Jabs EW - Search Results

1

Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice.

Motch Perrine SM, Cole TM 3rd, Martínez-Abadías N, Aldridge K, Jabs EW, Richtsmeier JT. Motch Perrine SM, et al. Among authors: jabs ew. BMC Dev Biol. 2014 Feb 28;14:8. doi: 10.1186/1471-213X-14-8. BMC Dev Biol. 2014. PMID: 24580805 Free PMC article.

2

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: jabs ew. 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.

3

From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome.

Martínez-Abadías N, Holmes G, Pankratz T, Wang Y, Zhou X, Jabs EW, Richtsmeier JT. Martínez-Abadías N, et al. Among authors: jabs ew. Dis Model Mech. 2013 May;6(3):768-79. doi: 10.1242/dmm.010397. Epub 2013 Mar 8. Dis Model Mech. 2013. PMID: 23519026 Free PMC article.

4

Embryonic craniofacial bone volume and bone mineral density in Fgfr2(+/P253R) and nonmutant mice.

Percival CJ, Huang Y, Jabs EW, Li R, Richtsmeier JT. Percival CJ, et al. Among authors: jabs ew. Dev Dyn. 2014 Apr;243(4):541-51. doi: 10.1002/dvdy.24095. Epub 2014 Feb 7. Dev Dyn. 2014. PMID: 24504751 Free PMC article.

5

Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues.

Heuzé Y, Singh N, Basilico C, Jabs EW, Holmes G, Richtsmeier JT. Heuzé Y, et al. Among authors: jabs ew. Bone. 2014 Jun;63:101-9. doi: 10.1016/j.bone.2014.03.003. Epub 2014 Mar 13. Bone. 2014. PMID: 24632501 Free PMC article.

6

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: jabs ew. Development. 2018 Oct 5;145(19):dev166488. doi: 10.1242/dev.166488. Development. 2018. PMID: 30228104 Free PMC article.

7

Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice.

Motch Perrine SM, Wu M, Stephens NB, Kriti D, van Bakel H, Jabs EW, Richtsmeier JT. Motch Perrine SM, et al. Among authors: jabs ew. Dis Model Mech. 2019 May 30;12(5):dmm038513. doi: 10.1242/dmm.038513. Dis Model Mech. 2019. PMID: 31064775 Free PMC article.

8

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

9

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: jabs ew. BMC Dev Biol. 2010 Feb 22;10:22. doi: 10.1186/1471-213X-10-22. BMC Dev Biol. 2010. PMID: 20175913 Free PMC article.

10

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

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