-
1
-
-
66249088004
-
Catalytically-active complex of HIV-1 integrase with a viral DNA substrate binds anti-integrase drugs
-
Alian A., Griner S.L., Chiang V., Tsiang M., Jones G., Birkus G., Geleziunas R., Leavitt A.D., and Stroud R.M. Catalytically-active complex of HIV-1 integrase with a viral DNA substrate binds anti-integrase drugs. Proceedings of the National Academy of Sciences United States of America 106 (2009) 8192-8197
-
(2009)
Proceedings of the National Academy of Sciences United States of America
, vol.106
, pp. 8192-8197
-
-
Alian, A.1
Griner, S.L.2
Chiang, V.3
Tsiang, M.4
Jones, G.5
Birkus, G.6
Geleziunas, R.7
Leavitt, A.D.8
Stroud, R.M.9
-
2
-
-
39049101609
-
Tenofovir disoproxil fumarate, emtricitabine, and efavirenz compared with zidovudine/lamivudine and efavirenz in treatment-naive patients: 144-week analysis
-
Arribas J.R., Pozniak A.L., Gallant J.E., Dejesus E., Gazzard B., Campo R.E., Chen S.S., McColl D., Holmes C.B., Enejosa J., Toole J.J., and Cheng A.K. Tenofovir disoproxil fumarate, emtricitabine, and efavirenz compared with zidovudine/lamivudine and efavirenz in treatment-naive patients: 144-week analysis. Journal of Acquired Immune Deficiency Syndromes (JAIDS) 47 (2008) 74-78
-
(2008)
Journal of Acquired Immune Deficiency Syndromes (JAIDS)
, vol.47
, pp. 74-78
-
-
Arribas, J.R.1
Pozniak, A.L.2
Gallant, J.E.3
Dejesus, E.4
Gazzard, B.5
Campo, R.E.6
Chen, S.S.7
McColl, D.8
Holmes, C.B.9
Enejosa, J.10
Toole, J.J.11
Cheng, A.K.12
-
3
-
-
34548220391
-
Comparative efficacy of nucleoside/nucleotide reverse transcriptase inhibitors in combination with efavirenz: results of a systematic overview
-
Bartlett J.A., Chen S.S., and Quinn J.B. Comparative efficacy of nucleoside/nucleotide reverse transcriptase inhibitors in combination with efavirenz: results of a systematic overview. HIV Clinical Trials 8 (2007) 221-226
-
(2007)
HIV Clinical Trials
, vol.8
, pp. 221-226
-
-
Bartlett, J.A.1
Chen, S.S.2
Quinn, J.B.3
-
5
-
-
0029990185
-
Alternate strand DNA triple helix-mediated inhibition of HIV-1 U5 long terminal repeat integration in vitro
-
Bouziane M., Cherny D.I., Mouscadet J.F., and Auclair C. Alternate strand DNA triple helix-mediated inhibition of HIV-1 U5 long terminal repeat integration in vitro. Journal of Biological Chemistry 271 (1996) 10359-10364
-
(1996)
Journal of Biological Chemistry
, vol.271
, pp. 10359-10364
-
-
Bouziane, M.1
Cherny, D.I.2
Mouscadet, J.F.3
Auclair, C.4
-
6
-
-
0027381647
-
Human immunodeficiency virus type 1 2-LTR circles reside in a nucleoprotein complex which is different from the preintegration complex
-
Bukrinsky M., Sharova N., and Stevenson M. Human immunodeficiency virus type 1 2-LTR circles reside in a nucleoprotein complex which is different from the preintegration complex. Journal of Virology 67 (1993) 6863-6865
-
(1993)
Journal of Virology
, vol.67
, pp. 6863-6865
-
-
Bukrinsky, M.1
Sharova, N.2
Stevenson, M.3
-
7
-
-
0026655897
-
Structural implications of spectroscopic characterization of a putative zinc finger peptide from HIV-1 integrase
-
Burke C.J., Sanyal G., Bruner M.W., Ryan J.A., LaFemina R.L., Robbins H.L., Zeft A.S., Middaugh C.R., and Cordingley M.G. Structural implications of spectroscopic characterization of a putative zinc finger peptide from HIV-1 integrase. Journal of Biological Chemistry 267 (1992) 9639-9644
-
(1992)
Journal of Biological Chemistry
, vol.267
, pp. 9639-9644
-
-
Burke, C.J.1
Sanyal, G.2
Bruner, M.W.3
Ryan, J.A.4
LaFemina, R.L.5
Robbins, H.L.6
Zeft, A.S.7
Middaugh, C.R.8
Cordingley, M.G.9
-
8
-
-
0032616706
-
Host proteins in retroviral cDNA integration
-
Bushman F.D. Host proteins in retroviral cDNA integration. Advances in Virus Research 52 (1999) 301-317
-
(1999)
Advances in Virus Research
, vol.52
, pp. 301-317
-
-
Bushman, F.D.1
-
9
-
-
0027456715
-
Domains of the integrase protein of human immunodeficiency virus type 1 responsible for polynucleotidyl transfer and zinc binding
-
Bushman F.D., Engelman A., Palmer I., Wingfield P., and Craigie R. Domains of the integrase protein of human immunodeficiency virus type 1 responsible for polynucleotidyl transfer and zinc binding. Proceedings of the National Academy of Sciences United States of America 90 (1993) 3428-3432
-
(1993)
Proceedings of the National Academy of Sciences United States of America
, vol.90
, pp. 3428-3432
-
-
Bushman, F.D.1
Engelman, A.2
Palmer, I.3
Wingfield, P.4
Craigie, R.5
-
10
-
-
0025133394
-
Retroviral DNA integration directed by HIV integration protein in vitro (Abstract)
-
Bushman F.D., Fujiwara T., and Craigie R. Retroviral DNA integration directed by HIV integration protein in vitro (Abstract). Science 249 (1990) 1555-1558
-
(1990)
Science
, vol.249
, pp. 1555-1558
-
-
Bushman, F.D.1
Fujiwara, T.2
Craigie, R.3
-
11
-
-
0030986376
-
Solution structure of the N-terminal zinc binding domain of HIV-1 integrase (Abstract)
-
Cai, M., Zheng, R., Cafferey, M., Craigie, R., Clore, G.M., A.M., G., 1997. Solution structure of the N-terminal zinc binding domain of HIV-1 integrase (Abstract). Nature Structural Biology 4, 567-577.
-
(1997)
Nature Structural Biology
, vol.4
, pp. 567-577
-
-
Cai, M.1
Zheng, R.2
Cafferey, M.3
Craigie, R.4
Clore, G.M.A.M.G.5
-
12
-
-
55049102952
-
Virological response and resistance in multi-experienced patients treated with raltegravir (poster 18)
-
Sitges, Spain
-
Ceccherini-Silberstein F., Armenia D., D'Arrigo R., Micheli V., Fabeni L., Meraviglia P., Capetti A., Zaccarelli M., Trotta M.P., Narciso P., Antinori A., and Perno C.F. Virological response and resistance in multi-experienced patients treated with raltegravir (poster 18). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Ceccherini-Silberstein, F.1
Armenia, D.2
D'Arrigo, R.3
Micheli, V.4
Fabeni, L.5
Meraviglia, P.6
Capetti, A.7
Zaccarelli, M.8
Trotta, M.P.9
Narciso, P.10
Antinori, A.11
Perno, C.F.12
-
13
-
-
73549088038
-
Nucleoside and nucleotide HIV reverse transcriptase inhibitors: 25 year after zidovudine
-
Cihlar T., and Ray A. Nucleoside and nucleotide HIV reverse transcriptase inhibitors: 25 year after zidovudine. Antiviral Research 85 (2010)
-
(2010)
Antiviral Research
, vol.85
-
-
Cihlar, T.1
Ray, A.2
-
14
-
-
0024278041
-
Sequence and spacing requirements of a retrovirus integration site (Abstract)
-
Colicelli J., and Goff S.P. Sequence and spacing requirements of a retrovirus integration site (Abstract). Journal of Molecular Biology 199 (1988) 47-59
-
(1988)
Journal of Molecular Biology
, vol.199
, pp. 47-59
-
-
Colicelli, J.1
Goff, S.P.2
-
15
-
-
47949114939
-
Subgroup and resistance analyses of raltegravir for resistance HIV-1 infection
-
Cooper D.A., Steigbigel R.T., Gatell J., Rockstroh J., Katlama C., Yeni P., Lazzarin A., Clotet B., Kumar P., Eron J.E., Schechter M., Markowitz M., Loutfy M.R., Lennox J.L., Zhao J., Chen J., Ryan D.M., Rhodes R.R., Killar J.A., Gilde L.R., Strohmaier K.M., Meibohm A.R., Miller M.D., Hazuda D.J., Nessly M.L., DiNubile M.J., Isaacs R.D., Teppler H., and Nguyen B. Subgroup and resistance analyses of raltegravir for resistance HIV-1 infection. New England Journal of Medicine 359 (2008) 355-365
-
(2008)
New England Journal of Medicine
, vol.359
, pp. 355-365
-
-
Cooper, D.A.1
Steigbigel, R.T.2
Gatell, J.3
Rockstroh, J.4
Katlama, C.5
Yeni, P.6
Lazzarin, A.7
Clotet, B.8
Kumar, P.9
Eron, J.E.10
Schechter, M.11
Markowitz, M.12
Loutfy, M.R.13
Lennox, J.L.14
Zhao, J.15
Chen, J.16
Ryan, D.M.17
Rhodes, R.R.18
Killar, J.A.19
Gilde, L.R.20
Strohmaier, K.M.21
Meibohm, A.R.22
Miller, M.D.23
Hazuda, D.J.24
Nessly, M.L.25
DiNubile, M.J.26
Isaacs, R.D.27
Teppler, H.28
Nguyen, B.29
more..
-
16
-
-
0033821651
-
Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets
-
Chen I.J., Neamati N., Nicklaus M.C., Orr A., Anderson L., Barchi Jr. J.J., Kelley J.A., Pommier Y., and MacKerell Jr. A.D. Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets. Bioorganic and Medicinal Chemistry 8 (2000) 2385-2398
-
(2000)
Bioorganic and Medicinal Chemistry
, vol.8
, pp. 2385-2398
-
-
Chen, I.J.1
Neamati, N.2
Nicklaus, M.C.3
Orr, A.4
Anderson, L.5
Barchi Jr., J.J.6
Kelley, J.A.7
Pommier, Y.8
MacKerell Jr., A.D.9
-
17
-
-
44949212848
-
Modeling, analysis, and validation of a novel HIV integrase structure provide insights into the binding modes of potent integrase inhibitors
-
Chen X., Tsiang M., Yu F., Hung M., Jones G.S., Zeynalzadegan A., Qi X., Jin H., Kim C.U., Swaminathan S., and Chen J.M. Modeling, analysis, and validation of a novel HIV integrase structure provide insights into the binding modes of potent integrase inhibitors. Journal of Molecular Biology 380 (2008) 504-519
-
(2008)
Journal of Molecular Biology
, vol.380
, pp. 504-519
-
-
Chen, X.1
Tsiang, M.2
Yu, F.3
Hung, M.4
Jones, G.S.5
Zeynalzadegan, A.6
Qi, X.7
Jin, H.8
Kim, C.U.9
Swaminathan, S.10
Chen, J.M.11
-
18
-
-
55049134970
-
Mutational patterns in the HIV-1 integrase related to virological failures on raltegravir-containing regimens (poster 12)
-
Sitges, Spain
-
Da Silva D., Pellegrin I., Anies G., Breilh D., Wittkop L., Morlat P., Dupon M., Neau D., Pellegrin J.L., Fleury H., and Masquelier B. Mutational patterns in the HIV-1 integrase related to virological failures on raltegravir-containing regimens (poster 12). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Da Silva, D.1
Pellegrin, I.2
Anies, G.3
Breilh, D.4
Wittkop, L.5
Morlat, P.6
Dupon, M.7
Neau, D.8
Pellegrin, J.L.9
Fleury, H.10
Masquelier, B.11
-
19
-
-
0034616993
-
Three-dimensional structure of the Tn5 synaptic complex transposition intermediate
-
Davies D.R., Goryshin I.Y., Reznikoff W.S., and Rayment I. Three-dimensional structure of the Tn5 synaptic complex transposition intermediate. Science 289 (2000) 77-85
-
(2000)
Science
, vol.289
, pp. 77-85
-
-
Davies, D.R.1
Goryshin, I.Y.2
Reznikoff, W.S.3
Rayment, I.4
-
20
-
-
73549115378
-
Non-nucleoside reverse transcriptase inhibitors (NNRTIs), their discovery, development, and use in the treatment of HIV-1 infection: a review of the last 20 years (1989-2009)
-
XX-XX
-
de Bethune M.P. Non-nucleoside reverse transcriptase inhibitors (NNRTIs), their discovery, development, and use in the treatment of HIV-1 infection: a review of the last 20 years (1989-2009). Antiviral Research 85 (2010) XX-XX
-
(2010)
Antiviral Research
, vol.85
-
-
de Bethune, M.P.1
-
21
-
-
33748113778
-
The HIV integrase inhibitor GS-9137 (JTK-303) exhibits potent antiviral activity in treatment-naïve and experienced patients (oral number 36)
-
DeJesus E., Berger D., Markowitz M., Cohen C., Hawkins T., Ruane P., Elion R., Farthing C., Cheng A., and Kearney B. The HIV integrase inhibitor GS-9137 (JTK-303) exhibits potent antiviral activity in treatment-naïve and experienced patients (oral number 36). Journal of Acquired Immune Deficiency Syndromes 43 (2006) 1-5
-
(2006)
Journal of Acquired Immune Deficiency Syndromes
, vol.43
, pp. 1-5
-
-
DeJesus, E.1
Berger, D.2
Markowitz, M.3
Cohen, C.4
Hawkins, T.5
Ruane, P.6
Elion, R.7
Farthing, C.8
Cheng, A.9
Kearney, B.10
-
22
-
-
33748113778
-
Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients
-
DeJesus E., Berger D., Markowitz M., Cohen C., Hawkins T., Ruane P., Elion R., Farthing C., Zhong L., Cheng A.K., McColl D., and Kearney B.P. Antiviral activity, pharmacokinetics, and dose response of the HIV-1 integrase inhibitor GS-9137 (JTK-303) in treatment-naive and treatment-experienced patients. Journal of Acquired Immune Deficiency Syndromes (JAIDS) 43 (2006) 1-5
-
(2006)
Journal of Acquired Immune Deficiency Syndromes (JAIDS)
, vol.43
, pp. 1-5
-
-
DeJesus, E.1
Berger, D.2
Markowitz, M.3
Cohen, C.4
Hawkins, T.5
Ruane, P.6
Elion, R.7
Farthing, C.8
Zhong, L.9
Cheng, A.K.10
McColl, D.11
Kearney, B.P.12
-
23
-
-
0026740842
-
Identification of amino acid residues critical for endonuclease and integration activities of HIV-1 IN protein in Vitro (Abstract)
-
Drelich M., Wilhelm R., and Mous J. Identification of amino acid residues critical for endonuclease and integration activities of HIV-1 IN protein in Vitro (Abstract). Virology 188 (1992) 459-468
-
(1992)
Virology
, vol.188
, pp. 459-468
-
-
Drelich, M.1
Wilhelm, R.2
Mous, J.3
-
24
-
-
0028584269
-
Crystal structure of the catalytic domain of HIV-1 integrase: similarity to other polynucleotidyl transferases (Abstract)
-
Dyda F., Hickman A.B., Jenkins T.M., Engelman A., Craigie R., and Davies D.R. Crystal structure of the catalytic domain of HIV-1 integrase: similarity to other polynucleotidyl transferases (Abstract). Science 266 (1994) 1981-1986
-
(1994)
Science
, vol.266
, pp. 1981-1986
-
-
Dyda, F.1
Hickman, A.B.2
Jenkins, T.M.3
Engelman, A.4
Craigie, R.5
Davies, D.R.6
-
25
-
-
0028888455
-
An essential interaction between distinct domains of HIV-1 integrase mediates assembly of the active multimer
-
Ellison V., Gerton J., Vincent K.A., and Brown P.O. An essential interaction between distinct domains of HIV-1 integrase mediates assembly of the active multimer. Journal of Biological Chemistry 270 (1995) 3320-3326
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 3320-3326
-
-
Ellison, V.1
Gerton, J.2
Vincent, K.A.3
Brown, P.O.4
-
26
-
-
0027179694
-
Identification of discrete functional domains of HIV-1 integrase and their organization within an active multimeric complex
-
Engelman A., Bushman F.D., and Craigie R. Identification of discrete functional domains of HIV-1 integrase and their organization within an active multimeric complex. EMBO Journal 12 (1993) 3269-3275
-
(1993)
EMBO Journal
, vol.12
, pp. 3269-3275
-
-
Engelman, A.1
Bushman, F.D.2
Craigie, R.3
-
27
-
-
0026649557
-
Identification of conserved amino acid residues critical for human immunodeficiency virus type 1 integrase function in vitro
-
Engelman A., and Craigie R. Identification of conserved amino acid residues critical for human immunodeficiency virus type 1 integrase function in vitro. Journal of Virology 66 (1992) 6361-6369
-
(1992)
Journal of Virology
, vol.66
, pp. 6361-6369
-
-
Engelman, A.1
Craigie, R.2
-
28
-
-
68949186494
-
Switching from stable lopinavir/ritonavir-based to raltegravir-based combination ART resulted in a superior lipid profile at week 12 but did not demonstrate non-inferior virologic efficacy at week 24 (abstract 70aLB)
-
Montréal, Canada
-
Eron J., Andrade J., Zajdenverg R., Workman C., Cooper D., Young B., Xu X., Nguyen B.Y., Leavitt R., and Sklar P. Switching from stable lopinavir/ritonavir-based to raltegravir-based combination ART resulted in a superior lipid profile at week 12 but did not demonstrate non-inferior virologic efficacy at week 24 (abstract 70aLB). 16th Conference on Retroviruses and Opportunistic Infections (CROI). Montréal, Canada (2009)
-
(2009)
16th Conference on Retroviruses and Opportunistic Infections (CROI)
-
-
Eron, J.1
Andrade, J.2
Zajdenverg, R.3
Workman, C.4
Cooper, D.5
Young, B.6
Xu, X.7
Nguyen, B.Y.8
Leavitt, R.9
Sklar, P.10
-
29
-
-
12944270496
-
HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase
-
Espeseth A.S., Felock P., Wolfe A., Witmer M., Grobler J., Anthony N., Egbertson M., Melamed J.Y., Young S., Hamill T., Cole J.L., and Hazuda D.J. HIV-1 integrase inhibitors that compete with the target DNA substrate define a unique strand transfer conformation for integrase. Proceeding of the National Academy of Sciences United States of America 97 (2000) 11244-11249
-
(2000)
Proceeding of the National Academy of Sciences United States of America
, vol.97
, pp. 11244-11249
-
-
Espeseth, A.S.1
Felock, P.2
Wolfe, A.3
Witmer, M.4
Grobler, J.5
Anthony, N.6
Egbertson, M.7
Melamed, J.Y.8
Young, S.9
Hamill, T.10
Cole, J.L.11
Hazuda, D.J.12
-
30
-
-
0031004162
-
HIV-1 cDNA integration: requirement of HMG I(Y) protein for function of preintegration complexes in vitro
-
Farnet C.M., and Bushman F.D. HIV-1 cDNA integration: requirement of HMG I(Y) protein for function of preintegration complexes in vitro. Cell 88 (1997) 483-492
-
(1997)
Cell
, vol.88
, pp. 483-492
-
-
Farnet, C.M.1
Bushman, F.D.2
-
32
-
-
7744240084
-
Multiple mutations in human immunodeficiency virus-1 integrase confer resistance to the clinical trial drug S-1360
-
Fikkert V., Hombrouck A., Van Remoortel B., De Maeyer M., Pannecouque C., De Clercq E., Debyser Z., and Witvrouw M. Multiple mutations in human immunodeficiency virus-1 integrase confer resistance to the clinical trial drug S-1360. AIDS 18 (2004) 2019-2028
-
(2004)
AIDS
, vol.18
, pp. 2019-2028
-
-
Fikkert, V.1
Hombrouck, A.2
Van Remoortel, B.3
De Maeyer, M.4
Pannecouque, C.5
De Clercq, E.6
Debyser, Z.7
Witvrouw, M.8
-
33
-
-
10744226580
-
Development of resistance against diketo derivatives of human immunodeficiency virus type 1 by progressive accumulation of integrase mutations
-
Fikkert V., Van Maele B., Vercammen J., Hantson A., Van Remoortel B., Michiels M., Gurnari C., Pannecouque C., De Maeyer M., Engelborghs Y., De Clercq E., Debyser Z., and Witvrouw M. Development of resistance against diketo derivatives of human immunodeficiency virus type 1 by progressive accumulation of integrase mutations. Journal of Virology 77 (2003) 11459-11470
-
(2003)
Journal of Virology
, vol.77
, pp. 11459-11470
-
-
Fikkert, V.1
Van Maele, B.2
Vercammen, J.3
Hantson, A.4
Van Remoortel, B.5
Michiels, M.6
Gurnari, C.7
Pannecouque, C.8
De Maeyer, M.9
Engelborghs, Y.10
De Clercq, E.11
Debyser, Z.12
Witvrouw, M.13
-
34
-
-
52749088638
-
Loss of raltegravir susceptibility in treated patients is conferred by multiple non-overlapping genetic pathways (poster 7)
-
Sitges, Spain
-
Fransen S., Gupta S., Danovich R., Hazuda D., Miller M., Witmer M., Petropoulos C.J., Parkin N.T., and Huang W. Loss of raltegravir susceptibility in treated patients is conferred by multiple non-overlapping genetic pathways (poster 7). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Fransen, S.1
Gupta, S.2
Danovich, R.3
Hazuda, D.4
Miller, M.5
Witmer, M.6
Petropoulos, C.J.7
Parkin, N.T.8
Huang, W.9
-
35
-
-
0037227942
-
Cofactors for human immunodeficiency virus type 1 cDNA integration in vitro
-
Gao K., Gorelick R.J., Johnson D.G., and Bushman F. Cofactors for human immunodeficiency virus type 1 cDNA integration in vitro. Journal of Virology 77 (2003) 1598-1603
-
(2003)
Journal of Virology
, vol.77
, pp. 1598-1603
-
-
Gao, K.1
Gorelick, R.J.2
Johnson, D.G.3
Bushman, F.4
-
36
-
-
40549145842
-
The naphthyridinone GSK-364735 is a novel, potent human immunodeficiency virus type 1 integrase inhibitor and antiretroviral
-
Garvey E.P., Johns B.A., Gartland M.J., Foster S.A., Miller W.H., Ferris R.G., Hazen R.J., Underwood M.R., Boros E.E., Thompson J.B., Weatherhead J.G., Koble C.S., Allen S.H., Schaller L.T., Sherrill R.G., Yoshinaga T., Kobayashi M., Wakasa-Morimoto C., Miki S., Nakahara K., Noshi T., Sato A., and Fujiwara T. The naphthyridinone GSK-364735 is a novel, potent human immunodeficiency virus type 1 integrase inhibitor and antiretroviral. Antimicrobial Agents and Chemotherapy 52 (2008) 901-908
-
(2008)
Antimicrobial Agents and Chemotherapy
, vol.52
, pp. 901-908
-
-
Garvey, E.P.1
Johns, B.A.2
Gartland, M.J.3
Foster, S.A.4
Miller, W.H.5
Ferris, R.G.6
Hazen, R.J.7
Underwood, M.R.8
Boros, E.E.9
Thompson, J.B.10
Weatherhead, J.G.11
Koble, C.S.12
Allen, S.H.13
Schaller, L.T.14
Sherrill, R.G.15
Yoshinaga, T.16
Kobayashi, M.17
Wakasa-Morimoto, C.18
Miki, S.19
Nakahara, K.20
Noshi, T.21
Sato, A.22
Fujiwara, T.23
more..
-
37
-
-
55049108574
-
Resistance mutations in HIV-1 integrase selected with raltegravir or elvitegravir confer reduced susceptibility to a diverse panel of integrase inhibitors (poster 9)
-
Sitges, Spain
-
Goethals O., Clayton R., Wagemans E., Van Ginderen M., Cummings M., Geluykens P., Dockx K., Smits V., Meersseman G., Jochmans D., Hallenberger S., and Hertogs K. Resistance mutations in HIV-1 integrase selected with raltegravir or elvitegravir confer reduced susceptibility to a diverse panel of integrase inhibitors (poster 9). XVII International HIV Drug Resistance Workshop (IHDRW). Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop (IHDRW)
-
-
Goethals, O.1
Clayton, R.2
Wagemans, E.3
Van Ginderen, M.4
Cummings, M.5
Geluykens, P.6
Dockx, K.7
Smits, V.8
Meersseman, G.9
Jochmans, D.10
Hallenberger, S.11
Hertogs, K.12
-
38
-
-
0027102597
-
Genetics of retroviral integration (Abstract)
-
Goff S.P. Genetics of retroviral integration (Abstract). Annual Review of Genetics 26 (1992) 527-544
-
(1992)
Annual Review of Genetics
, vol.26
, pp. 527-544
-
-
Goff, S.P.1
-
39
-
-
13044295993
-
Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: a platform for antiviral drug design
-
Goldgur Y., Craigie R., Cohen G.H., Fujiwara T., Yoshinaga T., Fujishita T., Sugimoto H., Endo T., Murai H., and Davies D.R. Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: a platform for antiviral drug design. Proceedings of National Academy of Sciences United States of America 96 (1999) 13040-13043
-
(1999)
Proceedings of National Academy of Sciences United States of America
, vol.96
, pp. 13040-13043
-
-
Goldgur, Y.1
Craigie, R.2
Cohen, G.H.3
Fujiwara, T.4
Yoshinaga, T.5
Fujishita, T.6
Sugimoto, H.7
Endo, T.8
Murai, H.9
Davies, D.R.10
-
40
-
-
52749097450
-
Integrase inhibitor resistance involves complex interactions among primary and secondary resistance mutations: a novel mutation L68V/I associates with E92Q and increases resistance (poster 13)
-
Stiges, Spain
-
Goodman D.D., Hluhanich R., Waters J.M., Margot N.A., Fransen S., Gupta S., Huang W., Parkin N., Borroto-Esoda K., Svarovskaia E.S., Miller M.D., and McColl D.J. Integrase inhibitor resistance involves complex interactions among primary and secondary resistance mutations: a novel mutation L68V/I associates with E92Q and increases resistance (poster 13). XVII International HIV Drug Resistance Workshop. Stiges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Goodman, D.D.1
Hluhanich, R.2
Waters, J.M.3
Margot, N.A.4
Fransen, S.5
Gupta, S.6
Huang, W.7
Parkin, N.8
Borroto-Esoda, K.9
Svarovskaia, E.S.10
Miller, M.D.11
McColl, D.J.12
-
41
-
-
52349108864
-
48 week efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus (abstract H-173)
-
Chicago, IL, USA
-
Grinsztejn B., Nguyen B., Katlama C., Gatell J., Lazzarain A., Vittecoq D., Gonzalex C., Chen J., and Isaacs R. 48 week efficacy and safety of MK-0518, a novel HIV-1 integrase inhibitor, in patients with triple-class resistant virus (abstract H-173). 47th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC). Chicago, IL, USA (2007)
-
(2007)
47th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC)
-
-
Grinsztejn, B.1
Nguyen, B.2
Katlama, C.3
Gatell, J.4
Lazzarain, A.5
Vittecoq, D.6
Gonzalex, C.7
Chen, J.8
Isaacs, R.9
-
42
-
-
0037076324
-
Diketo acid inhibitor mechanism and HIV-1 integrase: implications for metal binding in the active site of phosphotransferase enzymes
-
Grobler J.A., Stillmock K., Hu B., Witmer M., Felock P., Espeseth A.S., Wolfe A., Egbertson M., Bourgeois M., Melamed J., Wai J.S., Young S., Vacca J., and Hazuda D.J. Diketo acid inhibitor mechanism and HIV-1 integrase: implications for metal binding in the active site of phosphotransferase enzymes. Proceedings of the National Academy of Sciences United States of America 99 (2002) 6661-6666
-
(2002)
Proceedings of the National Academy of Sciences United States of America
, vol.99
, pp. 6661-6666
-
-
Grobler, J.A.1
Stillmock, K.2
Hu, B.3
Witmer, M.4
Felock, P.5
Espeseth, A.S.6
Wolfe, A.7
Egbertson, M.8
Bourgeois, M.9
Melamed, J.10
Wai, J.S.11
Young, S.12
Vacca, J.13
Hazuda, D.J.14
-
43
-
-
55049140537
-
Virologic and immunologic outcomes in a cohort of subjects failing integrase inhibitors (poster 2725)
-
Sitges, Spain
-
Hatano H., Lampiris H., Huang W., Hoh R., Gupta S., Fransen S., Martin J.N., Petropoulous C., and Deeks S.G. Virologic and immunologic outcomes in a cohort of subjects failing integrase inhibitors (poster 2725). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Hatano, H.1
Lampiris, H.2
Huang, W.3
Hoh, R.4
Gupta, S.5
Fransen, S.6
Martin, J.N.7
Petropoulous, C.8
Deeks, S.G.9
-
44
-
-
0032922813
-
Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites (Abstract)
-
Hazuda D., Blau C.U., Felock P., Hastings J., Pramanik B., Wolfe A., Bushman F., Famet C., Goetz M., Williams M., Silverman K., Lingham R., and Singh S. Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites (Abstract). Antiviral Chemistry and Chemotherapy 10 (1999) 63-70
-
(1999)
Antiviral Chemistry and Chemotherapy
, vol.10
, pp. 63-70
-
-
Hazuda, D.1
Blau, C.U.2
Felock, P.3
Hastings, J.4
Pramanik, B.5
Wolfe, A.6
Bushman, F.7
Famet, C.8
Goetz, M.9
Williams, M.10
Silverman, K.11
Lingham, R.12
Singh, S.13
-
45
-
-
3843108916
-
A naphthyridine carboxamide provides evidence for discordant resistance between mechanistically identical inhibitors of HIV-1 integrase
-
Hazuda D.J., Anthony N.J., Gomez R.P., Jolly S.M., Wai J.S., Zhuang L., Fisher T.E., Embrey M., Guare Jr. J.P., Egbertson M.S., Vacca J.P., Huff J.R., Felock P.J., Witmer M.V., Stillmock K.A., Danovich R., Grobler J., Miller M.D., Espeseth A.S., Jin L., Chen I.W., Lin J.H., Kassahun K., Ellis J.D., Wong B.K., Xu W., Pearson P.G., Schleif W.A., Cortese R., Emini E., Summa V., Holloway M.K., and Young S.D. A naphthyridine carboxamide provides evidence for discordant resistance between mechanistically identical inhibitors of HIV-1 integrase. Proceedings of the National Academy of Sciences United States of America 101 (2004) 11233-11238
-
(2004)
Proceedings of the National Academy of Sciences United States of America
, vol.101
, pp. 11233-11238
-
-
Hazuda, D.J.1
Anthony, N.J.2
Gomez, R.P.3
Jolly, S.M.4
Wai, J.S.5
Zhuang, L.6
Fisher, T.E.7
Embrey, M.8
Guare Jr., J.P.9
Egbertson, M.S.10
Vacca, J.P.11
Huff, J.R.12
Felock, P.J.13
Witmer, M.V.14
Stillmock, K.A.15
Danovich, R.16
Grobler, J.17
Miller, M.D.18
Espeseth, A.S.19
Jin, L.20
Chen, I.W.21
Lin, J.H.22
Kassahun, K.23
Ellis, J.D.24
Wong, B.K.25
Xu, W.26
Pearson, P.G.27
Schleif, W.A.28
Cortese, R.29
Emini, E.30
Summa, V.31
Holloway, M.K.32
Young, S.D.33
more..
-
46
-
-
0034723439
-
Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells
-
Hazuda D.J., Felock P., Witmer M., Wolfe A., Stillmock K., Grobler J.A., Espeseth A., Gabryelski L., Schleif W., Blau C., and Miller M.D. Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells. Science 287 (2000) 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
Espeseth, A.7
Gabryelski, L.8
Schleif, W.9
Blau, C.10
Miller, M.D.11
-
48
-
-
35648950291
-
Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase 2 study in patients with triple-class resistant HIV-1 infection (poster #8)
-
Bridgetown, Barbados
-
Hazuda D.J., Miller M.D., Nguyen B.Y., and Zhao J. Resistance to the HIV-integrase inhibitor raltegravir: analysis of protocol 005, a phase 2 study in patients with triple-class resistant HIV-1 infection (poster #8). 16th International HIV Drug Resistance Workshop. Bridgetown, Barbados (2007)
-
(2007)
16th International HIV Drug Resistance Workshop
-
-
Hazuda, D.J.1
Miller, M.D.2
Nguyen, B.Y.3
Zhao, J.4
-
49
-
-
44449155764
-
Mutations in HIV-1 integrase confer resistance to the naphthyridine L-870,810 and cross resistance to the clinical trial drug GS-9137
-
Hombrouck A., Voet A., Van Remoortel B., Desadeleer C., De Maeyer M., Debyser Z., and Witvrouw M. Mutations in HIV-1 integrase confer resistance to the naphthyridine L-870,810 and cross resistance to the clinical trial drug GS-9137. Antimicrobial Agents and Chemotherapy (2008)
-
(2008)
Antimicrobial Agents and Chemotherapy
-
-
Hombrouck, A.1
Voet, A.2
Van Remoortel, B.3
Desadeleer, C.4
De Maeyer, M.5
Debyser, Z.6
Witvrouw, M.7
-
50
-
-
33644861936
-
Integration requires a specific interaction of the donor DNA terminal 5′-cytosine with glutamine 148 of the HIV-1 integrase flexible loop
-
Johnson A.A., Santos W., Pais G.C., Marchand C., Amin R., Burke Jr. T.R., Verdine G., and Pommier Y. Integration requires a specific interaction of the donor DNA terminal 5′-cytosine with glutamine 148 of the HIV-1 integrase flexible loop. Journal of Biological Chemistry 281 (2006) 461-467
-
(2006)
Journal of Biological Chemistry
, vol.281
, pp. 461-467
-
-
Johnson, A.A.1
Santos, W.2
Pais, G.C.3
Marchand, C.4
Amin, R.5
Burke Jr., T.R.6
Verdine, G.7
Pommier, Y.8
-
51
-
-
34248203565
-
In vitro resistance profile of HIV-1 mutants selected by the HIV-1 integrase inhibitor GS-9137 (JTK-303) (slides-poster #627)
-
Los Angeles, CA, USA
-
Jones G., Ledford R.M., Yu F., Chen X., Miller M.D., Tsiang M., and McColl D.J. In vitro resistance profile of HIV-1 mutants selected by the HIV-1 integrase inhibitor GS-9137 (JTK-303) (slides-poster #627). 14th Conference on Retroviruses and Opportunistic Infections. Los Angeles, CA, USA (2007)
-
(2007)
14th Conference on Retroviruses and Opportunistic Infections
-
-
Jones, G.1
Ledford, R.M.2
Yu, F.3
Chen, X.4
Miller, M.D.5
Tsiang, M.6
McColl, D.J.7
-
52
-
-
62949153971
-
Preclinical evaluation of GS-9160, a novel inhibitor of human immunodeficiency virus type 1 integrase
-
Jones G.S., Yu F., Zeynalzadegan A., Hesselgesser J., Chen X., Chen J., Jin H., Kim C.U., Wright M., Geleziunas R., and Tsiang M. Preclinical evaluation of GS-9160, a novel inhibitor of human immunodeficiency virus type 1 integrase. Antimicrobial Agents and Chemotherapy 53 (2009) 1194-1203
-
(2009)
Antimicrobial Agents and Chemotherapy
, vol.53
, pp. 1194-1203
-
-
Jones, G.S.1
Yu, F.2
Zeynalzadegan, A.3
Hesselgesser, J.4
Chen, X.5
Chen, J.6
Jin, H.7
Kim, C.U.8
Wright, M.9
Geleziunas, R.10
Tsiang, M.11
-
53
-
-
0028566214
-
Binding and stimulation of HIV-1 integrase by a human homolog of yeast transcription factor SNF5 (Abstract)
-
Kalpana G.V., Marmon S., Wang W., Crabtree G.R., and Goff S.P. Binding and stimulation of HIV-1 integrase by a human homolog of yeast transcription factor SNF5 (Abstract). Science 266 (1994) 2002-2006
-
(1994)
Science
, vol.266
, pp. 2002-2006
-
-
Kalpana, G.V.1
Marmon, S.2
Wang, W.3
Crabtree, G.R.4
Goff, S.P.5
-
54
-
-
0027377121
-
Crystal structure of Esherichia coli RNase HI in complex with Mg2+ at 2.8 A resolution: proof for a single Mg(2+)-binding site (Abstract)
-
Katayanagi K., Okumara M., and Morikawa K. Crystal structure of Esherichia coli RNase HI in complex with Mg2+ at 2.8 A resolution: proof for a single Mg(2+)-binding site (Abstract). Proteins 17 (1993) 337-346
-
(1993)
Proteins
, vol.17
, pp. 337-346
-
-
Katayanagi, K.1
Okumara, M.2
Morikawa, K.3
-
55
-
-
55049106358
-
Virological evolution in HIV treatment-experienced patients with raltegravir-based salvage regimens (poster 11)
-
Sitges, Spain
-
Katlama C., Caby F., Schneider L., Andrade R.M., Tubiana A., Valantin M.A., Ktorza N., Malet I., Peytavin G., Canestri A., and Calvez V. Virological evolution in HIV treatment-experienced patients with raltegravir-based salvage regimens (poster 11). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Katlama, C.1
Caby, F.2
Schneider, L.3
Andrade, R.M.4
Tubiana, A.5
Valantin, M.A.6
Ktorza, N.7
Malet, I.8
Peytavin, G.9
Canestri, A.10
Calvez, V.11
-
56
-
-
33745198847
-
Safety and pharmacokinetics of single oral dose of JTK-303/GS-9137, a novel HIV integrase inhibitor, in healthy volunteers (poster number 580)
-
Denver, CO, USA
-
Kawaguchi I., Ishikawa T., Ishibashi M., Irie S., and Kakee A. Safety and pharmacokinetics of single oral dose of JTK-303/GS-9137, a novel HIV integrase inhibitor, in healthy volunteers (poster number 580). 13th Conference on Retroviruses and Opportunistic Infections. Denver, CO, USA (2006)
-
(2006)
13th Conference on Retroviruses and Opportunistic Infections
-
-
Kawaguchi, I.1
Ishikawa, T.2
Ishibashi, M.3
Irie, S.4
Kakee, A.5
-
57
-
-
33746816830
-
Pharmacokinetics/pharmacodynamics of GS-9137 an HIV integrase inhibitor in treatment-naïve and experienced patients (abstract 73)
-
Lisbon, Portugal
-
Kearney B.P., Mathias A., Zhong L., DeJesus E., Markowitz M., Hawkins T., and Cheng A. Pharmacokinetics/pharmacodynamics of GS-9137 an HIV integrase inhibitor in treatment-naïve and experienced patients (abstract 73). 7th International Workshop on Clinical Pharmacology of HIV Therapy. Lisbon, Portugal (2006)
-
(2006)
7th International Workshop on Clinical Pharmacology of HIV Therapy
-
-
Kearney, B.P.1
Mathias, A.2
Zhong, L.3
DeJesus, E.4
Markowitz, M.5
Hawkins, T.6
Cheng, A.7
-
58
-
-
0037293099
-
Human immunodeficiency virus type-1 integrase containing a glycine to serine mutation at position 140 is attenuated for catalysis and resistant to integrase inhibitors
-
King P.J., Lee D.J., Reinke R.A., Victoria J.G., Beale K., and Robinson Jr. W.E. Human immunodeficiency virus type-1 integrase containing a glycine to serine mutation at position 140 is attenuated for catalysis and resistant to integrase inhibitors. Virology 306 (2003) 147-161
-
(2003)
Virology
, vol.306
, pp. 147-161
-
-
King, P.J.1
Lee, D.J.2
Reinke, R.A.3
Victoria, J.G.4
Beale, K.5
Robinson Jr., W.E.6
-
59
-
-
0031685017
-
Resistance to the anti-human immunodeficiency virus type 1 compound L-chicoric acid results from a single mutation at amino acid 140 of integrase
-
King P.J., and Robinson Jr. W.E. Resistance to the anti-human immunodeficiency virus type 1 compound L-chicoric acid results from a single mutation at amino acid 140 of integrase. Journal of Virology 72 (1998) 8420-8424
-
(1998)
Journal of Virology
, vol.72
, pp. 8420-8424
-
-
King, P.J.1
Robinson Jr., W.E.2
-
60
-
-
53249087908
-
Selection of diverse and clinically relevant integrase inhibitor-resistant human immunodeficiency virus type 1 mutants
-
doi: 10.1016/j.antiviral.2008.06012
-
Kobayashi M., Nakahara K., Seki T., Miki S., Kawauchi S., Suyama A., Wakasa-Morimoto C., Kodama M., Endoh T., Oosugi E., Matsushita Y., Murai H., Fujishita T., Yoshinaga T., Garvey E., Foster S., Underwood M., Johns B., Sato A., and Fujiwara T. Selection of diverse and clinically relevant integrase inhibitor-resistant human immunodeficiency virus type 1 mutants. Antiviral Research (2008) doi: 10.1016/j.antiviral.2008.06012
-
(2008)
Antiviral Research
-
-
Kobayashi, M.1
Nakahara, K.2
Seki, T.3
Miki, S.4
Kawauchi, S.5
Suyama, A.6
Wakasa-Morimoto, C.7
Kodama, M.8
Endoh, T.9
Oosugi, E.10
Matsushita, Y.11
Murai, H.12
Fujishita, T.13
Yoshinaga, T.14
Garvey, E.15
Foster, S.16
Underwood, M.17
Johns, B.18
Sato, A.19
Fujiwara, T.20
more..
-
61
-
-
0026719238
-
Residues critical for retroviral integrative recombination in a region that is highly conserved among retroviral/retrotransposon integrases and bacterial insertion sequence transposases
-
Kulkosky J., Jones K.S., Katz R.A., Mack J.P., and Skalka A.M. Residues critical for retroviral integrative recombination in a region that is highly conserved among retroviral/retrotransposon integrases and bacterial insertion sequence transposases. Molecular and Cellular Biology 12 (1992) 2331-2338
-
(1992)
Molecular and Cellular Biology
, vol.12
, pp. 2331-2338
-
-
Kulkosky, J.1
Jones, K.S.2
Katz, R.A.3
Mack, J.P.4
Skalka, A.M.5
-
62
-
-
0026072804
-
Substrate specificity of recombinant human immunodeficiency virus integrase protein
-
LaFemina R.L., Callahan P.L., and Cordingley M.G. Substrate specificity of recombinant human immunodeficiency virus integrase protein. Journal of Virology 65 (1991) 5624-5630
-
(1991)
Journal of Virology
, vol.65
, pp. 5624-5630
-
-
LaFemina, R.L.1
Callahan, P.L.2
Cordingley, M.G.3
-
63
-
-
70350166248
-
Potent antiviral activity of S/GSK1349572, a next generation integrase inhibitor (INI), in INI-Naïve HIV-1-infected patients: ING111521 Protocol (Abstract TUAB105)
-
Cape Town, South Africa
-
Lalezari J., Sloan L., DeJesus E., Hawkins T., McCurdy L., Song I., Borland J., Stroder R., Chen S., Lou Y., Underwood M., Fujiwara T., Piscitelli S., and Min S. Potent antiviral activity of S/GSK1349572, a next generation integrase inhibitor (INI), in INI-Naïve HIV-1-infected patients: ING111521 Protocol (Abstract TUAB105). IAS 2009-5th Conference on HIV Pathogenesis, Treatment and Prevention. Cape Town, South Africa (2009)
-
(2009)
IAS 2009-5th Conference on HIV Pathogenesis, Treatment and Prevention
-
-
Lalezari, J.1
Sloan, L.2
DeJesus, E.3
Hawkins, T.4
McCurdy, L.5
Song, I.6
Borland, J.7
Stroder, R.8
Chen, S.9
Lou, Y.10
Underwood, M.11
Fujiwara, T.12
Piscitelli, S.13
Min, S.14
-
64
-
-
34347354196
-
Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-2: 24-week results from a randomised, double-blind, placebo-controlled trial
-
Lazzarin A., Campbell T., Clotet B., Johnson M., Katlama C., Moll A., Towner W., Trottier B., Peeters M., Vingerhoets J., de Smedt G., Baeten B., Beets G., Sinha R., and Woodfall B. Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-2: 24-week results from a randomised, double-blind, placebo-controlled trial. Lancet 370 (2007) 39-48
-
(2007)
Lancet
, vol.370
, pp. 39-48
-
-
Lazzarin, A.1
Campbell, T.2
Clotet, B.3
Johnson, M.4
Katlama, C.5
Moll, A.6
Towner, W.7
Trottier, B.8
Peeters, M.9
Vingerhoets, J.10
de Smedt, G.11
Baeten, B.12
Beets, G.13
Sinha, R.14
Woodfall, B.15
-
65
-
-
0026537415
-
Both substrate and target oligonucleotide sequences affect in vitro integration mediated by human immunodeficiency virus type 1 integrase protein produced in Saccharomyces cerevisiae
-
Leavitt A.D., Rose R.B., and Varmus H.E. Both substrate and target oligonucleotide sequences affect in vitro integration mediated by human immunodeficiency virus type 1 integrase protein produced in Saccharomyces cerevisiae. Journal of Virology 66 (1992) 2359-2368
-
(1992)
Journal of Virology
, vol.66
, pp. 2359-2368
-
-
Leavitt, A.D.1
Rose, R.B.2
Varmus, H.E.3
-
66
-
-
77953913027
-
Raltegravir demonstrates durable efficacy through 96 weeks: results from STARTMRK, a phase III study of raltegravir-based vs. efavirenz-based therapy in treatment-naïve HIV+ patients (Poster H924b)
-
San Francisco, CA, USA
-
Lennox J., DeJesus E., Lazzarin A., Berger D., Pollard R., Madruga J., Zhao J., Gilbert C., Rodgers A., Teppler H., Nguyen B.Y., Leavitt R., and Sklar P. Raltegravir demonstrates durable efficacy through 96 weeks: results from STARTMRK, a phase III study of raltegravir-based vs. efavirenz-based therapy in treatment-naïve HIV+ patients (Poster H924b). 49th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC). San Francisco, CA, USA (2009)
-
(2009)
49th Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC)
-
-
Lennox, J.1
DeJesus, E.2
Lazzarin, A.3
Berger, D.4
Pollard, R.5
Madruga, J.6
Zhao, J.7
Gilbert, C.8
Rodgers, A.9
Teppler, H.10
Nguyen, B.Y.11
Leavitt, R.12
Sklar, P.13
-
67
-
-
69449101785
-
Safety and efficacy of raltegravir-based versus efavirenz-based combination therapy in treatment-naive patients with HIV-1 infection: a multicentre, double-blind randomised controlled trial
-
Lennox J.L., DeJesus E., Lazzarin A., Pollard R.B., Madruga J.V., Berger D.S., Zhao J., Xu X., Williams-Diaz A., Rodgers A.J., Barnard R.J., Miller M.D., DiNubile M.J., Nguyen B.Y., Leavitt R., and Sklar P. Safety and efficacy of raltegravir-based versus efavirenz-based combination therapy in treatment-naive patients with HIV-1 infection: a multicentre, double-blind randomised controlled trial. Lancet 374 (2009) 796-806
-
(2009)
Lancet
, vol.374
, pp. 796-806
-
-
Lennox, J.L.1
DeJesus, E.2
Lazzarin, A.3
Pollard, R.B.4
Madruga, J.V.5
Berger, D.S.6
Zhao, J.7
Xu, X.8
Williams-Diaz, A.9
Rodgers, A.J.10
Barnard, R.J.11
Miller, M.D.12
DiNubile, M.J.13
Nguyen, B.Y.14
Leavitt, R.15
Sklar, P.16
-
68
-
-
0034467084
-
Retroviral cDNA integration: stimulation by HMG I family proteins
-
Li L., Yoder K., Hansen M.S., Olvera J., Miller M.D., and Bushman F.D. Retroviral cDNA integration: stimulation by HMG I family proteins. Journal of Virology 74 (2000) 10965-10974
-
(2000)
Journal of Virology
, vol.74
, pp. 10965-10974
-
-
Li, L.1
Yoder, K.2
Hansen, M.S.3
Olvera, J.4
Miller, M.D.5
Bushman, F.D.6
-
69
-
-
0344211405
-
The barrier-to-autointegration factor is a component of functional human immunodeficiency virus type 1 preintegration complexes
-
Lin C.W., and Engelman A. The barrier-to-autointegration factor is a component of functional human immunodeficiency virus type 1 preintegration complexes. Journal of Virology 77 (2003) 5030-5036
-
(2003)
Journal of Virology
, vol.77
, pp. 5030-5036
-
-
Lin, C.W.1
Engelman, A.2
-
70
-
-
20844459881
-
Antiretroviral effect of L-000870810, a novel HIV-1 integrase inhibitor, in HIV-1 infected patients (abstract 161)
-
Protocol 004 Study Team. Boston, MA, USA
-
Little S., Drusano G., Schooley R., Haas D., Kumar P., Hammer S., McMahon D., Squires K., Asfour R., Richman D., Chen J., Saah A., Leavitt R., Hazuda D., Nguyen B.Y., and Protocol 004 Study Team. Antiretroviral effect of L-000870810, a novel HIV-1 integrase inhibitor, in HIV-1 infected patients (abstract 161). 12th Conference on Retroviruses and Opportunistic Infections. Boston, MA, USA (2005)
-
(2005)
12th Conference on Retroviruses and Opportunistic Infections
-
-
Little, S.1
Drusano, G.2
Schooley, R.3
Haas, D.4
Kumar, P.5
Hammer, S.6
McMahon, D.7
Squires, K.8
Asfour, R.9
Richman, D.10
Chen, J.11
Saah, A.12
Leavitt, R.13
Hazuda, D.14
Nguyen, B.Y.15
-
71
-
-
0342569810
-
Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor
-
Lubkowski J., Yang F., Alexandratos J., Wlodawer A., Zhao H., Burke Jr. T.R., Neamati N., Pommier Y., Merkel G., and Skalka A.M. Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor. Proceedings of the National Academy of Sciences United States of America 95 (1998) 4831-4836
-
(1998)
Proceedings of the National Academy of Sciences United States of America
, vol.95
, pp. 4831-4836
-
-
Lubkowski, J.1
Yang, F.2
Alexandratos, J.3
Wlodawer, A.4
Zhao, H.5
Burke Jr., T.R.6
Neamati, N.7
Pommier, Y.8
Merkel, G.9
Skalka, A.M.10
-
72
-
-
34347327010
-
Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-1: 24-week results from a randomised, double-blind, placebo-controlled trial
-
Madruga J.V., Cahn P., Grinsztejn B., Haubrich R., Lalezari J., Mills A., Pialoux G., Wilkin T., Peeters M., Vingerhoets J., de Smedt G., Leopold L., Trefiglio R., and Woodfall B. Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-1: 24-week results from a randomised, double-blind, placebo-controlled trial. Lancet 370 (2007) 29-38
-
(2007)
Lancet
, vol.370
, pp. 29-38
-
-
Madruga, J.V.1
Cahn, P.2
Grinsztejn, B.3
Haubrich, R.4
Lalezari, J.5
Mills, A.6
Pialoux, G.7
Wilkin, T.8
Peeters, M.9
Vingerhoets, J.10
de Smedt, G.11
Leopold, L.12
Trefiglio, R.13
Woodfall, B.14
-
73
-
-
0041856142
-
LEDGF/p75 is essential for nuclear and chromosomal targeting of HIV-1 integrase in human cells
-
Maertens G., Cherepanov P., Pluymers W., Busschots K., De Clercq E., Debyser Z., and Engelborghs Y. LEDGF/p75 is essential for nuclear and chromosomal targeting of HIV-1 integrase in human cells. Journal of Biological Chemistry 278 (2003) 33528-33539
-
(2003)
Journal of Biological Chemistry
, vol.278
, pp. 33528-33539
-
-
Maertens, G.1
Cherepanov, P.2
Pluymers, W.3
Busschots, K.4
De Clercq, E.5
Debyser, Z.6
Engelborghs, Y.7
-
74
-
-
0041353616
-
-
Marchand, C., Johnson, A.A., Karki, R.G., Pais, G.C., Zhang, X., Cowansage, K., Patel, T.A., Nicklaus, M.C., Burke, T.R., Pommier, Y., 2003. Metal-dependent inhibition of HIV-1 integrase by beta-diketo acids and resistance of the soluble double-mutant (F185K/C280S) 64, 600-609.
-
(2003)
Metal-dependent inhibition of HIV-1 integrase by beta-diketo acids and resistance of the soluble double-mutant (F185K/C280S)
, vol.64
, pp. 600-609
-
-
Marchand, C.1
Johnson, A.A.2
Karki, R.G.3
Pais, G.C.4
Zhang, X.5
Cowansage, K.6
Patel, T.A.7
Nicklaus, M.C.8
Burke, T.R.9
Pommier, Y.10
-
75
-
-
0037066730
-
Structural determinants for HIV-1 integrase inhibition by beta-diketo acids
-
Marchand C., Zhang X., Pais G.C., Cowansage K., Neamati N., Burke Jr. T.R., and Pommier Y. Structural determinants for HIV-1 integrase inhibition by beta-diketo acids. Journal of Biological Chemistry 277 (2002) 12596-12603
-
(2002)
Journal of Biological Chemistry
, vol.277
, pp. 12596-12603
-
-
Marchand, C.1
Zhang, X.2
Pais, G.C.3
Cowansage, K.4
Neamati, N.5
Burke Jr., T.R.6
Pommier, Y.7
-
76
-
-
33845366857
-
Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals
-
Markowitz M., Morales-Ramirez J.O., Nguyen B.Y., Kovacs C.M., Steigbigel R.T., Cooper D.A., Liporace R., Schwartz R., Isaacs R., Gilde L.R., Wenning L., Zhao J., and Teppler H. Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals. Journal of Acquired Immune Deficiency Syndromes (JAIDS) 43 (2006) 509-515
-
(2006)
Journal of Acquired Immune Deficiency Syndromes (JAIDS)
, vol.43
, pp. 509-515
-
-
Markowitz, M.1
Morales-Ramirez, J.O.2
Nguyen, B.Y.3
Kovacs, C.M.4
Steigbigel, R.T.5
Cooper, D.A.6
Liporace, R.7
Schwartz, R.8
Isaacs, R.9
Gilde, L.R.10
Wenning, L.11
Zhao, J.12
Teppler, H.13
-
77
-
-
34748860363
-
Rapid and durable antiretroviral effect of the HIV-1 Integrase inhibitor raltegravir as part of combination therapy in treatment-naive patients with HIV-1 infection: results of a 48-week controlled study
-
Markowitz M., Nguyen B.Y., Gotuzzo E., Mendo F., Ratanasuwan W., Kovacs C., Prada G., Morales-Ramirez J.O., Crumpacker C.S., Isaacs R.D., Gilde L.R., Wan H., Miller M.D., Wenning L.A., and Teppler H. Rapid and durable antiretroviral effect of the HIV-1 Integrase inhibitor raltegravir as part of combination therapy in treatment-naive patients with HIV-1 infection: results of a 48-week controlled study. Journal of Acquired Immune Deficiency Syndromes (JAIDS) 46 (2007) 125-133
-
(2007)
Journal of Acquired Immune Deficiency Syndromes (JAIDS)
, vol.46
, pp. 125-133
-
-
Markowitz, M.1
Nguyen, B.Y.2
Gotuzzo, E.3
Mendo, F.4
Ratanasuwan, W.5
Kovacs, C.6
Prada, G.7
Morales-Ramirez, J.O.8
Crumpacker, C.S.9
Isaacs, R.D.10
Gilde, L.R.11
Wan, H.12
Miller, M.D.13
Wenning, L.A.14
Teppler, H.15
-
78
-
-
35648940077
-
Resistance and cross-resistance to first generation integrase inhibitors: Insights from a phase 2 study of Elvitegravir (GS-9137) (abstract number 9)
-
Bridgetown, Barbados
-
McColl D.J., Fransen S., Gupta S., Parkin N., Margot N., Ledford R., Chen J., Chuck S., Cheng A.K., and Miller M.D. Resistance and cross-resistance to first generation integrase inhibitors: Insights from a phase 2 study of Elvitegravir (GS-9137) (abstract number 9). 16th International HIV Drug Resistance Workshop. Bridgetown, Barbados (2007)
-
(2007)
16th International HIV Drug Resistance Workshop
-
-
McColl, D.J.1
Fransen, S.2
Gupta, S.3
Parkin, N.4
Margot, N.5
Ledford, R.6
Chen, J.7
Chuck, S.8
Cheng, A.K.9
Miller, M.D.10
-
79
-
-
0031875905
-
Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells
-
Mekouar K., Mouscadet J.F., Desmaele D., Subra F., Leh H., Savoure D., Auclair C., and d'Angelo J. Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells. Journal of Medicinal Chemistry 41 (1998) 2846-2857
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, pp. 2846-2857
-
-
Mekouar, K.1
Mouscadet, J.F.2
Desmaele, D.3
Subra, F.4
Leh, H.5
Savoure, D.6
Auclair, C.7
d'Angelo, J.8
-
80
-
-
52749085595
-
Longitudinal analysis of resistance to the HIV-1 integrase inhibitor raltegravir: results from P005, a phase 2 study in treatment experienced patients (poster)
-
Sitges, Spain
-
Miller M.D., Danovich R.M., Ke Y., Witmer M., Zhao J., Harvey C., Nguyen B.-Y., and Hazuda D. Longitudinal analysis of resistance to the HIV-1 integrase inhibitor raltegravir: results from P005, a phase 2 study in treatment experienced patients (poster). XVII International HIV Drug Resistance Workshop. Sitges, Spain (2008)
-
(2008)
XVII International HIV Drug Resistance Workshop
-
-
Miller, M.D.1
Danovich, R.M.2
Ke, Y.3
Witmer, M.4
Zhao, J.5
Harvey, C.6
Nguyen, B.-Y.7
Hazuda, D.8
-
81
-
-
0030972160
-
Human immunodeficiency virus type 1 preintegration complexes: studies of organization and composition
-
Miller M.D., Farnet C.M., and Bushman F.D. Human immunodeficiency virus type 1 preintegration complexes: studies of organization and composition. Journal of Virology 71 (1997) 5382-5390
-
(1997)
Journal of Virology
, vol.71
, pp. 5382-5390
-
-
Miller, M.D.1
Farnet, C.M.2
Bushman, F.D.3
-
82
-
-
14444276046
-
Salicylhydrazine-containing inhibitors of HIV-1 integrase: implication for a selective chelation in the integrase active site
-
Neamati N., Hong H., Owen J.M., Sunder S., Winslow H.E., Christensen J.L., Zhao H., Burke Jr. T.R., Milne G.W., and Pommier Y. Salicylhydrazine-containing inhibitors of HIV-1 integrase: implication for a selective chelation in the integrase active site. Journal of Medicinal Chemistry 41 (1998) 3202-3209
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, pp. 3202-3209
-
-
Neamati, N.1
Hong, H.2
Owen, J.M.3
Sunder, S.4
Winslow, H.E.5
Christensen, J.L.6
Zhao, H.7
Burke Jr., T.R.8
Milne, G.W.9
Pommier, Y.10
-
83
-
-
0030891601
-
HIV-1 integrase pharmacophore: discovery of inhibitors through three-dimensional database searching
-
Nicklaus M.C., Neamati N., Hong H., Mazumder A., Sunder S., Chen J., Milne G.W., and Pommier Y. HIV-1 integrase pharmacophore: discovery of inhibitors through three-dimensional database searching. Journal of Medicinal Chemistry 40 (1997) 920-929
-
(1997)
Journal of Medicinal Chemistry
, vol.40
, pp. 920-929
-
-
Nicklaus, M.C.1
Neamati, N.2
Hong, H.3
Mazumder, A.4
Sunder, S.5
Chen, J.6
Milne, G.W.7
Pommier, Y.8
-
85
-
-
0029840318
-
Targeting sites within HIV-1 cDNA with a DNA-cleaving ribozyme
-
Raillard S.A., and Joyce G.F. Targeting sites within HIV-1 cDNA with a DNA-cleaving ribozyme. Biochemistry 35 (1996) 11693-11701
-
(1996)
Biochemistry
, vol.35
, pp. 11693-11701
-
-
Raillard, S.A.1
Joyce, G.F.2
-
87
-
-
0029129435
-
Structure of the bacteriophage Mu transposase core: a common structural motif for DNA transposition and retroviral integration
-
Rice P., and Mizuuchi K. Structure of the bacteriophage Mu transposase core: a common structural motif for DNA transposition and retroviral integration. Cell 82 (1995) 209-220
-
(1995)
Cell
, vol.82
, pp. 209-220
-
-
Rice, P.1
Mizuuchi, K.2
-
88
-
-
10244260392
-
Dicaffeoylquinic acid inhibitors of human immunodeficiency virus integrase: inhibition of the core catalytic domain of human immunodeficiency virus integrase
-
Robinson Jr. W.E., Cordeiro M., Abdel-Malek S., Jia Q., Chow S.A., Reinecke M.G., and Mitchell W.M. Dicaffeoylquinic acid inhibitors of human immunodeficiency virus integrase: inhibition of the core catalytic domain of human immunodeficiency virus integrase. Molecular Pharmacology 50 (1996) 846-855
-
(1996)
Molecular Pharmacology
, vol.50
, pp. 846-855
-
-
Robinson Jr., W.E.1
Cordeiro, M.2
Abdel-Malek, S.3
Jia, Q.4
Chow, S.A.5
Reinecke, M.G.6
Mitchell, W.M.7
-
89
-
-
33644863638
-
Novel HIV-1 integrase inhibitors derived from quinolone antibiotics
-
Sato M., Motomura T., Aramaki H., Matsuda T., Yamashita M., Ito Y., Kawakami H., Matsuzaki Y., Watanabe W., Yamataka K., Ikeda S., Kodama E., Matsuoka M., and Shinkai H. Novel HIV-1 integrase inhibitors derived from quinolone antibiotics. Journal of Medicinal Chemistry 49 (2006) 1506-1508
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, pp. 1506-1508
-
-
Sato, M.1
Motomura, T.2
Aramaki, H.3
Matsuda, T.4
Yamashita, M.5
Ito, Y.6
Kawakami, H.7
Matsuzaki, Y.8
Watanabe, W.9
Yamataka, K.10
Ikeda, S.11
Kodama, E.12
Matsuoka, M.13
Shinkai, H.14
-
90
-
-
0037076711
-
Tenofovir DF in antiretroviral-experienced patients: results from a 48-week, randomized, double-blind study
-
Schooley R.T., Ruane P., Myers R.A., Beall G., Lampiris H., Berger D., Chen S.-S., Miller M.D., Isaacson E., and Cheng A.K. Tenofovir DF in antiretroviral-experienced patients: results from a 48-week, randomized, double-blind study. AIDS 16 (2002) 1257-1263
-
(2002)
AIDS
, vol.16
, pp. 1257-1263
-
-
Schooley, R.T.1
Ruane, P.2
Myers, R.A.3
Beall, G.4
Lampiris, H.5
Berger, D.6
Chen, S.-S.7
Miller, M.D.8
Isaacson, E.9
Cheng, A.K.10
-
91
-
-
0025366844
-
Human immunodeficiency virus integration protein expressed in Escherichia coli possesses selective DNA cleaving activity
-
Sherman P.A., and Fyfe J.A. Human immunodeficiency virus integration protein expressed in Escherichia coli possesses selective DNA cleaving activity. Proceedings of the National Academy of Sciences United States of America 87 (1990) 5119-5123
-
(1990)
Proceedings of the National Academy of Sciences United States of America
, vol.87
, pp. 5119-5123
-
-
Sherman, P.A.1
Fyfe, J.A.2
-
92
-
-
37849002059
-
Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137)
-
Shimura K., Kodama E., Sakagami Y., Matsuzaki Y., Watanabe W., Yamataka K., Watanabe Y., Ohata Y., Doi S., Sato M., Kano M., Ikeda S., and Matsuoka M. Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137). Journal of Virology 82 (2008) 764-774
-
(2008)
Journal of Virology
, vol.82
, pp. 764-774
-
-
Shimura, K.1
Kodama, E.2
Sakagami, Y.3
Matsuzaki, Y.4
Watanabe, W.5
Yamataka, K.6
Watanabe, Y.7
Ohata, Y.8
Doi, S.9
Sato, M.10
Kano, M.11
Ikeda, S.12
Matsuoka, M.13
-
93
-
-
0037294186
-
Four novel bis-(naphtho-gamma-pyrones) isolated from Fusarium species as inhibitors of HIV-1 integrase
-
Singh S.B., Zink D.L., Bills G.F., Teran A., Silverman K.C., Lingham R.B., Felock P., and Hazuda D.J. Four novel bis-(naphtho-gamma-pyrones) isolated from Fusarium species as inhibitors of HIV-1 integrase. Bioorganic & Medicinal Chemistry Letters 13 (2003) 713-717
-
(2003)
Bioorganic & Medicinal Chemistry Letters
, vol.13
, pp. 713-717
-
-
Singh, S.B.1
Zink, D.L.2
Bills, G.F.3
Teran, A.4
Silverman, K.C.5
Lingham, R.B.6
Felock, P.7
Hazuda, D.J.8
-
94
-
-
0025864336
-
Prevention of human immunodeficiency virus type 1 integrase expression in Escherichia coli by a ribozyme
-
Sioud M., and Drlica K. Prevention of human immunodeficiency virus type 1 integrase expression in Escherichia coli by a ribozyme. Proceedings of the National Academy of Sciences United States of America 88 (1991) 7303-7307
-
(1991)
Proceedings of the National Academy of Sciences United States of America
, vol.88
, pp. 7303-7307
-
-
Sioud, M.1
Drlica, K.2
-
95
-
-
66949155479
-
96-Week results from BENCHMRK 1&2, phase III studies of raltegravir (RAL) in patients (pts) failing antiretroviral therapy (ART) with triple-class resistant HIV (Poster 571b)
-
Montréal, Canada
-
Steigbigel R.T., Cooper D.A., Eron J.E., Gatell J.M., Kumar P.N., Rockstroh J.K., Wan H., Sklar P., Teppler H., and Nguyen B.Y. 96-Week results from BENCHMRK 1&2, phase III studies of raltegravir (RAL) in patients (pts) failing antiretroviral therapy (ART) with triple-class resistant HIV (Poster 571b). 16th Conference on Retroviruses and Opportunistic Infections (CROI). Montréal, Canada (2009)
-
(2009)
16th Conference on Retroviruses and Opportunistic Infections (CROI)
-
-
Steigbigel, R.T.1
Cooper, D.A.2
Eron, J.E.3
Gatell, J.M.4
Kumar, P.N.5
Rockstroh, J.K.6
Wan, H.7
Sklar, P.8
Teppler, H.9
Nguyen, B.Y.10
-
96
-
-
47949120697
-
Raltegravir with optimized background therapy for resistant HIV-1 infection
-
Steigbigel R.T., Cooper D.A., Kumar P.N., Eron J.E., Schechter M., Markowitz M., Loutfy M.R., Lennox J.L., Gatell J.M., Rockstroh J.K., Katlama C., Yeni P., Lazzarin A., Clotet B., Zhao J., Chen J., Ryan D.M., Rhodes R.R., Killar J.A., Gilde L.R., Strohmaier K.M., Neibohm A.R., Miller M.D., Hazuda D.J., Nessly M.L., DiNubile M.J., Isaacs R.D., Nguyen B.Y., and Teppler H. Raltegravir with optimized background therapy for resistant HIV-1 infection. New England Journal of Medicine 359 (2008) 339-353
-
(2008)
New England Journal of Medicine
, vol.359
, pp. 339-353
-
-
Steigbigel, R.T.1
Cooper, D.A.2
Kumar, P.N.3
Eron, J.E.4
Schechter, M.5
Markowitz, M.6
Loutfy, M.R.7
Lennox, J.L.8
Gatell, J.M.9
Rockstroh, J.K.10
Katlama, C.11
Yeni, P.12
Lazzarin, A.13
Clotet, B.14
Zhao, J.15
Chen, J.16
Ryan, D.M.17
Rhodes, R.R.18
Killar, J.A.19
Gilde, L.R.20
Strohmaier, K.M.21
Neibohm, A.R.22
Miller, M.D.23
Hazuda, D.J.24
Nessly, M.L.25
DiNubile, M.J.26
Isaacs, R.D.27
Nguyen, B.Y.28
Teppler, H.29
more..
-
97
-
-
52449097240
-
Discovery of raltegravir, a potent, selective orally bioavailable HIV-integrase inhibitor for the treatment of HIV-AIDS infection
-
Summa V., Petrocchi A., Bonelli F., Crescenzi B., Donghi M., Ferrara M., Fiore F., Gardelli C., Gonzalez Paz O., Hazuda D.J., Jones P., Kinzel O., Laufer R., Monteagudo E., Muraglia E., Nizi E., Orvieto F., Pace P., Pescatore G., Scarpelli R., Stillmock K., Witmer M.V., and Rowley M. Discovery of raltegravir, a potent, selective orally bioavailable HIV-integrase inhibitor for the treatment of HIV-AIDS infection. Journal of Medicinal Chemistry 51 (2008) 5843-5855
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, pp. 5843-5855
-
-
Summa, V.1
Petrocchi, A.2
Bonelli, F.3
Crescenzi, B.4
Donghi, M.5
Ferrara, M.6
Fiore, F.7
Gardelli, C.8
Gonzalez Paz, O.9
Hazuda, D.J.10
Jones, P.11
Kinzel, O.12
Laufer, R.13
Monteagudo, E.14
Muraglia, E.15
Nizi, E.16
Orvieto, F.17
Pace, P.18
Pescatore, G.19
Scarpelli, R.20
Stillmock, K.21
Witmer, M.V.22
Rowley, M.23
more..
-
98
-
-
73549092165
-
Entry inhibitors in the treatment of HIV-1 infection
-
Tilton J.C., and Doms R.W. Entry inhibitors in the treatment of HIV-1 infection. Antiviral Research 85 (2010)
-
(2010)
Antiviral Research
, vol.85
-
-
Tilton, J.C.1
Doms, R.W.2
-
99
-
-
73549088975
-
S/GSK1349572: a next generation integrase inhibitor with activity against integrase inhibitor-resistant clinical isolates from patients experiencing virologic failure while on raltegravir therapy (Poster WEPEA098)
-
Cape Town, South Africa
-
Underwood M., Johns B., Sato A., Fujiwara T., and Spreen W. S/GSK1349572: a next generation integrase inhibitor with activity against integrase inhibitor-resistant clinical isolates from patients experiencing virologic failure while on raltegravir therapy (Poster WEPEA098). IAS 2009-5th Conference on HIV Pathogenesis, Treatment and Prevention. Cape Town, South Africa (2009)
-
(2009)
IAS 2009-5th Conference on HIV Pathogenesis, Treatment and Prevention
-
-
Underwood, M.1
Johns, B.2
Sato, A.3
Fujiwara, T.4
Spreen, W.5
-
100
-
-
46949109542
-
Discovery of MK-2048-subtle changes confer unique resistance properties to a series of tricyclic hydroxypyrrole integrase strand transfer inhibitors (Abstract)
-
Sydney, Australia
-
Vacca J., Wai J., Fisher T., Embrey M., Hazuda D., Miller M., Felock P., Witmer M., Gabryelski L., and Lyle T. Discovery of MK-2048-subtle changes confer unique resistance properties to a series of tricyclic hydroxypyrrole integrase strand transfer inhibitors (Abstract). 4th IAS Conference on HIV Pathogenesis, Treatment and Prevention incorporating the 19th ASHM Conference. Sydney, Australia (2007)
-
(2007)
4th IAS Conference on HIV Pathogenesis, Treatment and Prevention incorporating the 19th ASHM Conference
-
-
Vacca, J.1
Wai, J.2
Fisher, T.3
Embrey, M.4
Hazuda, D.5
Miller, M.6
Felock, P.7
Witmer, M.8
Gabryelski, L.9
Lyle, T.10
-
101
-
-
0027179416
-
Identification of amino acids in HIV-2 integrase involved in site-specific hydrolysis and alcoholysis of viral DNA termini
-
van Gent D.C., Oude Groeneger A.A., and Plasterk R.H. Identification of amino acids in HIV-2 integrase involved in site-specific hydrolysis and alcoholysis of viral DNA termini. Nucleic Acids Research 21 (1993) 3373-3377
-
(1993)
Nucleic Acids Research
, vol.21
, pp. 3373-3377
-
-
van Gent, D.C.1
Oude Groeneger, A.A.2
Plasterk, R.H.3
-
102
-
-
0027508068
-
The human immunodeficiency virus integrase protein (Abstract)
-
Vink C., and Plasterek R.H. The human immunodeficiency virus integrase protein (Abstract). Trends Genetics 9 (1993) 443-448
-
(1993)
Trends Genetics
, vol.9
, pp. 443-448
-
-
Vink, C.1
Plasterek, R.H.2
-
103
-
-
34248217447
-
Next generation of inhibitors of HIV-1 integrase strand transfer inhibitor: structural diversity and resistance profiles (Abstract 87)
-
Los Angeles, CA, USA
-
Wai J., Fisher T., Embrey M., Egbertson M., Vacca J., Hazuda D., Miller M., Witmer M., Gabryelski L., and Lyle T. Next generation of inhibitors of HIV-1 integrase strand transfer inhibitor: structural diversity and resistance profiles (Abstract 87). 14th Conference on Retroviruses and Opportunistic Infections. Los Angeles, CA, USA (2007)
-
(2007)
14th Conference on Retroviruses and Opportunistic Infections
-
-
Wai, J.1
Fisher, T.2
Embrey, M.3
Egbertson, M.4
Vacca, J.5
Hazuda, D.6
Miller, M.7
Witmer, M.8
Gabryelski, L.9
Lyle, T.10
-
104
-
-
73549114053
-
Evolution of resistance to the HIV integrase inhibitor (INI) elvitegravir can involve genotypic switching among primary INI resistance patterns (Poster P116)
-
Fort Myers, Florida
-
Waters J.M., Margot N., Hluhanich R., Svarovskaia J., Harris J., Borroto-Esoda K., Miller M.D., and McColl D.J. Evolution of resistance to the HIV integrase inhibitor (INI) elvitegravir can involve genotypic switching among primary INI resistance patterns (Poster P116). XVIII International HIV Drug Resistance Workshop. Fort Myers, Florida (2009)
-
(2009)
XVIII International HIV Drug Resistance Workshop
-
-
Waters, J.M.1
Margot, N.2
Hluhanich, R.3
Svarovskaia, J.4
Harris, J.5
Borroto-Esoda, K.6
Miller, M.D.7
McColl, D.J.8
-
105
-
-
73549120207
-
-
Wensing, A.M.J., van Maarseveen, N.M., Nijhuys, M., 2010. HIV protease inhibitors. Antiviral Research 85.
-
Wensing, A.M.J., van Maarseveen, N.M., Nijhuys, M., 2010. HIV protease inhibitors. Antiviral Research 85.
-
-
-
-
106
-
-
52749091840
-
In vitro resistance selection studies using raltegravir: a novel inhibitor of HIV-1 integrase (abstract #17)
-
Richmond, VA, USA
-
Witmer M., Danovich R., Ke Y., Day A., Gabryelski L., Ecto L., Lu M., Lai M.-T., McKenna P., DiStefano D., Miller M., and Hazuda D. In vitro resistance selection studies using raltegravir: a novel inhibitor of HIV-1 integrase (abstract #17). 8th Annual Symposium on Antiviral Drug Resistance. Richmond, VA, USA (2007)
-
(2007)
8th Annual Symposium on Antiviral Drug Resistance
-
-
Witmer, M.1
Danovich, R.2
Ke, Y.3
Day, A.4
Gabryelski, L.5
Ecto, L.6
Lu, M.7
Lai, M.-T.8
McKenna, P.9
DiStefano, D.10
Miller, M.11
Hazuda, D.12
-
107
-
-
0034468560
-
Repair of gaps in retroviral DNA integration intermediates
-
Yoder K.E., and Bushman F.D. Repair of gaps in retroviral DNA integration intermediates. Journal of Virology 74 (2000) 11191-11200
-
(2000)
Journal of Virology
, vol.74
, pp. 11191-11200
-
-
Yoder, K.E.1
Bushman, F.D.2
-
108
-
-
0030478950
-
Zinc folds the N-terminal domain of HIV-1 integrase, promotes multimerization, and enhances catalytic activity
-
Zheng R., Jenkins T.M., and Craigie R. Zinc folds the N-terminal domain of HIV-1 integrase, promotes multimerization, and enhances catalytic activity. Proceedings of the National Academy of Sciences United States of America 93 (1996) 13659-13664
-
(1996)
Proceedings of the National Academy of Sciences United States of America
, vol.93
, pp. 13659-13664
-
-
Zheng, R.1
Jenkins, T.M.2
Craigie, R.3
-
109
-
-
0037434509
-
Design and synthesis of 8-hydroxy-(1,6)naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells
-
Zhuang L., Wai J.S., Embrey M.W., Fisher T.E., Egbertson M.S., Payne L.S., Guare Jr. J.P., Vacca J.P., Hazuda D.J., Felock P.J., Wolfe A.L., Stillmock K.A., Witmer M.V., Moyer G., Schleif W.A., Gabryelski L.J., Leonard Y.M., Lynch Jr. J.J., Michelson S.R., and Young S.D. Design and synthesis of 8-hydroxy-(1,6)naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells. Journal of Medicinal Chemistry 46 (2003) 453-456
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, pp. 453-456
-
-
Zhuang, L.1
Wai, J.S.2
Embrey, M.W.3
Fisher, T.E.4
Egbertson, M.S.5
Payne, L.S.6
Guare Jr., J.P.7
Vacca, J.P.8
Hazuda, D.J.9
Felock, P.J.10
Wolfe, A.L.11
Stillmock, K.A.12
Witmer, M.V.13
Moyer, G.14
Schleif, W.A.15
Gabryelski, L.J.16
Leonard, Y.M.17
Lynch Jr., J.J.18
Michelson, S.R.19
Young, S.D.20
more..
-
110
-
-
55049114155
-
The HIV integrase inhibitor elvitegravir (EVG/r) has potent and durable antiretroviral activity in treatment-experienced patients with active optimized background therapy (OBT) (Oral Presentation)
-
Chicago, IL
-
Zolopa A.R., Lampiris H., Blick G., Walworth C., Zhong L., Chuck S.L., Enejosa J., Kearney B.P., and Cheng A.K. The HIV integrase inhibitor elvitegravir (EVG/r) has potent and durable antiretroviral activity in treatment-experienced patients with active optimized background therapy (OBT) (Oral Presentation). 47th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC). Chicago, IL (2007)
-
(2007)
47th Annual Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC)
-
-
Zolopa, A.R.1
Lampiris, H.2
Blick, G.3
Walworth, C.4
Zhong, L.5
Chuck, S.L.6
Enejosa, J.7
Kearney, B.P.8
Cheng, A.K.9
-
111
-
-
34248199833
-
The HIV integrase inhibitor GS-9137 has potent antiretroviral activity in treatment-experienced patients (oral presentation 143LB)
-
Los Angeles, CA, USA
-
Zolopa, A.R., Mullen, M., Berger, D., Ruane, P., Hawkins, T., Zhong, L., Chuck, S.L., Enejosa, J., Kearney, B.P., K, C.A., 2007b. The HIV integrase inhibitor GS-9137 has potent antiretroviral activity in treatment-experienced patients (oral presentation 143LB). In: 14th Conference on Retroviruses and Opportunistic Infections, Los Angeles, CA, USA.
-
(2007)
14th Conference on Retroviruses and Opportunistic Infections
-
-
Zolopa, A.R.1
Mullen, M.2
Berger, D.3
Ruane, P.4
Hawkins, T.5
Zhong, L.6
Chuck, S.L.7
Enejosa, J.8
Kearney, B.P.K.C.A.9
-
112
-
-
0034692178
-
Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture
-
Zouhiri F., Mouscadet J.F., Mekouar K., Desmaele D., Savoure D., Leh H., Subra F., Le Bret M., Auclair C., and d'Angelo J. Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture. Journal of Medicinal Chemistry 43 (2000) 1533-1540
-
(2000)
Journal of Medicinal Chemistry
, vol.43
, pp. 1533-1540
-
-
Zouhiri, F.1
Mouscadet, J.F.2
Mekouar, K.3
Desmaele, D.4
Savoure, D.5
Leh, H.6
Subra, F.7
Le Bret, M.8
Auclair, C.9
d'Angelo, J.10
|