ba0006p132 | (1) | ICCBH2017
Palmisano Biagio
, Labella Rossella
, Spica Emanuela
, Remoli Cristina
, Corsi Alessandro
, Robey Pamela
, Riminucci Mara
Fibrous dysplasia of bone (FD) is a crippling skeletal disease caused by activating mutations (R201C, R201H) of the Gsα gene. We recently generated GsαR201C transgenic mice that develop a FD skeletal phenotype. The analyses of these mice demonstrated that increased bone resorption is one of the main morbidity factors in FD and that RANKL is the major molecular mediator of osteolysis at affected skeletal sites.Ob...