The hope is that modified adenovirus could play a role in gene therapy, used as a vector (carrier) for delivering therapeutic genes to the interior of cells.
人们希望，改构后的腺病毒在基因治疗方面能起到重要的作用，例如，作为载体基因携带治疗性基因到达细胞内。
This new research modified the introduced dystrophin gene to increase the efficiency of dystrophin protein production in the cells.
这一新的经过改造的方法，增强了抗肌萎缩蛋白在肌肉细胞内产生的有效性。
Objective: To explore the therapeutic effects of the vaccine, B7 1 gene modified tumor cells, on gastric cancer in mice.
目的：探讨B7 - 1基因修饰的肿瘤细胞作为瘤苗对小鼠胃癌的治疗效果。
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