Altered FGF signalling in congenital craniofacial and skeletal disorders
S Moosa, B Wollnik - Seminars in cell & developmental biology, 2016 - Elsevier
The fibroblast growth factor (FGF) signalling pathway has been the focus of intense genetic
and functional research for several decades. The emerging data implicate FGF signalling in …
and functional research for several decades. The emerging data implicate FGF signalling in …
FGF signaling in craniofacial biological control and pathological craniofacial development
NE Hatch - Critical Reviews™ in Eukaryotic Gene Expression, 2010 - dl.begellhouse.com
Fibroblast growth factor receptors comprise a family of four evolutionarily conserved
transmembrane proteins (FGFR1, FGFR2, FGFR3 and FGFR4) known to be critical for the …
transmembrane proteins (FGFR1, FGFR2, FGFR3 and FGFR4) known to be critical for the …
[PDF][PDF] Roles of FGF signaling in skeletal development and human genetic diseases
L Chen, CX Deng - Front Biosci, 2005 - article.imrpress.com
Fibroblast growth factor receptors (FGFRs) exist as a gene family of 4 membrane bound
receptor tyrosine kinases (FGFR1-4) that mediate signals of at least 22 fibroblast growth …
receptor tyrosine kinases (FGFR1-4) that mediate signals of at least 22 fibroblast growth …
FGF signalling in craniofacial development and developmental disorders
X Nie, K Luukko, P Kettunen - Oral diseases, 2006 - Wiley Online Library
The Fgf signalling pathway is highly conserved in evolution and plays crucial roles in
development. In the craniofacial region, it is involved in almost all structure development …
development. In the craniofacial region, it is involved in almost all structure development …
[HTML][HTML] Fibroblast growth factor (FGF) signaling in development and skeletal diseases
CM Teven, EM Farina, J Rivas, RR Reid - Genes & diseases, 2014 - Elsevier
Fibroblast growth factors (FGF) and their receptors serve many functions in both the
developing and adult organism. Humans contain 18 FGF ligands and four FGF receptors …
developing and adult organism. Humans contain 18 FGF ligands and four FGF receptors …
FGF signaling in the developing endochondral skeleton
DM Ornitz - Cytokine & growth factor reviews, 2005 - Elsevier
Mutations in fibroblast growth factor receptors (Fgfrs) are the etiology of many
craniosynostosis and chondrodysplasia syndromes in humans. The phenotypes associated …
craniosynostosis and chondrodysplasia syndromes in humans. The phenotypes associated …
FGF and FGFR signaling in chondrodysplasias and craniosynostosis
The first experimental mouse model for FGF2 in bone dysplasia was made serendipitously
by overexpression of FGF from a constitutive promoter. The results were not widely …
by overexpression of FGF from a constitutive promoter. The results were not widely …
Signaling by fibroblast growth factors (FGF) and fibroblast growth factor receptor 2 (FGFR2)–activating mutations blocks mineralization and induces apoptosis in …
A Mansukhani, P Bellosta, M Sahni… - The Journal of cell …, 2000 - rupress.org
Fibroblast growth factors (FGF) play a critical role in bone growth and development affecting
both chondrogenesis and osteogenesis. During the process of intramembranous …
both chondrogenesis and osteogenesis. During the process of intramembranous …
FGF signaling regulates development by processes beyond canonical pathways
AT Ray, P Mazot, JR Brewer, C Catela… - Genes & …, 2020 - genesdev.cshlp.org
FGFs are key developmental regulators that engage a signal transduction cascade through
receptor tyrosine kinases, prominently engaging ERK1/2 but also other pathways. However …
receptor tyrosine kinases, prominently engaging ERK1/2 but also other pathways. However …
Tissue‐specific responses to aberrant FGF signaling in complex head phenotypes
N Martínez‐Abadías, SM Motch… - Developmental …, 2013 - Wiley Online Library
BACKGROUND: The role of fibroblast growth factor and receptor (FGF/FGFR) signaling in
bone development is well studied, partly because mutations in FGFRs cause human …
bone development is well studied, partly because mutations in FGFRs cause human …