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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Detalles Bibliográficos
Autores principales: Bai, Shanshan, Li, Dong, Xu, Liang, Duan, Huichuan, Yuan, Jie, Wei, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research
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

Internet

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

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