Craniosynostoses: Lessons Learned from Animal Models
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-31512-6_57-1
Reference33 articles.
1. Behr B, Longaker MT, Quarto N (2011) Craniosynostosis of coronal suture in twist1 mice occurs through endochondral ossification recapitulating the physiological closure of posterior frontal suture. Front Physiol 2:37. https://doi.org/10.3389/fphys.2011.00037
2. Bialek P, Kern B, Yang X, Schrock M, Sosic D, Hong N, Wu H, Yu K, Ornitz DM, Olson EN, Justice MJ, Karsenty G (2004) A twist code determines the onset of osteoblast differentiation. Dev Cell 6:423–435
3. Bourgeois P, Bolcato-Bellemin AL, Danse JM, Bloch-Zupan A, Yoshiba K, Stoetzel C, Perrin-Schmitt F (1998) The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome. Hum Mol Genet 7:945–957
4. Carlton MB, Colledge WH, Evans MJ (1998) Crouzon-like craniofacial dysmorphology in the mouse is caused by an insertional mutation at the Fgf3/Fgf4 locus. Dev Dyn Off Publ Am Assoc Anat 212:242–249. https://doi.org/10.1002/(SICI)1097-0177(199806)212:2<242::AID-AJA8>3.0.CO;2-H
5. Carver EA, Oram KF, Gridley T (2002) Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome. Anat Rec 268:90–92. https://doi.org/10.1002/ar.10124
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