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Adult Brtl/+ Mouse Model of Osteogenesis Imperfecta Demonstrates Anabolic Response to Sclerostin Antibody Treatment with Increased Bone Mass and Strength

PURPOSE: Osteogenesis imperfecta (OI) is a heritable collagen-related bone dysplasia, characterized by brittle bones with increased fracture risk. Although OI fracture risk is greatest before puberty, adults with OI remain at risk of fracture. Anti-resorptive bisphosphonates are commonly used to tre...

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Detalhes bibliográficos
Publicado no:Osteoporos Int
Main Authors: Sinder, Benjamin P., White, Logan E., Salemi, Joseph D., Ominsky, Michael S., Caird, Michelle S., Marini, Joan C., Kozloff, Kenneth M.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4415164/
https://ncbi.nlm.nih.gov/pubmed/24803333
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00198-014-2737-y
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