颅面
发病机制
病因学
医学
机制(生物学)
生物信息学
遗传学
生物
病理
哲学
认识论
作者
Si Di Zhang,Yue You,Mei Lin Yao,Bing Shi,Zhong Lin Jia
出处
期刊:PubMed
日期:2024-03-28
卷期号:27 (1): 29-38
标识
DOI:10.3290/j.cjdr.b5128515
摘要
Non-syndromic orofacial clefts (NSOCs) are the most common craniofacial malformation. In the complex aetiology and pathogenesis of NSOCs, genetic factors play a crucial role and IRF6, located at chromosome 1q32.2, is the best documented NSOC susceptibility gene. IRF6 is a key factor in oral maxillofacial development and known to contribute the most in NSOCs. It is essential to conduct a complete review of the existing results on IRF6 to further understand its role in the pathogenesis of NSOCs. Thus, the present authors summarised the research progress on the mechanism of IRF6 in NSOCs from both genetic and functional perspectives in this review.
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