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Fibrillin-1 directly regulates osteoclast formation and function by a dual mechanism
Mutations in the fibrillin-1 gene give rise to a number of heritable disorders, which are all characterized by various malformations of bone as well as manifestations in other tissues. However, the role of fibrillin-1 in the development and homeostasis of bone is not well understood. Here, we examin...
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| Publicado no: | J Cell Sci |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4961468/ https://ncbi.nlm.nih.gov/pubmed/24039232 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/jcs.127571 |
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