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Osteoblast-specific expression of the fibrous dysplasia (FD)-causing mutation Gsα(R201C) produces a high bone mass phenotype but does not reproduce FD in the mouse.
Remoli C, Michienzi S, Sacchetti B, Consiglio AD, Cersosimo S, Spica E, Robey PG, Holmbeck K, Cumano A, Boyde A, Davis G, Saggio I, Riminucci M, Bianco P. Remoli C, et al. Among authors: saggio i. J Bone Miner Res. 2015 Jun;30(6):1030-43. doi: 10.1002/jbmr.2425. J Bone Miner Res. 2015. PMID: 25487351 Free PMC article.
Fibrous dysplasia as a stem cell disease.
Riminucci M, Saggio I, Robey PG, Bianco P. Riminucci M, et al. Among authors: saggio i. J Bone Miner Res. 2006 Dec;21 Suppl 2:P125-31. doi: 10.1359/jbmr.06s224. J Bone Miner Res. 2006. PMID: 17229001 Free article. Review.
No Identical "Mesenchymal Stem Cells" at Different Times and Sites: Human Committed Progenitors of Distinct Origin and Differentiation Potential Are Incorporated as Adventitial Cells in Microvessels.
Sacchetti B, Funari A, Remoli C, Giannicola G, Kogler G, Liedtke S, Cossu G, Serafini M, Sampaolesi M, Tagliafico E, Tenedini E, Saggio I, Robey PG, Riminucci M, Bianco P. Sacchetti B, et al. Among authors: saggio i. Stem Cell Reports. 2016 Jun 14;6(6):897-913. doi: 10.1016/j.stemcr.2016.05.011. Stem Cell Reports. 2016. PMID: 27304917 Free PMC article.
66 results