-
1
-
-
77249134151
-
Twenty-six years of anti-HIV drug discovery: Where do we stand and where do we go?
-
Mehellou, Y.; De Clercq, E. Twenty-six years of anti-HIV drug discovery: where do we stand and where do we go? J. Med. Chem. 2010, 53, 521-38
-
(2010)
J. Med. Chem.
, vol.53
, pp. 521-538
-
-
Mehellou, Y.1
De Clercq, E.2
-
2
-
-
15844419153
-
Identification of a major co-receptor for primary isolates of HIV-1
-
DOI 10.1038/381661a0
-
Deng, H.; Liu, R.; Ellmeier, W.; Choe, S.; Unutmaz, D.; Burkhart, M.; Di Marzio, P.; Marmon, S.; Sutton, R. E.; Hill, C. M.; Davis, C. B.; Peiper, S. C.; Schall, T. J.; Littman, D. R.; Landau, N. R. Identification of a major co-receptor for primary isolates of HIV-1 Nature 1996, 381, 661-6 (Pubitemid 26197679)
-
(1996)
Nature
, vol.381
, Issue.6584
, pp. 661-666
-
-
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.E.9
Mark Hill, C.10
Davis, C.B.11
Peiper, S.C.12
Schall, T.J.13
Littman, D.R.14
Landau, N.R.15
-
3
-
-
15844389650
-
+ cells is mediated by the chemokine receptor CC-CKR-5
-
DOI 10.1038/381667a0
-
Dragic, T.; Litwin, V.; Allaway, G. P.; Martin, S. R.; Huang, Y.; Nagashima, K. A.; Cayanan, C.; Maddon, P. J.; Koup, R. A.; Moore, J. P.; Paxton, W. A. HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5 Nature 1996, 381, 667-73 (Pubitemid 26197680)
-
(1996)
Nature
, vol.381
, Issue.6584
, 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
-
4
-
-
0030932188
-
Chemokine receptors as fusion cofactors fat human immunodeficiency virus type 1 (HIV-1)
-
Doranz, B. J.; Berson, J. F.; Rucker, J.; Doms, R. W. Chemokine receptors as fusion cofactors for human immunodeficiency virus type 1 (HIV-1) Immunol. Res. 1997, 16, 15-28 (Pubitemid 27129627)
-
(1997)
Immunologic Research
, vol.16
, Issue.1
, pp. 15-28
-
-
Doranz, B.J.1
Berson, J.F.2
Rucker, J.3
Doms, R.W.4
-
6
-
-
35549007987
-
CCR5 antagonists in the treatment of treatment-naive patients infected with CCR5 tropic HIV-1
-
Bredeek, U. F.; Harbour, M. J. CCR5 antagonists in the treatment of treatment-naive patients infected with CCR5 tropic HIV-1 Eur. J. Med. Res. 2007, 12, 427-34 (Pubitemid 350011455)
-
(2007)
European Journal of Medical Research
, vol.12
, Issue.9
, pp. 427-434
-
-
Bredeek, U.F.1
Harbour, M.J.2
-
8
-
-
77953616686
-
Pharmacotherapy of HIV-1 Infection: Focus on CCR5 Antagonist Maraviroc
-
Latinovic, O.; Kuruppu, J.; Davis, C.; Le, N.; Heredia, A. Pharmacotherapy of HIV-1 Infection: Focus on CCR5 Antagonist Maraviroc Clin. Med. Ther. 2009, 1, 1497-1510
-
(2009)
Clin. Med. Ther.
, vol.1
, pp. 1497-1510
-
-
Latinovic, O.1
Kuruppu, J.2
Davis, C.3
Le, N.4
Heredia, A.5
-
9
-
-
84864658614
-
Update on clinical and methodological recommendations for genotypic determination of HIV tropism to guide the usage of CCR5 antagonists
-
Poveda, E.; Paredes, R.; Moreno, S.; Alcami, J.; Cordoba, J.; Delgado, R.; Gutierrez, F.; Llibre, J. M.; Garcia Deltoro, M.; Hernandez-Quero, J.; Pulido, F.; Iribarren, J. A.; Garcia, F. Update on clinical and methodological recommendations for genotypic determination of HIV tropism to guide the usage of CCR5 antagonists AIDS Rev. 2012, 14, 208-17
-
(2012)
AIDS Rev.
, vol.14
, pp. 208-217
-
-
Poveda, E.1
Paredes, R.2
Moreno, S.3
Alcami, J.4
Cordoba, J.5
Delgado, R.6
Gutierrez, F.7
Llibre, J.M.8
Garcia Deltoro, M.9
Hernandez-Quero, J.10
Pulido, F.11
Iribarren, J.A.12
Garcia, F.13
-
10
-
-
84863680262
-
Blockade of lymphocyte chemotaxis in visceral graft-versus-host disease
-
Reshef, R.; Luger, S. M.; Hexner, E. O.; Loren, A. W.; Frey, N. V.; Nasta, S. D.; Goldstein, S. C.; Stadtmauer, E. A.; Smith, J.; Bailey, S.; Mick, R.; Heitjan, D. F.; Emerson, S. G.; Hoxie, J. A.; Vonderheide, R. H.; Porter, D. L. Blockade of lymphocyte chemotaxis in visceral graft-versus-host disease N. Engl. J. Med. 2012, 367, 135-45
-
(2012)
N. Engl. J. Med.
, vol.367
, pp. 135-145
-
-
Reshef, R.1
Luger, S.M.2
Hexner, E.O.3
Loren, A.W.4
Frey, N.V.5
Nasta, S.D.6
Goldstein, S.C.7
Stadtmauer, E.A.8
Smith, J.9
Bailey, S.10
Mick, R.11
Heitjan, D.F.12
Emerson, S.G.13
Hoxie, J.A.14
Vonderheide, R.H.15
Porter, D.L.16
-
11
-
-
84871814560
-
CCR5 is a receptor for Staphylococcus aureus leukotoxin ED
-
Alonzo, F., 3rd; Kozhaya, L.; Rawlings, S. A.; Reyes-Robles, T.; DuMont, A. L.; Myszka, D. G.; Landau, N. R.; Unutmaz, D.; Torres, V. J. CCR5 is a receptor for Staphylococcus aureus leukotoxin ED Nature 2013, 493, 51-5
-
(2013)
Nature
, vol.493
, pp. 51-55
-
-
Kozhaya, L.1
Rawlings, S.A.2
Reyes-Robles, T.3
Dumont, A.L.4
Myszka, D.G.5
Landau, N.R.6
Unutmaz, D.7
Torres, V.J.8
-
12
-
-
0038641840
-
Chemically programmed monoclonal antibodies for cancer therapy: Adaptor immunotherapy based on a covalent antibody catalyst
-
DOI 10.1073/pnas.0931308100
-
Rader, C.; Sinha, S. C.; Popkov, M.; Lerner, R. A.; Barbas, C. F., 3rd Chemically programmed monoclonal antibodies for cancer therapy: adaptor immunotherapy based on a covalent antibody catalyst Proc. Natl. Acad. Sci. U. S. A. 2003, 100, 5396-400 (Pubitemid 36542716)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.9
, pp. 5396-5400
-
-
Rader, C.1
Sinha, S.C.2
Popkov, M.3
Lerner, R.A.4
Barbas III, C.F.5
-
13
-
-
33746344379
-
Small molecule drug activity in melanoma models may be dramatically enhanced with an antibody effector
-
DOI 10.1002/ijc.21924
-
Popkov, M.; Rader, C.; Gonzalez, B.; Sinha, S. C.; Barbas, C. F., 3rd. Small molecule drug activity in melanoma models may be dramatically enhanced with an antibody effector Int. J. Cancer 2006, 119, 1194-207 (Pubitemid 44116929)
-
(2006)
International Journal of Cancer
, vol.119
, Issue.5
, pp. 1194-1207
-
-
Popkov, M.1
Rader, C.2
Gonzalez, B.3
Sinha, S.C.4
Barbas III, C.F.5
-
14
-
-
60449100413
-
Beta-lactam-based approach for the chemical programming of aldolase antibody 38C2
-
Gavrilyuk, J. I.; Wuellner, U.; Barbas, C. F., 3rd Beta-lactam-based approach for the chemical programming of aldolase antibody 38C2 Bioorg. Med. Chem. Lett. 2009, 19, 1421-4
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 1421-1424
-
-
Gavrilyuk, J.I.1
Wuellner, U.2
Barbas III, C.F.3
-
15
-
-
77955575201
-
Expanding the concept of chemically programmable antibodies to RNA aptamers: Chemically programmed biotherapeutics
-
Wuellner, U.; Gavrilyuk, J. I.; Barbas, C. F., 3rd Expanding the concept of chemically programmable antibodies to RNA aptamers: chemically programmed biotherapeutics Angew. Chem., Int. Ed. Engl. 2010, 49, 5934-7
-
(2010)
Angew. Chem., Int. Ed. Engl.
, vol.49
, pp. 5934-5937
-
-
Wuellner, U.1
Gavrilyuk, J.I.2
Barbas III, C.F.3
-
16
-
-
79751517940
-
Potent inhibition of HIV-1 entry with a chemically programmed antibody aided by an efficient organocatalytic synthesis
-
Gavrilyuk, J.; Uehara, H.; Otsubo, N.; Hessell, A.; Burton, D. R.; Barbas, C. F., 3rd Potent inhibition of HIV-1 entry with a chemically programmed antibody aided by an efficient organocatalytic synthesis ChemBioChem 2010, 11, 2113-8
-
(2010)
ChemBioChem
, vol.11
, pp. 2113-2118
-
-
Gavrilyuk, J.1
Uehara, H.2
Otsubo, N.3
Hessell, A.4
Burton, D.R.5
Barbas III, C.F.6
-
17
-
-
79952271693
-
Specifically targeting angiopoietin-2 inhibits angiogenesis, Tie2-expressing monocyte infiltration, and tumor growth
-
Huang, H.; Lai, J. Y.; Do, J.; Liu, D.; Li, L.; Del Rosario, J.; Doppalapudi, V. R.; Pirie-Shepherd, S.; Levin, N.; Bradshaw, C.; Woodnutt, G.; Lappe, R.; Bhat, A. Specifically targeting angiopoietin-2 inhibits angiogenesis, Tie2-expressing monocyte infiltration, and tumor growth Clin. Cancer Res.: Off. J. Am. Assoc. Cancer Res. 2011, 17, 1001-11
-
(2011)
Clin. Cancer Res.: Off. J. Am. Assoc. Cancer Res.
, vol.17
, pp. 1001-1011
-
-
Huang, H.1
Lai, J.Y.2
Do, J.3
Liu, D.4
Li, L.5
Del Rosario, J.6
Doppalapudi, V.R.7
Pirie-Shepherd, S.8
Levin, N.9
Bradshaw, C.10
Woodnutt, G.11
Lappe, R.12
Bhat, A.13
-
18
-
-
84867214330
-
A chemically programmed antibody is a long-lasting and potent inhibitor of influenza neuraminidase
-
Hayakawa, M.; Toda, N.; Carrillo, N.; Thornburg, N. J.; Crowe, J. E., Jr.; Barbas, C. F., 3rd A chemically programmed antibody is a long-lasting and potent inhibitor of influenza neuraminidase ChemBioChem 2012, 13, 2191-5
-
(2012)
ChemBioChem
, vol.13
, pp. 2191-2195
-
-
Hayakawa, M.1
Toda, N.2
Carrillo, N.3
Thornburg, N.J.4
Crowe, Jr.J.E.5
Barbas III, C.F.6
-
19
-
-
84877708005
-
Chemically Programmed Antibodies as HIV-1 Attachment Inhibitors
-
Sato, S.; Inokuma, T.; Otsubo, N.; Burton, D. R.; Barbas, C. F., 3rd. Chemically Programmed Antibodies as HIV-1 Attachment Inhibitors ACS Med. Chem. Lett. 2013, 4, 460-465
-
(2013)
ACS Med. Chem. Lett.
, vol.4
, pp. 460-465
-
-
Sato, S.1
Inokuma, T.2
Otsubo, N.3
Burton, D.R.4
-
20
-
-
0029590066
-
Efficient aldolase catalytic antibodies that use the enamine mechanism of natural enzymes
-
Wagner, J.; Lerner, R. A.; Barbas, C. F., 3rd Efficient aldolase catalytic antibodies that use the enamine mechanism of natural enzymes Science 1995, 270, 1797-800 (Pubitemid 26007222)
-
(1995)
Science
, vol.270
, Issue.5243
, pp. 1797-1800
-
-
Wagner, J.1
Lerner, R.A.2
Barbas III, C.F.3
-
21
-
-
0033576651
-
Broadening the aldolase catalytic antibody repertoire by combining reactive immunization and transition state theory: New enantio- and diastereoselectivities
-
DOI 10.1002 /(SICI) 1521-3773 (19991216)38:24<3738::AID-ANIE3738>3. 0.CO;2-2
-
Zhong, G.; Lerner, R. A.; Barbas, I. C. Broadening the Aldolase Catalytic Antibody Repertoire by Combining Reactive Immunization and Transition State Theory: New Enantio- and Diastereoselectivities Angew. Chem., Int. Ed. Engl. 1999, 38, 3738-3741 (Pubitemid 30022002)
-
(1999)
Angewandte Chemie - International Edition
, vol.38
, Issue.24
, pp. 3738-3741
-
-
Zhong, G.1
Lerner, R.A.2
Barbas III, C.F.3
-
22
-
-
0033536048
-
Multiple event activation of a generic prodrug trigger by antibody catalysis
-
DOI 10.1073/pnas.96.12.6925
-
Shabat, D.; Rader, C.; List, B.; Lerner, R. A.; Barbas, C. F., 3rd. Multiple event activation of a generic prodrug trigger by antibody catalysis Proc. Natl. Acad. Sci. U. S. A. 1999, 96, 6925-30 (Pubitemid 29274986)
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, Issue.12
, pp. 6925-6930
-
-
Shabat, D.1
Rader, C.2
List, B.3
Lerner, R.A.4
Barbas III, C.F.5
-
23
-
-
0032833799
-
27-35 peptide: Implications for peptide vaccines
-
DOI 10.1002 /(SICI) 1097-0215 (19991029)83:3<326::AID-IJC7>3.0. CO;2-X
-
Brinckerhoff, L. H.; Kalashnikov, V. V.; Thompson, L. W.; Yamshchikov, G. V.; Pierce, R. A.; Galavotti, H. S.; Engelhard, V. H.; Slingluff, C. L., Jr. Terminal modifications inhibit proteolytic degradation of an immunogenic MART-1(27-35) peptide: implications for peptide vaccines Int. J. Cancer 1999, 83, 326-34 (Pubitemid 29455755)
-
(1999)
International Journal of Cancer
, vol.83
, Issue.3
, pp. 326-334
-
-
Brinckerhoff, L.H.1
Kalashnikov, V.V.2
Thompson, L.W.3
Yamshchikov, G.V.4
Pierce, R.A.5
Galavotti, H.S.6
Engelhard, V.H.7
Slingluff Jr., C.L.8
-
24
-
-
0030843862
-
Poly(ethylene glycol) modification of β-glucuronidase-antibody conjugates for solid-tumor therapy by targeted activation of glucuronide prodrugs
-
DOI 10.1007/s002620050387
-
Cheng, T. L.; Chen, B. M.; Chan, L. Y.; Wu, P. Y.; Chern, J. W.; Roffler, S. R. Poly(ethylene glycol) modification of beta-glucuronidase-antibody conjugates for solid-tumor therapy by targeted activation of glucuronide prodrugs Cancer Immunol. Immunother. 1997, 44, 305-15 (Pubitemid 27364610)
-
(1997)
Cancer Immunology Immunotherapy
, vol.44
, Issue.6
, pp. 305-315
-
-
Cheng, T.-L.1
Chen, B.-M.2
Chan, L.-Y.3
Wu, P.-Y.4
Chern, J.-W.5
Roffler, S.R.6
-
25
-
-
0026659050
-
IgG antibody response to polyethylene glycol-modified adenosine deaminase in patients with adenosine deaminase deficiency
-
Chaffee, S.; Mary, A.; Stiehm, E. R.; Girault, D.; Fischer, A.; Hershfield, M. S. IgG antibody response to polyethylene glycol-modified adenosine deaminase in patients with adenosine deaminase deficiency J. Clin. Invest. 1992, 89, 1643-51
-
(1992)
J. Clin. Invest.
, vol.89
, pp. 1643-1651
-
-
Chaffee, S.1
Mary, A.2
Stiehm, E.R.3
Girault, D.4
Fischer, A.5
Hershfield, M.S.6
-
26
-
-
0037124398
-
Structural and biological characterization of pegylated recombinant interferon alpha-2b and its therapeutic implications
-
DOI 10.1016/S0169-409X(02)00027-3, PII S0169409X02000273
-
Wang, Y. S.; Youngster, S.; Grace, M.; Bausch, J.; Bordens, R.; Wyss, D. F. Structural and biological characterization of pegylated recombinant interferon alpha-2b and its therapeutic implications Adv. Drug Delivery Rev. 2002, 54, 547-70 (Pubitemid 34618512)
-
(2002)
Advanced Drug Delivery Reviews
, vol.54
, Issue.4
, pp. 547-570
-
-
Wang, Y.-S.1
Youngster, S.2
Grace, M.3
Bausch, J.4
Bordens, R.5
Wyss, D.F.6
-
27
-
-
0029948533
-
Drug delivery systems. 2. Camptothecin 20-O-poly(ethylene glycol) ester transport forms
-
DOI 10.1021/jm9600555
-
Greenwald, R. B.; Pendri, A.; Conover, C.; Gilbert, C.; Yang, R.; Xia, J. Drug delivery systems. 2. Camptothecin 20-O-poly(ethylene glycol) ester transport forms J. Med. Chem. 1996, 39, 1938-40 (Pubitemid 26157293)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.10
, pp. 1938-1940
-
-
Greenwald, R.B.1
Pendri, A.2
Conover, C.3
Gilbert, C.4
Yang, R.5
Xia, J.6
-
28
-
-
19944434038
-
Design, synthesis, and analysis of a polyethelene glycol-modified (PEGylated) small molecule inhibitor of integrin α4β1 with improved pharmaceutical properties
-
DOI 10.1124/jpet.104.075648
-
Pepinsky, R. B.; Lee, W. C.; Cornebise, M.; Gill, A.; Wortham, K.; Chen, L. L.; Leone, D. R.; Giza, K.; Dolinski, B. M.; Perper, S.; Nickerson-Nutter, C.; Lepage, D.; Chakraborty, A.; Whalley, E. T.; Petter, R. C.; Adams, S. P.; Lobb, R. R.; Scott, D. M. Design, synthesis, and analysis of a polyethelene glycol-modified (PEGylated) small molecule inhibitor of integrin {alpha}4{beta}1 with improved pharmaceutical properties J. Pharmacol. Exp. Ther. 2005, 312, 742-50 (Pubitemid 40189574)
-
(2005)
Journal of Pharmacology and Experimental Therapeutics
, vol.312
, Issue.2
, pp. 742-750
-
-
Pepinsky, R.B.1
Lee, W.-C.2
Cornebise, M.3
Gill, A.4
Wortham, K.5
Chen, L.L.6
Leone, D.R.7
Giza, K.8
Dolinski, B.M.9
Perper, S.10
Nickerson-Nutter, C.11
Lepage, D.12
Chakraborty, A.13
Whalley, E.T.14
Petter, R.C.15
Adams, S.P.16
Lobb, R.R.17
Scott, D.M.18
-
29
-
-
40849098660
-
Molecular interactions of CCR5 with major classes of small-molecule anti-HIV CCR5 antagonists
-
DOI 10.1124/mol.107.042101
-
Kondru, R.; Zhang, J.; Ji, C.; Mirzadegan, T.; Rotstein, D.; Sankuratri, S.; Dioszegi, M. Molecular interactions of CCR5 with major classes of small-molecule anti-HIV CCR5 antagonists Mol. Pharmacol. 2008, 73, 789-800 (Pubitemid 351397884)
-
(2008)
Molecular Pharmacology
, vol.73
, Issue.3
, pp. 789-800
-
-
Kondru, R.1
Zhang, J.2
Ji, C.3
Mirzadegan, T.4
Rotstein, D.5
Sankuratri, S.6
Dioszegi, M.7
-
30
-
-
34347272702
-
Preparation of integrin α(v)β(3)-targeting Ab 38C2 constructs
-
DOI 10.1038/nprot.2007.3, PII NPROT.2007.3
-
Sinha, S. C.; Das, S.; Li, L. S.; Lerner, R. A.; Barbas, C. F., 3rd. Preparation of integrin alpha(v)beta3-targeting Ab 38C2 constructs Nat. Protoc. 2007, 2, 449-56 (Pubitemid 47040060)
-
(2007)
Nature Protocols
, vol.2
, Issue.2
, pp. 449-456
-
-
Sinha, S.C.1
Das, S.2
Li, L.-S.3
Lerner, R.A.4
Barbas III, C.F.5
-
31
-
-
27744548649
-
The discovery of the CCR5 receptor antagonist, UK-427,857, a new agent for the treatment of HIV infection and AIDS
-
Wood, A.; Armour, D. The discovery of the CCR5 receptor antagonist, UK-427,857, a new agent for the treatment of HIV infection and AIDS Prog. Med. Chem. 2005, 43, 239-71
-
(2005)
Prog. Med. Chem.
, vol.43
, pp. 239-271
-
-
Wood, A.1
Armour, D.2
-
32
-
-
0028337034
-
Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice
-
DOI 10.1002/jps.2600830432
-
Yamaoka, T.; Tabata, Y.; Ikada, Y. Distribution and tissue uptake of poly(ethylene glycol) with different molecular weights after intravenous administration to mice J. Pharm. Sci. 1994, 83, 601-6 (Pubitemid 24222392)
-
(1994)
Journal of Pharmaceutical Sciences
, vol.83
, Issue.4
, pp. 601-606
-
-
Yamaoka, T.1
Tabata, Y.2
Ikada, Y.3
-
33
-
-
0032211606
-
Polyethylene glycol-conjugated pharmaceutical proteins
-
Bailon, P. B. W. Polyethylene glycol-conjugated pharmaceutical proteins Pharm. Sci. Technol. Today 1998, 1, 352-356
-
(1998)
Pharm. Sci. Technol. Today
, vol.1
, pp. 352-356
-
-
Bailon, P.B.W.1
-
34
-
-
66249109940
-
Affinity and avidity in antibody-based tumor targeting
-
Rudnick, S. I.; Adams, G. P. Affinity and avidity in antibody-based tumor targeting Cancer Biother. Radiopharm. 2009, 24, 155-61
-
(2009)
Cancer Biother. Radiopharm.
, vol.24
, pp. 155-161
-
-
Rudnick, S.I.1
Adams, G.P.2
-
35
-
-
63149182641
-
Instant immunity through chemically programmable vaccination and covalent self-assembly
-
Popkov, M.; Gonzalez, B.; Sinha, S. C.; Barbas, C. F., 3rd. Instant immunity through chemically programmable vaccination and covalent self-assembly Proc. Natl. Acad. Sci. U. S. A. 2009, 106, 4378-83
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 4378-4383
-
-
Popkov, M.1
Gonzalez, B.2
Sinha, S.C.3
-
36
-
-
84876326554
-
Antibody conjugation approach enhances breadth and potency of neutralization of anti-HIV-1 antibodies and CD4-IgG
-
Gavrilyuk, J.; Ban, H.; Uehara, H.; Sirk, S. J.; Saye-Francisco, K.; Cuevas, A.; Zablowsky, E.; Oza, A.; Seaman, M. S.; Burton, D. R.; Barbas, C. F., 3rd. Antibody conjugation approach enhances breadth and potency of neutralization of anti-HIV-1 antibodies and CD4-IgG J. Virol. 2013, 87, 4985-93
-
(2013)
J. Virol.
, vol.87
, pp. 4985-4993
-
-
Gavrilyuk, J.1
Ban, H.2
Uehara, H.3
Sirk, S.J.4
Saye-Francisco, K.5
Cuevas, A.6
Zablowsky, E.7
Oza, A.8
Seaman, M.S.9
Burton, D.R.10
|