CRISPR/Cas9 editing of HIV-1 transcription factor binding sites on the 5’ long terminal repeats to permanently inactivate latent provirus

Journal article

Open access

Peer reviewed

B. Wigdahl, C.-H. Chung, A.G. Allen, A.J. Atkins, R. Costello, N.T. Sullivan, M.R. Nonnemacher and W.N. Dampier

Journal of Virus Eradication, v 5, pp 54-55

Dec 2019

Files and links (2)

url

https://doi.org/10.1016/s2055-6640(20)30218-1View

Published, Version of Record (VoR) Open

url

https://doi.org/10.1016/S2055-6640(20)30218-1View

Published, Version of Record (VoR) Open

7 Record Views

Title: CRISPR/Cas9 editing of HIV-1 transcription factor binding sites on the 5’ long terminal repeats to permanently inactivate latent provirus
Creators: B. Wigdahl
C.-H. Chung
A.G. Allen
A.J. Atkins
R. Costello
N.T. Sullivan
M.R. Nonnemacher
W.N. Dampier
Publication Details: Journal of Virus Eradication, v 5, pp 54-55
Publisher: Elsevier
Resource Type: Journal article
Language: English
Academic Unit: Microbiology and Immunology
Other Identifier: 991020111331504721