Gender-Related Impact of Sclerostin Antibody on Bone in the Osteogenesis Imperfecta Mouse

Osteogenesis imperfecta (OI), which is most often due to a collagen type 1 gene mutation, is characterized by low bone density and bone fragility. In OI patients, gender-related differences were reported, but data in the literature are not convergent. We previously observed that sclerostin antibody...

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Detalles Bibliográficos
Autores principales: Cardinal, Mickaël, Chretien, Antoine, Roels, Thomas, Lafont, Sébastien, Ominsky, Michael S., Devogelaer, Jean-Pierre, Manicourt, Daniel H., Behets, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383339/
https://www.ncbi.nlm.nih.gov/pubmed/34447412
http://dx.doi.org/10.3389/fgene.2021.705505

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383339/
https://www.ncbi.nlm.nih.gov/pubmed/34447412
http://dx.doi.org/10.3389/fgene.2021.705505

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