Further Analysis of the Crouzon Mouse: Effects of the FGFR2C342Y Mutation Are Cranial Bone–Dependent

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

Craniofacial reconstruction as a treatment for elevated intracranial pressure

(2011) Lissa C. Baird et al.   CHILDS NERVOUS SYSTEM

Treatment for delayed presentation of sagittal synostosis: challenges pertaining to occult intracranial hypertension

(2011) Mitchel Seruya et al.   Journal of Neurosurgery-Pediatrics

FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models

(2011) Neus Martínez-Abadías et al.   PLoS One

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

(2010) Yingli Wang et al.   BMC DEVELOPMENTAL BIOLOGY

Different endogenous threshold levels of Fibroblast Growth Factor-ligands determine the healing potential of frontal and parietal bones

(2010) Björn Behr et al.   BONE

Further biochemical and molecular characterization of primary rat parietal bone cell cultures

(2010) Thomas L. McCarthy et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Expression of bone morphogenetic protein messenger RNA in prolonged cultures of fetal rat calvarial cells

(2010) S.E. Harris et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Guidelines for assessment of bone microstructure in rodents using micro-computed tomography

(2010) Mary L Bouxsein et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis

(2010) A. O. M. Wilkie et al.   PEDIATRICS

Activation of FGF Signaling Mediates Proliferative and Osteogenic Differences between Neural Crest Derived Frontal and Mesoderm Parietal Derived Bone

(2010) Shuli Li et al.   PLoS One

Differential FGF Ligands and FGF Receptors Expression Pattern in Frontal and Parietal Calvarial Bones

(2009) Natalina Quarto et al.   CELLS TISSUES ORGANS

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

(2009) Greg Holmes et al.   DEVELOPMENTAL BIOLOGY

Intellectual Outcomes Following Protocol Management in Crouzon, Pfeiffer, and Muenke Syndromes

(2009) Walter J. Flapper et al.   JOURNAL OF CRANIOFACIAL SURGERY

Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome

(2008) Stephen R. F. Twigg et al.   DEVELOPMENTAL DYNAMICS

FGF2 Stimulation of the Pyrophosphate-Generating Enzyme, PC-1, in Pre-Osteoblast Cells Is Mediated by RUNX2

(2008) Nan E Hatch et al.   JOURNAL OF BONE AND MINERAL RESEARCH

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

(2007) Liangjun Yin et al.   BONE