Conclusion: Liposome mediated gene transfer in bone marrow cells is highly efficient and the expression of the transferred gene is stable.
结论：利用脂质体介导的基因转移方法介导骨髓细胞基因转移可获得高效、稳定的表达。
Objective to study efficiency and security of the recombinant adenoviral-mediated gene transfer to the donor heart during the heart transplantation.
目的探讨大鼠心脏移植过程中，重组腺病毒介导的外源基因转移至供心的可行性及安全性。
Objective: to assess the feasibility, efficiency and selectivity of adenovirus mediated gene transfer to local arterial wall by protein coated metallic stent.
目的：评估在腺病毒介导下，由蛋白涂层金属支架向局部动脉壁转基因的可行性、效率和选择性。
In order to use retroviral-mediated gene transfer technology in clinical application, retroviral vector must be of high titer and free of detectable replication-competent retroviruses.
逆转录病毒介导的基因转移技术要过渡到临床应用，主要解决如何使病毒载体具有高滴度而不具有复制活性。
Objective: To observe the transduction efficiency of adenoviral-mediated gene transfer in human breast cancer cells and the effect of viral transduction on the growth of the cancer cells.
目的：观察腺病毒介导的基因转移在乳腺癌细胞的转导效率及腺病毒转导对细胞生长的影响。
This article briefly reviews the recent developments on receptor-mediated gene transfer technology, including its main types, effect factors and tactics to augment gene transfer efficiency.
简要综述了受体介导基因转移的主要类型、影响受体介导基因转移的因素和提高基因转移效率的策略等方面的进展。
The direct gene transfer systems involved the chemical method (PEG), electroporation, microinjection, particle bombardment, pollen-mediated gene transfer and other systems using various vectors.
阐述了化学导入法(PEG)、电穿孔法、注射法，粒子轰击法、花粉管萌导法及使用其它载体系统的成功实例。
For example, transfer of virulence gene and transmission of drug-resistant gene mediated by a phage results in gene polymorphism of bacteria, which is an important problem in medicine and genetics.
如由噬菌体介导的细菌毒力基因的转移、细菌耐药基因的传递等导致了病原菌基因表型的多态性，这在医学与遗传学中是一个日益严峻的重要问题。
Objective to investigate the effects of erythropoietin (EPO) gene transfer into skeleton muscle mediated by electroporation on renal anemia.
目的研究电脉冲介导的质粒红细胞生成素(EPO)基因肌肉转移效率以及对肾性贫血的治疗作用。
Conclusion GE7 system-mediated gene therapy system can transfer target gene to pituitary adenoma effectively and specifically.
结论GE7基因治疗系统能够达到靶向性治疗垂体腺瘤的目的。
They were treated with transduced autologous hematopoietic stem cells transfected with the ADA gene, inserted via retroviral-mediated transfer.
以反转录调节基因转殖，转换具有ADA基因的自体造血干细胞对他们进行治疗。
They were treated with transduced autologous hematopoietic stem cells transfected with the ADA gene, inserted via retroviral-mediated transfer.
以反转录调节基因转殖，转换具有ADA基因的自体造血干细胞对他们进行治疗。
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