Skeletal phenotypes in secreted frizzled-related protein 4 gene knockout mice mimic skeletal architectural abnormalities in subjects with Pyle’s disease from SFRP4 mutations

Mutations in SFRP4 cause Pyle’s bone disease with wide metaphyses and increased skeletal fragility. The WNT signaling pathway plays important roles in determining skeletal architecture and SFRP4 is a secreted Frizzled decoy receptor that inhibits WNT signaling. Seven cohorts of male and female Sfrp4...

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Detalles Bibliográficos
Autores principales: Brommage, Robert, Liu, Jeff, Powell, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941579/
https://www.ncbi.nlm.nih.gov/pubmed/36808149
http://dx.doi.org/10.1038/s41413-022-00242-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941579/
https://www.ncbi.nlm.nih.gov/pubmed/36808149
http://dx.doi.org/10.1038/s41413-022-00242-9

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