-
1
-
-
0029786905
-
The K65R mutation confers increased DNA polymerase processivity to HIV-1 reverse transcriptase
-
Arion, D., G. Borkow, Z. Gu, M. A. Wainberg, and M. A. Parniak. 1996. The K65R mutation confers increased DNA polymerase processivity to HIV-1 reverse transcriptase. J. Biol. Chem. 271:19860-19864.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 19860-19864
-
-
Arion, D.1
Borkow, G.2
Gu, Z.3
Wainberg, M.A.4
Parniak, M.A.5
-
2
-
-
0032506055
-
Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′-deoxythymidine (AZT): Increased polymerization processivity and enhanced sensitivity to pyrophosphate of the mutant viral reverse transcriptase
-
Axion, D., N. Kaushik, S. McCormick, G. Borkow, and M. A. Parniak. 1998. Phenotypic mechanism of HIV-1 resistance to 3′-azido-3′-deoxythymidine (AZT): increased polymerization processivity and enhanced sensitivity to pyrophosphate of the mutant viral reverse transcriptase. Biochemistry 37:15908-15917.
-
(1998)
Biochemistry
, vol.37
, pp. 15908-15917
-
-
Axion, D.1
Kaushik, N.2
McCormick, S.3
Borkow, G.4
Parniak, M.A.5
-
3
-
-
0028176053
-
Comparison of deoxyoligonucleotide and tRNA(Lys-3) as primers in an endogenous human immunodeficiency virus-1 in vitro reverse transcription/template-switching reaction
-
Arts, E. J., X. Li, Z. Gu, L. Kleiman, M. A. Parniak, and M. A. Wainberg. 1994. Comparison of deoxyoligonucleotide and tRNA(Lys-3) as primers in an endogenous human immunodeficiency virus-1 in vitro reverse transcription/template-switching reaction. J. Biol. Chem. 269:14672-14680.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 14672-14680
-
-
Arts, E.J.1
Li, X.2
Gu, Z.3
Kleiman, L.4
Parniak, M.A.5
Wainberg, M.A.6
-
4
-
-
0029757751
-
Reduced replication of 3TC-resistant HIV-1 variants in primary cells due to a processivity defect of the reverse transcriptase enzyme
-
Back, N. K. T., M. Nijhuis, W. Keulen, C. A. B. Boucher, B. O. Oude Essink, A. B. P. van Kuilenburg, A. H. van Gennip, and B. Berkhout. 1996. Reduced replication of 3TC-resistant HIV-1 variants in primary cells due to a processivity defect of the reverse transcriptase enzyme. EMBO J. 15:4040-4049.
-
(1996)
EMBO J.
, vol.15
, pp. 4040-4049
-
-
Back, N.K.T.1
Nijhuis, M.2
Keulen, W.3
Boucher, C.A.B.4
Oude Essink, B.O.5
Van Kuilenburg, A.B.P.6
Van Gennip, A.H.7
Berkhout, B.8
-
6
-
-
0033921632
-
In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-β-D-dioxolane-guanosine and suppress resistance to 3′-azido-3′-deoxythymidine
-
Bazmi, H., J. Hammond, S. Cavalcanti, C. Chu, R. Schinazi, and J. Mellors. 2000. In vitro selection of mutations in the human immunodeficiency virus type 1 reverse transcriptase that decrease susceptibility to (-)-β-D-dioxolane-guanosine and suppress resistance to 3′-azido-3′-deoxythymidine. Antimicrob. Agents Chemother. 44:1783-1788.
-
(2000)
Antimicrob. Agents Chemother.
, vol.44
, pp. 1783-1788
-
-
Bazmi, H.1
Hammond, J.2
Cavalcanti, S.3
Chu, C.4
Schinazi, R.5
Mellors, J.6
-
7
-
-
0000941474
-
Patterns of HIV drug resistance in routine clinical practice: A survey of almost 12000 samples from the USA in 1999
-
Bloor, S., S. D. Kemp, K. Hertogs, T. Alcorn, and B. A. Larder. 2000. Patterns of HIV drug resistance in routine clinical practice: a survey of almost 12000 samples from the USA in 1999. Antivir. Ther. 5(Suppl. 3):169.
-
(2000)
Antivir. Ther.
, vol.5
, Issue.SUPPL. 3
, pp. 169
-
-
Bloor, S.1
Kemp, S.D.2
Hertogs, K.3
Alcorn, T.4
Larder, B.A.5
-
8
-
-
0029816733
-
Human immunodeficiency virus type 1 drug susceptibility determination by using recombinant viruses generated from patient sera tested in a cell-killing assay
-
Boucher, C. A. B., W. Keulen, T. van Bommel, M. Nijhuis, D. de Jong, M. D. de Jong, P. Schipper, and N. K. T. Back. 1996. Human immunodeficiency virus type 1 drug susceptibility determination by using recombinant viruses generated from patient sera tested in a cell-killing assay. Antimicrob. Agents Chemother. 40:2404-2409.
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 2404-2409
-
-
Boucher, C.A.B.1
Keulen, W.2
Van Bommel, T.3
Nijhuis, M.4
De Jong, D.5
De Jong, M.D.6
Schipper, P.7
Back, N.K.T.8
-
9
-
-
0035031936
-
Selective excision of AZTMP by drug-resistant human immunodeficiency virus reverse transcriptase
-
Boyer, P. L., S. G. Sarafianos, E. Arnold, and S. H. Hughes. 2001. Selective excision of AZTMP by drug-resistant human immunodeficiency virus reverse transcriptase. J. Virol. 75:4832-4842.
-
(2001)
J. Virol.
, vol.75
, pp. 4832-4842
-
-
Boyer, P.L.1
Sarafianos, S.G.2
Arnold, E.3
Hughes, S.H.4
-
10
-
-
15844392150
-
Comparative kinetic analysis of interaction of inhibitors with Rauscher murine leukemia virus and human immunodeficiency virus reverse transcriptases
-
Cherrington, J. M., M. D. Fuller, A. S. Mulato, S. J. W. Allen, S. C. Kunder, M. A. Ussery, Z. Lesnikowski, R. F. Schinazi, J.-P. Sommadossi, and M. S. Chen. 1996. Comparative kinetic analysis of interaction of inhibitors with Rauscher murine leukemia virus and human immunodeficiency virus reverse transcriptases. Antimicrob. Agents Chemother. 40:1270-1273.
-
(1996)
Antimicrob. Agents Chemother.
, vol.40
, pp. 1270-1273
-
-
Cherrington, J.M.1
Fuller, M.D.2
Mulato, A.S.3
Allen, S.J.W.4
Kunder, S.C.5
Ussery, M.A.6
Lesnikowski, Z.7
Schinazi, R.F.8
Sommadossi, J.-P.9
Chen, M.S.10
-
11
-
-
0030982931
-
1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity
-
Daluge, S. M., S. S. Good, M. B. Faletto, W. H. Miller, M. H. St Clair, L. R. Boone, M. Tisdale, N. R. Parry, J. E. Reardon, R. E. Dornsife, D. R. Averett, and T. A. Krenitsky. 1997. 1592U89, a novel carbocyclic nucleoside analog with potent, selective anti-human immunodeficiency virus activity. Antimicrob. Agents Chemother. 41:1082-1093.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1082-1093
-
-
Daluge, S.M.1
Good, S.S.2
Faletto, M.B.3
Miller, W.H.4
St Clair, M.H.5
Boone, L.R.6
Tisdale, M.7
Parry, N.R.8
Reardon, J.E.9
Dornsife, R.E.10
Averett, D.R.11
Krenitsky, T.A.12
-
12
-
-
0030840407
-
Mutations in the pol gene of human immunodeficiency virus type 1 in infected patients receiving didanosine and hydroxyurea combination therapy
-
De Antoni, A., A. Foli, J. Lisziewicz, and F. Lori. 1997. Mutations in the pol gene of human immunodeficiency virus type 1 in infected patients receiving didanosine and hydroxyurea combination therapy. J. Infect. Dis. 176:899-903.
-
(1997)
J. Infect. Dis.
, vol.176
, pp. 899-903
-
-
De Antoni, A.1
Foli, A.2
Lisziewicz, J.3
Lori, F.4
-
13
-
-
0035864943
-
Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia
-
Deeks, S. G., T. Wrin, T. Liegler~ R. Hoh, M. Hayden, J. D. Barbour, N. S. Hellmann, C. J. Petropoulos, J. M. McCune, M. K. Hellerstein, and R. M. Grant. 2001. Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia. N. Engl. J. Med. 344:472-480.
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 472-480
-
-
Deeks, S.G.1
Wrin, T.2
Liegler, T.3
Hoh, R.4
Hayden, M.5
Barbour, J.D.6
Hellmann, N.S.7
Petropoulos, C.J.8
McCune, J.M.9
Hellerstein, M.K.10
Grant, R.M.11
-
14
-
-
0030903443
-
Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89
-
Faletto, M. B., M. W. Miller, E. P. Garvey, M. H. St. Clair, S. M. Daluge, and S. S. Good. 1997. Unique intracellular activation of the potent anti-human immunodeficiency virus agent 1592U89. Antimicrob. Agents Chemother. 41:1099-1107.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1099-1107
-
-
Faletto, M.B.1
Miller, M.W.2
Garvey, E.P.3
St. Clair, M.H.4
Daluge, S.M.5
Good, S.S.6
-
15
-
-
0035162759
-
Mechanism of action of I-β-D-2,6-diaminopurine dioxalane, a prodrug of the human immunodeficiency virus type I inhibitor 1-β-D-dioxolane guanosine
-
Furman, P., J. Jeffrey, L. Kiefer, J. Feng, K. Anderson, K. Borroto-Esoda, E. Hill, W. Copeland, C. Chu, J. Sommadossi, L Liberman, R. Schinazi, and G. Painter. 2001. Mechanism of action of I-β-D-2,6-diaminopurine dioxalane, a prodrug of the human immunodeficiency virus type I inhibitor 1-β-D-dioxolane guanosine. Antimicrob. Agents Chemother. 45:158-165.
-
(2001)
Antimicrob. Agents Chemother.
, vol.45
, pp. 158-165
-
-
Furman, P.1
Jeffrey, J.2
Kiefer, L.3
Feng, J.4
Anderson, K.5
Borroto-Esoda, K.6
Hill, E.7
Copeland, W.8
Chu, C.9
Sommadossi, J.10
Liberman, L.11
Schinazi, R.12
Painter, G.13
-
16
-
-
0142100752
-
The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue of chain-terminated DNA synthesis
-
Gotte, M., D. Axion, M. A. Parniak, and M. A. Wainberg. 2000. The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue of chain-terminated DNA synthesis. J. Virol. 74:3579-3585.
-
(2000)
J. Virol.
, vol.74
, pp. 3579-3585
-
-
Gotte, M.1
Axion, D.2
Parniak, M.A.3
Wainberg, M.A.4
-
17
-
-
0028034266
-
The K65R mutant reverse transcriptase of HIV-1 cross-resistant to 2′,3′-dideoxycytidine, 2′,3′-dideoxy-3′-thiacytidine, and 2′,3′-dideoxyinosine shows reduced sensitivity to specific dideoxynucleoside triphosphate inhibitors in vitro
-
Gu, Z., R. S. Fletcher, E. J. Arts, M. A. Wainberg, and M. A. Parniak. 1994. The K65R mutant reverse transcriptase of HIV-1 cross-resistant to 2′,3′-dideoxycytidine, 2′,3′-dideoxy-3′-thiacytidine, and 2′,3′-dideoxyinosine shows reduced sensitivity to specific dideoxynucleoside triphosphate inhibitors in vitro. J. Biol. Chem. 269:28118-28122.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 28118-28122
-
-
Gu, Z.1
Fletcher, R.S.2
Arts, E.J.3
Wainberg, M.A.4
Parniak, M.A.5
-
18
-
-
0028057581
-
Identification of a mutation of codon 65 in the IKKK motif of reverse transcriptase that encodes human immunodeficiency virus resistance to 2′,3′-dideoxycytidine and 2′,3′-dideoxy-3′-thiacytidine
-
Gu, Z., Q. Gao, H. Fang, H. Salomon, M. A. Parniak, E. Goldberg, J. Cameron, and M. A. Wainberg. 1994. Identification of a mutation of codon 65 in the IKKK motif of reverse transcriptase that encodes human immunodeficiency virus resistance to 2′,3′-dideoxycytidine and 2′,3′-dideoxy-3′-thiacytidine. Antimicrob. Agents Chemother. 38:275-281.
-
(1994)
Antimicrob. Agents Chemother.
, vol.38
, pp. 275-281
-
-
Gu, Z.1
Gao, Q.2
Fang, H.3
Salomon, H.4
Parniak, M.A.5
Goldberg, E.6
Cameron, J.7
Wainberg, M.A.8
-
19
-
-
0032823357
-
Mechanism of action and in vitro activity of 1′,3′-dioxolanyipurine nucleoside analogues against sensitive and drug-resistant human immunodeficiency virus type 1 variants
-
Gu, Z., M. Wainberg, N. Nguyen-Ba, L. L'Heureux, J. De Muys, T. Bowlin, and R. Rando. 1999. Mechanism of action and in vitro activity of 1′,3′-dioxolanyipurine nucleoside analogues against sensitive and drug-resistant human immunodeficiency virus type 1 variants. Antimicrob. Agents Chemother. 43:2376-2382.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 2376-2382
-
-
Gu, Z.1
Wainberg, M.2
Nguyen-Ba, N.3
L'Heureux, L.4
De Muys, J.5
Bowlin, T.6
Rando, R.7
-
20
-
-
0033056651
-
Anti-HIV-1 activities of 1,3-dioxolane guanine and 2,6-diaminopurine dixolane
-
Gu, Z., M. A. Wainberg, P. Nguyen-Ba, L. L'Heureux, J.-M. de Muys, and R. F. Rando. 1999. Anti-HIV-1 activities of 1,3-dioxolane guanine and 2,6-diaminopurine dixolane. Nucleosides Nucleotides 18:891-892.
-
(1999)
Nucleosides Nucleotides
, vol.18
, pp. 891-892
-
-
Gu, Z.1
Wainberg, M.A.2
Nguyen-Ba, P.3
L'Heureux, L.4
De Muys, J.-M.5
Rando, R.F.6
-
21
-
-
0023242380
-
RNase H activity associated with bacterially expressed reverse transcriptase of human T-cell tropic virus III/lymphadenopathy-associated virus
-
Hansen, J., T. Schulze, and K. Moellin. 1987. RNase H activity associated with bacterially expressed reverse transcriptase of human T-cell tropic virus III/lymphadenopathy-associated virus. J. Biol. Chem. 262:12393-12396.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 12393-12396
-
-
Hansen, J.1
Schulze, T.2
Moellin, K.3
-
22
-
-
0034088720
-
Resistance profile of the human immunodeficiency virus type 1 reverse transcriptase inhibitor abacavir (1592U89) after monotherapy and combination therapy
-
Harrigan, P., C. Stone, P. Griffin, I. Najera, S. Bloor, S. Kemp, M. Tisdale, and B. Larder. 2000. Resistance profile of the human immunodeficiency virus type 1 reverse transcriptase inhibitor abacavir (1592U89) after monotherapy and combination therapy. J. Infect. Dis. 181:912-920.
-
(2000)
J. Infect. Dis.
, vol.181
, pp. 912-920
-
-
Harrigan, P.1
Stone, C.2
Griffin, P.3
Najera, I.4
Bloor, S.5
Kemp, S.6
Tisdale, M.7
Larder, B.8
-
23
-
-
0015718863
-
Analysis of nucleotide pools in animal cells
-
Hauschka, P. V. 1973, Analysis of nucleotide pools in animal cells. Methods Cell Biol. 7:361-462.
-
(1973)
Methods Cell Biol.
, vol.7
, pp. 361-462
-
-
Hauschka, P.V.1
-
24
-
-
0032573488
-
Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance
-
Huang, H., R. Chopra, G. L. Verdine, and S. C. Harrison. 1998. Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance. Science 282:1669-1675.
-
(1998)
Science
, vol.282
, pp. 1669-1675
-
-
Huang, H.1
Chopra, R.2
Verdine, G.L.3
Harrison, S.C.4
-
25
-
-
0027530506
-
1,3-Dioxolanylpurine nucleosides (2R.4R) and (2R,4S) with selective anti-HIV-1 activity in human lymphocytes
-
Kim, H., R. Schinazi, S. Nampalli, K. Shanmuganathan, D. Cannon, A. Alves, L. Jeong, J. Beach, and C. Chu. 1993. 1,3-Dioxolanylpurine nucleosides (2R.4R) and (2R,4S) with selective anti-HIV-1 activity in human lymphocytes. J. Med. Chem. 36:30-37.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 30-37
-
-
Kim, H.1
Schinazi, R.2
Nampalli, S.3
Shanmuganathan, K.4
Cannon, D.5
Alves, A.6
Jeong, L.7
Beach, J.8
Chu, C.9
-
26
-
-
0037076708
-
Genotypic and phenotypic analyses of HIV-1 in antiretroviral-experienced patients treated with tenofovir DF
-
Margot, N. A., E. Isaacson, I. McGowan, A. K. Cheng, R. T. Schooley, and M. D. Miller. 2002. Genotypic and phenotypic analyses of HIV-1 in antiretroviral-experienced patients treated with tenofovir DF. AIDS 16:1227-1235.
-
(2002)
AIDS
, vol.16
, pp. 1227-1235
-
-
Margot, N.A.1
Isaacson, E.2
McGowan, I.3
Cheng, A.K.4
Schooley, R.T.5
Miller, M.D.6
-
27
-
-
0036156325
-
Dioxolane guanosine, the active form of the prodrug diaminopurine dioxolane, is a potent inhibitor of drug-resistant HIV-1 isolates from patients for whom standard nucleoside therapy fails
-
Mewshaw, J. P., F. T. Myrick, D. A. Wakefield, B. J. Hooper, J. L. Harris, B. McCreedy, and K. Borroto-Esoda. 2002. Dioxolane guanosine, the active form of the prodrug diaminopurine dioxolane, is a potent inhibitor of drug-resistant HIV-1 isolates from patients for whom standard nucleoside therapy fails. J. Acquir. Immune Defic. Syndr. 29:11-20.
-
(2002)
J. Acquir. Immune Defic. Syndr.
, vol.29
, pp. 11-20
-
-
Mewshaw, J.P.1
Myrick, F.T.2
Wakefield, D.A.3
Hooper, B.J.4
Harris, J.L.5
McCreedy, B.6
Borroto-Esoda, K.7
-
28
-
-
0033165851
-
A mechanism of AZT resistance: An increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase
-
Meyer, P. R., S. E. Matsuura, A. M. Mian, A. G. So, and W. A. Scott. 1999. A mechanism of AZT resistance: an increase in nucleotide-dependent primer unblocking by mutant HIV-1 reverse transcriptase. Mol. Cell 4:3543.
-
(1999)
Mol. Cell
, vol.4
, pp. 3543
-
-
Meyer, P.R.1
Matsuura, S.E.2
Mian, A.M.3
So, A.G.4
Scott, W.A.5
-
29
-
-
0032937011
-
Human immunodeficiency virus type 1 expressing the lamivudine-associated M184V mutation in reverse transcriptase shows increased susceptibility to adefovir and decreased replication capability in vitro
-
Miller, M. D., K. E. Anton, A. S. Mulato, P. D. Lamy, and J. M. Cherrington. 1999. Human immunodeficiency virus type 1 expressing the lamivudine-associated M184V mutation in reverse transcriptase shows increased susceptibility to adefovir and decreased replication capability in vitro. J. Infect. Dis. 179:92-100.
-
(1999)
J. Infect. Dis.
, vol.179
, pp. 92-100
-
-
Miller, M.D.1
Anton, K.E.2
Mulato, A.S.3
Lamy, P.D.4
Cherrington, J.M.5
-
30
-
-
0031848831
-
Human immunodeficiency virus type 1 reverse transcriptase expressing the K70E mutation exhibits a decrease in specific activity and processivity
-
Miller, M. D., P. D. Lamy, M. D. Fuller, A. S. Mulato, N. A. Margot, T. Cihlar, and J. M. Cherrington. 1998. Human immunodeficiency virus type 1 reverse transcriptase expressing the K70E mutation exhibits a decrease in specific activity and processivity. Mol. Pharmacol. 54:291-297.
-
(1998)
Mol. Pharmacol.
, vol.54
, pp. 291-297
-
-
Miller, M.D.1
Lamy, P.D.2
Fuller, M.D.3
Mulato, A.S.4
Margot, N.A.5
Cihlar, T.6
Cherrington, J.M.7
-
31
-
-
0033995190
-
HIV-1 reverse transcriptase (RT) genotype and susceptibility to RT inhibitors during abacavir monotherapy and combination therapy
-
Miller, V., M. Ait-Khaled, C. Stone, P. Griffin, D. Mesogiti, A. Cutrell, R. Harrigan, S. Staszewski, C. Katlama, G. Pearce, and M. Tisdale. 2000. HIV-1 reverse transcriptase (RT) genotype and susceptibility to RT inhibitors during abacavir monotherapy and combination therapy. AIDS 14:163-171.
-
(2000)
AIDS
, vol.14
, pp. 163-171
-
-
Miller, V.1
Ait-Khaled, M.2
Stone, C.3
Griffin, P.4
Mesogiti, D.5
Cutrell, A.6
Harrigan, R.7
Staszewski, S.8
Katlama, C.9
Pearce, G.10
Tisdale, M.11
-
32
-
-
0001287124
-
Altered drug susceptibility of HIV-1 RT mutants containing M184V and zidovudine-resi stance mutations: Analysis of RT processivity, viral replication, and chain-terminator removal
-
Naeger, L. K., N. A. Margot, and M. D. Miller. 2001. Altered drug susceptibility of HIV-1 RT mutants containing M184V and zidovudine-resi stance mutations: analysis of RT processivity, viral replication, and chain-terminator removal. Antivir. Ther. 6:111-123.
-
(2001)
Antivir. Ther.
, vol.6
, pp. 111-123
-
-
Naeger, L.K.1
Margot, N.A.2
Miller, M.D.3
-
33
-
-
0035984790
-
ATP-dependent removal of nucleoside reverse transcriptase inhibitors by human immunodeficiency virus type 1 reverse transcriptase
-
Naeger, L. K., N. A. Margot, and M. D. Miller. 2002. ATP-dependent removal of nucleoside reverse transcriptase inhibitors by human immunodeficiency virus type 1 reverse transcriptase. Antimicrob. Agents Chemother. 46:2179-2184.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 2179-2184
-
-
Naeger, L.K.1
Margot, N.A.2
Miller, M.D.3
-
34
-
-
0035061595
-
Mechanisms of HIV-1 nucleoside reverse transcriptase inhibitor resistance: Is it all figured out?
-
Naeger, L. K., and M. D. Miller. 2001. Mechanisms of HIV-1 nucleoside reverse transcriptase inhibitor resistance: is it all figured out? Curr. Opin. Investig. Drugs 2:335-339.
-
(2001)
Curr. Opin. Investig. Drugs
, vol.2
, pp. 335-339
-
-
Naeger, L.K.1
Miller, M.D.2
-
35
-
-
0029896847
-
Endogenous reverse transcription assays reveal high-level resistance to the triphosphate of (-)-2′-dideoxy-3′-thiacytidine by mutated M184V human immunodeficiency virus type 1
-
Quan, Y., Z. Gu, X. Li, Z. Li, C. D. Morrow, and M. A. Wainberg. 1996. Endogenous reverse transcription assays reveal high-level resistance to the triphosphate of (-)-2′-dideoxy-3′-thiacytidine by mutated M184V human immunodeficiency virus type 1. J. Virol. 70:5642-5645.
-
(1996)
J. Virol.
, vol.70
, pp. 5642-5645
-
-
Quan, Y.1
Gu, Z.2
Li, X.3
Li, Z.4
Morrow, C.D.5
Wainberg, M.A.6
-
36
-
-
0003507870
-
-
International Medical Press, London, United Kingdom
-
Richman, D., and S. Staszewski. 2000. A practical guide to HIV drug resistance and its implications for antiretroviral treatment strategies, 2nd ed. International Medical Press, London, United Kingdom.
-
(2000)
A practical guide to HIV drug resistance and its implications for antiretroviral treatment strategies, 2nd ed.
-
-
Richman, D.1
Staszewski, S.2
-
37
-
-
0033133780
-
Touching the heart of HIV-1 drug resistance: The fingers close down on the dNTP at the polymerase active site
-
Sarafianos, S. G., K. Das, J. Ding, P. L. Boyer, S. H. Hughes, and E. Arnold. 1999. Touching the heart of HIV-1 drug resistance: the fingers close down on the dNTP at the polymerase active site. Chem. Biol. 6:R137-R146.
-
(1999)
Chem. Biol.
, vol.6
-
-
Sarafianos, S.G.1
Das, K.2
Ding, J.3
Boyer, P.L.4
Hughes, S.H.5
Arnold, E.6
-
38
-
-
0035930584
-
Mechanism-based suppression of dideoxvnucleotide resistance by K65R human immunodeficiency virus reverse transcriptase using an alpha-boranophosphate nucleoside analogue
-
Selmi, B., J. Boretto, S. R. Sarfati, C. Guerreiro, and B. Canard. 2001. Mechanism-based suppression of dideoxvnucleotide resistance by K65R human immunodeficiency virus reverse transcriptase using an alpha-boranophosphate nucleoside analogue. J. Biol. Chem. 276:48466-48472.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 48466-48472
-
-
Selmi, B.1
Boretto, J.2
Sarfati, S.R.3
Guerreiro, C.4
Canard, B.5
-
39
-
-
0034282409
-
Differential influence of nucleoside analog-resistance mutations K65R and L74V on the overall mutation rate and error specificity of human immunodeficiency virus type 1 reverse transcriptase
-
Shah, F. S., K. A. Curr, M. E. Hamburgh, M. Parniak, H. Mitsuya, J. G. Arnez, and V. R. Prasad. 2000. Differential influence of nucleoside analog-resistance mutations K65R and L74V on the overall mutation rate and error specificity of human immunodeficiency virus type 1 reverse transcriptase. J. Biol. Chem. 275:27037-27044.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 27037-27044
-
-
Shah, F.S.1
Curr, K.A.2
Hamburgh, M.E.3
Parniak, M.4
Mitsuya, H.5
Arnez, J.G.6
Prasad, V.R.7
-
40
-
-
0032875344
-
Decreased processivity of human immunodeficiency virus type 1 reverse transcriptase (RT) containing didanosine-selected mutation Leu74Val: A comparative analysis of RT variants Leu74Val and lamivudine-selected Met184Val
-
Sharma, P. L., and C. S. Crumpacker. 1999. Decreased processivity of human immunodeficiency virus type 1 reverse transcriptase (RT) containing didanosine-selected mutation Leu74Val: a comparative analysis of RT variants Leu74Val and lamivudine-selected Met184Val. J. Virol. 73:8448-8456.
-
(1999)
J. Virol.
, vol.73
, pp. 8448-8456
-
-
Sharma, P.L.1
Crumpacker, C.S.2
-
41
-
-
0027183976
-
Antiviral optically pure dioxolane purine nucleoside analogs
-
Siddiqui, M., W. Brown, N. Nguyen-Ba, D. Dixit, and T. Mansour. 1993. Antiviral optically pure dioxolane purine nucleoside analogs. Bioorg. Med. Chem. Lett. 3:1543-1546.
-
(1993)
Bioorg. Med. Chem. Lett.
, vol.3
, pp. 1543-1546
-
-
Siddiqui, M.1
Brown, W.2
Nguyen-Ba, N.3
Dixit, D.4
Mansour, T.5
-
42
-
-
0030945276
-
Combination of mutations in human immunodeficiency virus type 1 reverse transcriptase required for resistance to the carbocyclic nucleoside 1592U89
-
Tisdale, M., T. Alnadaf, and D. Cousens. 1997. Combination of mutations in human immunodeficiency virus type 1 reverse transcriptase required for resistance to the carbocyclic nucleoside 1592U89. Antimicrob. Agents Chemother. 41:1094-1098.
-
(1997)
Antimicrob. Agents Chemother.
, vol.41
, pp. 1094-1098
-
-
Tisdale, M.1
Alnadaf, T.2
Cousens, D.3
-
43
-
-
0028143584
-
Physiological concentrations of purines and pyrimidines
-
Traut, T. 1994. Physiological concentrations of purines and pyrimidines. Mol. Cell. Biochem. 140:1-22.
-
(1994)
Mol. Cell. Biochem.
, vol.140
, pp. 1-22
-
-
Traut, T.1
-
44
-
-
0031046557
-
Comparative enzymatic study of HIV-1 reverse transcriptase resistant to 2′,3′-dideoxynucleotide analogs using the single-nucleotide incorporation assay
-
Ueno, T., and H. Mitsuya. 1997. Comparative enzymatic study of HIV-1 reverse transcriptase resistant to 2′,3′-dideoxynucleotide analogs using the single-nucleotide incorporation assay. Biochemistry 36:1092-1099.
-
(1997)
Biochemistry
, vol.36
, pp. 1092-1099
-
-
Ueno, T.1
Mitsuya, H.2
-
45
-
-
20644436472
-
In vitro selection and characterization of HIV-1 with reduced susceptibility to PMPA
-
Wainberg, M. A., M. D. Miller, Y. Quan, H. Salomon, A. S. Mulato, P. D. Lamy, N. A. Margot, K. E. Anton, and J. M. Cherrington. 1999. In vitro selection and characterization of HIV-1 with reduced susceptibility to PMPA, Antivir. Ther. 4:87-94.
-
(1999)
Antivir. Ther.
, vol.4
, pp. 87-94
-
-
Wainberg, M.A.1
Miller, M.D.2
Quan, Y.3
Salomon, H.4
Mulato, A.S.5
Lamy, P.D.6
Margot, N.A.7
Anton, K.E.8
Cherrington, J.M.9
-
46
-
-
0029920290
-
Human Immunodeficiency virus type-1 reverse transcriptase contribution of Met-184 to binding of nucleoside 5′-triphosphate
-
Wilson, J. E., A. Aulabaugh, B. Caligan, S. McPherson, J. K. Wakefield, S. Jablonski, C. D. Morrow, J. E. Reardon, and P. A. Furman. 1996. Human Immunodeficiency virus type-1 reverse transcriptase contribution of Met-184 to binding of nucleoside 5′-triphosphate. J. Biol. Chem. 271:13656-13662.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 13656-13662
-
-
Wilson, J.E.1
Aulabaugh, A.2
Caligan, B.3
McPherson, S.4
Wakefield, J.K.5
Jablonski, S.6
Morrow, C.D.7
Reardon, J.E.8
Furman, P.A.9
|