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Title
Craniofacial Shape Variation inTwist1+/−Mutant Mice
Authors
Keywords
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Journal
Anatomical Record-Advances in Integrative Anatomy and Evolutionary Biology
Volume 297, Issue 5, Pages 826-833
Publisher
Wiley
Online
2014-06-09
DOI
10.1002/ar.22899
References
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Related references
Note: Only part of the references are listed.- Second family with the boston-type craniosynostosis syndrome: Novel mutation and expansion of the clinical spectrum
- (2013) Alexander Janssen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Postnatal brain and skull growth in an Apert syndrome mouse model
- (2013) Cheryl A. Hill et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome
- (2013) N. Martinez-Abadias et al. Disease Models & Mechanisms
- Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis
- (2013) Vikram P Sharma et al. NATURE GENETICS
- Analysis of Snail1 function and regulation by Twist1 in palatal fusion
- (2013) Wenli Yu et al. Frontiers in Physiology
- Interrelationship of Cranial Suture Fusion, Basicranial Development, and Resynostosis Following Suturectomy in Twist1+/− Mice, a Murine Model of Saethre-Chotzen Syndrome
- (2012) Christopher D. Hermann et al. CALCIFIED TISSUE INTERNATIONAL
- Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome
- (2012) Greg Holmes et al. DEVELOPMENTAL BIOLOGY
- The mesenchymal architecture of the cranial mesoderm of mouse embryos is disrupted by the loss of Twist1 function
- (2012) Heidi Bildsoe et al. DEVELOPMENTAL BIOLOGY
- Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with hand2
- (2012) Yanping Zhang et al. DEVELOPMENTAL DYNAMICS
- Tissue-specific responses to aberrant FGF signaling in complex head phenotypes
- (2012) Neus Martínez-Abadías et al. DEVELOPMENTAL DYNAMICS
- A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
- (2012) Cristina M Justice et al. NATURE GENETICS
- Facial suture synostosis of newborn Fgfr1P250R/+ and Fgfr2S252W/+ mouse models of Pfeiffer and Apert syndromes
- (2011) Roopa Purushothaman et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
- Normal and disease-related biological functions of Twist1 and underlying molecular mechanisms
- (2011) Qian Qin et al. CELL RESEARCH
- Persistent expression of Twist1 in chondrocytes causes growth plate abnormalities and dwarfism in mice
- (2011) Rosa M. Guzzo et al. INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY
- Beyond the closed suture in apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth
- (2010) Neus Martínez-Abadías et al. DEVELOPMENTAL DYNAMICS
- Pivotal role of Twist in skeletal biology and pathology
- (2010) Hichem Miraoui et al. GENE
- MorphoJ: an integrated software package for geometric morphometrics
- (2010) CHRISTIAN PETER KLINGENBERG Molecular Ecology Resources
- Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
- (2010) A. O. M. Wilkie et al. PEDIATRICS
- Requirement for Twist1 in frontonasal and skull vault development in the mouse embryo
- (2009) Heidi Bildsoe et al. DEVELOPMENTAL BIOLOGY
- A population-based study of craniosynostosis in metropolitan Atlanta, 1989–2003
- (2008) Sheree L. Boulet et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
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