组学
特发性肺纤维化
肺纤维化
计算生物学
医学
生物信息学
生物
纤维化
肺
病理
内科学
作者
Zhuofeng Wen,Wenpeng Liang,Zhongxia Yang,Junjie Liu,Jing Yang,Rui-Ming Xu,Kun‐Ta Lin,Pan Jia,Zisheng Chen
标识
DOI:10.1186/s12967-025-06368-8
摘要
We identified six key genes-ANO9, BRCA1, CCDC200, EZH1, FAM13A, and SFR1-as potential drug targets for IPF. Molecular docking revealed strong drug affinities, while PheW-MR analysis highlighted therapeutic potential and associated risks. These findings offer new insights for IPF treatment and further investigation of potential side effects.
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