药物发现
银屑病
药品
计算生物学
医学
药物重新定位
数据科学
计算机科学
药理学
生物信息学
生物
皮肤病科
作者
Zih‐Chan Lin,Shih-Chun Yang,Thi Thu Phuong Tran,Jia-You Fang
标识
DOI:10.1080/17460441.2025.2528959
摘要
Despite extensive model development, no single system fully mimics human psoriatic disease. The imiquimod-induced model remains widely used due to its practicality, although it better reflects acute inflammation compared with chronic pathology. The combination of complementary models and the incorporation of human-derived tissues or immune components may improve translational relevance. Advances in genome editing and humanized systems are likely to shape the future of psoriasis research and therapeutic discovery.
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