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.
本文综述了包括肿瘤坏死因子抑制剂、白细胞介素1抑制剂、干细胞移植及基因治疗等生物治疗在类风湿性关节炎治疗中的作用。
This article reviews the effect of biotherapy in ra including tumor necrosis factor inhibitor, IL-1inhibitor, stem cell transplantation genetic therapy and so on.
目的探讨CT导引下肝细胞生长因子（HGF）基因治疗脑缺血的可行性。
Objectives To investigate the feasibility of CT guided hepatocyte growth factor(HGF)gene therapy for cerebral ischemic diseases.
探讨利用基因枪技术转移肝细胞生长因子基因治疗大鼠肢体闭塞性血管病的可行性。
To explore the feasibility of gene therapy with hepatocyte growth factor (HGF) transferred using gene gun technique in treatment of peripheral vascular disease of rat limb.
目的研究转人IL2基因对原代肾细胞癌(RCC)细胞致瘤性的影响，为RCC的基因治疗提供依据。
Objective to study the influence on tumorigenicity of human renal cell carcinoma (RCC) cells transduced with human IL 2 gene, and to intend in forming a basis for RCC gene therapy.
因此，骨髓基质细胞被认为是一种理想的治疗性细胞和基因治疗中的靶细胞。
So the cells have been regarded as the ideal cells to be used for cell and gene therapy.
这些阶段变化表明在细胞整个发育过程中表观修饰的复杂性和可能的基因治疗的新的研究领域。
These waves indicated the complexity of epigenetic modifications throughout the cell development process as well as a possible new research area for gene therapy.
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.
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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