外源基因自己不能主动进入细胞，欲进入细胞内必须借助一定的技术方法。通常把基因治疗中将治疗基因导入细胞内的运载工具称作基因转移系统或载体（vector）。它分为病毒载体和非病毒载体两大类（见表1）。
目的构建并评价受体靶向性基因导入系统对垂体腺瘤的靶向性治疗作用。
Objective to construct and evaluate the receptor targeted gene therapy system for pituitary adenoma.
进行系统的分子生物学研究，为麻黄的优良基因导入、表达及高产与高含碱量新种质的选育奠定坚实的理论基础。
To establish the stable theory bases of choiceness gene induced, expression and breeding of high yield and high ephedrine content through series research the molecular biology.
使用本发明的载体将基因导入到呼吸道上皮组织干细胞可基因治疗囊性纤维症等遗传性呼吸系统疾病。
This gene transfer into airway epithelial stem cells with the use of the vector as described above is useful in gene therapy for a hereditary respiratory disease such as cystic fibrosis.
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