Effect of sclerostin inactivation in a mouse model of severe dominant osteogenesis imperfecta

Abstract Osteogenesis imperfecta (OI) is a rare bone disease that is associated with fractures and low bone mass. Sclerostin inhibition is being evaluated as a potential approach to increase bone mass in OI. We had previously found that in Col1a1 Jrt/+ mice, a model of severe OI, treatment with an a...

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Bibliographic Details
Main Authors: Juliana Marulanda, Josephine T. Tauer, Iris Boraschi-Diaz, Ghalib Bardai, Frank Rauch
Format: Article
Language:English
Published: Nature Portfolio 2023-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-32221-3

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