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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–...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905175/ https://www.ncbi.nlm.nih.gov/pubmed/29665811 http://dx.doi.org/10.1186/s12967-018-1454-2 |