-
1
-
-
80455175886
-
Reverse Transcriptase. Cold Spring Harbor Monogr
-
Skalka AM, Goff SP, (1993) Reverse Transcriptase. Cold Spring Harbor Monogr. Ser. Vol 23: 492.
-
(1993)
Ser
, vol.23
, pp. 492
-
-
Skalka, A.M.1
Goff, S.P.2
-
2
-
-
36749088862
-
HIV drug development: the next 25 years
-
Flexner C, (2007) HIV drug development: the next 25 years. Nat Rev 6: 959-966.
-
(2007)
Nat Rev
, vol.6
, pp. 959-966
-
-
Flexner, C.1
-
3
-
-
0037624182
-
Twenty years of therapy for HIV-1 infection
-
Pomerantz R, Horn DL, (2003) Twenty years of therapy for HIV-1 infection. Nat Med 9: 867-873.
-
(2003)
Nat Med
, vol.9
, pp. 867-873
-
-
Pomerantz, R.1
Horn, D.L.2
-
4
-
-
0035800026
-
Highly active antiretroviral therapy decreases mortality and morbidity in patients with advanced HIV disease
-
Murphy EL, Collier AC, Kalish LA, Assmann SF, Para MF, et al. (2001) Highly active antiretroviral therapy decreases mortality and morbidity in patients with advanced HIV disease. Ann Intern Med 135: 17-26.
-
(2001)
Ann Intern Med
, vol.135
, pp. 17-26
-
-
Murphy, E.L.1
Collier, A.C.2
Kalish, L.A.3
Assmann, S.F.4
Para, M.F.5
-
5
-
-
4544381403
-
HIV fusion and its inhibition in antiretroviral therapy
-
Greenberg M, Cammack N, Salgo M, Smiley L, (2004) HIV fusion and its inhibition in antiretroviral therapy. Rev Med Virol 14: 321-337.
-
(2004)
Rev Med Virol
, vol.14
, pp. 321-337
-
-
Greenberg, M.1
Cammack, N.2
Salgo, M.3
Smiley, L.4
-
6
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
-
Dorr P, Westby M, Dobbs S, Griffin P, Irvine B, et al. (2005) Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob Agents Chemother 49: 4721-4732.
-
(2005)
Antimicrob Agents Chemother
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
Westby, M.2
Dobbs, S.3
Griffin, P.4
Irvine, B.5
-
7
-
-
0034723439
-
Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells
-
Hazuda DJ, Felock P, Witmer M, Wolfe A, Stillmock K, Grobler JA, et al. (2000) Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells. Science 287: 646-650.
-
(2000)
Science
, vol.287
, pp. 646-650
-
-
Hazuda, D.J.1
Felock, P.2
Witmer, M.3
Wolfe, A.4
Stillmock, K.5
Grobler, J.A.6
-
8
-
-
0029150042
-
Human immunodeficiency virus reverse transcriptase substrate-induced conformational changes and the mechanism of inhibition by nonnucleoside inhibitors Proc Natl Acad Sci USA
-
Rittinger K, Divita G, Goody RS, (1995) Human immunodeficiency virus reverse transcriptase substrate-induced conformational changes and the mechanism of inhibition by nonnucleoside inhibitors Proc Natl Acad Sci USA 92: 8046-8049.
-
(1995)
, vol.92
, pp. 8046-8049
-
-
Rittinger, K.1
Divita, G.2
Goody, R.S.3
-
9
-
-
0028925773
-
Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors
-
Spence RA, Kati WM, Anderson KS, Johnson KA, (1995) Mechanism of inhibition of HIV-1 reverse transcriptase by nonnucleoside inhibitors. Science 267: 988-993.
-
(1995)
Science
, vol.267
, pp. 988-993
-
-
Spence, R.A.1
Kati, W.M.2
Anderson, K.S.3
Johnson, K.A.4
-
10
-
-
30844469498
-
Nucleoside and nucleotide inhibitors of HIV-1 replication
-
Vivet-Boudou V, Didierjean J, Isel C, Marquet R, (2006) Nucleoside and nucleotide inhibitors of HIV-1 replication. Cell Mol Life Sci 63: 163-186.
-
(2006)
Cell Mol Life Sci
, vol.63
, pp. 163-186
-
-
Vivet-Boudou, V.1
Didierjean, J.2
Isel, C.3
Marquet, R.4
-
12
-
-
58149133507
-
Structure and function of HIV-1 reverse transcriptase: Molecular mechanisms of polymerization and inhibition
-
Sarafianos S, Marchand B, Das K, Himmel D, Parniak M, et al. (2009) Structure and function of HIV-1 reverse transcriptase: Molecular mechanisms of polymerization and inhibition. J Mol Biol 385: 693-713.
-
(2009)
J Mol Biol
, vol.385
, pp. 693-713
-
-
Sarafianos, S.1
Marchand, B.2
Das, K.3
Himmel, D.4
Parniak, M.5
-
13
-
-
0024267430
-
Fidelity of HIV-1 reverse transcriptase
-
Preston BD, Poiesz BJ, Loeb LA, (1988) Fidelity of HIV-1 reverse transcriptase. Science 242: 1168-1171.
-
(1988)
Science
, vol.242
, pp. 1168-1171
-
-
Preston, B.D.1
Poiesz, B.J.2
Loeb, L.A.3
-
14
-
-
0024273119
-
The accuracy of reverse transcriptase from HIV-1
-
Roberts JD, Bebenek K, Kunkel TA, (1988) The accuracy of reverse transcriptase from HIV-1. Science 242: 1171-1173.
-
(1988)
Science
, vol.242
, pp. 1171-1173
-
-
Roberts, J.D.1
Bebenek, K.2
Kunkel, T.A.3
-
15
-
-
43049105858
-
Mechanisms of resistance to nucleoside analogue inhibitors of HIV-1 reverse transcriptase
-
Menendez-Arias L, (2008) Mechanisms of resistance to nucleoside analogue inhibitors of HIV-1 reverse transcriptase. Virus Res 134: 124-146.
-
(2008)
Virus Res
, vol.134
, pp. 124-146
-
-
Menendez-Arias, L.1
-
16
-
-
77957817451
-
The role of nucleotide excision by reverse transcriptase in HIV drug resistance
-
Acosta-Hoyos A, Scott W, (2010) The role of nucleotide excision by reverse transcriptase in HIV drug resistance. Viruses 2: 372-394.
-
(2010)
Viruses
, vol.2
, pp. 372-394
-
-
Acosta-Hoyos, A.1
Scott, W.2
-
17
-
-
2942560771
-
Primer unblocking by HIV-1 reverse transcriptase and resistance to nucleoside RT inhibitors (NRTIs)
-
Goldschmidt V, Marquet R, (2004) Primer unblocking by HIV-1 reverse transcriptase and resistance to nucleoside RT inhibitors (NRTIs). Int J Biochem Cell Biol 36: 1687-1705.
-
(2004)
Int J Biochem Cell Biol
, vol.36
, pp. 1687-1705
-
-
Goldschmidt, V.1
Marquet, R.2
-
18
-
-
9644259018
-
Fixed conformation nucleoside analogs effectively inhibit excision-proficient HIV-1 reverse transcriptase
-
Boyer P, Julias JG, Marquez V, Hughes S, (2005) Fixed conformation nucleoside analogs effectively inhibit excision-proficient HIV-1 reverse transcriptase. J Mol Biol 345: 441-450.
-
(2005)
J Mol Biol
, vol.345
, pp. 441-450
-
-
Boyer, P.1
Julias, J.G.2
Marquez, V.3
Hughes, S.4
-
19
-
-
33747108083
-
The history of N-methanocarbathymidine: The investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent
-
Marquez VE, Hughes SH, Sei S, Agbaria R, (2006) The history of N-methanocarbathymidine: The investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent. Antiviral Res 71: 268-275.
-
(2006)
Antiviral Res
, vol.71
, pp. 268-275
-
-
Marquez, V.E.1
Hughes, S.H.2
Sei, S.3
Agbaria, R.4
-
20
-
-
0035342161
-
4′-C-Substituted-2′-deoxynucleosides: a family of antiretroviral agents which are potent against drug-resistant HIV variants
-
Ohrui H, Mitsuya H, (2001) 4′-C-Substituted-2′-deoxynucleosides: a family of antiretroviral agents which are potent against drug-resistant HIV variants. Curr Drug Targets: Infectious Disorders 1: 1-10.
-
(2001)
Curr Drug Targets: Infectious Disorders
, vol.1
, pp. 1-10
-
-
Ohrui, H.1
Mitsuya, H.2
-
21
-
-
0034744423
-
4 -Ethynyl nucleoside analogs: potent inhibitors of multidrug resistant human immunodeficiency virus variants in vitro
-
Kodama E, Kohgo S, Kitano K, Machida H, Gatanaga H, et al. (2001) 4-Ethynyl nucleoside analogs: potent inhibitors of multidrug resistant human immunodeficiency virus variants in vitro. Antimicrob Agents Chemother 45: 1539-1546.
-
(2001)
Antimicrob Agents Chemother
, vol.45
, pp. 1539-1546
-
-
Kodama, E.1
Kohgo, S.2
Kitano, K.3
Machida, H.4
Gatanaga, H.5
-
22
-
-
48349089930
-
2′-Deoxy-4′-C-ethynyl-2-halo-adenosines active against drug-resistant human immunodeficiency virus type 1 variants
-
Kawamoto A, Kodama E, Sarafianos S, Sakagami Y, Kohgo S, et al. (2008) 2′-Deoxy-4′-C-ethynyl-2-halo-adenosines active against drug-resistant human immunodeficiency virus type 1 variants. Int J Biochem Cell B 40: 2410-2420.
-
(2008)
Int J Biochem Cell B
, vol.40
, pp. 2410-2420
-
-
Kawamoto, A.1
Kodama, E.2
Sarafianos, S.3
Sakagami, Y.4
Kohgo, S.5
-
23
-
-
33746109349
-
2′-Deoxy-4′-C-ethynyl-2-fluoroadenosine, a nucleoside reverse transcriptase inhibitor, is highly potent against all human immunodeficiency viruses type 1 and has low toxicity
-
Ohrui H, (2006) 2′-Deoxy-4′-C-ethynyl-2-fluoroadenosine, a nucleoside reverse transcriptase inhibitor, is highly potent against all human immunodeficiency viruses type 1 and has low toxicity. Chem Record 6: 133-143.
-
(2006)
Chem Record
, vol.6
, pp. 133-143
-
-
Ohrui, H.1
-
24
-
-
72149100464
-
Mechanism of inhibition of HIV-1 reverse transcriptase by 4′-ethynyl-2-fluoro-2′-deoxyadenosine triphosphate, a translocation-defective reverse transcriptase inhibitor
-
Michailidis E, Marchand B, Kodama E, Singh K, Matsuoka M, et al. (2009) Mechanism of inhibition of HIV-1 reverse transcriptase by 4′-ethynyl-2-fluoro-2′-deoxyadenosine triphosphate, a translocation-defective reverse transcriptase inhibitor. J Biol Chem 284: 35681-35691.
-
(2009)
J Biol Chem
, vol.284
, pp. 35681-35691
-
-
Michailidis, E.1
Marchand, B.2
Kodama, E.3
Singh, K.4
Matsuoka, M.5
-
25
-
-
34547118863
-
The nucleoside analogs 4′ C-methyl thymidine and 4′ C-ethyl thymidine block DNA synthesis by wild-type HIV-1 RT and excision proficient NRTI resistant RT variants
-
Boyer P, Julias JG, Ambrose Z, Siddiqui M, Marquez V, et al. (2007) The nucleoside analogs 4′ C-methyl thymidine and 4′ C-ethyl thymidine block DNA synthesis by wild-type HIV-1 RT and excision proficient NRTI resistant RT variants. J Mol Biol 371: 873-882.
-
(2007)
J Mol Biol
, vol.371
, pp. 873-882
-
-
Boyer, P.1
Julias, J.G.2
Ambrose, Z.3
Siddiqui, M.4
Marquez, V.5
-
26
-
-
79955527089
-
4′-C-Methyl-2′-deoxyadenosine and 4′-C-ethyl-2′-deoxyadenosine inhibit HIV-1 replication
-
Vu BC, Boyer PL, Siddiqui MA, Marquez VE, Hughes SH, (2011) 4′-C-Methyl-2′-deoxyadenosine and 4′-C-ethyl-2′-deoxyadenosine inhibit HIV-1 replication. Antimicrob Agents Chemother 55: 2379-2389.
-
(2011)
Antimicrob Agents Chemother
, vol.55
, pp. 2379-2389
-
-
Vu, B.C.1
Boyer, P.L.2
Siddiqui, M.A.3
Marquez, V.E.4
Hughes, S.H.5
-
27
-
-
57749104132
-
Delayed chain termination protects the anti-hepatitis B virus drug Entecavir from excision by HIV-1 reverse transcriptase
-
Tchesnokov EP, Obikhod A, Schinazi RF, Gotte M, (2008) Delayed chain termination protects the anti-hepatitis B virus drug Entecavir from excision by HIV-1 reverse transcriptase. J Biol Chem 283: 34218-34228.
-
(2008)
J Biol Chem
, vol.283
, pp. 34218-34228
-
-
Tchesnokov, E.P.1
Obikhod, A.2
Schinazi, R.F.3
Gotte, M.4
-
28
-
-
47649130103
-
A case of HIV co-infected with hepatitis B virus precore/core deletion mutant treated by entecavir
-
Fukushima K, Ueno Y, Inoue J, Wakui Y, Obara N, et al. (2008) A case of HIV co-infected with hepatitis B virus precore/core deletion mutant treated by entecavir. Hepatol Res 38: 842-846.
-
(2008)
Hepatol Res
, vol.38
, pp. 842-846
-
-
Fukushima, K.1
Ueno, Y.2
Inoue, J.3
Wakui, Y.4
Obara, N.5
-
29
-
-
34250722018
-
The HBV drug entecavir - effects on HIV-1 replication and resistance
-
McMahon MA, Jilek BL, Brennan TP, Shen L, Zhou Y, et al. (2007) The HBV drug entecavir- effects on HIV-1 replication and resistance. N Engl J Med 356: 2614-2621.
-
(2007)
N Engl J Med
, vol.356
, pp. 2614-2621
-
-
McMahon, M.A.1
Jilek, B.L.2
Brennan, T.P.3
Shen, L.4
Zhou, Y.5
-
30
-
-
0031039885
-
A minor groove binding track in reverse transcriptase
-
Bebenek K, Beard WA, Darden TA, Li L, Prasad R, et al. (1997) A minor groove binding track in reverse transcriptase. Nat Struct Biol 4: 194-197.
-
(1997)
Nat Struct Biol
, vol.4
, pp. 194-197
-
-
Bebenek, K.1
Beard, W.A.2
Darden, T.A.3
Li, L.4
Prasad, R.5
-
31
-
-
33744821955
-
Cross-coupling reactions of unprotected halopurine bases, nucleosides, nucleotides and nucleoside triphosphates with 4-boronophenylalanine in water. Synthesis of (purin-8-yl)- and (purin-6-yl)phenylalanines
-
Capek P, Pohl R, Hocek M, (2006) Cross-coupling reactions of unprotected halopurine bases, nucleosides, nucleotides and nucleoside triphosphates with 4-boronophenylalanine in water. Synthesis of (purin-8-yl)- and (purin-6-yl)phenylalanines. Org Biomol Chem 4: 2278-2284.
-
(2006)
Org Biomol Chem
, vol.4
, pp. 2278-2284
-
-
Capek, P.1
Pohl, R.2
Hocek, M.3
-
32
-
-
0014129273
-
Purine nucleosides. XV. Synthesis of 8-amino- and 8-substituted aminopurine nucleosides
-
Long RA, Robins RK, Townsend LB, (1967) Purine nucleosides. XV. Synthesis of 8-amino- and 8-substituted aminopurine nucleosides. J Org Chem 32: 2751-2756.
-
(1967)
J Org Chem
, vol.32
, pp. 2751-2756
-
-
Long, R.A.1
Robins, R.K.2
Townsend, L.B.3
-
33
-
-
0028339344
-
Synthesis and antiviral activities of 8-alkynyl-, 8-alkenyl-, and 8-alkyl-2′-deoxyadenosine analogs
-
Sagi G, Otvos L, Ikeda S, Andrei G, Snoeck R, et al. (1994) Synthesis and antiviral activities of 8-alkynyl-, 8-alkenyl-, and 8-alkyl-2′-deoxyadenosine analogs. J Med Chem 37: 1307-1311.
-
(1994)
J Med Chem
, vol.37
, pp. 1307-1311
-
-
Sagi, G.1
Otvos, L.2
Ikeda, S.3
Andrei, G.4
Snoeck, R.5
-
34
-
-
0032573488
-
Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance
-
Huang H, Chopra R, Verdine GL, Harrison SC, (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
-
35
-
-
14244253595
-
8-Vinyl-deoxyadenosine, an alternative fluorescent nucleoside analog to 2′-deoxyribosyl-2-aminopurine with improved properties
-
Ben Gaied N, Glasser N, Ramalanjaona N, Beltz H, Wolff P, et al. (2005) 8-Vinyl-deoxyadenosine, an alternative fluorescent nucleoside analog to 2′-deoxyribosyl-2-aminopurine with improved properties. Nucleic Acids Res 33: 1031-1039.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 1031-1039
-
-
Ben Gaied, N.1
Glasser, N.2
Ramalanjaona, N.3
Beltz, H.4
Wolff, P.5
-
36
-
-
69949102329
-
The nucleoside analogue D-carba T blocks HIV-1 reverse transcription
-
Boyer PL, Vu BC, Ambrose Z, Julias JG, Warnecke S, et al. (2009) The nucleoside analogue D-carba T blocks HIV-1 reverse transcription. J Med Chem 52: 5356-5364.
-
(2009)
J Med Chem
, vol.52
, pp. 5356-5364
-
-
Boyer, P.L.1
Vu, B.C.2
Ambrose, Z.3
Julias, J.G.4
Warnecke, S.5
-
37
-
-
77649196705
-
5-Modified-2′-dU and 2′-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity
-
El Safadi Y, Paillart J-C, Laumond G, Aubertin A-M, Burger A, et al. (2010) 5-Modified-2′-dU and 2′-dC as mutagenic anti HIV-1 proliferation agents: synthesis and activity. J Med Chem 53: 1534-1545.
-
(2010)
J Med Chem
, vol.53
, pp. 1534-1545
-
-
El Safadi, Y.1
Paillart, J.-C.2
Laumond, G.3
Aubertin, A.-M.4
Burger, A.5
-
38
-
-
0027431083
-
Antiviral activity of C-alkylated purine nucleosides obtained by cross-coupling with tetraalkyltin reagents
-
Van Aerschot AA, Mamos P, Weyns NJ, Ikeda S, De Clercq E, et al. (1993) Antiviral activity of C-alkylated purine nucleosides obtained by cross-coupling with tetraalkyltin reagents. J Med Chem 36: 2938-2942.
-
(1993)
J Med Chem
, vol.36
, pp. 2938-2942
-
-
Van Aerschot, A.A.1
Mamos, P.2
Weyns, N.J.3
Ikeda, S.4
De Clercq, E.5
-
39
-
-
0028333978
-
Dimerization of human immunodeficiency virus type 1 RNA involves sequences located upstream of the splice donor site
-
Marquet R, Paillart J-C, Skripkin E, Ehresmann C, Ehresmann B, (1994) Dimerization of human immunodeficiency virus type 1 RNA involves sequences located upstream of the splice donor site. Nucleic Acids Res 22: 145-151.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 145-151
-
-
Marquet, R.1
Paillart, J.-C.2
Skripkin, E.3
Ehresmann, C.4
Ehresmann, B.5
-
40
-
-
0028016271
-
Mutagenesis of the conserved aspartic acid 443, glutamic acid 478, asparagine 494, and aspartic acid 498 residues in the ribonuclease H domain of p66/p51 human immunodeficiency virus type I reverse transcriptase. Expression and biochemical analysis
-
Mizrahi V, Brooksbank RL, Nkabinde NC, (1994) Mutagenesis of the conserved aspartic acid 443, glutamic acid 478, asparagine 494, and aspartic acid 498 residues in the ribonuclease H domain of p66/p51 human immunodeficiency virus type I reverse transcriptase. Expression and biochemical analysis. J Biol Chem 269: 19245-19249.
-
(1994)
J Biol Chem
, vol.269
, pp. 19245-19249
-
-
Mizrahi, V.1
Brooksbank, R.L.2
Nkabinde, N.C.3
-
41
-
-
0036229823
-
Structural basis for inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant
-
Lindberg J, Sigurdsson S, Lowgren S, Andersson HO, Sahlberg C, et al. (2002) Structural basis for inhibitory efficacy of efavirenz (DMP-266), MSC194 and PNU142721 towards the HIV-1 RT K103N mutant. Eur J Biochem 269: 1670-1677.
-
(2002)
Eur J Biochem
, vol.269
, pp. 1670-1677
-
-
Lindberg, J.1
Sigurdsson, S.2
Lowgren, S.3
Andersson, H.O.4
Sahlberg, C.5
|