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K70Q adds high-level tenofovir resistance to "Q151M complex" HIV reverse transcriptase through the enhanced discrimination mechanismCurrent perspectives on HIV-1 antiretroviral drug resistanceCommon and unique features of viral RNA-dependent polymerasesHIV-1 reverse transcriptionHIV-1 Reverse Transcriptase (RT) Polymorphism 172K Suppresses the Effect of Clinically Relevant Drug Resistance Mutations to Both Nucleoside and Non-nucleoside RT InhibitorsComplexes of HIV-1 RT, NNRTI and RNA/DNA hybrid reveal a structure compatible with RNA degradationStructural and Inhibition Studies of the RNase H Function of Xenotropic Murine Leukemia Virus-Related Virus Reverse TranscriptaseHIV-1 reverse transcriptase complex with DNA and nevirapine reveals non-nucleoside inhibition mechanismApproved Antiviral Drugs over the Past 50 YearsMechanism of ganciclovir-induced chain termination revealed by resistant viral polymerase mutants with reduced exonuclease activityHIV-1 polymerase inhibition by nucleoside analogs: cellular- and kinetic parameters of efficacy, susceptibility and resistance selectionZidovudine (AZT) monotherapy selects for the A360V mutation in the connection domain of HIV-1 reverse transcriptaseMolecular dynamics study of HIV-1 RT-DNA-nevirapine complexes explains NNRTI inhibition and resistance by connection mutationsPrediction of HIV drug resistance from genotype with encoded three-dimensional protein structureClicking 3'-azidothymidine into novel potent inhibitors of human immunodeficiency virus.Patterns of recombination in HIV-1M are influenced by selection disfavouring the survival of recombinants with disrupted genomic RNA and protein structuresA cell-intrinsic inhibitor of HIV-1 reverse transcription in CD4(+) T cells from elite controllersRecent findings on the mechanisms involved in tenofovir resistance.HIV-1 reverse transcriptase and antiviral drug resistance. Part 2.4'-C-methyl-2'-deoxyadenosine and 4'-C-ethyl-2'-deoxyadenosine inhibit HIV-1 replicationThe base component of 3'-azido-2',3'-dideoxynucleosides influences resistance mutations selected in HIV-1 reverse transcriptase.Structures of reverse transcriptase pre- and post-excision complexes shed new light on HIV-1 AZT resistanceSubstrate mimicry: HIV-1 reverse transcriptase recognizes 6-modified-3'-azido-2',3'-dideoxyguanosine-5'-triphosphates as adenosine analogs.HIV-1 and HIV-2 reverse transcriptases: different mechanisms of resistance to nucleoside reverse transcriptase inhibitors.Role of induced fit in limiting discrimination against AZT by HIV reverse transcriptaseUnderstanding the molecular mechanism of sequence dependent tenofovir removal by HIV-1 reverse transcriptase: differences in primer binding site versus polypurine tractBioinformatic Identification of Rare Codon Clusters (RCCs) in HBV Genome and Evaluation of RCCs in Proteins Structure of Hepatitis B Virus.Analysis of the Zidovudine Resistance Mutations T215Y, M41L, and L210W in HIV-1 Reverse Transcriptase.NTP-mediated nucleotide excision activity of hepatitis C virus RNA-dependent RNA polymerase.The structural biology of HIV-1: mechanistic and therapeutic insightsFormation of a quaternary complex of HIV-1 reverse transcriptase with a nucleotide-competing inhibitor and its ATP enhancer.Design, Synthesis, and Biological Evaluations of Hydroxypyridonecarboxylic Acids as Inhibitors of HIV Reverse Transcriptase Associated RNase H.Hypersusceptibility mechanism of Tenofovir-resistant HIV to EFdA.Conformational Plasticity of the NNRTI-Binding Pocket in HIV-1 Reverse Transcriptase: A Fluorine Nuclear Magnetic Resonance Study.Clinical significance of HIV reverse-transcriptase inhibitor-resistance mutations.The lysine 65 residue in HIV-1 reverse transcriptase function and in nucleoside analog drug resistance.Biochemical characterization of a multi-drug resistant HIV-1 subtype AG reverse transcriptase: antagonism of AZT discrimination and excision pathways and sensitivity to RNase H inhibitors.Structural Insights into HIV Reverse Transcriptase Mutations Q151M and Q151M Complex That Confer Multinucleoside Drug Resistance.Molecular basis and potential activity of HIV-1 reverse transcriptase toward trimethylamine-based compounds.Conformational States of HIV-1 Reverse Transcriptase for Nucleotide Incorporation vs Pyrophosphorolysis-Binding of Foscarnet.
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Structural basis of HIV-1 resistance to AZT by excision
@ast
Structural basis of HIV-1 resistance to AZT by excision
@en
Structural basis of HIV-1 resistance to AZT by excision
@nl
type
label
Structural basis of HIV-1 resistance to AZT by excision
@ast
Structural basis of HIV-1 resistance to AZT by excision
@en
Structural basis of HIV-1 resistance to AZT by excision
@nl
prefLabel
Structural basis of HIV-1 resistance to AZT by excision
@ast
Structural basis of HIV-1 resistance to AZT by excision
@en
Structural basis of HIV-1 resistance to AZT by excision
@nl
P2093
P2860
P50
P3181
P356
P1476
Structural basis of HIV-1 resistance to AZT by excision
@en
P2093
Arthur D Clark
Barbara L Gaffney
Joseph D Bauman
Paul L Boyer
Qianwei Han
Roger A Jones
Xiaorong Hou
Xiongying Tu
Yulia V Frenkel
P2860
P2888
P304
P3181
P356
10.1038/NSMB.1908
P407
P577
2010-10-01T00:00:00Z
P5875
P6179
1010007278