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Recombinant mouse periostin ameliorates coronal sutures fusion in Twist1(+/−) mice
BACKGROUND: Saethre–Chotzen syndrome is an autosomal dominantly inherited disorder caused by mutations in the twist family basic helix-loop-helix transcription factor 1 (TWIST1) gene. Surgical procedures are frequently required to reduce morphological and functional defects in patients with Saethre–...
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| Publicado no: | J Transl Med |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5905175/ https://ncbi.nlm.nih.gov/pubmed/29665811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12967-018-1454-2 |
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