基因转移
载体(分子生物学)
基因传递
病毒载体
遗传增强
计算生物学
计算机科学
生物
风险分析(工程)
基因
医学
遗传学
重组DNA
作者
Alan L. Parker,Christopher Newman,Simon S. Briggs,Leonard W. Seymour,Paul Sheridan
出处
期刊:Expert Reviews in Molecular Medicine
[Cambridge University Press]
日期:2003-09-03
卷期号:5 (22): 1-15
被引量:107
标识
DOI:10.1017/s1462399403006562
摘要
Medical research continues to illuminate the origins of many human diseases. Gene therapy has been widely proposed as a novel strategy by which this knowledge can be used to deliver new and improved therapies. Viral gene transfer is relatively efficient but there are concerns relating to the use of viral vectors in humans. Conversely, nonviral vectors appear safe but inefficient. Therefore, the development of an efficient nonviral vector remains a highly desirable goal. This review focuses on the numerous challenges preventing efficient nonviral gene transfer in vivo and discusses the many technologies that have been adopted to overcome these problems.
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