Literature DB >> 12221714

Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome.

Ethan A Carver1, Kathleen F Oram, Thomas Gridley.   

Abstract

Saethre-Chotzen syndrome is a common autosomal dominant form of craniosynostosis, the premature fusion of the sutures of the calvarial bones of the skull. Most Saethre-Chotzen syndrome cases are caused by haploinsufficiency for the TWIST gene. Mice heterozygous for a null mutation of the Twist gene replicate certain features of Saethre-Chotzen syndrome, but have not been reported to exhibit craniosynostosis. We demonstrate that Twist heterozygous mice exhibit fusions of the coronal suture and other cranial suture abnormalities, indicating that Twist heterozygous mice constitute a better animal model for Saethre-Chotzen syndrome than was previously appreciated. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12221714     DOI: 10.1002/ar.10124

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  32 in total

1.  Jagged1 functions downstream of Twist1 in the specification of the coronal suture and the formation of a boundary between osteogenic and non-osteogenic cells.

Authors:  Hai-Yun Yen; Man-Chun Ting; Robert E Maxson
Journal:  Dev Biol       Date:  2010-08-19       Impact factor: 3.582

Review 2.  The role of vertebrate models in understanding craniosynostosis.

Authors:  Greg Holmes
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 3.  Neural crest cell signaling pathways critical to cranial bone development and pathology.

Authors:  Yuji Mishina; Taylor Nicholas Snider
Journal:  Exp Cell Res       Date:  2014-02-06       Impact factor: 3.905

4.  TWIST1 Homodimers and Heterodimers Orchestrate Lineage-Specific Differentiation.

Authors:  Xiaochen Fan; Ashley J Waardenberg; Madeleine Demuth; Pierre Osteil; Jane Q J Sun; David A F Loebel; Mark Graham; Patrick P L Tam; Nicolas Fossat
Journal:  Mol Cell Biol       Date:  2020-05-14       Impact factor: 4.272

5.  Gli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiation.

Authors:  David P C Rice; Elaine C Connor; Jacqueline M Veltmaat; Eva Lana-Elola; Lotta Veistinen; Yukiho Tanimoto; Saverio Bellusci; Ritva Rice
Journal:  Hum Mol Genet       Date:  2010-06-22       Impact factor: 6.150

6.  Candidate Gene Analyses of Skeletal Variation in Malocclusion.

Authors:  C S G da Fontoura; S F Miller; G L Wehby; B A Amendt; N E Holton; T E Southard; V Allareddy; L M Moreno Uribe
Journal:  J Dent Res       Date:  2015-04-24       Impact factor: 6.116

7.  Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.

Authors:  Yingli Wang; Miao Sun; Victoria L Uhlhorn; Xueyan Zhou; Inga Peter; Neus Martinez-Abadias; Cheryl A Hill; Christopher J Percival; Joan T Richtsmeier; David L Huso; Ethylin Wang Jabs
Journal:  BMC Dev Biol       Date:  2010-02-22       Impact factor: 1.978

8.  Unexpected functional redundancy between Twist and Slug (Snail2) and their feedback regulation of NF-kappaB via Nodal and Cerberus.

Authors:  Chi Zhang; Michael W Klymkowsky
Journal:  Dev Biol       Date:  2009-04-21       Impact factor: 3.582

9.  Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology.

Authors:  Greg Holmes; Gerson Rothschild; Upal Basu Roy; Chu-Xia Deng; Alka Mansukhani; Claudio Basilico
Journal:  Dev Biol       Date:  2009-01-29       Impact factor: 3.582

10.  Rapid re-synostosis following suturectomy in pediatric mice is age and location dependent.

Authors:  Christopher D Hermann; Kelsey Lawrence; Rene Olivares-Navarrete; Joseph K Williams; Robert E Guldberg; Barbara D Boyan; Zvi Schwartz
Journal:  Bone       Date:  2012-11-28       Impact factor: 4.398

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