Richtsmeier JT - Search Results

1

Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.

Holmes G, O'Rourke C, Motch Perrine SM, Lu N, van Bakel H, Richtsmeier JT, Jabs EW. Holmes G, et al. Among authors: richtsmeier jt. Development. 2018 Oct 5;145(19):dev166488. doi: 10.1242/dev.166488. Development. 2018. PMID: 30228104 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

Developmental aspects of the upper airway: report from an NHLBI Workshop, March 5-6, 2009.

Marcus CL, Smith RJ, Mankarious LA, Arens R, Mitchell GS, Elluru RG, Forte V, Goudy S, Jabs EW, Kane AA, Katz E, Paydarfar D, Pereira K, Reeves RH, Richtsmeier JT, Ruiz RL, Thach BT, Tunkel DE, Whitsett JA, Wootton D, Blaisdell CJ. Marcus CL, et al. Among authors: richtsmeier jt. Proc Am Thorac Soc. 2009 Sep 15;6(6):513-20. doi: 10.1513/pats.200905-024CB. Proc Am Thorac Soc. 2009. PMID: 19741259 Free PMC article.

4

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.

5

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.

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

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.

9

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.

10

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. Among authors: richtsmeier jt. 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.

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