Substrate Discrimination by Formamidopyrimidine-DNA Glycosylase:  Distinguishing Interactions within the Active Site by Perlow-Poehnelt, Rebecca A, Zharkov, Dmitry O, Grollman, Arthur P, Broyde, Suse

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The spacious active site of a Y-family DNA polymerase facilitates promiscuous nucleotide incorporation opposite a bulky carcinogen-DNA adduct: elucidating the structure-function re... by Perlow-Poehnelt, Rebecca A, Likhterov, Ilya, Scicchitano, David A, Geacintov, Nicholas E, Broyde, Suse

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Increased Flexibility Enhances Misincorporation: TEMPERATURE EFFECTS ON NUCLEOTIDE INCORPORATION OPPOSITE A BULKY CARCINOGEN-DNA ADDUCT BY A Y-FAMILY DNA POLYMERASE by Perlow-Poehnelt, Rebecca A, Likhterov, Ilya, Wang, Lihua, Scicchitano, David A, Geacintov, Nicholas E, Broyde, Suse

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Increased Flexibility Enhances Misincorporation by Perlow-Poehnelt, Rebecca A., Likhterov, Ilya, Wang, Lihua, Scicchitano, David A., Geacintov, Nicholas E., Broyde, Suse

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The Spacious Active Site of a Y-Family DNA Polymerase Facilitates Promiscuous Nucleotide Incorporation Opposite a Bulky Carcinogen-DNA Adduct by Perlow-Poehnelt, Rebecca A., Likhterov, Ilya, Scicchitano, David A., Geacintov, Nicholas E., Broyde, Suse

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Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: Aryl substituted pyrazole as a surrogate for the pyrazolopyridine motif by Su, Dai-Shi, Lim, John J., Tinney, Elizabeth, Tucker, Thomas J., Saggar, Sandeep, Sisko, John T., Wan, Bang-Lin, Young, Mary Beth, Anderson, Kenneth D., Rudd, Deanne, Munshi, Vandna, Bahnck, Carolyn, Felock, Peter J., Lu, Meiquing, Lai, Ming-Tain, Touch, Sinoeun, Moyer, Gregory, DiStefano, Daniel J., Flynn, Jessica A., Liang, Yuexia, Sanchez, Rosa, Perlow-Poehnelt, Rebecca, Miller, Mike, Vacca, Joe P., Williams, Theresa M., Anthony, Neville J.

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Discovery of 3-{5-[(6-Amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): A Potent, Orally Bioavailable HIV-1 Non-Nucleoside Reverse Tra... by Tucker, Thomas J, Sisko, John T, Tynebor, Robert M, Williams, Theresa M, Felock, Peter J, Flynn, Jessica A, Lai, Ming-Tain, Liang, Yuexia, McGaughey, Georgia, Liu, Meiquing, Miller, Mike, Moyer, Gregory, Munshi, Vandna, Perlow-Poehnelt, Rebecca, Prasad, Sridhar, Reid, John C, Sanchez, Rosa, Torrent, Maricel, Vacca, Joseph P, Wan, Bang-Lin, Yan, Youwei

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Biaryl Ethers as Novel Non-nucleoside Reverse Transcriptase Inhibitors with Improved Potency against Key Mutant Viruses by Su, Dai-Shi, Lim, John J, Tinney, Elizabeth, Wan, Bang-Lin, Young, Mary Beth, Anderson, Kenneth D, Rudd, Deanne, Munshi, Vandna, Bahnck, Carolyn, Felock, Peter J, Lu, Meiquing, Lai, Ming-Tain, Touch, Sinoeun, Moyer, Gregory, DiStefano, Daniel J, Flynn, Jessica A, Liang, Yuexia, Sanchez, Rosa, Perlow-Poehnelt, Rebecca, Miller, Mike, Vacca, Joe P, Williams, Theresa M, Anthony, Neville J

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The design and synthesis of diaryl ether second generation HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) with enhanced potency versus key clinical mutations by Tucker, Thomas J., Saggar, Sandeep, Sisko, John T., Tynebor, Robert M., Williams, Theresa M., Felock, Peter J., Flynn, Jessica A., Lai, Ming-Tain, Liang, Yuexia, McGaughey, Georgia, Liu, Meiquing, Miller, Mike, Moyer, Gregory, Munshi, Vandna, Perlow-Poehnelt, Rebecca, Prasad, Sridhar, Sanchez, Rosa, Torrent, Maricel, Vacca, Joseph P., Wan, Bang-Lin, Yan, Youwei

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Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutants by Su, Dai-Shi, Lim, John J., Tinney, Elizabeth, Wan, Bang-Lin, Young, Mary Beth, Anderson, Kenneth D., Rudd, Deanne, Munshi, Vandna, Bahnck, Carolyn, Felock, Peter J., Lu, Meiqing, Lai, Ming-Tain, Touch, Sinoeun, Moyer, Gregory, DiStefano, Daniel J., Flynn, Jessica A., Liang, Yuexia, Sanchez, Rosa, Prasad, Sridhar, Yan, Youwei, Perlow-Poehnelt, Rebecca, Torrent, Maricel, Miller, Mike, Vacca, Joe P., Williams, Theresa M., Anthony, Neville J.

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