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Suppression of toxic transgene expression by optimized artificial miRNAs increases AAV vector yields in HEK-293 cells

Molecular Therapy - Methods & Clinical Development Pub Date : 2024-06-01 DOI:10.1016/j.omtm.2024.101280
Gina Blahetek, Christine Mayer, Johannes Zuber, Martin Lenter, Benjamin Strobel
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用优化的人工 miRNA 抑制毒性转基因表达，提高 HEK-293 细胞中 AAV 载体的产量
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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Molecular Therapy - Methods & Clinical Development
Molecular Therapy - Methods & Clinical Development
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