The Wnt1G177C mutation impairs mechanically induced bone formation via Nr4a2
Objectives: Wnt1 plays a crucial role in mediating the skeletal response to mechanical load, but its mechanisms, especially concerning the Wnt1 mutation associated with osteogenesis imperfecta type XV (OI-XV), remain elusive. We investigated the impact of the Wnt1G177C loss-of-function mutation during [for full text, please go to the a.m. URL]
Institutions
- Universität Hamburg (DE)
- University Medical Center Hamburg-Eppendorf (DE)
Publication Details
- Journal
- German Medical Science (German Research Foundation)
- Published
- 2024-10-21
- DOI
- https://doi.org/10.3205/24dkou045
- Primary Topic
- Connective tissue disorders research
- Type
- article
- Field-Weighted Citation Impact
- 0.00