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Updated: May 11, 2025

Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats
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在早产婴儿中解码支气管肺功能障碍症通过表观遗传透镜

Seyed Alireza Dastgheib1, Reza Bahrami2, Mohammad Golshan-Tafti3

  • 1Department of Medical Genetics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

Frontiers in medicine
|April 18, 2025
PubMed
概括

像DNA甲基化和RNA调节这样的表观遗传变化是早产婴儿支气管肺功能障碍 (BPD) 发展的关键. 这些变化为早期检测和针对性干预提供了潜在的生物标志物.

关键词:
通过DNA甲基化.在RUNX3中使用RUNX3支气管肺功能失育症 支气管肺功能失育症表观遗传学是指表观遗传学.长长的非编码RNAs.微RNAs 是一个微型RNA.

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