Results 211 to 220 of about 118,861 (266)

Targeting the AKT pathway: Repositioning HIV protease inhibitors as radiosensitizers.

open access: yesIndian J Med Res, 2016
Goda JS   +4 more
europepmc   +1 more source

Two cases of possible transmitted HIV drug resistance to all currently available integrase inhibitors, the Netherlands, 2025. [PDF]

open access: yesEuro Surveill
van Kampen J   +13 more
europepmc   +1 more source

Residue-Level Affinity Decomposition via Quantum Electron Density: A Multivariable Framework Applied to HIV-1 Protease Inhibitors. [PDF]

open access: yesJ Phys Chem B
Gutiérrez-Flores J   +7 more
europepmc   +1 more source

Tracking the evolution of multiple in vitro HCV replicon mutants under protease inhibitor selection pressure by 454 ultra deep sequencing. [PDF]

open access: yes
Claes, Marijke   +8 more
core  

HIV-Protease Inhibitors

New England Journal of Medicine, 1998
Inhibitors of human immunodeficiency virus (HIV)–encoded protease, combined with nucleoside analogues with antiretroviral activity, cause profound and sustained suppression of viral replication, reduce morbidity, and prolong life in patients with HIV infection.1–3 Recent guidelines recommend that initial treatment of all HIV-infected patients include ...
Charles W Flexner
exaly   +6 more sources

HIV Protease Inhibitors

Current Pharmaceutical Design, 1996
The protease encoded by the human immunodeficiency virus (HIV protease) mediates the maturation of newly formed HIV particles through proteolytic processing of the gag and gag-pol gene products. Because of its essential role in the HIV replication cycle, this enzyme represents a logical target for the treatment of HIV infection.
A, Carr, D A, Cooper
exaly   +7 more sources

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