The bone phenotype associated with cherubism is independent of Caspase-1-dependent inflammasome activation in the mouse.

Cherubism is a rare genetic disorder caused by SH3BP2 mutations. This sterile autoinflammatory disease is characterized by jaw osteolysis, in which bone tissue is replaced by multinucleated giant cells containing fibrous tissue. The cherubism mouse model (Sh3bp2 KI) is characterized by systemic bone...

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Bibliographic Details
Main Authors: Badre-Victor Rabhi, Sylvie Thomasseau, Xavier Decrouy, Martine Cohen-Solal, Marcel Deckert, Amélie E Coudert, François Brial
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2025-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0318826
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