Lv21
108 积分 2022-09-19 加入
Highly Efficient and Selective CAR-Gene Transfer Using CD4- and CD8-Targeted Lentiviral Vectors
4小时前
已完结
Tumour-derived small extracellular vesicles act as a barrier to therapeutic nanoparticle delivery
7个月前
已完结
An exhaustive pre-clinical study of a circRNA drug candidate (cmRNA1210) encoding IL-12sc for anti-tumor therapeutics
9个月前
已关闭
Tailor made: the art of therapeutic mRNA design
11个月前
已完结
Engineered exosome-mediated messenger RNA and single-chain variable fragment delivery for human chimeric antigen receptor T-cell engineering
1年前
已完结
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