机制(生物学)
疾病
冠心病
重性抑郁障碍
医学
计算生物学
生物
内科学
物理
扁桃形结构
量子力学
作者
Yuling Zhang,Guiting Zhou,Qing Miao,Chuchu Shen,Yujie Hua,Wanwen Kong,Kunsheng Wu,Peijian Liu,Qingmin Chu,Rui Peng
标识
DOI:10.1016/j.compbiomed.2025.110456
摘要
This study identifies S1PR3 as a critical therapeutic target for the comorbidity of CHD and MDD. GXN has the potential to treat CHD and MDD by regulating S1PR3 expression levels. Although further validation through animal and cell-based experiments is needed, our findings provide a foundational understanding of the molecular mechanisms and highlight the therapeutic potential of GXN in dual heart therapy.
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