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- The retroviral genetransfer system is nicely fit for the ex vivo gene therapy for mesangio-proliferative glomerular disease. 结论：该逆转录病毒载体基因转移系统能很好地适用于系膜增殖性肾小球疾病的间接体内基因治疗研究。
- Suppression of articular cartilage breakdown in osteoarthritis by interleukin-1 receptor antagonist using ex vivo gene therapy 白细胞介素1受体拮抗蛋白间接体内转基因抑制骨关节炎软骨破坏
- ex vivo gene transfer 先体外后体内基因转移
- Animal experiment study of in vivo gene therapy for growth hormone-secreting somatotroph adenomas 垂体生长激素腺瘤基因治疗的动物实验研究
- Yajun Guo, Immunogene Therapy: Both in vitro and in vivo gene transfer approaches. 沈锋，郭亚军。多基因转染在肿瘤治疗中的作用。
- In vitro and ex vivo antihydroxyl radical activity of green and roasted coffee. 研究课题:新鲜绿色咖啡豆及烘烤咖啡豆体内外抗羟基自由基效果。
- Can the gene be fixed with gene therapy? 这种基因能用基因疗法治疗吗?
- Is Gene Therapy for Hypertension Possible? （基因治疗高血压可能吗？）
- To increase AHS injection volume can obviously enlarge the destruction zone by single RFA in ex vivo bovine liver. 增加AHS注射剂量可以明显增大离体牛肝RFA一次性毁损体积。
- Objective To study the effect of human embryonic chorion extract(HECE) on the growth of NCI446 cells cultured ex vivo. 目的:探讨人胚绒毛提取液对NCI446细胞生长的影响。
- Conclusion: The recombinant adenovirus generated is E1 and E3 deleted which can be further used in gene therapy in vivo. 结论：所获重组腺病毒为E1，E3缺陷型，可进一步用于基因治疗研究。
- These limitations could be re- solved by gene therapy which could express endostatin in vivo and obviate the dis- advantages in front. 但研究和治疗发现，内皮抑素性质不稳定，极易失活，难以大量制备，治疗中需要反复用药，很不方便，且非常昂贵。
- METHODS: Liver DCs were isolated without expansion in cytokines from human liver allowing us to study unmanipulated tissue-resident DCs ex vivo. 方法：从人肝脏中没有表达细胞因子肝树状突细胞被分离出来，允许我们在体外研究未经过处理的组织原位的树状突细胞。
- Preliminary succes has been achieved in application of ex vivo expanded hematopoietic cells in animal model and clinical trials. 扩增后的造血细胞在动物模型和临床上的应用已取得了初步成效。
- Finally I should say a word about germline gene therapy. 最后，我应当提一句生殖系基因疗法。
- Objective To study the application of the ex vivo ATP-bioluminescence assay(ATP-TCA) in the chemotherapy of digestive tract malignant solid tumor. 目的探讨ATP-生物荧光法（ATP-TCA系统）在消化道恶性实体肿瘤体外药物敏感性试验中的应用。
- Adenovirus mediated angiostatin gene therapy for rat glioma. 重组腺病毒载体介导血管抑素基因治疗大鼠脑胶质瘤的实验研究。
- The result of ex vivo sensitive rate is listed follows: wilm's tumor: VCR+ ACTD (94.12%),ACTD(82.35%),ADM(52.94%),VCR (47.06%),VP-16 (29.41%),HCPT(29.41%). 各种小儿恶性实体瘤对药物的敏感性分别为;肾母细胞瘤:长春新碱+放线菌素D (94.;12%25)、放线菌素D (82
- Gene therapy is a new therapy technique for human being. 基因治疗是用于人类疾病治疗的一种新方法。
- Using a defective retroviral vector, the investigators transduced ex vivo CD34+ bone marrow cells from five boys with this SCID, resulting in no adverse effects. 调查者使用一种有缺陷的逆转录病毒载体，把5名重症联合免疫缺陷患儿的CD34+骨髓细胞取出体外并进行转换。
