Mutations in the SH3-domain binding protein 2 (SH3BP2) are known to cause a rare childhood disorder called cherubism that is characterized by inflammation and bone loss in the jaw, but the mechanism has remained unclear. In this issue, Ueki et al. (Ueki et al., 2007) now demonstrate that a cherubism mutation activates mouse Sh3bp2 resulting in enhanced production of the cytokine TNF-α by myeloid cells, leading to both bone loss and inflammation
SH3BP2 is a signaling adapter protein which regulates immune and skeletal systems. Gain-of-function ...
Cherubism is a rare developmental lesion of the jaw that is generally inherited as an autosomal domi...
SummaryCherubism is an autosomal-dominant syndrome characterized by inflammatory destructive bony le...
Cherubism (OMIM# 118400) is a genetic disorder with excessive jawbone resorption caused by mutations...
SummaryCherubism is caused by mutations in SH3BP2. Studies of cherubism mice showed that tumor necro...
Cherubism is a rare bone dysplasia that is characterized by symmetrical bone resorption limited to t...
International audienceCherubism is a rare autoinflammatory bone disorder that is associated with poi...
Cherubism is a rare autosomal dominant craniofacial disorder affecting pre-pubertal children. It is ...
Cherubism is a rare bone dysplasia that is characterized by symmetrical bone resorption limited to t...
We describe a novel missense mutation (Aspartic acid to Asparagine, p.D419N (g.1371G>A, c.1255G&g...
Cherubism (OMIM#118400) is a craniofacial disorder characterized by destructive jaw expansion. Gain‐...
Cherubism (CBM) is characterized by multiple fibro-osseous lesions in jawbones and caused by mutatio...
Cherubism is a human genetic disorder that affects children around the ages of 3-4 years. It causes ...
Cherubism (MIM 118400) is an autosomal dominant inherited syndrome characterized by excessive bone d...
SH3BP2 is a signaling adapter protein which regulates immune and skeletal systems. Gain-of-function ...
SH3BP2 is a signaling adapter protein which regulates immune and skeletal systems. Gain-of-function ...
Cherubism is a rare developmental lesion of the jaw that is generally inherited as an autosomal domi...
SummaryCherubism is an autosomal-dominant syndrome characterized by inflammatory destructive bony le...
Cherubism (OMIM# 118400) is a genetic disorder with excessive jawbone resorption caused by mutations...
SummaryCherubism is caused by mutations in SH3BP2. Studies of cherubism mice showed that tumor necro...
Cherubism is a rare bone dysplasia that is characterized by symmetrical bone resorption limited to t...
International audienceCherubism is a rare autoinflammatory bone disorder that is associated with poi...
Cherubism is a rare autosomal dominant craniofacial disorder affecting pre-pubertal children. It is ...
Cherubism is a rare bone dysplasia that is characterized by symmetrical bone resorption limited to t...
We describe a novel missense mutation (Aspartic acid to Asparagine, p.D419N (g.1371G>A, c.1255G&g...
Cherubism (OMIM#118400) is a craniofacial disorder characterized by destructive jaw expansion. Gain‐...
Cherubism (CBM) is characterized by multiple fibro-osseous lesions in jawbones and caused by mutatio...
Cherubism is a human genetic disorder that affects children around the ages of 3-4 years. It causes ...
Cherubism (MIM 118400) is an autosomal dominant inherited syndrome characterized by excessive bone d...
SH3BP2 is a signaling adapter protein which regulates immune and skeletal systems. Gain-of-function ...
SH3BP2 is a signaling adapter protein which regulates immune and skeletal systems. Gain-of-function ...
Cherubism is a rare developmental lesion of the jaw that is generally inherited as an autosomal domi...
SummaryCherubism is an autosomal-dominant syndrome characterized by inflammatory destructive bony le...