近日,北京大学未来技术学院邬一谦研究团队在hLife上发表了题为"Boosting CAR-T cell therapy with CRISPR ...

Gene therapy pioneer Jim Wilson and researcher Kiran Musunuru are using contrasting approaches to overcome “irrational ...

At meeting on human embryo editing, CRISPR pioneer says science is a long way from knowing if germline DNA can be safely ...

The therapy, EPI-321, is intended to treat cases of facioscapulohumeral muscular dystrophy, a genetic neuromuscular disorder.

研究人员针对年龄相关性黄斑变性（AMD），用 CRISPR 技术在 ARPE-19 细胞中靶向相关 SNP，实现补体系统操控，为治疗提供新方向。

Human extracellular matrices can be edited in their composition using the CRISPR/Cas9 system, leading to materials exhibiting tailored regenerative capacities.

Targeted CRISPR lipid nanoparticles eliminated 50% of tumors in mice with head and neck cancer.

撰文丨王聪编辑丨王多鱼排版丨水成文近年来，以 PD-1/PD-L1 抑制剂为代表的免疫检查点疗法彻底改变了癌症治疗格局，然而，相当一部分癌症患者对这些癌症免疫治疗“无动于衷”，癌细胞究竟用了什么“隐身术”来逃避免疫系统的追杀？近日，国际顶级学术期刊 ...

The Department of Health - Abu Dhabi (DoH), the regulator of the healthcare sector in the emirate, has announced the ...

CM. Read why NTLA stock has potential with upcoming 2025 data and a growing $12B market for Transthyretin Amyloidosis.