Effect of immunosuppressants on a mouse model of osteogenesis imperfecta type V harboring a heterozygous Ifitm5 c.-14C > T mutation

Osteogenesis imperfecta (OI) type V is an autosomal dominant disorder caused by the c.-14C > T mutation in the interferon-induced transmembrane protein 5 gene (IFITM5), however, its onset mechanism remains unclear. In this study, heterozygous c.-14C > T mutant mice were developed to investigat...

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Detalles Bibliográficos
Autores principales: Hanagata, Nobutaka, Takemura, Taro, Kamimura, Keiko, Koda, Toshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713238/
https://www.ncbi.nlm.nih.gov/pubmed/33273604
http://dx.doi.org/10.1038/s41598-020-78403-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713238/
https://www.ncbi.nlm.nih.gov/pubmed/33273604
http://dx.doi.org/10.1038/s41598-020-78403-1

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