Latent HIV-1 provirus in vitro suppression using combinatorial CRISPR/Cas9 strategy-Reference-Cited by-同舟云学术

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Latent HIV-1 provirus in vitro suppression using combinatorial CRISPR/Cas9 strategy

Published:2022-12 Issue: Volume:29 Page:101686
ISSN:2452-0144
Container-title:Gene Reports
language:en
Short-container-title:Gene Reports

Author:

Kalidasan V.,Ravichantar Nithya,Muhd Besari Alwi,Yunus Muhammad Amir,Mohd Yusoff Narazah,Mohamed Zeehaida,Theva Das Kumitaa

Funder

Hospital Universiti Sains Malaysia

Ministry of Higher Education, Malaysia

Universiti Sains Malaysia

Publisher

Elsevier BV

Subject

Genetics

Reference54 articles.

1. Highly active antiretroviral therapies are effective against HIV-1 cell-to-cell transmission;Agosto;PLoS Pathog.,2014

2. HIV-1 tat: role in bystander toxicity;Ajasin;Front. Cell. Infect. Microbiol.,2020

3. Gene editing of HIV-1 co-receptors to prevent and/or cure virus infection;Allen;Front. Microbiol.,2018

4. HIV-1 Vpr: mechanisms of G2 arrest and apoptosis;Andersen;Exp. Mol. Pathol.,2008

5. HIV-1 subtype D infection is associated with faster disease progression than subtype A in spite of similar plasma HIV-1 loads;Baeten;J. Infect. Dis.,2007

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