基因治疗的方式 体细胞基因治疗(somatic cell gene therapy) 性细胞基因治疗(germ line gene therapy) Molecular Hybridization & Blotting Technology 分子杂交与印迹技术的原理 核酸分子杂交(nucleic acid hybridization ) ： ...
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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。
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.
对非人类的灵长类动物的研究为aids活体病毒感染模型的干细胞基因治疗法在实验上提供解决基本问题的可能性办法。
Studies in nonhuman primates offer the opportunity to experimentally address basic questions regarding stem cell gene therapy for AIDS in an in vivo disease model.
此外，由于具有多能性，间充质干细胞还是很好的基因载体，在创伤修复的基因治疗中有广阔的应用前景。
In addition, for its multi potential to differentiate into lineages of mesenchymal tissues, MSC could be used as gene vehicle for gene therapy of trauma care.
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