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...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Mol Endocrinol
Glavni autori: Chamoux, Estelle, Couture, Julie, Bisson, Martine, Morissette, Jean, Brown, Jacques P., Roux, Sophie
Format: Artigo
Jezik:Inglês
Izdano: Endocrine Society 2009
Teme:
Original Research
Online pristup: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
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items