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Title
Phenotype profile of a genetic mouse model for Muenke syndrome
Authors
Keywords
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Journal
CHILDS NERVOUS SYSTEM
Volume 28, Issue 9, Pages 1483-1493
Publisher
Springer Nature
Online
2012-08-07
DOI
10.1007/s00381-012-1778-9
References
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Related references
Note: Only part of the references are listed.- Palatal and Oral Manifestations of Muenke Syndrome (FGFR3-Related Craniosynostosis)
- (2012) Nneamaka Barbara Agochukwu et al. JOURNAL OF CRANIOFACIAL SURGERY
- Muenke Syndrome Mutation, FgfR3P244R, Causes TMJ Defects
- (2012) T. Yasuda et al. JOURNAL OF DENTAL RESEARCH
- Audiological Profile of Children and Young Adults With Syndromic and Complex Craniosynostosis
- (2011) Tim de Jong ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
- The Muenke syndrome mutation (FgfR3P244R) causes cranial base shortening associated with growth plate dysfunction and premature perichondrial ossification in murine basicranial synchondroses
- (2011) Jason Laurita et al. DEVELOPMENTAL DYNAMICS
- Craniofacial Growth in Patients With FGFR3Pro250Arg Mutation After Fronto-Orbital Advancement in Infancy
- (2011) Emily B. Ridgway et al. JOURNAL OF CRANIOFACIAL SURGERY
- Additional Phenotypic Features of Muenke Syndrome in 2 Dutch Families
- (2011) Tim de Jong et al. JOURNAL OF CRANIOFACIAL SURGERY
- Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
- (2010) A. O. M. Wilkie et al. PEDIATRICS
- Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene
- (2009) Xiao-lin Wu et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Significant phenotypic variability of Muenke syndrome in identical twins
- (2009) Luis F. Escobar et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Critical roles of the TGF-β type I receptor ALK5 in perichondrial formation and function, cartilage integrity, and osteoblast differentiation during growth plate development
- (2009) Tomoya Matsunobu et al. DEVELOPMENTAL BIOLOGY
- FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusion
- (2009) Masayo Harada et al. NATURE GENETICS
- Inner Ear Anomalies and Conductive Hearing Loss in Children With Apert Syndrome
- (2009) Guangwei Zhou et al. OTOLOGY & NEUROTOLOGY
- The Natural History of Patients Treated for FGFR3-Associated (Muenke-Type) Craniosynostosis
- (2009) M Barbera Honnebier et al. PLASTIC AND RECONSTRUCTIVE SURGERY
- A population-based study of craniosynostosis in metropolitan Atlanta, 1989–2003
- (2008) Sheree L. Boulet et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Fibroblast growth factor inhibits interferon γ-STAT1 and interleukin 6-STAT3 signaling in chondrocytes
- (2008) P KREJCI et al. CELLULAR SIGNALLING
- Development and tissue origins of the mammalian cranial base
- (2008) B. McBratney-Owen et al. DEVELOPMENTAL BIOLOGY
- Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome
- (2008) Stephen R. F. Twigg et al. DEVELOPMENTAL DYNAMICS
- Hearing loss in a mouse model of Muenke syndrome
- (2008) Suzanne L. Mansour et al. HUMAN MOLECULAR GENETICS
- FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway
- (2008) T. Matsushita et al. HUMAN MOLECULAR GENETICS
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