Morphological and mechanical characterization of bone phenotypes in the Amish G610C murine model of osteogenesis imperfecta

Osteogenesis imperfecta (OI) is a hereditary bone disease where gene mutations affect Type I collagen formation resulting in osteopenia and increased fracture risk. There are several established mouse models of OI, but some are severe and result in spontaneous fractures or early animal death. The Am...

Descripción completa

Detalles Bibliográficos
Autores principales: Kohler, Rachel, Tastad, Carli A., Creecy, Amy, Wallace, Joseph M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396767/
https://www.ncbi.nlm.nih.gov/pubmed/34449800
http://dx.doi.org/10.1371/journal.pone.0255315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396767/
https://www.ncbi.nlm.nih.gov/pubmed/34449800
http://dx.doi.org/10.1371/journal.pone.0255315

Ejemplares similares