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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Mol Endocrinol
Autors principals: Chamoux, Estelle, Couture, Julie, Bisson, Martine, Morissette, Jean, Brown, Jacques P., Roux, Sophie
Format: Artigo
Idioma:Inglês
Publicat: Endocrine Society 2009
Matèries:
Original Research
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars