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The study of abnormal bone development in the Apert syndrome Fgfr2(+/S252W) mouse using a 3D hydrogel culture model
Apert syndrome is caused by mutations in fibroblast growth factor receptor 2 (Fgfr2) and is characterized by craniosynostosis and other skeletal abnormalities. The Apert syndrome Fgfr2(+/S252W) mouse model exhibits perinatal lethality. A 3D hydrogel culture model, derived from tissue engineering str...
Tallennettuna:
| Päätekijät: | , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2743143/ https://ncbi.nlm.nih.gov/pubmed/18407821 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2008.02.008 |
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