-
1
-
-
34250169806
-
A novel bis-tetrahydrofuranylurethane- Containing nonpeptidic protease inhibitor (PI), GRL-98065, is potent against multiple-PI-resistant human immunodeficiency virus in vitro
-
Amano, M., Y. Koh, D. Das, J. Li, S. Leschenko, Y. F. Wang, P. I. Boross, I. T. Weber, A. K. Ghosh, and H. Mitsuya. 2007. A novel bis- tetrahydrofuranylurethane- containing nonpeptidic protease inhibitor (PI), GRL-98065, is potent against multiple-PI-resistant human immunodeficiency virus in vitro. Antimicrob. Agents Chemother. 51:2143-2155.
-
(2007)
Antimicrob. Agents Chemother.
, vol.51
, pp. 2143-2155
-
-
Amano, M.1
Koh, Y.2
Das, D.3
Li, J.4
Leschenko, S.5
Wang, Y.F.6
Boross, P.I.7
Weber, I.T.8
Ghosh, A.K.9
Mitsuya, H.10
-
2
-
-
46349111534
-
Changes in the risk of death after HIV seroconversion compared with mortality in the general population
-
DOI 10.1001/jama.300.1.51
-
Bhaskaran, K., O. Hamouda, M. Sannes, F. Boufassa, A. M. Johnson, P. C. Lambert, and K. Porter. 2008. Changes in the risk of death after HIV seroconversion compared with mortality in the general population. JAMA 300:51-59. (Pubitemid 351920404)
-
(2008)
JAMA - Journal of the American Medical Association
, vol.300
, Issue.1
, pp. 51-59
-
-
Bhaskaran, K.1
Hamouda, O.2
Sannes, M.3
Boufassa, F.4
Johnson, A.M.5
Lambert, P.C.6
Porter, K.7
-
3
-
-
0043069555
-
Toxicity of antiretroviral therapy and implications for drug development
-
Carr, A. 2003. Toxicity of antiretroviral therapy and implications for drug development. Nat. Rev. Drug Discov. 2:624-634.
-
(2003)
Nat. Rev. Drug Discov.
, vol.2
, pp. 624-634
-
-
Carr, A.1
-
4
-
-
0036776359
-
Crystal structures of zidovudine-or lamivudine-resistant human immunodeficiency virus type 1 reverse transcriptases containing mutations at codons 41, 184, and 215
-
Chamberlain, P. P., J. Ren, C. E. Nichols, L. Douglas, J. Lennerstrand, B. A. Larder, D. I. Stuart, and D. K. Stammers. 2002. Crystal structures of zidovudine-or lamivudine-resistant human immunodeficiency virus type 1 reverse transcriptases containing mutations at codons 41, 184, and 215. J. Virol. 76:10015-10019.
-
(2002)
J. Virol.
, vol.76
, pp. 10015-10019
-
-
Chamberlain, P.P.1
Ren, J.2
Nichols, C.E.3
Douglas, L.4
Lennerstrand, J.5
Larder, B.A.6
Stuart, D.I.7
Stammers, D.K.8
-
5
-
-
0023052240
-
Isolation of a new human retrovirus from West African patients with AIDS
-
Clavel, F., D. Guetard, F. Brun-Vezinet, S. Chamaret, M. A. Rey, M. O. Santos-Ferreira, A. G. Laurent, C. Dauguet, C. Katlama, C. Rouzioux, et al. 1986. Isolation of a new human retrovirus from West African patients with AIDS. Science 233:343-346.
-
(1986)
Science
, vol.233
, pp. 343-346
-
-
Clavel, F.1
Guetard, D.2
Brun-Vezinet, F.3
Chamaret, S.4
Rey, M.A.5
Santos-Ferreira, M.O.6
Laurent, A.G.7
Dauguet, C.8
Katlama, C.9
Rouzioux, C.10
-
6
-
-
77649202344
-
Highlights in the discovery of antiviral drugs: A personal retrospective
-
De Clercq, E. 2010. Highlights in the discovery of antiviral drugs: a personal retrospective. J. Med. Chem. 53:1438-1450.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 1438-1450
-
-
De Clercq, E.1
-
7
-
-
0029899093
-
Second locus involved in human immunodeficiency virus type 1 resistance to protease inhibitors
-
Doyon, L., G. Croteau, D. Thibeault, F. Poulin, L. Pilote, and D. Lamarre. 1996. Second locus involved in human immunodeficiency virus type 1 resistance to protease inhibitors. J. Virol. 70:3763-3769. (Pubitemid 26161824)
-
(1996)
Journal of Virology
, vol.70
, Issue.6
, pp. 3763-3769
-
-
Doyon, L.1
Croteau, G.2
Thibeault, D.3
Poulin, F.4
Pilote, L.5
Lamarre, D.6
-
8
-
-
46449115901
-
The exploration of macrocycles for drug discovery-an underexploited structural class
-
Driggers, E. M., S. P. Hale, J. Lee, and N. K. Terrett. 2008. The exploration of macrocycles for drug discovery-an underexploited structural class. Nat. Rev. Drug Discov. 7:608-624.
-
(2008)
Nat. Rev. Drug Discov.
, vol.7
, pp. 608-624
-
-
Driggers, E.M.1
Hale, S.P.2
Lee, J.3
Terrett, N.K.4
-
9
-
-
0032957538
-
PCR-mediated recombination: A general method applied to construct chimeric infectious molecular clones of plasma-derived HIV-1 RNA
-
Fang, G., B. Weiser, A. Visosky, T. Moran, and H. Burger. 1999. PCR-mediated recombination: a general method applied to construct chimeric infectious molecular clones of plasma-derived HIV-1 RNA. Nat. Med. 5:239-242.
-
(1999)
Nat. Med.
, vol.5
, pp. 239-242
-
-
Fang, G.1
Weiser, B.2
Visosky, A.3
Moran, T.4
Burger, H.5
-
10
-
-
0037443127
-
Genotype and phenotype at baseline and at failure in human immunodeficiency virus-infected antiretroviral-naive patients in a randomized trial comparing zidovudine and lamivudine plus nelfinavir or nevirapine
-
Ferrer, E., D. Podzamczer, M. Arnedo, E. Fumero, P. McKenna, A. Rinehart, J. L. Perez, M. J. Barbera, T. Pumarola, J. M. Gatell, and F. Gudiol. 2003. Genotype and phenotype at baseline and at failure in human immunodeficiency virus-infected antiretroviral-naive patients in a randomized trial comparing zidovudine and lamivudine plus nelfinavir or nevirapine. J. Infect. Dis. 187:687-690.
-
(2003)
J. Infect. Dis.
, vol.187
, pp. 687-690
-
-
Ferrer, E.1
Podzamczer, D.2
Arnedo, M.3
Fumero, E.4
McKenna, P.5
Rinehart, A.6
Perez, J.L.7
Barbera, M.J.8
Pumarola, T.9
Gatell, J.M.10
Gudiol, F.11
-
11
-
-
0242539778
-
New patterns of HIV-1 resistance during HAART
-
Fumero, E., and D. Podzamczer. 2003. New patterns of HIV-1 resistance during HAART. Clin. Microbiol. Infect. 9:1077-1084.
-
(2003)
Clin. Microbiol. Infect.
, vol.9
, pp. 1077-1084
-
-
Fumero, E.1
Podzamczer, D.2
-
12
-
-
0037155193
-
Amino acid substitutions in Gag protein at non-cleavage sites are indispensable for the development of a high multitude of HIV-1 resistance against protease inhibitors
-
Gatanaga, H., Y. Suzuki, H. Tsang, K. Yoshimura, M. F. Kavlick, K. Nagashima, R. J. Gorelick, S. Mardy, C. Tang, M. F. Summers, and H. Mitsuya. 2002. Amino acid substitutions in Gag protein at non-cleavage sites are indispensable for the development of a high multitude of HIV-1 resistance against protease inhibitors. J. Biol. Chem. 277:5952-5961.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 5952-5961
-
-
Gatanaga, H.1
Suzuki, Y.2
Tsang, H.3
Yoshimura, K.4
Kavlick, M.F.5
Nagashima, K.6
Gorelick, R.J.7
Mardy, S.8
Tang, C.9
Summers, M.F.10
Mitsuya, H.11
-
13
-
-
4344716145
-
Stereoselective chloroacetate aldol reactions: Syntheses of acetate aldol equivalents and darzens glycidic esters
-
Ghosh, A. K., and J. H. Kim. 2004. Stereoselective chloroacetate aldol reactions: syntheses of acetate aldol equivalents and darzens glycidic esters. Org. Lett. 6:2725-2728.
-
(2004)
Org. Lett.
, vol.6
, pp. 2725-2728
-
-
Ghosh, A.K.1
Kim, J.H.2
-
14
-
-
0032539842
-
Potent HIV protease inhibitors incorporating high-affinity P2-ligands and (R)-(hydroxyethylamino) sulfonamide isostere
-
Ghosh, A. K., J. F. Kincaid, W. Cho, D. E. Walters, K. Krishnan, K. A. Hussain, Y. Koo, H. Cho, C. Rudall, L. Holland, and J. Buthod. 1998. Potent HIV protease inhibitors incorporating high-affinity P2-ligands and (R)-(hydroxyethylamino) sulfonamide isostere. Bioorg. Med. Chem. Lett. 8:687-690.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 687-690
-
-
Ghosh, A.K.1
Kincaid, J.F.2
Cho, W.3
Walters, D.E.4
Krishnan, K.5
Hussain, K.A.6
Koo, Y.7
Cho, H.8
Rudall, C.9
Holland, L.10
Buthod, J.11
-
15
-
-
0032554691
-
Structure based design: Novel spirocyclic ethers as nonpeptidal P2-ligands for HIV protease inhibitors
-
Ghosh, A. K., K. Krishnan, D. E. Walters, W. Cho, H. Cho, Y. Koo, J. Trevino, L. Holland, and J. Buthod. 1998. Structure based design: novel spirocyclic ethers as nonpeptidal P2-ligands for HIV protease inhibitors. Bioorg. Med. Chem. Lett. 8:979-982.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 979-982
-
-
Ghosh, A.K.1
Krishnan, K.2
Walters, D.E.3
Cho, W.4
Cho, H.5
Koo, Y.6
Trevino, J.7
Holland, L.8
Buthod, J.9
-
16
-
-
72249085558
-
Design, synthesis, protein-ligand X-ray structure, and biological evaluation of a series of novel macrocyclic human immunodeficiency virus-1 protease inhibitors to combat drug resistance
-
Ghosh, A. K., S. Kulkarni, D. D. Anderson, L. Hong, A. Baldridge, Y. F. Wang, A. A. Chumanevich, A. Y. Kovalevsky, Y. Tojo, M. Amano, Y. Koh, J. Tang, I. T. Weber, and H. Mitsuya. 2009. Design, synthesis, protein-ligand X-ray structure, and biological evaluation of a series of novel macrocyclic human immunodeficiency virus-1 protease inhibitors to combat drug resistance. J. Med. Chem. 52:7689-7705.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7689-7705
-
-
Ghosh, A.K.1
Kulkarni, S.2
Anderson, D.D.3
Hong, L.4
Baldridge, A.5
Wang, Y.F.6
Chumanevich, A.A.7
Kovalevsky, A.Y.8
Tojo, Y.9
Amano, M.10
Koh, Y.11
Tang, J.12
Weber, I.T.13
Mitsuya, H.14
-
17
-
-
8644220502
-
Stereoselective photochemical 1,3-dioxolane addition to 5-alkoxymethyl-2(5H)-furanone: Synthesis of bis-tetrahydrofuranyl ligand for HIV protease inhibitor UIC-94017 (TMC-114)
-
Ghosh, A. K., S. Leshchenko, and M. Noetzel. 2004. Stereoselective photochemical 1,3-dioxolane addition to 5-alkoxymethyl-2(5H)-furanone: synthesis of bis-tetrahydrofuranyl ligand for HIV protease inhibitor UIC-94017 (TMC-114). J. Org Chem. 69:7822-7829.
-
(2004)
J. Org Chem.
, vol.69
, pp. 7822-7829
-
-
Ghosh, A.K.1
Leshchenko, S.2
Noetzel, M.3
-
18
-
-
0141706723
-
Mutations E44D and V118I in the reverse transcriptase of HIV-1 play distinct mechanistic roles in dual resistance to AZT and 3TC
-
Girouard, M., K. Diallo, B. Marchand, S. McCormick, and M. Gotte. 2003. Mutations E44D and V118I in the reverse transcriptase of HIV-1 play distinct mechanistic roles in dual resistance to AZT and 3TC. J. Biol. Chem. 278:34403-34410.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 34403-34410
-
-
Girouard, M.1
Diallo, K.2
Marchand, B.3
McCormick, S.4
Gotte, M.5
-
19
-
-
0142100752
-
The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue of chain-terminated DNA synthesis
-
Gotte, M., D. Arion, 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
Arion, D.2
Parniak, M.A.3
Wainberg, M.A.4
-
20
-
-
49449099010
-
Emergence of drug resistance in HIV type 1-infected patients after receipt of first-line highly active antiretroviral therapy: A systematic review of clinical trials
-
Gupta, R., A. Hill, A. W. Sawyer, and D. Pillay. 2008. Emergence of drug resistance in HIV type 1-infected patients after receipt of first-line highly active antiretroviral therapy: a systematic review of clinical trials. Clin. Infect. Dis. 47:712-722.
-
(2008)
Clin. Infect. Dis.
, vol.47
, pp. 712-722
-
-
Gupta, R.1
Hill, A.2
Sawyer, A.W.3
Pillay, D.4
-
21
-
-
47649115323
-
Life expectancy of individuals on combination antiretroviral therapy in high-income countries: A collaborative analysis of 14 cohort studies
-
Hog, R. 2008. Life expectancy of individuals on combination antiretroviral therapy in high-income countries: a collaborative analysis of 14 cohort studies. Lancet 372:293-299.
-
(2008)
Lancet
, vol.372
, pp. 293-299
-
-
Hog, R.1
-
22
-
-
62949083325
-
GRL-02031, a novel nonpeptidic protease inhibitor (PI) containing a stereochemically defined fused cyclopentanyltetrahydrofuran potent against multi-PI-resistant human immunodeficiency virus type 1 in vitro
-
Koh, Y., D. Das, S. Leschenko, H. Nakata, H. Ogata-Aoki, M. Amano, M. Nakayama, A. K. Ghosh, and H. Mitsuya. 2009. GRL-02031, a novel nonpeptidic protease inhibitor (PI) containing a stereochemically defined fused cyclopentanyltetrahydrofuran potent against multi-PI-resistant human immunodeficiency virus type 1 in vitro. Antimicrob. Agents Chemother. 53: 997-1006.
-
(2009)
Antimicrob. Agents Chemother.
, vol.53
, pp. 997-1006
-
-
Koh, Y.1
Das, D.2
Leschenko, S.3
Nakata, H.4
Ogata-Aoki, H.5
Amano, M.6
Nakayama, M.7
Ghosh, A.K.8
Mitsuya, H.9
-
23
-
-
35348960903
-
Potent inhibition of HIV-1 replication by novel non-peptidyl small molecule inhibitors of protease dimerization
-
Koh, Y., S. Matsumi, D. Das, M. Amano, D. A. Davis, J. Li, S. Leschenko, A. Baldridge, T. Shioda, R. Yarchoan, A. K. Ghosh, and H. Mitsuya. 2007. Potent inhibition of HIV-1 replication by novel non-peptidyl small molecule inhibitors of protease dimerization. J. Biol. Chem. 282:28709-28720.
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 28709-28720
-
-
Koh, Y.1
Matsumi, S.2
Das, D.3
Amano, M.4
Davis, D.A.5
Li, J.6
Leschenko, S.7
Baldridge, A.8
Shioda, T.9
Yarchoan, R.10
Ghosh, A.K.11
Mitsuya, H.12
-
24
-
-
10744226241
-
Novel bistetrahydrofuranylurethane- containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro
-
Koh, Y., H. Nakata, K. Maeda, H. Ogata, G. Bilcer, T. Devasamudram, J. F. Kincaid, P. Boross, Y. F. Wang, Y. Tie, P. Volarath, L. Gaddis, R. W. Harrison, I. T. Weber, A. K. Ghosh, and H. Mitsuya. 2003. Novel bistetrahydrofuranylurethane- containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro. Antimicrob. Agents Chemother. 47:3123-3129.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, pp. 3123-3129
-
-
Koh, Y.1
Nakata, H.2
Maeda, K.3
Ogata, H.4
Bilcer, G.5
Devasamudram, T.6
Kincaid, J.F.7
Boross, P.8
Wang, Y.F.9
Tie, Y.10
Volarath, P.11
Gaddis, L.12
Harrison, R.W.13
Weber, I.T.14
Ghosh, A.K.15
Mitsuya, H.16
-
25
-
-
54549105456
-
Solution kinetics measurements suggest HIV-1 protease has two binding sites for darunavir and amprenavir
-
Kovalevsky, A. Y., A. K. Ghosh, and I. T. Weber. 2008. Solution kinetics measurements suggest HIV-1 protease has two binding sites for darunavir and amprenavir. J. Med. Chem. 51:6599-6603.
-
(2008)
J. Med. Chem.
, vol.51
, pp. 6599-6603
-
-
Kovalevsky, A.Y.1
Ghosh, A.K.2
Weber, I.T.3
-
26
-
-
0029028067
-
Potential mechanism for sustained antiretroviral efficacy of AZT-3TC combination therapy
-
Larder, B. A., S. D. Kemp, and P. R. Harrigan. 1995. Potential mechanism for sustained antiretroviral efficacy of AZT-3TC combination therapy. Science 269:696-699.
-
(1995)
Science
, vol.269
, pp. 696-699
-
-
Larder, B.A.1
Kemp, S.D.2
Harrigan, P.R.3
-
27
-
-
0037043652
-
Antiretroviral-drug resistance among patients recently infected with HIV
-
Little, S. J., S. Holte, J. P. Routy, E. S. Daar, M. Markowitz, A. C. Collier, R. A. Koup, J. W. Mellors, E. Connick, B. Conway, M. Kilby, L. Wang, J. M. Whitcomb, N. S. Hellmann, and D. D. Richman. 2002. Antiretroviral-drug resistance among patients recently infected with HIV. N. Engl. J. Med. 347:385-394.
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 385-394
-
-
Little, S.J.1
Holte, S.2
Routy, J.P.3
Daar, E.S.4
Markowitz, M.5
Collier, A.C.6
Koup, R.A.7
Mellors, J.W.8
Connick, E.9
Conway, B.10
Kilby, M.11
Wang, L.12
Whitcomb, J.M.13
Hellmann, N.S.14
Richman, D.D.15
-
28
-
-
0035860744
-
Novel low molecular weight spirodiketopiperazine derivatives potently inhibit R5 HIV-1 infection through their antagonistic effects on CCR5
-
Maeda, K., K. Yoshimura, S. Shibayama, H. Habashita, H. Tada, K. Sagawa, T. Miyakawa, M. Aoki, D. Fukushima, and H. Mitsuya. 2001. Novel low molecular weight spirodiketopiperazine derivatives potently inhibit R5 HIV-1 infection through their antagonistic effects on CCR5. J. Biol. Chem. 276:35194-35200.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 35194-35200
-
-
Maeda, K.1
Yoshimura, K.2
Shibayama, S.3
Habashita, H.4
Tada, H.5
Sagawa, K.6
Miyakawa, T.7
Aoki, M.8
Fukushima, D.9
Mitsuya, H.10
-
29
-
-
0002052695
-
Discovery and development of antiretroviral therapeutics for HIV infection
-
T. C. Merigan, J. G. Bartlet, and D. Bolognesi (ed.), The Williams & Wilkins Co., Baltimore, MD
-
Mitsuya, H., and J. Erickson. 1999. Discovery and development of antiretroviral therapeutics for HIV infection, p. 751-780. In T. C. Merigan, J. G. Bartlet, and D. Bolognesi (ed.), Textbook of AIDS medicine. The Williams & Wilkins Co., Baltimore, MD.
-
(1999)
Textbook of AIDS Medicine
, pp. 751-780
-
-
Mitsuya, H.1
Erickson, J.2
-
30
-
-
0035800026
-
Highly active antiretroviral therapy decreases mortality and morbidity in patients with advanced HIV disease
-
Murphy, E. L., A. C. Collier, L. A. Kalish, S. F. Assmann, M. F. Para, T. P. Flanigan, P. N. Kumar, L. Mintz, F. R. Wallach, and G. J. Nemo. 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
Flanigan, T.P.6
Kumar, P.N.7
Mintz, L.8
Wallach, F.R.9
Nemo, G.J.10
-
31
-
-
33845925741
-
Food and Drug Administration analysis of tipranavir clinical resistance in HIV-1-infected treatment-experienced patients
-
Naeger, L. K., and K. A. Struble. 2007. Food and Drug Administration analysis of tipranavir clinical resistance in HIV-1-infected treatment-experienced patients. AIDS 21:179-185.
-
(2007)
AIDS
, vol.21
, pp. 179-185
-
-
Naeger, L.K.1
Struble, K.A.2
-
32
-
-
0027398296
-
Changes in drug sensitivity of human immunodeficiency virus type 1 during therapy with azidothymidine, dideoxycytidine, and dideoxyinosine: An in vitro comparative study
-
Shirasaka, T., R. Yarchoan, M. C. O'Brien, R. N. Husson, B. D. Anderson, E. Kojima, T. Shimada, S. Broder, and H. Mitsuya. 1993. Changes in drug sensitivity of human immunodeficiency virus type 1 during therapy with azidothymidine, dideoxycytidine, and dideoxyinosine: an in vitro comparative study. Proc. Natl. Acad. Sci. U. S. A. 90:562-566.
-
(1993)
Proc. Natl. Acad. Sci. U. S. A.
, vol.90
, pp. 562-566
-
-
Shirasaka, T.1
Yarchoan, R.2
O'Brien, M.C.3
Husson, R.N.4
Anderson, B.D.5
Kojima, E.6
Shimada, T.7
Broder, S.8
Mitsuya, H.9
-
33
-
-
3543125970
-
A long-term latent reservoir for HIV-1: Discovery and clinical implications
-
Siliciano, J. D., and R. F. Siliciano. 2004. A long-term latent reservoir for HIV-1: discovery and clinical implications. J. Antimicrob. Chemother. 54: 6-9.
-
(2004)
J. Antimicrob. Chemother.
, vol.54
, pp. 6-9
-
-
Siliciano, J.D.1
Siliciano, R.F.2
-
34
-
-
11144354478
-
High resolution crystal structures of HIV-1 protease with a potent non-peptide inhibitor (UIC-94017) active against multi-drug-resistant clinical strains
-
Tie, Y., P. I. Boross, Y. F. Wang, L. Gaddis, A. K. Hussain, S. Leshchenko, A. K. Ghosh, J. M. Louis, R. W. Harrison, and I. T. Weber. 2004. High resolution crystal structures of HIV-1 protease with a potent non-peptide inhibitor (UIC-94017) active against multi-drug-resistant clinical strains. J. Mol. Biol. 338:341-352.
-
(2004)
J. Mol. Biol.
, vol.338
, pp. 341-352
-
-
Tie, Y.1
Boross, P.I.2
Wang, Y.F.3
Gaddis, L.4
Hussain, A.K.5
Leshchenko, S.6
Ghosh, A.K.7
Louis, J.M.8
Harrison, R.W.9
Weber, I.T.10
-
35
-
-
33745222568
-
The survival benefits of AIDS treatment in the United States
-
Walensky, R. P., A. D. Paltiel, E. Losina, L. M. Mercincavage, B. R. Schackman, P. E. Sax, M. C. Weinstein, and K. A. Freedberg. 2006. The survival benefits of AIDS treatment in the United States. J. Infect. Dis. 194:11-19.
-
(2006)
J. Infect. Dis.
, vol.194
, pp. 11-19
-
-
Walensky, R.P.1
Paltiel, A.D.2
Losina, E.3
Mercincavage, L.M.4
Schackman, B.R.5
Sax, P.E.6
Weinstein, M.C.7
Freedberg, K.A.8
-
36
-
-
0036145503
-
A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site
-
Yoshimura, K., R. Kato, M. F. Kavlick, A. Nguyen, V. Maroun, K. Maeda, K. A. Hussain, A. K. Ghosh, S. V. Gulnik, J. W. Erickson, and H. Mitsuya. 2002. A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site. J. Virol. 76:1349-1358. (Pubitemid 34066437)
-
(2002)
Journal of Virology
, vol.76
, Issue.3
, pp. 1349-1358
-
-
Yoshimura, K.1
Kato, R.2
Kavlick, M.F.3
Nguyen, A.4
Maroun, V.5
Maeda, K.6
Hussain, K.A.7
Ghosh, A.K.8
Gulnik, S.V.9
Erickson, J.W.10
Mitsuya, H.11
-
37
-
-
13044254785
-
JE-2147: A dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1
-
Yoshimura, K., R. Kato, K. Yusa, M. F. Kavlick, V. Maroun, A. Nguyen, T. Mimoto, T. Ueno, M. Shintani, J. Falloon, H. Masur, H. Hayashi, J. Erickson, and H. Mitsuya. 1999. JE-2147: a dipeptide protease inhibitor (PI) that potently inhibits multi-PI-resistant HIV-1. Proc. Natl. Acad. Sci. U. S. A. 96:8675-8680.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 8675-8680
-
-
Yoshimura, K.1
Kato, R.2
Yusa, K.3
Kavlick, M.F.4
Maroun, V.5
Nguyen, A.6
Mimoto, T.7
Ueno, T.8
Shintani, M.9
Falloon, J.10
Masur, H.11
Hayashi, H.12
Erickson, J.13
Mitsuya, H.14
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