نتایج جستجو برای: hiv 1 pr

تعداد نتایج: 2909370  

Journal: :Thorax 2004
R A M Breen C J Smith H Bettinson S Dart B Bannister M A Johnson M C I Lipman

BACKGROUND It has been suggested that deterioration of tuberculosis (TB) during appropriate treatment, termed a paradoxical reaction (PR), is more common and severe in HIV positive individuals on highly active antiretroviral therapy (HAART). METHOD A study was undertaken to determine the frequency of PR and its associated features in a population of HIV+TB+ patients and a similar sized group ...

Journal: :The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases 2010
Paula Virginia Michelon Toledo Denise Siqueira de Carvalho Luiza Romagnoli Gustavo Marcinko Clovis Arns da Cunha Margely Nunes de Souza Rodrigo Brindeiro Flávio de Queiroz-Telles

Antiretroviral therapy (ART) has reduced morbidity and mortality related to human immunodeficiency virus (HIV) infection, but in spite of this advance, HIV mutations decrease antiretroviral susceptibility, thus contributing to treatment failure in patients. Genotyping HIV-1 allows the selection of new drugs after initial drug failure. This study evaluated the genotypic profile of HIV-1 isolates...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
T Lee G S Laco B E Torbett H S Fox D L Lerner J H Elder C H Wong

The S3 and S3' subsite binding specificities of HIV and feline immunodeficiency virus proteases (FIV) proteases (PRs) have been explored by using C2-symmetric competitive inhibitors. The inhibitors evaluated contained (1S, 2R, 3R, 4S)-1,4-diamino-1, 4-dibenzyl-2,3-diol as P1 and P1' units, Val as P2 and P2' residues, and a variety of amino acids at the P3 and P3' positions. All inhibitors showe...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Mi Li Gary S Laco Mariusz Jaskolski Jan Rozycki Jerry Alexandratos Alexander Wlodawer Alla Gustchina

The successful development of a number of HIV-1 protease (PR) inhibitors for the treatment of AIDS has validated the utilization of retroviral PRs as drug targets and necessitated their detailed structural study. Here we report the structure of a complex of human T cell leukemia virus type 1 (HTLV-1) PR with a substrate-based inhibitor bound in subsites P5 through P5'. Although HTLV-1 PR exhibi...

Journal: :AIDS Research and Therapy 2007
Amisha Malhotra Sunanda Gaur Patricia Whitley-Williams Caitlin Loomis Anna Petrova

BACKGROUND Although the introduction of combined therapy with reverse transcriptase and protease inhibitors has resulted in considerable decrease in HIV related mortality; it has also induced the development of multiple drug-resistant HIV-1 variants. The few studies on HIV-1 mutagenesis in HIV infected children have not evaluated the impact of HIV-1 mutations on the clinical, virological and im...

2013
Mona S. Ellithey Namrita Lall Ahmed A. Hussein Debra Meyer

Bioassay-guided fractionation using different chromatographic and spectroscopic techniques in the analysis of the Red Sea soft coral Litophyton arboreum led to the isolation of nine compounds; sarcophytol M (1), alismol (2), 24-methylcholesta-5,24(28)-diene-3β-ol (3), 10-O-methyl alismoxide (4), alismoxide (5), (S)-chimyl alcohol (6), 7β-acetoxy-24-methylcholesta-5-24(28)-diene-3,19-diol (7), e...

2003
Yaakov Levy Amedeo Caflisch

The flexibility and stability of both monomeric and dimeric HIV-1 PR were explored by 100 ns implicit solvent molecular dynamics simulation at 350 K with the aim to correlate the monomer stability with the dimerization mechanism. The principal component analysis (PCA) was applied to visualize the available regions in the conformational space of the two HIV-1 PR forms, to compare their structura...

Journal: :Chemical communications 2007
Kagan Kerman Khaled A Mahmoud Heinz-Bernhard Kraatz

An electrochemical biosensor with a new bioorganometallic approach for the detection of human immunodeficiency virus (HIV) type 1 protease (HIV-1 PR) using surface-bound ferrocenoyl (Fc)-pepstatin conjugates is presented.

2017
Luiz Fernando Almeida Machado Iran Barros Costa Maria Nazaré Folha Anderson Levy Bessa da Luz Antonio Carlos Rosário Vallinoto Ricardo Ishak Marluisa Oliveira Guimarães Ishak

BACKGROUND The present study aimed to describe the genetic diversity of HIV-1, as well as the resistance profile of the viruses identified in HIV-1 infected pregnant women under antiretroviral therapy in the state of Pará, Northern Brazil. METHODS Blood samples were collected from 45 HIV-1 infected pregnant to determine the virus subtypes according to the HIV-1 protease (PR) gene and part of ...

Journal: :Bioorganic & medicinal chemistry 1996
R S Randad L Lubkowska A M Silva D M Guerin S V Gulnik B Yu J W Erickson

A combination of structure-activity studies, kinetic analysis, X-ray crystallographic analysis, and modeling were employed in the design of a novel series of HIV-1 protease (HIV PR) inhibitors. The crystal structure of a complex of HIV PR with SRSS-2,5-bis[N-(tert-butyloxycarbonyl)amino]-3,4-dihydroxy-1, 6-diphenylhexane (1) delineated a crucial water-mediated hydrogen bond between the tert-but...

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