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Journal Abstract Search

163 related items for PubMed ID: 35011517

  • 1. Biophysical Characterization of Novel DNA Aptamers against K103N/Y181C Double Mutant HIV-1 Reverse Transcriptase.
    Ratanabunyong S, Seetaha S, Hannongbua S, Yanaka S, Yagi-Utsumi M, Kato K, Paemanee A, Choowongkomon K.
    Molecules; 2022 Jan 03; 27(1):. PubMed ID: 35011517
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  • 2. Use of Capillary Electrophoresis to Study the Binding Interaction of Aptamers with Wild-Type, K103N, and Double Mutant (K103N/Y181C) HIV-1 RT : Studying the Binding Interaction of Wild-Type, K103N, and Double Mutant (K103N/Y181C) HIV-1 RT with Aptamers by Performing the Capillary Electrophoresis.
    Aeksiri N, Warakulwit C, Hannongbua S, Unajak S, Choowongkomon K.
    Appl Biochem Biotechnol; 2017 Jun 03; 182(2):546-558. PubMed ID: 27900665
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  • 6. Novel indolylarylsulfone derivatives as covalent HIV-1 reverse transcriptase inhibitors specifically targeting the drug-resistant mutant Y181C.
    Gao P, Song S, Frutos-Beltrán E, Li W, Sun B, Kang D, Zou J, Zhang J, Pannecouque C, De Clercq E, Menéndez-Arias L, Zhan P, Liu X.
    Bioorg Med Chem; 2021 Jan 15; 30():115927. PubMed ID: 33352387
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  • 8. RNA-protein interactions govern antiviral specificity and encapsidation of broad spectrum anti-HIV reverse transcriptase aptamers.
    Lange MJ, Nguyen PDM, Callaway MK, Johnson MC, Burke DH.
    Nucleic Acids Res; 2017 Jun 02; 45(10):6087-6097. PubMed ID: 28334941
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  • 9. Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1.
    Chan JH, Freeman GA, Tidwell JH, Romines KR, Schaller LT, Cowan JR, Gonzales SS, Lowell GS, Andrews CW, Reynolds DJ, St Clair M, Hazen RJ, Ferris RG, Creech KL, Roberts GB, Short SA, Weaver K, Koszalka GW, Boone LR.
    J Med Chem; 2004 Feb 26; 47(5):1175-82. PubMed ID: 14971897
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  • 13. Effect of a bound non-nucleoside RT inhibitor on the dynamics of wild-type and mutant HIV-1 reverse transcriptase.
    Zhou Z, Madrid M, Evanseck JD, Madura JD.
    J Am Chem Soc; 2005 Dec 14; 127(49):17253-60. PubMed ID: 16332074
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  • 16. HIV-1 reverse transcriptase (RT) polymorphism 172K suppresses the effect of clinically relevant drug resistance mutations to both nucleoside and non-nucleoside RT inhibitors.
    Hachiya A, Marchand B, Kirby KA, Michailidis E, Tu X, Palczewski K, Ong YT, Li Z, Griffin DT, Schuckmann MM, Tanuma J, Oka S, Singh K, Kodama EN, Sarafianos SG.
    J Biol Chem; 2012 Aug 24; 287(35):29988-99. PubMed ID: 22761416
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  • 17. Potent inhibition of human immunodeficiency virus type 1 replication by template analog reverse transcriptase inhibitors derived by SELEX (systematic evolution of ligands by exponential enrichment).
    Joshi P, Prasad VR.
    J Virol; 2002 Jul 24; 76(13):6545-57. PubMed ID: 12050367
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  • 19. 4-Benzyl and 4-benzoyl-3-dimethylaminopyridin-2(1H)-ones: in vitro evaluation of new C-3-amino-substituted and C-5,6-alkyl-substituted analogues against clinically important HIV mutant strains.
    Benjahad A, Croisy M, Monneret C, Bisagni E, Mabire D, Coupa S, Poncelet A, Csoka I, Guillemont J, Meyer C, Andries K, Pauwels R, de Béthune MP, Himmel DM, Das K, Arnold E, Nguyen CH, Grierson DS.
    J Med Chem; 2005 Mar 24; 48(6):1948-64. PubMed ID: 15771439
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  • 20. Identification of novel bifunctional HIV-1 reverse transcriptase inhibitors.
    Lai MT, Tawa P, Auger A, Wang D, Su HP, Yan Y, Hazuda DJ, Miller MD, Asante-Appiah E, Melnyk RA.
    J Antimicrob Chemother; 2018 Jan 01; 73(1):109-117. PubMed ID: 29029095
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