Lv1
30 积分 2025-05-22 加入
Targeted delivery of genome editors in vivo
5个月前
已完结
CRISPR–Cas9 genome editing in human cells occurs via the Fanconi anemia pathway
6个月前
已完结
CRISPR-Cas9 gene repair of hematopoietic stem cells from patients with X-linked chronic granulomatous disease
6个月前
已完结
Adenovirus dodecahedron, a new vector for human gene transfer
7个月前
已完结
Virus-like particle-mediated intracellular delivery of mRNA cap analog with in vivo activity against hepatocellular carcinoma
7个月前
已完结
In vivo HSC Gene Therapy Using BaEVRLess-Pseudotyped Alpha-Retroviral and Lentiviral Vectors
9个月前
已完结
Gene editing by ferrying of CRISPR/Cas ribonucleoprotein complexes in enveloped virus-derived particles
9个月前
已完结
Lentiviral delivery of co-packaged Cas9 mRNA and a Vegfa-targeting guide RNA prevents wet age-related macular degeneration in mice
10个月前
已完结
In-vivo B-cell maturation antigen CAR T-cell therapy for relapsed or refractory multiple myeloma
1年前
已完结
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