Carregant...
Kindlin-3 Mutation in Mesenchymal Stem Cells Results in Enhanced Chondrogenesis
Identifying patient mutations driving skeletal development disorders has driven our understanding of bone development. Integrin adhesion deficiency disease is caused by a Kindlin-3 (fermitin family member 3) mutation, and its inactivation results in bleeding disorders and osteopenia. In this study,...
Guardat en:
| Publicat a: | Exp Cell Res |
|---|---|
| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2021
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7874523/ https://ncbi.nlm.nih.gov/pubmed/33417921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2020.112456 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|