The design of drugs for HIV and HCV
ED Clercq - Nature reviews Drug discovery, 2007 - nature.com
Since the discovery of the human immunodeficiency virus (HIV) in 1983, dramatic progress
has been made in the development of novel antiviral drugs. The HIV epidemic fuelled the …
has been made in the development of novel antiviral drugs. The HIV epidemic fuelled the …
HIV entry inhibitors
JA Esté, A Telenti - The Lancet, 2007 - thelancet.com
The need for new classes of antiretroviral drugs has become apparent because of
increasing concern about the long-term toxic effects of existing drugs, the need to combat …
increasing concern about the long-term toxic effects of existing drugs, the need to combat …
Current perspectives on HIV-1 antiretroviral drug resistance
P Iyidogan, KS Anderson - Viruses, 2014 - mdpi.com
Current advancements in antiretroviral therapy (ART) have turned HIV-1 infection into a
chronic and manageable disease. However, treatment is only effective until HIV-1 develops …
chronic and manageable disease. However, treatment is only effective until HIV-1 develops …
Entry inhibitors in the treatment of HIV-1 infection
Infection of target cells by HIV is a complex, multi-stage process involving attachment to host
cells and CD4 binding, coreceptor binding, and membrane fusion. Drugs that block HIV …
cells and CD4 binding, coreceptor binding, and membrane fusion. Drugs that block HIV …
Entry inhibitors and their use in the treatment of HIV-1 infection
AA Haqqani, JC Tilton - Antiviral research, 2013 - Elsevier
Entry of HIV into target cells is a complex, multi-stage process involving sequential
attachment and CD4 binding, coreceptor binding, and membrane fusion. HIV entry inhibitors …
attachment and CD4 binding, coreceptor binding, and membrane fusion. HIV entry inhibitors …
The remarkable frequency of human immunodeficiency virus type 1 genetic recombination
A Onafuwa-Nuga, A Telesnitsky - Microbiology and Molecular …, 2009 - Am Soc Microbiol
The genetic diversity of human immunodeficiency virus type 1 (HIV-1) results from a
combination of point mutations and genetic recombination, and rates of both processes are …
combination of point mutations and genetic recombination, and rates of both processes are …
Design of a Potent d-Peptide HIV-1 Entry Inhibitor with a Strong Barrier to Resistance
BD Welch, JN Francis, JS Redman, S Paul… - Journal of …, 2010 - Am Soc Microbiol
The HIV gp41 N-trimer pocket region is an ideal viral target because it is extracellular, highly
conserved, and essential for viral entry. Here, we report on the design of a pocket-specific d …
conserved, and essential for viral entry. Here, we report on the design of a pocket-specific d …
Protease‐resistant peptide design—empowering nature's fragile warriors against HIV
MT Weinstock, JN Francis, JS Redman… - Peptide Science, 2012 - Wiley Online Library
Peptides have great potential as therapeutic agents, but their use is often limited by
susceptibility to proteolysis and their resulting in vivo fragility. In this review, we focus on …
susceptibility to proteolysis and their resulting in vivo fragility. In this review, we focus on …
[HTML][HTML] HIV-1 entry, inhibitors, and resistance
MA Lobritz, AN Ratcliff, EJ Arts - Viruses, 2010 - mdpi.com
Entry inhibitors represent a new class of antiretroviral agents for the treatment of infection
with HIV-1. While resistance to other HIV drug classes has been well described, resistance …
with HIV-1. While resistance to other HIV drug classes has been well described, resistance …
[HTML][HTML] HIV/AIDS e treinamento concorrente: a revisão sistemática
O uso da terapia anti-retroviral combinada (TARV) aumentou a expectativa de vida dos
portadores do vírus da imunodeficiência humana (HIV) e, como conseqüência, torna-se …
portadores do vírus da imunodeficiência humana (HIV) e, como conseqüência, torna-se …