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Monica Mottes

Showing results (41-50 of 45) with videos related to

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Scientific Reports|February 19, 2020
Publisher Correction: Runx2 stimulates neoangiogenesis through the Runt domain in melanomaDaniela Cecconi, Jessica Brandi, Marcello Manfredi, et al.
Scientific Reports|May 31, 2019
Runx2 stimulates neoangiogenesis through the Runt domain in melanomaDaniela Cecconi, Jessica Brandi, Marcello Manfredi, et al.
Cells|November 23, 2018
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and MigrationMichela Deiana, Luca Dalle Carbonare, Michela Serena, et al.
Cell Communication and Signaling : CCS|November 27, 2025
Extracellular vesicles from long COVID patients promote RUNX2-mediated cellular stress via dysregulated miR-204 and p53 pathway activationLuca Dalle Carbonare, Arianna Minoia, Sharazed Zouari, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
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Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
Scientific Reports|February 19, 2020
Publisher Correction: Runx2 stimulates neoangiogenesis through the Runt domain in melanomaDaniela Cecconi, Jessica Brandi, Marcello Manfredi, et al.
Scientific Reports|May 31, 2019
Runx2 stimulates neoangiogenesis through the Runt domain in melanomaDaniela Cecconi, Jessica Brandi, Marcello Manfredi, et al.
Cells|November 23, 2018
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and MigrationMichela Deiana, Luca Dalle Carbonare, Michela Serena, et al.
Cell Communication and Signaling : CCS|November 27, 2025
Extracellular vesicles from long COVID patients promote RUNX2-mediated cellular stress via dysregulated miR-204 and p53 pathway activationLuca Dalle Carbonare, Arianna Minoia, Sharazed Zouari, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
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