Cargando…
Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes
Heart development is a complex process requiring dynamic transcriptional regulation. Disturbance of this process will lead to severe developmental defects such as congenital heart disease/defect (CHD). CHD is a group of complex disorder with high genetic heterogeneity, common pathways associated wit...
Autores principales: | Wang, Bo, You, Guoling, Fu, Qihua |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402266/ https://www.ncbi.nlm.nih.gov/pubmed/28436429 http://dx.doi.org/10.1038/srep46760 |
Ejemplares similares
-
Association between ABO Blood Group and Risk of Congenital Heart Disease: A 6-year large cohort study
por: Zu, Bailing, et al.
Publicado: (2017) -
Preeclampsia and Fetal Congenital Heart Defects
por: Ferreira, Bárbara D., et al.
Publicado: (2022) -
Weighted Gene Coexpression Network Analysis Identifies Crucial Genes Involved in Coronary Atherosclerotic Heart Disease
por: Bao, Jinli
Publicado: (2022) -
Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot
por: You, Guoling, et al.
Publicado: (2020) -
Identification of candidate genes for congenital heart defects on proximal chromosome 8p
por: Li, Tingting, et al.
Publicado: (2016)