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LITERATURE CITED

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  • Guenou H, Kaabeche K, Mee SL, Marie PJ. 2005. A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre–Chotzen syndrome. Hum Mol Genet 14:14291439.
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  • Hinoi E, Bialek P, Chen Y, Rached MT, Groner Y, Behringer RR, Ornitz DM, Karsenty G. 2006. Runx2 inhibits chondrocyte proliferation and hypertrophy through its expression in the perichondrium. Genes Dev 20:29372942.
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  • Marie PJ, Kaabeche K, Guenou H. 2008. Roles of FGFR2 and TWIST in human craniosynostosis: insights from genetic mutations in cranial osteoblasts. Front Oral Biol 12:144159.
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  • Martínez-Abadías N, Motch S, Pankratz T, Wang Y, Aldridge K, Jabs EW, Richtsmeier JT. 2013b. Tissue specific responses to aberrant FGF signaling in complex head phenotypes. Dev Dyn 242:8094.
  • Martínez-Abadías N, Percival C, Aldridge K, Hill CA, Ryan T, Sirivunnabood S, Wang Y, Jabs EW, Richtsmeier JT. 2010. Beyond the closed suture in apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth. Dev Dyn 239:30583071.
  • Miraoui H, Marie P. 2010. Pivotal role of Twist in skeletal biology and pathology. Gene 468:17.
  • Mooney MP, Siegel MI, Burrows AM, Smith TD, Losken HW, Dechant J, Cooper G, Kapucu MR. 1998. A rabbit model of human familial, nonsyndromic unicoronal suture synostosis. I. Synostotic onset, pathology, and sutural growth patterns. Childs Nerv Syst 14:236246.
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  • Seto M, Hing A, Chang J, Hu M, Kapp-Simon K, Patel P, Burton B, Kane AA, Smyth M, Hopper R, Ellenbogen R, Stevenson K, Speltz M, Cunningham ML. 2007. Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations. Am J Med Genet Part A 143A:678686.
  • Sharma VP, Fenwick AL, Brockop MS, McGowan SJ, Goos JAC, Hoogeboom AJM, Brady AF, Jeelani NO, Lynch SA, Mulliken JB, Murray DJ, Phipps JM, Sweeney E, Tomkins SE, Wilson LC, Bennett S, Cornall RJ, Broxholme J, Kanapin A, Johnson D, Wall SA, Spek P, Mathijssen IMJ, Maxson RE, Twigg SR, Wilkie AOM. 2013. Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Nat Genet 45:304307.
  • Wiley DF, Amenta N, Alcantara DA, Ghosh D, Kil YJ, Delson E, Harcourt-Smith W, Rohlf FJ, St. John K, Hamann B. 2005.Evolutionary morphing. Visualization, 2005. VIS 05. IEEE, Minneapolis, MN: 431438. doi:10.1109/VISUAL.2005.1532826.
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  • Yousfi M, Lasmoles F, El Ghouzzi V, Marie PJ. 2002a. Twist haploinsufficiency in Saethre–Chotzen syndrome induces calvarial osteoblast apoptosis due to increased TNFalpha expression and caspase-2 activation. Hum Mol Genet 11:359369.
  • Yousfi M, Lasmoles F, Lomri A, Delannoy P, Marie PJ. 2001. Increased bone formation and decreased osteocalcin expression induced by reduced TWIST dosage in Saethre–Chotzen syndrome. J Clin Invest 107:11531161.
  • Yousfi M, Lasmoles F, Marie PJ. 2002b. TWIST inactivation reduces CBFA1/RUNX2 expression and DNA binding to the osteocalcin promoter in osteoblasts. Biochem Biophys Res Commun 297:641644.
  • Yu W, Zhang Y, Ruest L, Svoboda K. 2013. Analysis of Snail1 function and regulation by Twist1 in palatal fusion. Front Physiol 4:110.
  • Zhang Y, Blackwell E, McKnight M, Knutsen G, Vu W, Ruest L. 2012. Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with Hand2. Dev Dyn 241:924940.