CRISPR-Cas9-mediated genome editing delivered by a single AAV9 vector inhibits HSV-1 reactivation in a latent rabbit keratitis model
利用单个AAV9载体递送的CRISPR-Cas9介导的基因组编辑可抑制潜伏性兔角膜炎模型中的HSV-1再激活。
期刊:Molecular Therapy-Methods & Clinical Development
影响因子:4.7
doi:10.1016/j.omtm.2024.101303
Amrani, Nadia; Luk, Kevin; Singh, Pankaj; Shipley, Mason; Isik, Meltem; Donadoni, Martina; Bellizzi, Anna; Khalili, Kamel; Sariyer, Ilker K; Neumann, Donna; Gordon, Jennifer; Ruan, Guo-Xiang
