Cargando…
Imprinting aberrations of SNRPN, ZAC1 and INPP5F genes involved in the pathogenesis of congenital heart disease with extracardiac malformations
Congenital heart disease (CHD) with extracardiac malformations (EM) is the most common multiple malformation, resulting from the interaction between genetic abnormalities and environmental factors. Most studies have attributed the causes of CHD with EM to chromosomal abnormalities. However, multi‐sy...
Autores principales: | Zhao, Xiaolei, Chang, Shaoyan, Liu, Xinli, Wang, Shuangxing, Zhang, Yueran, Lu, Xiaolin, Zhang, Ting, Zhang, Hui, Wang, Li |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520315/ https://www.ncbi.nlm.nih.gov/pubmed/32693431 http://dx.doi.org/10.1111/jcmm.15584 |
Ejemplares similares
-
Is there any effect on imprinted genes H19, PEG3, and SNRPN during AOA?
por: Liang, Rong, et al.
Publicado: (2022) -
Characterization of cis- and trans-acting elements in the imprinted human SNURF-SNRPN locus
por: Rodriguez-Jato, Sara, et al.
Publicado: (2005) -
Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability
por: Lorgen-Ritchie, Marlene, et al.
Publicado: (2019) -
Correction: Imprinting methylation in SNRPN and MEST1 in adult blood predicts cognitive ability
por: Lorgen-Ritchie, Marlene, et al.
Publicado: (2019) -
Zac1 and the Imprinted Gene Network program juvenile NAFLD in response to maternal metabolic syndrome
por: Baptissart, Marine, et al.
Publicado: (2022)