Targeting HIV-1 transcription factor binding sites using CRISPR/Cas9 to permanently deactivate latent provirus

被引：0
|
作者：
Chung, Cheng-Han [1 ,2 ]
Allen, Alexander G. [1 ,2 ]
Atkins, Andrew K. [1 ,2 ]
Costello, Robert [1 ,2 ]
Sullivan, Neil T. [1 ,2 ]
Nonnemacher, Michael R. [1 ,2 ,3 ]
Dampier, Will [1 ,2 ,4 ]
Wigdahl, Brian [1 ,2 ,3 ]
机构：
[1] Drexel Univ, Coll Med, Dept Microbiol & Immunol, Philadelphia, PA 19104 USA
[2] Drexel Univ, Coll Med, Inst Mol Med & Infect Dis, Ctr Mol Virol & Translat Neurosci, Philadelphia, PA 19104 USA
[3] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[4] Drexel Univ, Sch Biomed Engn Sci & Hlth Syst, Philadelphia, PA 19104 USA
来源：
JOURNAL OF NEUROVIROLOGY | 2019年 / 25卷 / SUPPL 1期
关键词：
D O I：
暂无
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
P30
引用
收藏
页码：S10 / S10
页数：1
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