Combined Antiretroviral Therapy and Immune Pressure Lead to In Vivo HIV-1 Recombination With Ancestral Viral Genomes-Reference-Cited by-同舟云学术

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Combined Antiretroviral Therapy and Immune Pressure Lead to In Vivo HIV-1 Recombination With Ancestral Viral Genomes

Published:2011-06-01 Issue:2 Volume:57 Page:109-117
ISSN:1525-4135
Container-title:JAIDS Journal of Acquired Immune Deficiency Syndromes
language:en
Short-container-title:

Author:

Buzón Maria José,Wrin Terri,Codoñer Francisco M,Dalmau Judith,Phung Pham,Bonjoch Anna,Coakley Eoin,Clotet Bonaventura,Martinez-Picado Javier

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Pharmacology (medical),Infectious Diseases

Reference48 articles.

1. Limited durability of viral control following treated acute HIV infection.;Kaufmann;PLoS Med,2004

2. Partial treatment interruption of protease inhibitor-based highly active antiretroviral therapy regimens in HIV-infected children.;Abadi;J Acquir Immune Defic Syndr,2006

3. Transient treatment exclusively containing nucleoside analogue reverse transcriptase inhibitors in highly antiretroviral-experienced patients preserves viral benefit when a fully active therapy was initiated.;Bonjoch;HIV Clin Trials,2008

4. Interruption of treatment with individual therapeutic drug classes in adults with multidrug-resistant HIV-1 infection.;Deeks;J Infect Dis,2005

5. Dynamics of viral load rebound and immunological changes after stopping effective antiretroviral therapy.;Garcia;AIDS,1999

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1. HIV-1–Specific Immunodominant T-Cell Responses Drive the Dynamics of HIV-1 Recombination Following Superinfection;Frontiers in Immunology;2022-01-14

2. Social, Epidemiological, and Virological Characteristics from Peruvian Subjects Living with HIV-1/AIDS with Different Sexual Risk Behavior;AIDS Research and Human Retroviruses;2021-11-22

3. Anti-HIV cytotoxicity enzyme inhibition and molecular docking studies of quinoline based chalcones as potential non-nucleoside reverse transcriptase inhibitors (NNRT);Bioorganic Chemistry;2016-04

4. Synthesis, structure–activity relationship and molecular docking of cyclohexenone based analogous as potent non-nucleoside reverse-transcriptase inhibitors;Journal of Molecular Structure;2015-04

5. Efavirenz Stimulates HIV-1 Reverse Transcriptase RNase H Activity by a Mechanism Involving Increased Substrate Binding and Secondary Cleavage Activity;Biochemistry;2013-07-09

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