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Nuclear FGF2 Isoforms Inhibit Bone Marrow Stromal Cell Mineralization through FGF23/FGFR/MAPK In Vitro
Fibroblast growth factor 23 (FGF23) is responsible for phosphate wasting and the phenotypic changes observed in human diseases such as X-Linked Hypophosphatemia (XLH). Targeted over-expression of nuclear high molecular weight fibroblast growth factor 2 isoforms (HMW isoforms) in osteoblasts resulted...
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| Autors principals: | , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3519956/ https://ncbi.nlm.nih.gov/pubmed/22836867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jbmr.1721 |
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