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 signalling in osteoarthritis and cartilage repair

Y Xie, A Zinkle, L Chen, M Mohammadi - Nature Reviews …, 2020 - nature.com
Regulated fibroblast growth factor (FGF) signalling is a prerequisite for the correct
development and homeostasis of articular cartilage, as evidenced by the fact that aberrant …

Craniosynostosis

D Johnson, AOM Wilkie - European Journal of Human Genetics, 2011 - nature.com
Craniosynostosis, defined as the premature fusion of the cranial sutures, presents many
challenges in classification and treatment. At least 20% of cases are caused by specific …

Cranial sutures as intramembranous bone growth sites

LA Opperman - … dynamics: an official publication of the …, 2000 - Wiley Online Library
Intramembranous bone growth is achieved through bone formation within a periosteum or
by bone formation at sutures. Sutures are formed during embryonic development at the sites …

Achondroplasia

WA Horton, JG Hall, JT Hecht - The Lancet, 2007 - thelancet.com
Achondroplasia is the most common form of short limb dwarfism in human beings, affecting
more than 250 000 individuals worldwide. More than 95% of patients have the same point …

Guideline for care of patients with the diagnoses of craniosynostosis: working group on craniosynostosis

IMJ Mathijssen - Journal of Craniofacial Surgery, 2015 - journals.lww.com
This guideline for care of children with craniosynostosis was developed by a national
working group with representatives of 11 matrix societies of specialties and the national …

Increase of prevalence of craniosynostosis

M Cornelissen, B den Ottelander, D Rizopoulos… - Journal of Cranio …, 2016 - Elsevier
Introduction Craniosynostosis represents premature closure of cranial sutures. Prevalence is
approximately 3.1–6.4 in 10.000 live births, which is reportedly rising. This epidemiologic …

Craniosynostosis: genes and mechanisms

AOM Wilkie - Human molecular genetics, 1997 - academic.oup.com
Enlargement of the skull vault occurs by appositional growth at the fibrous joints between the
bones, termed cranial sutures. Relatively little is known about the developmental biology of …

A population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003

SL Boulet, SA Rasmussen… - American Journal of …, 2008 - Wiley Online Library
Craniosynostosis is a birth defect characterized by premature fusion of one or more cranial
sutures. We describe the birth prevalence of craniosynostosis and related risk factors among …

Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis

AOM Wilkie, JC Byren, JA Hurst, J Jayamohan… - …, 2010 - publications.aap.org
OBJECTIVES: We describe the first cohort-based analysis of the impact of genetic disorders
in craniosynostosis. We aimed to refine the understanding of prognoses and pathogenesis …