期刊论文详细信息
Frontiers in Cardiovascular Medicine | |
Mechanism Sharing Between Genetic and Gestational Hypoxia-Induced Cardiac Anomalies | |
Olivia Moumne1  | |
关键词: cardiac anomaly; gestational hypoxia; genetic mutation; mouse models; nkx2-5; | |
DOI : 10.3389/fcvm.2018.00100 | |
学科分类:心脏病和心血管学 | |
来源: Frontiers | |
【 摘 要 】
Background: Cardiac development is a dynamic process both temporally and spatially. These complex processes are often disturbed and lead to congenital cardiac anomalies that affect approximately 1% of live births. Disease-causing variants in several genetic loci lead to cardiac anomalies, with variants in transcription factor NKX2-5 gene being one of the largest variants known. Gestational hypoxia, such as seen in high-altitude pregnancy, has been known to affect cardiac development, yet the incidence and underlying mechanisms are largely unknown.
【 授权许可】
CC BY
【 预 览 】
Files | Size | Format | View |
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RO201904022836712ZK.pdf | 2858KB | download |