scholarly article | Q13442814 |
P50 | author | Michael J Dapp | Q57555080 |
Lauren Beach | Q59784284 | ||
P2093 | author name string | Louis M Mansky | |
Richard H Heineman | |||
Jonathan M Rawson | |||
Steven E Patterson | |||
Jessica L Martin | |||
Erica K Schnettler | |||
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Lower in vivo mutation rate of human immunodeficiency virus type 1 than that predicted from the fidelity of purified reverse transcriptase | Q29619994 | ||
Unselected mutations in the human immunodeficiency virus type 1 genome are mostly nonsynonymous and often deleterious | Q31047702 | ||
Deoxyribonucleoside triphosphate pool imbalances in vivo are associated with an increased retroviral mutation rate | Q33784748 | ||
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5-Azacytidine can induce lethal mutagenesis in human immunodeficiency virus type 1. | Q35000909 | ||
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Lethal mutagenesis of HIV. | Q36008905 | ||
Mutagenicity of 5-aza-2'-deoxycytidine is mediated by the mammalian DNA methyltransferase | Q36145017 | ||
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Isolation, characterization, and properties of a labile hydrolysis product of the antitumor nucleoside, 5-azacytidine | Q39471085 | ||
Back to the future: revisiting HIV-1 lethal mutagenesis | Q39511261 | ||
5-Azacytidine Hydrolysis Kinetics Measured by High-Pressure Liquid Chromatography and 13C-NMR Spectroscopy | Q39554910 | ||
Delivery of 5-aza-2'-deoxycytidine to cells using oligodeoxynucleotides | Q40110178 | ||
Mutation Frequencies at Defined Single Codon Sites in Vesicular Stomatitis Virus and Poliovirus Can Be Increased Only Slightly by Chemical Mutagenesis | Q40110327 | ||
Combination of a mutagenic agent with a reverse transcriptase inhibitor results in systematic inhibition of HIV-1 infection | Q40412986 | ||
KP-1212/1461, a nucleoside designed for the treatment of HIV by viral mutagenesis | Q40423448 | ||
Lethal mutagenesis of the prototypic arenavirus lymphocytic choriomeningitis virus (LCMV). | Q40653667 | ||
Mutational analysis of HIV-1 long terminal repeats to explore the relative contribution of reverse transcriptase and RNA polymerase II to viral mutagenesis | Q40714016 | ||
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Anti-human immunodeficiency virus type 1 activity of hydroxyurea in combination with 2',3'-dideoxynucleosides | Q42282585 | ||
Hydroxyurea as an inhibitor of human immunodeficiency virus-type 1 replication | Q42282677 | ||
Anti-HIV-1 activity of resveratrol derivatives and synergistic inhibition of HIV-1 by the combination of resveratrol and decitabine | Q42400705 | ||
Synergistic inhibition of HIV-1 in activated and resting peripheral blood mononuclear cells, monocyte-derived macrophages, and selected drug-resistant isolates with nucleoside analogues combined with a natural product, resveratrol | Q43511988 | ||
The broad-spectrum antiviral ribonucleoside ribavirin is an RNA virus mutagen | Q43545743 | ||
Mechanism of action of a novel viral mutagenic covert nucleotide: molecular interactions with HIV-1 reverse transcriptase and host cell DNA polymerases | Q43812620 | ||
Characterization of decomposition products and preclinical and low dose clinical pharmacokinetics of decitabine (5-aza-2'-deoxycytidine) by a new liquid chromatography/tandem mass spectrometry quantification method | Q46980232 | ||
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Changes of deoxyribonucleoside triphosphate pools induced by hydroxyurea and their relation to DNA synthesis | Q68917155 | ||
2'-Deoxy-2'-methylenecytidine and 2'-deoxy-2',2'-difluorocytidine 5'-diphosphates: potent mechanism-based inhibitors of ribonucleotide reductase | Q70215052 | ||
Role of ribonucleotide reductase in inhibition of mammalian cell growth by potent iron chelators | Q72639469 | ||
High-performance Liquid Chromatographic Analysis of Chemical Stability of 5-aza-2′-Deoxycytidine | Q72650148 | ||
Resveratrol, a remarkable inhibitor of ribonucleotide reductase | Q74191674 | ||
Safety, Tolerability, and Pharmacokinetics of KP-1461 in Phase I Clinical Studies: A Single Oral Dose Study in Non-HIV-Infected Adults, and a 14-Day Dose-Escalating Study in Highly Antiretroviral-Experienced HIV-Infected Adults | Q84142908 | ||
P433 | issue | 22 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 7222-7228 | |
P577 | publication date | 2013-08-20 | |
P1433 | published in | Bioorganic & Medicinal Chemistry | Q2904200 |
P1476 | title | 5,6-Dihydro-5-aza-2'-deoxycytidine potentiates the anti-HIV-1 activity of ribonucleotide reductase inhibitors | |
P478 | volume | 21 |
Q39514817 | 5-Azacytidine Enhances the Mutagenesis of HIV-1 by Reduction to 5-Aza-2'-Deoxycytidine. |
Q37547746 | Discovery of novel ribonucleoside analogs with activity against human immunodeficiency virus type 1 |
Q38705926 | Disparate Contributions of Human Retrovirus Capsid Subdomains to Gag-Gag Oligomerization, Virus Morphology, and Particle Biogenesis |
Q36725172 | Dual anti-HIV mechanism of clofarabine |
Q35834559 | HIV-1 and HIV-2 exhibit similar mutation frequencies and spectra in the absence of G-to-A hypermutation |
Q26749548 | New strategies against drug resistance to herpes simplex virus |
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Q38808216 | Rapid Determination of HIV-1 Mutant Frequencies and Mutation Spectra Using an mCherry/EGFP Dual-Reporter Viral Vector |
Q38610855 | Resveratrol, sirtuins, and viruses |
Q34303615 | Retroviral vectors for analysis of viral mutagenesis and recombination |
Q36371387 | Single-Strand Consensus Sequencing Reveals that HIV Type but not Subtype Significantly Impacts Viral Mutation Frequencies and Spectra. |
Q59356354 | The HIV-1 Reverse Transcriptase A62V Mutation Influences Replication Fidelity and Viral Fitness in the Context of Multi-Drug-Resistant Mutations |
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