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Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease

The fibroblast growth factor (FGF) regulatory axis is phylogenetically ancient, evolving into a large mammalian/human gene family of 22 ligands that bind to four receptor tyrosine kinases for a complex physiologic system controlling cell growth, differentiation, and metabolism. The tissue targets fo...

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Detalles Bibliográficos
Autores principales: Coffin, J Douglas, Homer-Bouthiette, Collin, Hurley, Marja Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009610/
https://www.ncbi.nlm.nih.gov/pubmed/29942929
http://dx.doi.org/10.1210/js.2018-00105
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author Coffin, J Douglas
Homer-Bouthiette, Collin
Hurley, Marja Marie
author_facet Coffin, J Douglas
Homer-Bouthiette, Collin
Hurley, Marja Marie
author_sort Coffin, J Douglas
collection PubMed
description The fibroblast growth factor (FGF) regulatory axis is phylogenetically ancient, evolving into a large mammalian/human gene family of 22 ligands that bind to four receptor tyrosine kinases for a complex physiologic system controlling cell growth, differentiation, and metabolism. The tissue targets for the primary FGF function are mainly in cartilage and in bone for morphogenesis, mineralization, and metabolism. A multitude of complexities in the FGF ligand-receptor signaling pathways have made translation into therapies for FGF-related bone disorders such as osteomalacia, osteoarthritis, and osteoporosis difficult but not impossible.
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spelling pubmed-60096102018-06-25 Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease Coffin, J Douglas Homer-Bouthiette, Collin Hurley, Marja Marie J Endocr Soc Mini-Reviews The fibroblast growth factor (FGF) regulatory axis is phylogenetically ancient, evolving into a large mammalian/human gene family of 22 ligands that bind to four receptor tyrosine kinases for a complex physiologic system controlling cell growth, differentiation, and metabolism. The tissue targets for the primary FGF function are mainly in cartilage and in bone for morphogenesis, mineralization, and metabolism. A multitude of complexities in the FGF ligand-receptor signaling pathways have made translation into therapies for FGF-related bone disorders such as osteomalacia, osteoarthritis, and osteoporosis difficult but not impossible. Endocrine Society 2018-05-28 /pmc/articles/PMC6009610/ /pubmed/29942929 http://dx.doi.org/10.1210/js.2018-00105 Text en Copyright © 2018 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mini-Reviews
Coffin, J Douglas
Homer-Bouthiette, Collin
Hurley, Marja Marie
Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title_full Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title_fullStr Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title_full_unstemmed Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title_short Fibroblast Growth Factor 2 and Its Receptors in Bone Biology and Disease
title_sort fibroblast growth factor 2 and its receptors in bone biology and disease
topic Mini-Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009610/
https://www.ncbi.nlm.nih.gov/pubmed/29942929
http://dx.doi.org/10.1210/js.2018-00105
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