The role of WNT and IL-1 signaling in osteoarthritis: therapeutic implications for platelet-rich plasma therapy
Antonio Tonutti(Humanitas University), Angela Ceribelli(Istituto di Sessuologia Clinica), Veronica Marrella(Institute of Genetic and Biomedical Research), Cristiano Sconza(Humanitas University), Cristina Sobacchi(Humanitas University), Valentina Granata(Institute of Genetic and Biomedical Research), Nicola Rani(Istituto Ortopedico Rizzoli), Rita Ragusa(Istituti di Ricovero e Cura a Carattere Scientifico), Berardo Di Matteo(Humanitas University)
Cited by 21
Related Papers
Osteopetrosis: genetics, treatment and new insights into osteoclast function
|Nature Reviews Endocrinology|2013|580
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL
|Nature Genetics|2007|387
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
|The American Journal of Human Genetics|2008|307
AIRE deficiency in thymus of 2 patients with Omenn syndrome
|Journal of Clinical Investigation|2005|152
AIRE deficiency in thymus of 2 patients with Omenn syndrome
|Journal of Clinical Investigation|2005|147