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NEWS
1. Dual-vector prodrug activator gene therapy displays synergistic cytocidal effects on cancer
2. No immunogenicity! Can the spring of AAV mediated gene therapy be far behind?
3. Retinitis pigmentosa (RP) patients may benefit from AAV mediated gene therapy
4. AAV mediated gene targeting in vivo through CRISPR-Cas9 repressors
5. Promising therapeutic approach for Duchenne muscular dystrophy-sarcolipin reduction
6. A dual-AAV approach rescues auditory function in deaf otoferlin knock-out mice
7. AAV CRISPR editing rescues cardiac and muscle function for 18 months in dystrophic mice
8. Correction of half the cardiomyocytes fully rescue Friedreich Ataxia mitochondrial cardiomyopathy
9. Deamidation of Amino Acids on the Surface of AAV Capsids Leads to Charge Heterogeneity and Altered Vector Function
10. Atrial-Specific Gene Delivery Using an AAV Vector
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