Cargando…
DNA methylation status of TBX20 in patients with tetralogy of Fallot
BACKGROUND: TBX20 plays an important role in heart development; however, its epigenetic regulation in the pathogenesis of tetralogy of Fallot (TOF) remains unclear. METHODS: The methylation levels of the TBX20 promoter region in the right ventricular myocardial tissues of TOF and control samples wer...
Autores principales: | Gong, Juan, Sheng, Wei, Ma, Duan, Huang, Guoying, Liu, Fang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6540552/ https://www.ncbi.nlm.nih.gov/pubmed/31138201 http://dx.doi.org/10.1186/s12920-019-0534-3 |
Ejemplares similares
-
LINE-1 methylation status and its association with tetralogy of fallot in infants
por: Sheng, Wei, et al.
Publicado: (2012) -
Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducing TBX5 expression
por: Ma, Jing, et al.
Publicado: (2020) -
DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot
por: Sheng, Wei, et al.
Publicado: (2013) -
Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot
por: Sheng, Wei, et al.
Publicado: (2014) -
TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus
por: Huang, Ri-Tai, et al.
Publicado: (2017)