Lv71
3370 积分 2023-04-01 加入
Genome engineering with Cas9 and AAV repair templates generates frequent concatemeric insertions of viral vectors
7天前
已完结
Ribozyme-activated mRNA trans-ligation enables large gene delivery to treat muscular dystrophies
7天前
已完结
Sequence basis of transcription initiation in the human genome
1个月前
已完结
Profound cellular defects attribute to muscular pathogenesis in the rhesus monkey model of Duchenne muscular dystrophy
2个月前
已完结
Decoding cellular mechanism of recombinant adeno-associated virus (rAAV) and engineering host-cell factories toward intensified viral vector manufacturing
2个月前
已完结
Split intein-mediated protein trans-splicing to express large dystrophins
3个月前
已完结
Structure-guided discovery of ancestral CRISPR-Cas13 ribonucleases
4个月前
已完结
Allogeneic CD19-targeted CAR-T therapy in patients with severe myositis and systemic sclerosis
4个月前
已完结
Precision RNA base editing with engineered and endogenous effectors
4个月前
已完结
Analysis of Off-target Effects and Risk Assessment Leading from Preclinical to Clinical Trials of Gene-edited Therapeutic Products
5个月前
已完结
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