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The p62 P392L Mutation Linked to Paget’s Disease Induces Activation of Human Osteoclasts
Mutations of the gene encoding p62/SQSTM1 have been described in Paget’s disease of bone (PDB), identifying p62 as an important player in osteoclast signaling. We investigated the phenotype of osteoclasts differentiated from peripheral blood monocytes obtained from healthy donors or PDB patients, al...
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| Publicado no: | Mol Endocrinol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5224938/ https://ncbi.nlm.nih.gov/pubmed/19589897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/me.2009-0066 |
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