-
1
-
-
0030018156
-
CC CKR5: A RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1
-
Alkhatib, G., C. Combadiere, C. C. Broder, Y. Feng, P. E. Kennedy, P. M. Murphy, and E. A. Berger. 1996. CC CKR5: a RANTES, MIP-1α, MIP-1β receptor as a fusion cofactor for macrophage-tropic HIV-1. Science 272:1955.
-
(1996)
Science
, vol.272
, pp. 1955
-
-
Alkhatib, G.1
Combadiere, C.2
Broder, C.C.3
Feng, Y.4
Kennedy, P.E.5
Murphy, P.M.6
Berger, E.A.7
-
2
-
-
0029062687
-
Expression and characterization of CD4-IgG2, a novel heterotetramer which neutralizes primary HIV-1 isolates
-
Allaway, G. P., K. L. Davis-Bruno, G. A. Beaudry, E. B. Garcia, E. L. Wong, A. M. Ryder, K. W. Hasel, M.-C. Gauduin, R. A. Koup, J. S. McDougal, and P. J. Maddon. 1995. Expression and characterization of CD4-IgG2, a novel heterotetramer which neutralizes primary HIV-1 isolates. AIDS Res. Hum. Retrovir. 11:533-539.
-
(1995)
AIDS Res. Hum. Retrovir.
, vol.11
, pp. 533-539
-
-
Allaway, G.P.1
Davis-Bruno, K.L.2
Beaudry, G.A.3
Garcia, E.B.4
Wong, E.L.5
Ryder, A.M.6
Hasel, K.W.7
Gauduin, M.-C.8
Koup, R.A.9
McDougal, J.S.10
Maddon, P.J.11
-
3
-
-
13044256383
-
A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity
-
Baba, M., O. Nishimura, N. Kanzaki, M. Okamoto, H. Sawada, Y. Iizawa, M. Shiraishi, Y. Aramaki, K. Okonogi, Y. Ogawa, K. Meguro, and M. Fujino. 1999. A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity. Proc. Natl. Acad. Sci. USA 96:5698-5703.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 5698-5703
-
-
Baba, M.1
Nishimura, O.2
Kanzaki, N.3
Okamoto, M.4
Sawada, H.5
Iizawa, Y.6
Shiraishi, M.7
Aramaki, Y.8
Okonogi, K.9
Ogawa, Y.10
Meguro, K.11
Fujino, M.12
-
4
-
-
1342325435
-
Defining a molecular mechanism of synergy between nucleoside and nonnucleoside AIDS drugs
-
Basavapathruni, A., C. M. Bailey, and K. S. Anderson. 2004. Defining a molecular mechanism of synergy between nucleoside and nonnucleoside AIDS drugs. J. Biol. Chem. 279:6221-6224.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 6221-6224
-
-
Basavapathruni, A.1
Bailey, C.M.2
Anderson, K.S.3
-
5
-
-
0032992656
-
The thiocarboxanilide nonnucleoside inhibitor UC781 restores antiviral activity of 3′-azido-3′-deoxythymidine (AZT) against AZT-resistant human immunodeficiency virus type 1
-
Borkow, G., D. Arion, M. A. Wainberg, and M. A. Parniak. 1999. The thiocarboxanilide nonnucleoside inhibitor UC781 restores antiviral activity of 3′-azido-3′-deoxythymidine (AZT) against AZT-resistant human immunodeficiency virus type 1. Antimicrob. Agents Chemother. 43:259-263.
-
(1999)
Antimicrob. Agents Chemother.
, vol.43
, pp. 259-263
-
-
Borkow, G.1
Arion, D.2
Wainberg, M.A.3
Parniak, M.A.4
-
7
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou, T. C., and P. Talalay. 1984. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv. Enzyme Regul. 22:27-55.
-
(1984)
Adv. Enzyme Regul.
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
8
-
-
0036333648
-
The crown and stem of the V3 loop play distinct roles in human immunodeficiency virus type 1 envelope glycoprotein interactions with the CCR5 coreceptor
-
Cormier, E. G., and T. Dragic. 2002. The crown and stem of the V3 loop play distinct roles in human immunodeficiency virus type 1 envelope glycoprotein interactions with the CCR5 coreceptor. J. Virol. 76:8953-8957.
-
(2002)
J. Virol.
, vol.76
, pp. 8953-8957
-
-
Cormier, E.G.1
Dragic, T.2
-
9
-
-
0028439090
-
Applications of standard error estimates in unrestricted factor analysis: Significance tests for factor loadings and correlations
-
Cudeck, R., and L. L. O'Dell. 1994. Applications of standard error estimates in unrestricted factor analysis: significance tests for factor loadings and correlations. Psychol. Bull. 115:475-487.
-
(1994)
Psychol. Bull.
, vol.115
, pp. 475-487
-
-
Cudeck, R.1
O'Dell, L.L.2
-
10
-
-
15844419153
-
Identification of a major co-receptor for primary isolates of HIV-1
-
Deng, H., R. Liu, W. Ellmeier, S. Choe, D. Unutmaz, M. Burkhart, P. Di Marzio, S. Marmon, R. Sutton, C. M. Hill, C. B. Davis, S. C. Peiper, T. J. Schall, D. R. Littman, and N. R. Landau. 1996. Identification of a major co-receptor for primary isolates of HIV-1. Nature 381:661.
-
(1996)
Nature
, vol.381
, pp. 661
-
-
Deng, H.1
Liu, R.2
Ellmeier, W.3
Choe, S.4
Unutmaz, D.5
Burkhart, M.6
Di Marzio, P.7
Marmon, S.8
Sutton, R.9
Hill, C.M.10
Davis, C.B.11
Peiper, S.C.12
Schall, T.J.13
Littman, D.R.14
Landau, N.R.15
-
11
-
-
27644510382
-
Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity
-
Dorr, P., M. Westby, S. Dobbs, P. Griffin, B. Irvine, M. Macartney, J. Mori, G. Rickett, C. Smith-Burchnell, C. Napier, R. Webster, D. Armour, D. Price, B. Stammen, A. Wood, and M. Perros. 2005. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob. Agents Chemother. 49:4721-4732.
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4721-4732
-
-
Dorr, P.1
Westby, M.2
Dobbs, S.3
Griffin, P.4
Irvine, B.5
Macartney, M.6
Mori, J.7
Rickett, G.8
Smith-Burchnell, C.9
Napier, C.10
Webster, R.11
Armour, D.12
Price, D.13
Stammen, B.14
Wood, A.15
Perros, M.16
-
12
-
-
15844389650
-
HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5
-
Dragic, T., V. Litwin, G. P. Allaway, S. R. Martin, Y. Huang, K. A. Nagashima, C. Cayanan, P. J. Maddon, R. A. Koup, J. P. Moore, and W. A. Paxton. 1996. HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5. Nature 381:667-673.
-
(1996)
Nature
, vol.381
, pp. 667-673
-
-
Dragic, T.1
Litwin, V.2
Allaway, G.P.3
Martin, S.R.4
Huang, Y.5
Nagashima, K.A.6
Cayanan, C.7
Maddon, P.J.8
Koup, R.A.9
Moore, J.P.10
Paxton, W.A.11
-
13
-
-
0034625144
-
A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5
-
Dragic, T., A. Trkola, D. A. Thompson, E. G. Cormier, F. A. Kajumo, E. Maxwell, S. W. Lin, W. Ying, S. O. Smith, T. P. Sakmar, and J. P. Moore. 2000. A binding pocket for a small molecule inhibitor of HIV-1 entry within the transmembrane helices of CCR5. Proc. Natl. Acad. Sci. USA 97:5639-5644.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5639-5644
-
-
Dragic, T.1
Trkola, A.2
Thompson, D.A.3
Cormier, E.G.4
Kajumo, F.A.5
Maxwell, E.6
Lin, S.W.7
Ying, W.8
Smith, S.O.9
Sakmar, T.P.10
Moore, J.P.11
-
14
-
-
30744447460
-
Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1
-
Fatkenheuer, G., A. L. Pozniak, M. A. Johnson, A. Plettenberg, S. Staszewski, A. I. M. Hoepelman, M. S. Saag, F. D. Goebel, J. K. Rockstroh, B. J. Dezube, T. M. Jenkins, C. Medhurst, J. F. Sullivan, C. Ridgway, S. Abel, I. T. James, M. Youle, and E. van der Ryst. 2005. Efficacy of short-term monotherapy with maraviroc, a new CCR5 antagonist, in patients infected with HIV-1. Nat. Med. 11:1170-1172.
-
(2005)
Nat. Med.
, vol.11
, pp. 1170-1172
-
-
Fatkenheuer, G.1
Pozniak, A.L.2
Johnson, M.A.3
Plettenberg, A.4
Staszewski, S.5
Hoepelman, A.I.M.6
Saag, M.S.7
Goebel, F.D.8
Rockstroh, J.K.9
Dezube, B.J.10
Jenkins, T.M.11
Medhurst, C.12
Sullivan, J.F.13
Ridgway, C.14
Abel, S.15
James, I.T.16
Youle, M.17
Van Der Ryst, E.18
-
15
-
-
0022480641
-
The role of mononuclear phagocytes in HTLV-III/LAV infection
-
Gartner, S., P. Markovits, D. M. Markovitz, M. H. Kaplan, R. C. Gallo, and M. Popovic. 1986. The role of mononuclear phagocytes in HTLV-III/LAV infection. Science 233:215-219.
-
(1986)
Science
, vol.233
, pp. 215-219
-
-
Gartner, S.1
Markovits, P.2
Markovitz, D.M.3
Kaplan, M.H.4
Gallo, R.C.5
Popovic, M.6
-
16
-
-
0032692850
-
Spontaneous and antigen-induced production of HIV-inhibitory beta-chemokines are associated with AIDS-free status
-
Garzino-Demo, A., R. B. Moss, J. B. Margolick, F. Cleghorn, A. Sill, W. A. Blattner, F. Cocchi, D. J. Carlo, A. L. DeVico, and R. C. Gallo. 1999. Spontaneous and antigen-induced production of HIV-inhibitory beta-chemokines are associated with AIDS-free status. Proc. Natl. Acad. Sci. USA 96:11986-11991.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 11986-11991
-
-
Garzino-Demo, A.1
Moss, R.B.2
Margolick, J.B.3
Cleghorn, F.4
Sill, A.5
Blattner, W.A.6
Cocchi, F.7
Carlo, D.J.8
Devico, A.L.9
Gallo, R.C.10
-
17
-
-
0036114281
-
Increased CCR5 affinity and reduced CCR5/CD4 dependence of a neurovirulent primary human immunodeficiency virus type 1 isolate
-
Gorry, P. R., J. Taylor, G. H. Holm, A. Mehle, T. Morgan, M. Cayabyab, M. Farzan, H. Wang, J. E. Bell, K. Kunstman, J. P. Moore, S. M. Wolinsky, and D. Gabuzda. 2002. Increased CCR5 affinity and reduced CCR5/CD4 dependence of a neurovirulent primary human immunodeficiency virus type 1 isolate. J. Virol. 76:6277-6292.
-
(2002)
J. Virol.
, vol.76
, pp. 6277-6292
-
-
Gorry, P.R.1
Taylor, J.2
Holm, G.H.3
Mehle, A.4
Morgan, T.5
Cayabyab, M.6
Farzan, M.7
Wang, H.8
Bell, J.E.9
Kunstman, K.10
Moore, J.P.11
Wolinsky, S.M.12
Gabuzda, D.13
-
18
-
-
0025991478
-
Two-drug combinations of zidovudine, didanosine, and recombinant interferon-alpha a inhibit replication of zidovudine-resistant human immunodeficiency virus type 1 synergistically in vitro
-
Johnson, V. A., D. P. Merrill, J. A. Videler, T. C. Chou, R. E. Byington, J. J. Eron, R. T. D'Aquila, and M. S. Hirsch. 1991. Two-drug combinations of zidovudine, didanosine, and recombinant interferon-alpha A inhibit replication of zidovudine-resistant human immunodeficiency virus type 1 synergistically in vitro. J. Infect. Dis. 164:646-655.
-
(1991)
J. Infect. Dis.
, vol.164
, pp. 646-655
-
-
Johnson, V.A.1
Merrill, D.P.2
Videler, J.A.3
Chou, T.C.4
Byington, R.E.5
Eron, J.J.6
D'Aquila, R.T.7
Hirsch, M.S.8
-
19
-
-
0034694084
-
Candidate microbicides block HIV-1 infection of human immature Langerhans cells within epithelial tissue explants
-
Kawamura, T., S. S. Cohen, D. L. Borris, E. A. Aquilino, S. Glushakova, L. B. Margolis, J. M. Orenstein, R. E. Offord, A. R. Neurath, and A. Blauvelt. 2000. Candidate microbicides block HIV-1 infection of human immature Langerhans cells within epithelial tissue explants. J. Exp. Med. 192:1491-1500.
-
(2000)
J. Exp. Med.
, vol.192
, pp. 1491-1500
-
-
Kawamura, T.1
Cohen, S.S.2
Borris, D.L.3
Aquilino, E.A.4
Glushakova, S.5
Margolis, L.B.6
Orenstein, J.M.7
Offord, R.E.8
Neurath, A.R.9
Blauvelt, A.10
-
20
-
-
12144289333
-
Genetic and phenotypic analyses of human immunodeficiency virus type 1 escape from a small-molecule CCR5 inhibitor
-
Kuhmann, S. E., P. Pugach, K. J. Kunstman, J. Taylor, R. L. Stanfield, A. Snyder, J. M. Strizki, J. Riley, B. M. Baroudy, I. A. Wilson, B. T. Korber, S. M. Wolinsky, and J. P. Moore. 2004. Genetic and phenotypic analyses of human immunodeficiency virus type 1 escape from a small-molecule CCR5 inhibitor. J. Virol. 78:2790-2807.
-
(2004)
J. Virol.
, vol.78
, pp. 2790-2807
-
-
Kuhmann, S.E.1
Pugach, P.2
Kunstman, K.J.3
Taylor, J.4
Stanfield, R.L.5
Snyder, A.6
Strizki, J.M.7
Riley, J.8
Baroudy, B.M.9
Wilson, I.A.10
Korber, B.T.11
Wolinsky, S.M.12
Moore, J.P.13
-
21
-
-
25844450042
-
Antiviral activity and safety of 873140, a novel CCR5 antagonist, during short-term monotherapy in HIV-infected adults
-
Lalezari, J., M. Thompson, P. Kumar, P. Piliero, R. Davey, K. Patterson, A. Shachoy-Clark, K. Adkison, J. Demarest, Y. Lou, M. Berrey, and S. Piscitelli. 2005. Antiviral activity and safety of 873140, a novel CCR5 antagonist, during short-term monotherapy in HIV-infected adults. AIDS 19:1443-1448.
-
(2005)
AIDS
, vol.19
, pp. 1443-1448
-
-
Lalezari, J.1
Thompson, M.2
Kumar, P.3
Piliero, P.4
Davey, R.5
Patterson, K.6
Shachoy-Clark, A.7
Adkison, K.8
Demarest, J.9
Lou, Y.10
Berrey, M.11
Piscitelli, S.12
-
22
-
-
0033515588
-
Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function
-
Lee, B., M. Sharron, C. Blanpain, B. J. Doranz, J. Vakili, P. Setoh, E. Berg, G. Liu, R. H. Guy, S. R. Durell, M. Parmentier, C. N. Chang, K. Price, M. Tsang, and R. W. Doms. 1999. Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function. J. Biol. Chem. 274:9617-9626.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 9617-9626
-
-
Lee, B.1
Sharron, M.2
Blanpain, C.3
Doranz, B.J.4
Vakili, J.5
Setoh, P.6
Berg, E.7
Liu, G.8
Guy, R.H.9
Durell, S.R.10
Parmentier, M.11
Chang, C.N.12
Price, K.13
Tsang, M.14
Doms, R.W.15
-
23
-
-
0141703204
-
A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding
-
Lin, P. F., W. Blair, T. Wang, T. Spicer, Q. Guo, N. Zhou, Y. F. Gong, H.-G. H. Wang, R. Rose, G. Yamanaka, B. Robinson, C. B. Li, R. Fridell, C. Deminie, G. Demers, Z. Yang, L. Zadjura, N. Meanwell, and R. Colonno. 2003. A small molecule HIV-1 inhibitor that targets the HIV-1 envelope and inhibits CD4 receptor binding. Proc. Natl. Acad. Sci. USA 100:11013-11018.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 11013-11018
-
-
Lin, P.F.1
Blair, W.2
Wang, T.3
Spicer, T.4
Guo, Q.5
Zhou, N.6
Gong, Y.F.7
Wang, H.-G.H.8
Rose, R.9
Yamanaka, G.10
Robinson, B.11
Li, C.B.12
Fridell, R.13
Deminie, C.14
Demers, G.15
Yang, Z.16
Zadjura, L.17
Meanwell, N.18
Colonno, R.19
-
24
-
-
9444291383
-
Human immunodeficiency virus type 1 membrane fusion mediated by a laboratory-adapted strain and a primary isolate analyzed by resonance energy transfer
-
Litwin, V., K. A. Nagashima, A. M. Ryder, C. H. Chang, J. M. Carver, W. C. Olson, M. Alizon, K. W. Hasel, P. J. Maddon, and G. P. Allaway. 1996. Human immunodeficiency virus type 1 membrane fusion mediated by a laboratory-adapted strain and a primary isolate analyzed by resonance energy transfer. J. Virol. 70:6437-6441.
-
(1996)
J. Virol.
, vol.70
, pp. 6437-6441
-
-
Litwin, V.1
Nagashima, K.A.2
Ryder, A.M.3
Chang, C.H.4
Carver, J.M.5
Olson, W.C.6
Alizon, M.7
Hasel, K.W.8
Maddon, P.J.9
Allaway, G.P.10
-
25
-
-
13044306739
-
Polymorphism in RANTES chemokine promoter affects HIV-1 disease progression
-
Liu, H., D. Chao, E. E. Nakayama, H. Taguchi, M. Goto, X. Xin, J. K. Takamatsu, H. Saito, Y. Ishikawa, T. Akaza, T. Juji, Y. Takebe, T. Ohishi, K. Fukutake, Y. Maruyama, S. Yashiki, S. Sonoda, T. Nakamura, Y. Nagai, A. Iwamoto, and T. Shioda. 1999. Polymorphism in RANTES chemokine promoter affects HIV-1 disease progression. Proc. Natl. Acad. Sci. USA 96:4581-4585.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 4581-4585
-
-
Liu, H.1
Chao, D.2
Nakayama, E.E.3
Taguchi, H.4
Goto, M.5
Xin, X.6
Takamatsu, J.K.7
Saito, H.8
Ishikawa, Y.9
Akaza, T.10
Juji, T.11
Takebe, Y.12
Ohishi, T.13
Fukutake, K.14
Maruyama, Y.15
Yashiki, S.16
Sonoda, S.17
Nakamura, T.18
Nagai, Y.19
Iwamoto, A.20
Shioda, T.21
more..
-
26
-
-
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
-
27
-
-
20644453529
-
Generation and properties of a human immunodeficiency virus type 1 isolate resistant to the small molecule CCR5 inhibitor, SCH-417690 (SCH-D)
-
Marozsan, A. J., S. E. Kuhmann, T. Morgan, C. Herrera, E. Rivera-Troche, S. Xu, B. M. Baroudy, J. Strizki, and J. P. Moore. 2005. Generation and properties of a human immunodeficiency virus type 1 isolate resistant to the small molecule CCR5 inhibitor, SCH-417690 (SCH-D). Virology 338:182-199.
-
(2005)
Virology
, vol.338
, pp. 182-199
-
-
Marozsan, A.J.1
Kuhmann, S.E.2
Morgan, T.3
Herrera, C.4
Rivera-Troche, E.5
Xu, S.6
Baroudy, B.M.7
Strizki, J.8
Moore, J.P.9
-
28
-
-
0035984802
-
In vitro antiviral interaction of lopinavir with other protease inhibitors
-
Molla, A., H. Mo, S. Vasavanonda, L. Han, C. T. Lin, A. Hsu, and D. J. Kempf. 2002. In vitro antiviral interaction of lopinavir with other protease inhibitors. Antimicrob. Agents Chemother. 46:2249-2253.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 2249-2253
-
-
Molla, A.1
Mo, H.2
Vasavanonda, S.3
Han, L.4
Lin, C.T.5
Hsu, A.6
Kempf, D.J.7
-
29
-
-
0035313589
-
Human immunodeficiency virus type 1 entry inhibitors PRO 542 and T-20 are potently synergistic in blocking virus-cell and cell-cell fusion
-
Nagashima, K. A., D. A. D. Thompson, S. I. Rosenfield, P. J. Maddon, T. Dragic, and W. C. Olson. 2001. Human immunodeficiency virus type 1 entry inhibitors PRO 542 and T-20 are potently synergistic in blocking virus-cell and cell-cell fusion. J. Infect. Dis. 183:1121-1125.
-
(2001)
J. Infect. Dis.
, vol.183
, pp. 1121-1125
-
-
Nagashima, K.A.1
Thompson, D.A.D.2
Rosenfield, S.I.3
Maddon, P.J.4
Dragic, T.5
Olson, W.C.6
-
30
-
-
27644446851
-
Analysis of binding sites for the new small-molecule CCR5 antagonist TAK-220 on human CCR5
-
Nishikawa, M., K. Takashima, T. Nishi, R. A. Furuta, N. Kanzaki, Y. Yamamoto, and J. Fujisawa. 2005. Analysis of binding sites for the new small-molecule CCR5 antagonist TAK-220 on human CCR5. Antimicrob. Agents Chemother. 49:4708-4715.
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 4708-4715
-
-
Nishikawa, M.1
Takashima, K.2
Nishi, T.3
Furuta, R.A.4
Kanzaki, N.5
Yamamoto, Y.6
Fujisawa, J.7
-
31
-
-
0025065099
-
HIV-1 tropism for mononuclear phagocytes can be determined by regions of gp120 outside the CD4-binding domain
-
O'Brien, W. A., Y. Koyanagi, A. Namazie, J. Q. Zhao, A. Diagne, K. Idler, J. A. Zack, and I. S. Chen. 1990. HIV-1 tropism for mononuclear phagocytes can be determined by regions of gp120 outside the CD4-binding domain. Nature 348:69-73.
-
(1990)
Nature
, vol.348
, pp. 69-73
-
-
O'Brien, W.A.1
Koyanagi, Y.2
Namazie, A.3
Zhao, J.Q.4
Diagne, A.5
Idler, K.6
Zack, J.A.7
Chen, I.S.8
-
33
-
-
0032902710
-
Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5
-
Olson, W. C., G. E. E. Rabut, K. A. Nagashima, D. N. H. Tran, D. J. Anselma, S. P. Monard, J. P. Segal, D. A. D. Thompson, F. Kajumo, Y. Guo, J. P. Moore, P. J. Maddon, and T. Dragic. 1999. Differential inhibition of human immunodeficiency virus type 1 fusion, gp120 binding, and CC-chemokine activity by monoclonal antibodies to CCR5. J. Virol. 73:4145-4155.
-
(1999)
J. Virol.
, vol.73
, pp. 4145-4155
-
-
Olson, W.C.1
Rabut, G.E.E.2
Nagashima, K.A.3
Tran, D.N.H.4
Anselma, D.J.5
Monard, S.P.6
Segal, J.P.7
Thompson, D.A.D.8
Kajumo, F.9
Guo, Y.10
Moore, J.P.11
Maddon, P.J.12
Dragic, T.13
-
34
-
-
2642709177
-
Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection
-
Palella, F. J., K. M. Delaney, A. C. Moorman, M. O. Loveless, J. Fuhrer, G. A. Satten, D. J. Aschman, S. D. Holmberg, and the HIV Outpatient Study Investigators. 1998. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. N. Engl. J. Med. 338:853.
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 853
-
-
Palella, F.J.1
Delaney, K.M.2
Moorman, A.C.3
Loveless, M.O.4
Fuhrer, J.5
Satten, G.A.6
Aschman, D.J.7
Holmberg, S.D.8
-
35
-
-
33645414100
-
HIV-1 coreceptors and their inhibitors
-
Ray, N., and R. W. Doms. 2006. HIV-1 coreceptors and their inhibitors. Curr. Top. Microbiol. Immunol. 303:97-120.
-
(2006)
Curr. Top. Microbiol. Immunol.
, vol.303
, pp. 97-120
-
-
Ray, N.1
Doms, R.W.2
-
36
-
-
33747045164
-
An anti-CCR5 monoclonal antibody and small molecule CCR5 antagonists synergize by inhibiting different stages of human immunodeficiency virus type 1 entry
-
in press
-
Safarian, D., X. Carnec, F. Tsamis, F. Kajumo, and T. Dragic. An anti-CCR5 monoclonal antibody and small molecule CCR5 antagonists synergize by inhibiting different stages of human immunodeficiency virus type 1 entry. Virology, in press.
-
Virology
-
-
Safarian, D.1
Carnec, X.2
Tsamis, F.3
Kajumo, F.4
Dragic, T.5
-
37
-
-
33646514864
-
Interaction of small molecule inhibitors of HIV-1 entry with CCR5
-
Seibert, C., W. Ying, S. Gavrilov, F. Tsamis, S. E. Kuhmann, A. Palani, J. R. Tagat, J. W. Clader, S. W. McCombie, B. M. Baroudy, S. O. Smith, T. Dragic, J. P. Moore, and T. P. Sakmar. 2006. Interaction of small molecule inhibitors of HIV-1 entry with CCR5. Virology 349:41-54.
-
(2006)
Virology
, vol.349
, pp. 41-54
-
-
Seibert, C.1
Ying, W.2
Gavrilov, S.3
Tsamis, F.4
Kuhmann, S.E.5
Palani, A.6
Tagat, J.R.7
Clader, J.W.8
McCombie, S.W.9
Baroudy, B.M.10
Smith, S.O.11
Dragic, T.12
Moore, J.P.13
Sakmar, T.P.14
-
38
-
-
0035866329
-
A luciferase-reporter gene-expressing T-cell line facilitates neutralization and drug-sensitivity assays that use either R5 or X4 strains of human immunodeficiency virus type 1
-
Spenlehauer, C., C. A. Gordon, A. Trkola, and J. P. Moore. 2001. A luciferase-reporter gene-expressing T-cell line facilitates neutralization and drug-sensitivity assays that use either R5 or X4 strains of human immunodeficiency virus type 1. Virology 280:292-300.
-
(2001)
Virology
, vol.280
, pp. 292-300
-
-
Spenlehauer, C.1
Gordon, C.A.2
Trkola, A.3
Moore, J.P.4
-
39
-
-
2342544143
-
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV. Discovery of 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]-4-[4-[2-methoxy-1(R) -4-(trifluoromethyl)phenyl]ethyl-3(S)-methyl-1-piperaz inyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective, and orally bioavailable CCR5 antagonist
-
Tagat, J. R., S. W. McCombie, D. Nazareno, M. A. Labroli, Y. Xiao, R. W. Steensma, J. M. Strizki, B. M. Baroudy, K. Cox, J. Lachowicz, G. Varty, and R. Watkins. 2004. Piperazine-based CCR5 antagonists as HIV-1 inhibitors. IV. Discovery of 1-[(4,6-dimethyl-5-pyrimidinyl)carbonyl]-4-[4-[2-methoxy-1(R)-4- (trifluoromethyl)phenyl]ethyl-3(S)-methyl-1-piperaz inyl]-4-methylpiperidine (Sch-417690/Sch-D), a potent, highly selective, and orally bioavailable CCR5 antagonist. J. Med. Chem. 47:2405-2408.
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2405-2408
-
-
Tagat, J.R.1
McCombie, S.W.2
Nazareno, D.3
Labroli, M.A.4
Xiao, Y.5
Steensma, R.W.6
Strizki, J.M.7
Baroudy, B.M.8
Cox, K.9
Lachowicz, J.10
Varty, G.11
Watkins, R.12
-
40
-
-
23044515844
-
Highly potent inhibition of human immunodeficiency virus type 1 replication by TAK-220, an orally bioavailable small-molecule CCR5 antagonist
-
Takashima, K., H. Miyake, N. Kanzaki, Y. Tagawa, X. Wang, Y. Sugihara, Y. Iizawa, and M. Baba. 2005. Highly potent inhibition of human immunodeficiency virus type 1 replication by TAK-220, an orally bioavailable small-molecule CCR5 antagonist. Antimicrob. Agents Chemother. 49:3474-3482.
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 3474-3482
-
-
Takashima, K.1
Miyake, H.2
Kanzaki, N.3
Tagawa, Y.4
Wang, X.5
Sugihara, Y.6
Iizawa, Y.7
Baba, M.8
-
41
-
-
0034298213
-
Strong in vitro synergy observed between the fusion inhibitor T-20 and a CXCR4 blocker AMD-3100
-
Tremblay, C., C. Kollman, F. Giguel, T. C. Chou, and M. S. Hirsch. 2000. Strong in vitro synergy observed between the fusion inhibitor T-20 and a CXCR4 blocker AMD-3100. J. Acquir. Immune Defic. Syndr. Hum. Retrovirol. 25:99-102.
-
(2000)
J. Acquir. Immune Defic. Syndr. Hum. Retrovirol.
, vol.25
, pp. 99-102
-
-
Tremblay, C.1
Kollman, C.2
Giguel, F.3
Chou, T.C.4
Hirsch, M.S.5
-
42
-
-
30444455633
-
TAK-652, a novel CCR5 inhibitor, has favourable drug interactions with other antiretrovirals in vitro
-
Tremblay, C. L., F. Giguel, T. C. Chou, H. Dong, K. Takashima, and M. S. Hirsch. 2005. TAK-652, a novel CCR5 inhibitor, has favourable drug interactions with other antiretrovirals in vitro. Antivir. Ther. 10:967-968.
-
(2005)
Antivir. Ther.
, vol.10
, pp. 967-968
-
-
Tremblay, C.L.1
Giguel, F.2
Chou, T.C.3
Dong, H.4
Takashima, K.5
Hirsch, M.S.6
-
43
-
-
23044484979
-
TAK-220, a novel small-molecule CCR5 antagonist, has favorable anti-human immunodeficiency virus interactions with other antiretrovirals in vitro
-
Tremblay, C. L., F. Giguel, Y. Guan, T.-C. Chou, K. Takashima, and M. S. Hirsch. 2005. TAK-220, a novel small-molecule CCR5 antagonist, has favorable anti-human immunodeficiency virus interactions with other antiretrovirals in vitro. Antimicrob. Agents Chemother. 49:3483-3485.
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 3483-3485
-
-
Tremblay, C.L.1
Giguel, F.2
Guan, Y.3
Chou, T.-C.4
Takashima, K.5
Hirsch, M.S.6
-
44
-
-
0036232981
-
Anti-human immunodeficiency virus interactions of SCH-C (SCH 351125), a CCR5 antagonist, with other antiretroviral agents in vitro
-
Tremblay, C. L., F. Giguel, C. Kollmann, Y. Guan, T.-C. Chou, B. M. Baroudy, and M. S. Hirsch. 2002. Anti-human immunodeficiency virus interactions of SCH-C (SCH 351125), a CCR5 antagonist, with other antiretroviral agents in vitro. Antimicrob. Agents Chemother. 46:1336-1339.
-
(2002)
Antimicrob. Agents Chemother.
, vol.46
, pp. 1336-1339
-
-
Tremblay, C.L.1
Giguel, F.2
Kollmann, C.3
Guan, Y.4
Chou, T.-C.5
Baroudy, B.M.6
Hirsch, M.S.7
-
45
-
-
0035173073
-
Potent, broad-spectrum inhibition of human immunodeficiency virus type 1 by the CCR5 monoclonal antibody PRO 140
-
Trkola, A., T. J. Ketas, K. A. Nagashima, L. Zhao, T. Cilliers, L. Morris, J. P. Moore, P. J. Maddon, and W. C. Olson. 2001. Potent, broad-spectrum inhibition of human immunodeficiency virus type 1 by the CCR5 monoclonal antibody PRO 140. J. Virol. 75:579-588.
-
(2001)
J. Virol.
, vol.75
, pp. 579-588
-
-
Trkola, A.1
Ketas, T.J.2
Nagashima, K.A.3
Zhao, L.4
Cilliers, T.5
Morris, L.6
Moore, J.P.7
Maddon, P.J.8
Olson, W.C.9
-
46
-
-
0032828730
-
A cell line-based neutralization assay for primary human immunodeficiency virus type 1 isolates that use either the CCR5 or the CXCR4 coreceptor
-
Trkola, A., J. Matthews, C. Gordon, T. Ketas, and J. P. Moore. 1999. A cell line-based neutralization assay for primary human immunodeficiency virus type 1 isolates that use either the CCR5 or the CXCR4 coreceptor. J. Virol. 73:8966-8974.
-
(1999)
J. Virol.
, vol.73
, pp. 8966-8974
-
-
Trkola, A.1
Matthews, J.2
Gordon, C.3
Ketas, T.4
Moore, J.P.5
-
47
-
-
0037404511
-
Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry
-
Tsamis, F., S. Gavrilov, F. Kajumo, C. Seibert, S. Kuhmann, T. Ketas, A. Trkola, A. Palani, J. W. Clader, J. R. Tagat, S. McCombie, B. Baroudy, J. P. Moore, T. P. Sakmar, and T. Dragic. 2003. Analysis of the mechanism by which the small-molecule CCR5 antagonists SCH-351125 and SCH-350581 inhibit human immunodeficiency virus type 1 entry. J. Virol. 77:5201-5208.
-
(2003)
J. Virol.
, vol.77
, pp. 5201-5208
-
-
Tsamis, F.1
Gavrilov, S.2
Kajumo, F.3
Seibert, C.4
Kuhmann, S.5
Ketas, T.6
Trkola, A.7
Palani, A.8
Clader, J.W.9
Tagat, J.R.10
McCombie, S.11
Baroudy, B.12
Moore, J.P.13
Sakmar, T.P.14
Dragic, T.15
-
48
-
-
15744391870
-
The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor
-
Watson, C., S. Jenkinson, W. Kazmierski, and T. Kenakin. 2005. The CCR5 receptor-based mechanism of action of 873140, a potent allosteric noncompetitive HIV entry inhibitor. Mol. Pharmacol. 67:1268-1282.
-
(2005)
Mol. Pharmacol.
, vol.67
, pp. 1268-1282
-
-
Watson, C.1
Jenkinson, S.2
Kazmierski, W.3
Kenakin, T.4
-
49
-
-
0026465468
-
A synthetic peptide inhibitor of human immunodeficiency virus replication: Correlation between solution structure and viral inhibition
-
Wild, C., T. Oas, C. McDanal, D. Bolognesi, and T. Matthews. 1992. A synthetic peptide inhibitor of human immunodeficiency virus replication: correlation between solution structure and viral inhibition. Proc. Natl. Acad. Sci. USA 89:10537-10541.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 10537-10541
-
-
Wild, C.1
Oas, T.2
McDanal, C.3
Bolognesi, D.4
Matthews, T.5
|