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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,...
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| Publicado no: | Exp Cell Res |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2021
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| Assuntos: | |
| Acesso em linha: | 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 |
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