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24 积分 2026-07-19 加入
Human promoter-driven AAV tools enable precision gene therapy targeting cochlear hair cells
6天前
已完结
Rational design of a Lfng-enhancer AAV construct drives specific and efficient gene expression in inner ear supporting cells
6天前
已完结
Natural history and phenotype–genotype correlations in GJB2-related hearing loss: a systematic and comprehensive review
24天前
已完结
A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity
1个月前
已完结
The new frontier of genome engineering with CRISPR-Cas9
1个月前
已完结
Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors
1个月前
已完结
Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage
1个月前
已完结
Treatment of monogenic and digenic dominant genetic hearing loss by CRISPR-Cas9 ribonucleoprotein delivery in vivo
1个月前
已完结
Gene therapy for deafness: we can do more
1个月前
已完结
Deafness: from genetic architecture to gene therapy
1个月前
已完结
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