Gene therapy for TH deficient mice through direct gene (PCI-hlL-2) transfer

Gene therapy for TH deficient mice through direct gene (PCI-hlL-2) transfer

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摘要 Objective: The objective of research is to explorethe prospective for direct gene transfer to be applied as aform of gene therapy. Materials and methods: ①Experimental animals: Male BALB/c mice, 0 - 8 weeksold;②Preparations of plasmid: PCI-hIL-2 plasmid isexpression vector for human IL-2 containing cytome-galovirus immediate-early enhance/promoter region andT7 promoer;③Injection of plasmids: Male

作者 Wei Liu, Jin-Zhu YinDepartment of Immunology, Beijing Medical University,Beijing 100083

出处《中国实验血液学杂志》 CAS CSCD 1997年第3期320-321,共2页 Journal of Experimental Hematology

关键词 cytome PLASMID IMMEDIATE promoter DEFICIENT Injection SRBC TITER prospective STAINING

分类号 R456 [医药卫生—治疗学]

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中国实验血液学杂志

1997年第3期

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Gene therapy for TH deficient mice through direct gene (PCI-hlL-2) transfer

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