In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
about
Bile pigments as HIV-1 protease inhibitors and their effects on HIV-1 viral maturation and infectivity in vitroGuidelines for antiretroviral therapy for HIV infection. Canadian HIV Trials Network Antiretroviral Working Group.Selection of high-level resistance to human immunodeficiency virus type 1 protease inhibitorsEngineering human immunodeficiency virus 1 protease heterodimers as macromolecular inhibitors of viral maturationVirus maturation as a new HIV-1 therapeutic targetAnti-AIDS agents 69. Moronic acid and other triterpene derivatives as novel potent anti-HIV agentsBroad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137)Assessment of FIV-C infection of cats as a function of treatment with the protease inhibitor, TL-3Selection of functional variants of the NS3-NS4A protease of hepatitis C virus by using chimeric sindbis virusesChimeric Sindbis viruses dependent on the NS3 protease of hepatitis C virusStructural and kinetic analysis of drug resistant mutants of HIV-1 proteaseInhibition of the HIV-1 and HIV-2 proteases by a monoclonal antibodyStructural studies of FIV and HIV-1 proteases complexed with an efficient inhibitor of FIV proteaseLack of synergy for inhibitors targeting a multi-drug-resistant HIV-1 proteaseThe structural bases of antibiotic resistance in the clinically derived mutant beta-lactamases TEM-30, TEM-32, and TEM-34Viability of a drug-resistant human immunodeficiency virus type 1 protease variant: structural insights for better antiviral therapyDesign and Synthesis of HIV-1 Protease Inhibitors Incorporating Oxazolidinones as P2/P2‘ Ligands in Pseudosymmetric Dipeptide IsosteresComputational design and experimental study of tighter binding peptides to an inactivated mutant of HIV-1 proteaseNinety-Nine Is Not Enough: Molecular Characterization of Inhibitor-Resistant Human Immunodeficiency Virus Type 1 Protease Mutants with Insertions in the Flap RegionHIV-1 Protease Inhibitors from Inverse Design in the Substrate Envelope Exhibit Subnanomolar Binding to Drug-Resistant VariantsEvaluating the Substrate-Envelope Hypothesis: Structural Analysis of Novel HIV-1 Protease Inhibitors Designed To Be Robust against Drug ResistanceAmprenavir complexes with HIV-1 protease and its drug-resistant mutants altering hydrophobic clustersStructure of the HIV-1 Frameshift Site RNA Bound to a Small Molecule Inhibitor of Viral ReplicationNine crystal structures determine the substrate envelope of the MDR HIV-1 proteaseStructural and Thermodynamic Basis of Amprenavir/Darunavir and Atazanavir Resistance in HIV-1 Protease with Mutations at Residue 50Extreme Multidrug Resistant HIV-1 Protease with 20 Mutations Is Resistant to Novel Protease Inhibitors with P1′-Pyrrolidinone or P2-Tris-tetrahydrofuranDual inhibition of HIV-1 replication by integrase-LEDGF allosteric inhibitors is predominant at the post-integration stage.Design, Synthesis, and Biological and Structural Evaluations of Novel HIV-1 Protease Inhibitors To Combat Drug ResistanceStructure of an inhibitor complex of the proteinase from feline immunodeficiency virusStructure of a G48H mutant of HIV-1 protease explains how glycine-48 replacements produce mutants resistant to inhibitor drugsMolecular recognition of cyclic urea HIV-1 protease inhibitorsIn vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-beta-D-dioxolane-guanosine and suppress resistance to 3'-azido-3'-deoxythymidineA potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site.In vitro resistance profile of the human immunodeficiency virus type 1 protease inhibitor BMS-232632In vitro selection and characterization of human immunodeficiency virus type 1 (HIV-1) isolates with reduced sensitivity to hydroxyethylamino sulfonamide inhibitors of HIV-1 aspartyl proteaseIn vitro selection and characterization of human immunodeficiency virus type 1 variants with increased resistance to ABT-378, a novel protease inhibitor.Genotypic and phenotypic characterization of human immunodeficiency virus type 1 variants isolated from patients treated with the protease inhibitor nelfinavir.T134, a small-molecule CXCR4 inhibitor, has no cross-drug resistance with AMD3100, a CXCR4 antagonist with a different structure.Characterization of human immunodeficiency virus type 1 resistant to modified cyclodextrin sulphate (mCDS71) in vitroAnti-human immunodeficiency virus (HIV) activities of halogenated gomisin J derivatives, new nonnucleoside inhibitors of HIV type 1 reverse transcriptase
P2860
Q24530002-0CA376C5-2165-4FDE-849D-3472181F1D87Q24534187-5F1A73D1-36AF-4EEE-8A43-476A4904857CQ24554340-587F2BE0-FDEF-4383-ACED-F4891F68F567Q24555227-6F6E3D7D-479B-4CA3-97C9-76699ADF8692Q24642446-F1979B78-60A2-455D-8630-56788E8CA52DQ24645221-0283983A-6C1D-42F8-A0DB-F1ED59171402Q24656978-24C89E1D-6789-41A3-BF9F-760AD5ED3C24Q24801797-FD704C30-9E49-4BD6-A638-2ADA1C9485E8Q27469337-D739313B-8328-4734-8E19-B8C3ECB57BBBQ27480780-52DA8196-6AA5-4590-ACFB-E61BD2B90812Q27619254-E7715EA8-CB6A-4972-9A45-9DBBD3C6A433Q27620967-DD6F25F0-8F88-4166-AA50-0FA0B9D9BA51Q27621075-FE57C0DD-0D85-4420-AB5A-B60E161E47D4Q27637329-23A26FEE-6085-4C50-B77D-5C945A08E5C0Q27639159-7CBF9333-7006-499D-83B4-E3568478058CQ27640250-024E02F7-B3B5-4827-8F62-69FABA8EA42BQ27647177-AD17D179-BA3E-40D9-8C78-3E1968AFB17FQ27647665-4ED898F9-E446-4772-B9F4-A793C4A8EDC8Q27650299-1B6AD367-62E2-4B99-99AE-F30058175FB3Q27650325-4AA74760-B49D-458D-B149-41ADAF944FC1Q27660267-8023357D-424D-4F06-B5BD-6D55058412ECQ27663981-0DC92962-2623-48C4-8A80-F434A3A7AE7AQ27666265-99134704-D421-45A8-A68A-0D9491E7A8B7Q27666929-1D9A0E62-42C0-4793-A7EE-98E0C69E5F12Q27676079-569E43BF-69E7-455D-ABE2-149AD1934E79Q27677405-B5CF4E11-0A71-4E34-B290-8092E3D6FEE9Q27680666-9F160580-0ED6-4C01-891F-60B21A896243Q27681219-AC0EC118-EAF0-4C76-B74D-0244C59C4B42Q27729877-B0F281DF-EFA3-4079-A46A-719BD4F280EBQ27748828-56FA2BB4-DE69-492D-ACE9-30F41D14085DQ27757042-BAC72D34-E88E-4C8D-A159-9F78E053D8FFQ28344355-8C4CA28C-9F09-49C2-AA35-F4A5CA3C53DCQ28344457-98EFCEFF-2C49-4EFF-A1A3-D4EFACEC09E1Q28344594-E554D288-2BDD-4905-A2C1-153766F7D7A6Q28367941-ECD88F34-4FCB-46F5-8D3E-CC72F433AB12Q28368369-B2D88628-2E3E-43F0-95BD-E7AD239E72ABQ28369030-F253637A-FDCF-4749-A1A9-CDD2B7C32AD7Q28369495-242E3447-44DC-4E9F-917B-6A67DB6B2655Q28371764-BE1E6F33-10A5-44EC-814C-9B949162F3B5Q28378745-4245016B-9AA6-4177-BABF-73E7F6D9FBE2
P2860
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
description
1995 nî lūn-bûn
@nan
1995 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@ast
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@en
type
label
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@ast
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@en
prefLabel
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@ast
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@en
P2093
P356
P1433
P1476
In vivo emergence of HIV-1 variants resistant to multiple protease inhibitors
@en
P2093
Gabryelski LJ
Quintero JC
Robbins HL
Schleif WA
Shivaprakash M
P2888
P304
P356
10.1038/374569A0
P407
P577
1995-04-06T00:00:00Z
P6179
1012077404