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Journal of Biomedical Engineering ; (6): 224-226, 2008.
Article in Chinese | WPRIM | ID: wpr-291261

ABSTRACT

Lentiviral vectors (Lv), known as holding lots of virtues (e.g. transfection to the dividing or non-dividing cells;large capacity of transfer gene fragments; long-term expression transfer genes; and low rate of immunological response) has come to be one of the hot-spots in gene therapy research. In this paper, taking the Lv derived from HIV-1 for example, we review the characteristics of frame, the developments and the advances in application of Lv.


Subject(s)
Animals , Humans , Animals, Genetically Modified , Genetic Therapy , Methods , Genetic Vectors , Genetics , HIV-1 , Genetics , RNA, Small Interfering , Genetics , Transduction, Genetic , Methods
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