Richtsmeier JT - Search Results

1

Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.

Ye X, Guilmatre A, Reva B, Peter I, Heuzé Y, Richtsmeier JT, Fox DJ, Goedken RJ, Jabs EW, Romitti PA. Ye X, et al. Among authors: richtsmeier jt. Plast Reconstr Surg. 2016 Mar;137(3):952-961. doi: 10.1097/01.prs.0000479978.75545.ee. Plast Reconstr Surg. 2016. PMID: 26910679 Free PMC article.

2

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. Among authors: richtsmeier jt. Development. 2005 Aug;132(15):3537-48. doi: 10.1242/dev.01914. Epub 2005 Jun 23. Development. 2005. PMID: 15975938

3

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: richtsmeier jt. Dev Dyn. 2010 Mar;239(3):987-97. doi: 10.1002/dvdy.22218. Dev Dyn. 2010. PMID: 20077479 Free PMC article.

4

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. Among authors: richtsmeier jt. BMC Dev Biol. 2010 Feb 22;10:22. doi: 10.1186/1471-213X-10-22. BMC Dev Biol. 2010. PMID: 20175913 Free PMC article.

5

New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis.

Heuzé Y, Boyadjiev SA, Marsh JL, Kane AA, Cherkez E, Boggan JE, Richtsmeier JT. Heuzé Y, et al. Among authors: richtsmeier jt. J Anat. 2010 Aug;217(2):85-96. doi: 10.1111/j.1469-7580.2010.01258.x. Epub 2010 Jun 22. J Anat. 2010. PMID: 20572900 Free PMC article.

6

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: richtsmeier jt. Dev Dyn. 2010 Nov;239(11):3058-71. doi: 10.1002/dvdy.22414. Dev Dyn. 2010. PMID: 20842696 Free PMC article.

7

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: richtsmeier jt. PLoS One. 2011;6(10):e26425. doi: 10.1371/journal.pone.0026425. Epub 2011 Oct 28. PLoS One. 2011. PMID: 22053191 Free PMC article.

8

Unilateral and bilateral expression of a quantitative trait: asymmetry and symmetry in coronal craniosynostosis.

Heuzé Y, Martínez-Abadías N, Stella JM, Senders CW, Boyadjiev SA, Lo LJ, Richtsmeier JT. Heuzé Y, et al. Among authors: richtsmeier jt. J Exp Zool B Mol Dev Evol. 2012 Mar;318(2):109-22. doi: 10.1002/jezb.21449. J Exp Zool B Mol Dev Evol. 2012. PMID: 22532473 Free PMC article.

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. Among authors: richtsmeier jt. 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: richtsmeier jt. 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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