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Application of Human Induced Pluripotent Stem Cells to Model Fibrodysplasia Ossificans Progressiva
Fibrodysplasia ossificans progressiva (FOP) is a genetic condition characterized by massive heterotopic ossification. FOP patients with mutations in the Activin A type I receptor (ACVR1), a bone morphogenetic protein (BMP) receptor. FOP is a progressive and debilitating disease characterized by bone...
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| Veröffentlicht in: | Bone |
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| Hauptverfasser: | , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5767535/ https://ncbi.nlm.nih.gov/pubmed/28716551 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2017.07.003 |
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