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Current and emerging treatments for the management of osteogenesis imperfecta.
Monti E, Mottes M, Fraschini P, Brunelli P, Forlino A, Venturi G, Doro F, Perlini S, Cavarzere P, Antoniazzi F. Monti E, et al. Among authors: antoniazzi f. Ther Clin Risk Manag. 2010 Sep 7;6:367-81. doi: 10.2147/tcrm.s5932. Ther Clin Risk Manag. 2010. PMID: 20856683 Free PMC article.
Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen.
Venturi G, Gandini A, Monti E, Dalle Carbonare L, Corradi M, Vincenzi M, Valenti MT, Valli M, Pelilli E, Boner A, Mottes M, Antoniazzi F. Venturi G, et al. Among authors: antoniazzi f. J Bone Miner Res. 2012 Mar;27(3):723-8. doi: 10.1002/jbmr.1480. J Bone Miner Res. 2012. PMID: 22113968 Free article.
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration.
Deiana M, Dalle Carbonare L, Serena M, Cheri S, Parolini F, Gandini A, Marchetto G, Innamorati G, Manfredi M, Marengo E, Brandi J, Cecconi D, Mori A, Mina MM, Antoniazzi F, Mottes M, Tiso N, Malerba G, Zipeto D, Valenti MT. Deiana M, et al. Among authors: antoniazzi f. Cells. 2018 Nov 20;7(11):220. doi: 10.3390/cells7110220. Cells. 2018. PMID: 30463392 Free PMC article.
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma.
Cecconi D, Brandi J, Manfredi M, Serena M, Dalle Carbonare L, Deiana M, Cheri S, Parolini F, Gandini A, Marchetto G, Innamorati G, Avanzi F, Antoniazzi F, Marengo E, Tiso N, Mottes M, Zipeto D, Valenti MT. Cecconi D, et al. Among authors: antoniazzi f. Sci Rep. 2019 May 29;9(1):8052. doi: 10.1038/s41598-019-44552-1. Sci Rep. 2019. PMID: 31142788 Free PMC article.
168 results