The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV

The recent identification of homozygous WNT1 mutations in individuals with osteogenesis imperfecta type XV (OI-XV) has suggested that WNT1 is a key ligand promoting the differentiation and function of bone-forming osteoblasts. Although such an influence was supported by subsequent studies, a mouse m...

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Veröffentlicht in:	Bone Research 2021-11, Vol.9 (1), p.48-48, Article 48
Hauptverfasser:	Vollersen, Nele, Zhao, Wenbo, Rolvien, Tim, Lange, Fabiola, Schmidt, Felix Nikolai, Sonntag, Stephan, Shmerling, Doron, von Kroge, Simon, Stockhausen, Kilian Elia, Sharaf, Ahmed, Schweizer, Michaela, Karsak, Meliha, Busse, Björn, Bockamp, Ernesto, Semler, Oliver, Amling, Michael, Oheim, Ralf, Schinke, Thorsten, Yorgan, Timur Alexander
Format:	Artikel
Sprache:	eng
Schlagworte:	631/443/811 692/699/317/821 Internal Medicine Medicine Medicine & Public Health Mutation Orthopedics
Online-Zugang:	Volltext
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