-
1
-
-
0019774135
-
An outbreak of community-acquired Pneumocystis carinii pneumonia: initial manifestation of cellular immune dysfunction
-
Masur H, Michelis MA, Greene JB, Onorato I, Stouwe RA, et al. (1981) An outbreak of community-acquired Pneumocystis carinii pneumonia: initial manifestation of cellular immune dysfunction. N Engl J Med. 305(24): 1431-8.
-
(1981)
N Engl J Med
, vol.305
, Issue.24
, pp. 1431-1438
-
-
Masur, H.1
Michelis, M.A.2
Greene, J.B.3
Onorato, I.4
Stouwe, R.A.5
-
2
-
-
84855718532
-
-
Joint United Nations Programme on HIV/AIDS (UNAIDS), ISBN: 978-92-9173-904-2 {pipe} UNAIDS/JC2216E
-
Joint United Nations Programme on HIV/AIDS (UNAIDS) (2011) World AIDS Day Report. ISBN: 978-92-9173-904-2 {pipe} UNAIDS/JC2216E.
-
(2011)
World AIDS Day Report
-
-
-
3
-
-
36749088862
-
HIV drug development: the next 25 years
-
Flexner C, (2007) HIV drug development: the next 25 years. Nat Rev Drug Discov. 6(12): 959-66.
-
(2007)
Nat Rev Drug Discov
, vol.6
, Issue.12
, pp. 959-966
-
-
Flexner, C.1
-
4
-
-
33746555576
-
HIV/AIDS epidemiology, pathogenesis, prevention, and treatment
-
Simon V, Ho DD, Abdool Karim Q, (2006) HIV/AIDS epidemiology, pathogenesis, prevention, and treatment. Lancet. 368(9534): 489-504.
-
(2006)
Lancet
, vol.368
, Issue.9534
, pp. 489-504
-
-
Simon, V.1
Ho, D.D.2
Abdool Karim, Q.3
-
5
-
-
0037043652
-
Antiretroviral-drug resistance among patients recently infected with HIV
-
Little SJ, Holte S, Routy JP, Daar ES, Markowitz M, et al. (2002) Antiretroviral-drug resistance among patients recently infected with HIV. N Engl J Med. 347(6): 385-94.
-
(2002)
N Engl J Med
, vol.347
, Issue.6
, pp. 385-394
-
-
Little, S.J.1
Holte, S.2
Routy, J.P.3
Daar, E.S.4
Markowitz, M.5
-
6
-
-
0242383496
-
Worldwide transmission of drug-resistant HIV
-
Wensing AM, Boucher CA, (2003) Worldwide transmission of drug-resistant HIV. AIDS Rev. 5(3): 140-55.
-
(2003)
AIDS Rev
, vol.5
, Issue.3
, pp. 140-155
-
-
Wensing, A.M.1
Boucher, C.A.2
-
7
-
-
20444376886
-
Confronting the emergence of drug-resistant HIV type 1 impact of antiretroviral therapy on individual and population resistance
-
Daar ES, Richman DD, (2005) Confronting the emergence of drug-resistant HIV type 1 impact of antiretroviral therapy on individual and population resistance. AIDS Res Hum Retorviruses. 21(5): 343-57.
-
(2005)
AIDS Res Hum Retorviruses
, vol.21
, Issue.5
, pp. 343-357
-
-
Daar, E.S.1
Richman, D.D.2
-
8
-
-
62249095476
-
The challenge of finding a cure for HIV infection
-
Richman DD, Margolis DM, Dalaney M, Greene WC, Hazuda D, et al. (2009) The challenge of finding a cure for HIV infection. Science 323(5919): 1304-7.
-
(2009)
Science
, vol.323
, Issue.5919
, pp. 1304-1307
-
-
Richman, D.D.1
Margolis, D.M.2
Dalaney, M.3
Greene, W.C.4
Hazuda, D.5
-
9
-
-
59849104542
-
Efficacy and tolerability of initial antiretroviral therapy: a systematic review
-
discussion 355-6
-
Carr A, Amin J (2009) Efficacy and tolerability of initial antiretroviral therapy: a systematic review. Aids, 23(3): 343-53; discussion 355-6.
-
(2009)
Aids
, vol.23
, Issue.3
, pp. 343-353
-
-
Carr, A.1
Amin, J.2
-
10
-
-
58449127521
-
Current HIV therapeutics: mechanistic and chemical determinants of toxicity
-
Chiao SK, Romero DL, Johnson DE, (2009) Current HIV therapeutics: mechanistic and chemical determinants of toxicity. Curr Opin Drug Discov Devel. 12(1): 53-60.
-
(2009)
Curr Opin Drug Discov Devel
, vol.12
, Issue.1
, pp. 53-60
-
-
Chiao, S.K.1
Romero, D.L.2
Johnson, D.E.3
-
11
-
-
24344470951
-
Cell-based and biochemical screening approaches for the discovery of novel HIV-1 inhibitors
-
Westby M, Nakayama GR, Butler SL, Blair WS, (2005) Cell-based and biochemical screening approaches for the discovery of novel HIV-1 inhibitors. Antiviral Res. 67(3): 121-40.
-
(2005)
Antiviral Res
, vol.67
, Issue.3
, pp. 121-140
-
-
Westby, M.1
Nakayama, G.R.2
Butler, S.L.3
Blair, W.S.4
-
12
-
-
10044285996
-
Ini1/hSNF5 is dispensable for retrovirus-induced cytoplasmic accumulation of PML and does not interfere with integration
-
Boese A, Sommer P, Gaussin A, Reimann A, Nehrbass U, (2004) Ini1/hSNF5 is dispensable for retrovirus-induced cytoplasmic accumulation of PML and does not interfere with integration. FEBS Lett. 578(3): 291-296.
-
(2004)
FEBS Lett
, vol.578
, Issue.3
, pp. 291-296
-
-
Boese, A.1
Sommer, P.2
Gaussin, A.3
Reimann, A.4
Nehrbass, U.5
-
13
-
-
7244226607
-
Anti-termination by SIV Tat requires flexibility of the nascent TAR structure
-
Sommer P, Vartanian JP, Wachsmuth M, Henry M, Guetard D, et al. (2004) Anti-termination by SIV Tat requires flexibility of the nascent TAR structure. J Mol Biol. 344(1): 11-28.
-
(2004)
J Mol Biol
, vol.344
, Issue.1
, pp. 11-28
-
-
Sommer, P.1
Vartanian, J.P.2
Wachsmuth, M.3
Henry, M.4
Guetard, D.5
-
14
-
-
33745158157
-
A simple method of estimating fifty percent endpoints
-
Reed LJ, Muench H, (1938) A simple method of estimating fifty percent endpoints. Am. J. Hyg. 27: 493-497.
-
(1938)
Am. J. Hyg
, vol.27
, pp. 493-497
-
-
Reed, L.J.1
Muench, H.2
-
15
-
-
0033003760
-
A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays
-
Zhang JH, Chung TD, Oldenburg KR, (1999) A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays. J Biomol Screen. 4(2): 67-73.
-
(1999)
J Biomol Screen
, vol.4
, Issue.2
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.2
Oldenburg, K.R.3
-
16
-
-
0034019566
-
A novel phenotypic drug susceptibility assay for human immunodeficiency virus type 1
-
Petropoulos CJ, Parkin NT, Limoli KL, Lie YS, Wrin T, et al. (2000) A novel phenotypic drug susceptibility assay for human immunodeficiency virus type 1. Antimicrob Agents Chemother. 44(4): 920-8.
-
(2000)
Antimicrob Agents Chemother
, vol.44
, Issue.4
, pp. 920-928
-
-
Petropoulos, C.J.1
Parkin, N.T.2
Limoli, K.L.3
Lie, Y.S.4
Wrin, T.5
-
17
-
-
0033954256
-
The Protein Data Bank
-
Berman HM, Westbrook Z, Feng Z, Gilliland G, Bhat TN, et al. (2000) The Protein Data Bank. Nucleic Acids Research. 28(1): 235-242.
-
(2000)
Nucleic Acids Research
, vol.28
, Issue.1
, pp. 235-242
-
-
Berman, H.M.1
Westbrook, Z.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
-
18
-
-
77953872635
-
Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-benzyl derivatives with broad potency against resistant mutant viruses
-
Kertesz DJ, Brontherton-Pleiss C, Yang M, Wang Z, Lin X, et al. (2010) Discovery of piperidin-4-yl-aminopyrimidines as HIV-1 reverse transcriptase inhibitors. N-benzyl derivatives with broad potency against resistant mutant viruses. Bioorg. Med. Chem. Lett. 20(14): 4215-4218.
-
(2010)
Bioorg. Med. Chem. Lett
, vol.20
, Issue.14
, pp. 4215-4218
-
-
Kertesz, D.J.1
Brontherton-Pleiss, C.2
Yang, M.3
Wang, Z.4
Lin, X.5
-
19
-
-
77952724079
-
Crystal structures of HIV-1 reverse transcriptase with etravirine (TMC125) and rilpivirine (TMC278): implications for drug design
-
Lansdon EB, Brendza KM, Hung M, Wang R, Mukund S, et al. (2010) Crystal structures of HIV-1 reverse transcriptase with etravirine (TMC125) and rilpivirine (TMC278): implications for drug design. J. Med. Chem. 53(10): 4295-4299.
-
(2010)
J. Med. Chem
, vol.53
, Issue.10
, pp. 4295-4299
-
-
Lansdon, E.B.1
Brendza, K.M.2
Hung, M.3
Wang, R.4
Mukund, S.5
-
20
-
-
54549125887
-
Discovery of 3-{5-[(6-amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): a potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses
-
Tucker TJ, Sisko JT, Tynebor RM, Williams TM, Felock PJ, et al. (2008) Discovery of 3-{5-[(6-amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): a potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses. J. Med. Chem. 51(20): 6503-6511.
-
(2008)
J. Med. Chem
, vol.51
, Issue.20
, pp. 6503-6511
-
-
Tucker, T.J.1
Sisko, J.T.2
Tynebor, R.M.3
Williams, T.M.4
Felock, P.J.5
-
21
-
-
84880440795
-
-
Protein Preparation Wizard, Schrödinger Suite 2011 Protein Preparation Wizard; Epik version 2.3, Schrödinger, LLC, New York, NY, 2012; Impact version 5.8, Schrödinger, LLC, New York, NY, 2012; Prime version 3.1, Schrödinger, LLC, New York, NY, 2012
-
Protein Preparation Wizard, Schrödinger Suite 2011 Protein Preparation Wizard; Epik version 2.3, Schrödinger, LLC, New York, NY, 2012; Impact version 5.8, Schrödinger, LLC, New York, NY, 2012; Prime version 3.1, Schrödinger, LLC, New York, NY, 2012.
-
-
-
-
22
-
-
84880396830
-
-
Glide (2012) version 5.8, Schrödinger, LLC, New York, NY
-
Glide (2012) version 5.8, Schrödinger, LLC, New York, NY.
-
-
-
-
23
-
-
84880431193
-
-
MacroModel (2012) version 9.9, Schrödinger, LLC, New York, NY
-
MacroModel (2012) version 9.9, Schrödinger, LLC, New York, NY.
-
-
-
-
24
-
-
0034869045
-
Differential susceptibility of retroviruses to nucleoside analogues
-
Rosenblum LL, Patton G, Grigg AR, Frater AJ, Cain D, et al. (2001) Differential susceptibility of retroviruses to nucleoside analogues. Antivir Chem Chemother. 12(2): 91-7.
-
(2001)
Antivir Chem Chemother
, vol.12
, Issue.2
, pp. 91-97
-
-
Rosenblum, L.L.1
Patton, G.2
Grigg, A.R.3
Frater, A.J.4
Cain, D.5
-
25
-
-
40349091258
-
High-resolution structures of HIV-1 reverse transcriptase/TMS278 complexes: strategic flexibility explains potency against resistance mutations
-
DAS k, Bauman JD, Clark A, Frenkel YV, Lewi PJ, et al. (2008) High-resolution structures of HIV-1 reverse transcriptase/TMS278 complexes: strategic flexibility explains potency against resistance mutations. Poc Natl Acad Sci U S A. 105(5): 1466-71.
-
(2008)
Poc Natl Acad Sci U S A
, vol.105
, Issue.5
, pp. 1466-1471
-
-
Das, K.1
Bauman, J.D.2
Clark, A.3
Frenkel, Y.V.4
Lewi, P.J.5
-
26
-
-
0030970697
-
Antagonism between human immunodeficiency virus type 1 protease inhibitors indanavir and saquinavir in vitro
-
Merrill DP, Manion DJ, Chou TC, Hirsch MS, (1997) Antagonism between human immunodeficiency virus type 1 protease inhibitors indanavir and saquinavir in vitro. J Infect Dis 176(1): 265-8.
-
(1997)
J Infect Dis
, vol.176
, Issue.1
, pp. 265-268
-
-
Merrill, D.P.1
Manion, D.J.2
Chou, T.C.3
Hirsch, M.S.4
-
27
-
-
0027447592
-
Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase
-
McMahon JB, Gulakowski RJ, Weislow OS, Schultz RJ, Narayanan VL, et al. (1993) Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase. Antimicrob Agents Chemother. 37(4): 754-60.
-
(1993)
Antimicrob Agents Chemother
, vol.37
, Issue.4
, pp. 754-760
-
-
McMahon, J.B.1
Gulakowski, R.J.2
Weislow, O.S.3
Schultz, R.J.4
Narayanan, V.L.5
-
28
-
-
7444224177
-
Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamides
-
Masuda N, Yamamoto O, Fujii M, Ohgami T, Fujuyasu J, et al. (2004) Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: Design and synthesis of thiazolidenebenzenesulfonamides. Bioorg Med Chem. 12(23): 6171-82.
-
(2004)
Bioorg Med Chem
, vol.12
, Issue.23
, pp. 6171-6182
-
-
Masuda, N.1
Yamamoto, O.2
Fujii, M.3
Ohgami, T.4
Fujuyasu, J.5
-
29
-
-
19944434039
-
Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivatives
-
Masuda N, Yamamoto O, Fujii M, Ohgami T, Fujiyasu J, et al. (2005) Studies of non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2: Synthesis and structure-activity relationships of 2-cyano and 2-hydroxy thiazolidenebenzenesulfonamide derivatives. Bioorg Med Chem. 13(4): 949-961.
-
(2005)
Bioorg Med Chem
, vol.13
, Issue.4
, pp. 949-961
-
-
Masuda, N.1
Yamamoto, O.2
Fujii, M.3
Ohgami, T.4
Fujiyasu, J.5
|