu J, et al. Calcif Tissue Int. 2013 May;92(5):451-66. doi: 10.1007/s00223-013-9701-2. Epub 2013 Jan 29. Calcif Tissue Int. 2013. PMID: 23358860 Free PMC article.

9

Attenuation of signaling pathways stimulated by pathologically activated FGF-receptor 2 mutants prevents craniosynostosis.

Eswarakumar VP, Ozcan F, Lew ED, Bae JH, Tomé F, Booth CJ, Adams DJ, Lax I, Schlessinger J. Eswarakumar VP, et al. Proc Natl Acad Sci U S A. 2006 Dec 5;103(49):18603-8. doi: 10.1073/pnas.0609157103. Epub 2006 Nov 28. Proc Natl Acad Sci U S A. 2006. PMID: 17132737 Free PMC article.

10

Minor Suture Fusion in Syndromic Craniosynostosis.

Runyan CM, Xu M D W, Alperovich M, Massie M D JP, Paek G, Cohen BA, Staffenberg DA, Flores RL, Taylor JA. Runyan CM, et al. Plast Reconstr Surg. 2017 Sep;140(3):434e-445e. doi: 10.1097/PRS.0000000000003586. Plast Reconstr Surg. 2017. PMID: 28574949

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