Wang Y - Search Results

1

Postnatal brain and skull growth in an Apert syndrome mouse model.

Hill CA, Martínez-Abadías N, Motch SM, Austin JR, Wang Y, Jabs EW, Richtsmeier JT, Aldridge K. Hill CA, et al. Among authors: wang y. Am J Med Genet A. 2013 Apr;161A(4):745-57. doi: 10.1002/ajmg.a.35805. Epub 2013 Mar 12. Am J Med Genet A. 2013. PMID: 23495236 Free PMC article.

2

Brain phenotypes in two FGFR2 mouse models for Apert syndrome.

Aldridge K, Hill CA, Austin JR, Percival C, Martinez-Abadias N, Neuberger T, Wang Y, Jabs EW, Richtsmeier JT. Aldridge K, et al. Among authors: wang y. Dev Dyn. 2010 Mar;239(3):987-97. doi: 10.1002/dvdy.22218. Dev Dyn. 2010. PMID: 20077479 Free PMC article.

3

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.

Wang Y, Sun M, Uhlhorn VL, Zhou X, Peter I, Martinez-Abadias N, Hill CA, Percival CJ, Richtsmeier JT, Huso DL, Jabs EW. Wang Y, et al. BMC Dev Biol. 2010 Feb 22;10:22. doi: 10.1186/1471-213X-10-22. BMC Dev Biol. 2010. PMID: 20175913 Free PMC article.

4

FGF/FGFR signaling coordinates skull development by modulating magnitude of morphological integration: evidence from Apert syndrome mouse models.

Martínez-Abadías N, Heuzé Y, Wang Y, Jabs EW, Aldridge K, Richtsmeier JT. Martínez-Abadías N, et al. Among authors: wang y. PLoS One. 2011;6(10):e26425. doi: 10.1371/journal.pone.0026425. Epub 2011 Oct 28. PLoS One. 2011. PMID: 22053191 Free PMC article.

5

Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse.

Wang Y, Xiao R, Yang F, Karim BO, Iacovelli AJ, Cai J, Lerner CP, Richtsmeier JT, Leszl JM, Hill CA, Yu K, Ornitz DM, Elisseeff J, Huso DL, Jabs EW. Wang Y, et al. Development. 2005 Aug;132(15):3537-48. doi: 10.1242/dev.01914. Epub 2005 Jun 23. Development. 2005. PMID: 15975938

6

The study of abnormal bone development in the Apert syndrome Fgfr2+/S252W mouse using a 3D hydrogel culture model.

Yang F, Wang Y, Zhang Z, Hsu B, Jabs EW, Elisseeff JH. Yang F, et al. Among authors: wang y. Bone. 2008 Jul;43(1):55-63. doi: 10.1016/j.bone.2008.02.008. Epub 2008 Feb 29. Bone. 2008. PMID: 18407821 Free PMC article.

7

Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth.

Martínez-Abadías N, Percival C, Aldridge K, Hill CA, Ryan T, Sirivunnabood S, Wang Y, Jabs EW, Richtsmeier JT. Martínez-Abadías N, et al. Among authors: wang y. Dev Dyn. 2010 Nov;239(11):3058-71. doi: 10.1002/dvdy.22414. Dev Dyn. 2010. PMID: 20842696 Free PMC article.

8

Genetic basis of potential therapeutic strategies for craniosynostosis.

Melville H, Wang Y, Taub PJ, Jabs EW. Melville H, et al. Among authors: wang y. Am J Med Genet A. 2010 Dec;152A(12):3007-15. doi: 10.1002/ajmg.a.33703. Am J Med Genet A. 2010. PMID: 21082653 Review.

9

p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.

Wang Y, Zhou X, Oberoi K, Phelps R, Couwenhoven R, Sun M, Rezza A, Holmes G, Percival CJ, Friedenthal J, Krejci P, Richtsmeier JT, Huso DL, Rendl M, Jabs EW. Wang Y, et al. J Clin Invest. 2012 Jun;122(6):2153-64. doi: 10.1172/JCI62644. Epub 2012 May 15. J Clin Invest. 2012. PMID: 22585574 Free PMC article.

10

The effect of a Beare-Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice.

Percival CJ, Wang Y, Zhou X, Jabs EW, Richtsmeier JT. Percival CJ, et al. Among authors: wang y. J Anat. 2012 Nov;221(5):434-42. doi: 10.1111/j.1469-7580.2012.01555.x. Epub 2012 Aug 12. J Anat. 2012. PMID: 22881429 Free PMC article.

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