Cargando…
Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects
BACKGROUND: Conotruncal defects (CTDs) are a type of heterogeneous congenital heart diseases (CHDs), but little is known about their etiology. Increasing evidence has demonstrated that fibroblast growth factor (FGF) 8 and FGF10 may be involved in the pathogenesis of CTDs. METHODS: The variants of FG...
Autores principales: | Zhou, Shuang, Wang, Qingjie, Meng, Zhuo, Peng, Jiayu, Zhou, Yue, Song, Wenting, Wang, Jian, Chen, Sun, Sun, Kun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362408/ https://www.ncbi.nlm.nih.gov/pubmed/32664970 http://dx.doi.org/10.1186/s12967-020-02445-2 |
Ejemplares similares
-
The Fgf8 subfamily (Fgf8, Fgf17 and Fgf18) is required for closure of the embryonic ventral body wall
por: Boylan, Michael, et al.
Publicado: (2020) -
TGF beta inhibits HGF, FGF7, and FGF10 expression in normal and IPF lung fibroblasts
por: Correll, Kelly A., et al.
Publicado: (2018) -
Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients
por: Mengmeng, Xu, et al.
Publicado: (2020) -
A loss‐of‐function mutation p.T256M in NDRG4 is implicated in the pathogenesis of pulmonary atresia with ventricular septal defect (PA/VSD) and tetralogy of Fallot (TOF)
por: Peng, Jiayu, et al.
Publicado: (2021) -
Fgf22 regulated by Fgf3/Fgf8 signaling is required for zebrafish midbrain development
por: Miyake, Ayumi, et al.
Publicado: (2013)