期刊文献+

基因治疗中外源基因的导入 被引量:2

The gene delivery technology in gene therapy
在线阅读 下载PDF
导出
摘要 基因治疗是将遗传物质导入靶细胞以达到治疗疾病的目的,目前基因治疗研究中的主要障碍是如何将外源基因导入靶细胞。本文介绍基因治疗的原理和外源基因导入靶细胞时的常用方法,包括显微注射法、电穿孔法、基因枪粒子轰击法等。对基因治疗的现状、存在的问题及未来发展前景作了简要探讨。 Gene therapy is defined as the introduction of genetic materials into cells to bring about a therapeutic ef-fect,the major stumbling block in the development of effective gene therapy is the delivery of the therapeutic gene to its target.As key issues,the principle and major delivery technology,which includes microinjection,electropora-tion,particle bombardment etc,were introduced in this paper,meanwhile,the present status,problems,and futher prospects were also presented and analyzed.
出处 《生物技术通讯》 CAS 2003年第3期235-237,共3页 Letters in Biotechnology
关键词 基因治疗 外源基因 导入 载体 靶细胞 基因枪 电穿孔法 显微注射法 gene therapy vector target gene delivery
  • 相关文献

参考文献19

  • 1顾泽宗.非病毒类基因转移技术在神经系统病变基因治疗以及生物机理研究方面的应用[A]..基因治疗的原理和实践[C].天津:天津科学技术出版社,2000.90.
  • 2PC.温特 GI.希基 HL.弗莱彻.遗传学[M].北京:科学出版社,2001.298.
  • 3杜宝恒.基因治疗概论[A]..基因治疗的原理和实践嗍[C].天津:天津科学技术出版社,2000.2.
  • 4杜涛.人类基因组计划[A]..基因治疗的原理和实践[C].天津:天津科学技术出版社,2000.103.
  • 5杨乃渡 崔虹.基因转移的方法[A]..基因治疗的原理和实践[C].天津:天津科学技术出版社,2000.69.
  • 6瞿礼嘉 顾红雅 胡苹 陈章良.现代生物技术导论[M].北京:高等教育出版社,施普林格出版社,1999.433.
  • 7张惠展.基因工程概论[M].上海:华东理工大学出版社,2000.436.
  • 8Abdallah B, Hassan A, Benoist C, et al. Human gene therapy: a powerful nonviral vector for in vivo gene transfer into the adult mammalian brain: polyethylenlmimine[J]. 1996,(7):1947.
  • 9Boussif O, Lezoulach F, Zanta MA, et al. A novel, versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo:polyethylenimine[J]. Prec Natl Acad Sci USA, 1995,(92):7297.
  • 10Goldman CK, Soroceanu L, Smith N, et al. In vitro and in vivo gene delivery mediated by a synthetic polycationic amino polymer [J]. Nature Biotechnol, 1997,(15):462.

共引文献5

同被引文献39

  • 1孙剑.RNA干扰在抗HIV感染中的研究进展[J].中国药学杂志,2005,40(2):84-86. 被引量:1
  • 2合作编辑者为:百科ROBOT,Rocy711,Wang12141210,等.基因治疗.[EB/OL].(2010-12-26)[2010-12-28].http://baike.baidu.com/view/94966.htm.
  • 3GABALLAH K, HILLS A, CURIEL D, et al. Lysis of dysplastie but not normal oral keratinocytes and tissue-engineered epithelia with conditionally replicating adenovimses[J]. Cancer Res, 2007, 67(15) : 7284-7294.
  • 4ANDERSON WF, BLAESE RM,CULVER K, et al. The ADA human gene therapy clinical protocol: Points to consider response with clinical protocol, July 6, 1990[J]. Hum Gene Ther, 1990, 1(3): 331-362.
  • 5杨鸿智.基因治疗的现状和存在的问题[EB/OL].(2008-12-01) [2010-12-10]. http://blog techllO.net/? Uid-975-actionviewspace-itemid- 18886.
  • 6Gene Therapy Clinical Trials Worldwide. Number of gene therapy clinical trials approved wordwide 1989-2010 [EB/OL]. (2010-06) [2010-12-09]. http://www.abedia.com/wiley/years. php;.
  • 7CAVAZZANA-CALVO M, HACEIN-BEY S, de SAINT BAS1LE G, et cal. Gene therapy of human severe combined immunodeficieney (SCID)-XI disease[J]. Science, 2000, 288 (5466): 669-672.
  • 8HACEIN-BEY-ABINA S, yon KALLE C, SCHMIDT M, et al. A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency[J]. N Engl J Med, 2003, 348 (3): 255-256.
  • 9FIRE A,XU S,MONTGOMERY M K,et al.Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans[J].Nature,1998,391(6669):806-811.
  • 10CAPLEN N J.Gene Therapy Progress and Prospects.Downregulating gene expression:the impact of RNA interference[J].Gene Therapy,2004,11(16):1241-1248.

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部