The fibroblast growth factor signaling pathway

DM Ornitz, N Itoh - Wiley Interdisciplinary Reviews …, 2015 - Wiley Online Library
The signaling component of the mammalian Fibroblast Growth Factor (FGF) family is
comprised of eighteen secreted proteins that interact with four signaling tyrosine kinase FGF …

Fibroblast growth factor signaling in skeletal development and disease

DM Ornitz, PJ Marie - Genes & development, 2015 - genesdev.cshlp.org
Fibroblast growth factor (FGF) signaling pathways are essential regulators of vertebrate
skeletal development. FGF signaling regulates development of the limb bud and formation of …

FGF receptors: cancer biology and therapeutics

M Katoh, H Nakagama - Medicinal research reviews, 2014 - Wiley Online Library
Fibroblast growth factors (FGFs) are involved in a variety of cellular processes, such as
stemness, proliferation, anti‐apoptosis, drug resistance, and angiogenesis. Here, FGF …

Therapeutics targeting FGF signaling network in human diseases

M Katoh - Trends in pharmacological sciences, 2016 - cell.com
Fibroblast growth factor (FGF) signaling through its receptors, FGFR1, FGFR2, FGFR3, or
FGFR4, regulates cell fate, angiogenesis, immunity, and metabolism. Dysregulated FGF …

[PDF][PDF] A genetic-pathophysiological framework for craniosynostosis

SRF Twigg, AOM Wilkie - The American Journal of Human Genetics, 2015 - cell.com
Craniosynostosis, the premature fusion of one or more cranial sutures of the skull, provides
a paradigm for investigating the interplay of genetic and environmental factors leading to …

[HTML][HTML] RUNX2-modifying enzymes: therapeutic targets for bone diseases

WJ Kim, HL Shin, BS Kim, HJ Kim… - Experimental & Molecular …, 2020 - nature.com
RUNX2 is a master transcription factor of osteoblast differentiation. RUNX2 expression in the
bone and osteogenic front of a suture is crucial for cranial suture closure and membranous …

Evidence-based medicine: craniosynostosis

JA Fearon - Plastic and reconstructive surgery, 2014 - journals.lww.com
This article provides an overview of the diagnosis and management of infants with
craniosynostosis. This review also incorporates some of the treatment philosophies followed …

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

CM Justice, G Yagnik, Y Kim, I Peter, EW Jabs… - Nature …, 2012 - nature.com
Sagittal craniosynostosis is the most common form of craniosynostosis, affecting
approximately one in 5,000 newborns. We conducted, to our knowledge, the first genome …

[HTML][HTML] Mutations in fam20b and xylt1 Reveal That Cartilage Matrix Controls Timing of Endochondral Ossification by Inhibiting Chondrocyte Maturation

BF Eames, YL Yan, ME Swartz, DS Levic… - PLoS …, 2011 - journals.plos.org
Differentiating cells interact with their extracellular environment over time. Chondrocytes
embed themselves in a proteoglycan (PG)-rich matrix, then undergo a developmental …

Evidence-based medicine: nonsyndromic craniosynostosis

Y Tahiri, SP Bartlett, MS Gilardino - Plastic and reconstructive …, 2017 - journals.lww.com
Craniosynostosis is a pathologic condition associated with the premature fusion of one or
more cranial sutures. When the cranial sutures fuse prematurely, the skull and the growing …