标题
Phenotype profile of a genetic mouse model for Muenke syndrome
作者
关键词
-
出版物
CHILDS NERVOUS SYSTEM
Volume 28, Issue 9, Pages 1483-1493
出版商
Springer Nature
发表日期
2012-08-07
DOI
10.1007/s00381-012-1778-9
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Palatal and Oral Manifestations of Muenke Syndrome (FGFR3-Related Craniosynostosis)
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- Muenke Syndrome Mutation, FgfR3P244R, Causes TMJ Defects
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- Audiological Profile of Children and Young Adults With Syndromic and Complex Craniosynostosis
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- 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
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- Additional Phenotypic Features of Muenke Syndrome in 2 Dutch Families
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- Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
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- Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene
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- (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
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- FGF9 monomer–dimer equilibrium regulates extracellular matrix affinity and tissue diffusion
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- Inner Ear Anomalies and Conductive Hearing Loss in Children With Apert Syndrome
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- 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
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- Development and tissue origins of the mammalian cranial base
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- 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
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