-
1
-
-
36749073433
-
The design of drugs for HIV and HCV
-
De Clercq E: The design of drugs for HIV and HCV. Nat. Rev. Drug Discov. 6, 1001-1018 (2007).
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 1001-1018
-
-
De Clercq, E.1
-
2
-
-
36749088862
-
HIV drug development: The next 25 years
-
Flexner C: HIV drug development: the next 25 years. Nat. Rev. Drug Discov. 6, 959-966 (2007).
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 959-966
-
-
Flexner, C.1
-
3
-
-
36749037438
-
From adefovir to Atripla™ via tenofovir, Viread™ and Truvada™
-
De Clercq E: From adefovir to Atripla™ via tenofovir, Viread™ and Truvada™. Future Virol. 1, 709-715 (2006).
-
(2006)
Future Virol
, vol.1
, pp. 709-715
-
-
De Clercq, E.1
-
4
-
-
38549137325
-
Antiviral treatment of chronic hepatitis B virus infections: The past, the present and the future
-
Ferir G, Kaptein S, Neyts J, De Clercq E: Antiviral treatment of chronic hepatitis B virus infections: the past, the present and the future. Rev Med. Virol. 18, 19-34 (2008).
-
(2008)
Rev Med. Virol
, vol.18
, pp. 19-34
-
-
Ferir, G.1
Kaptein, S.2
Neyts, J.3
De Clercq, E.4
-
5
-
-
34948857943
-
Evaluation of hexadecyloxypropyl-9-R-[2-(Phosphonomethoxy)propyl]-adenine, CMX157, as a potential treatment for human immunodeficiency virus type 1 and hepatitis B virus infections
-
Painter GR, Almond MR, Trost LC et al.: Evaluation of hexadecyloxypropyl-9-R-[2-(Phosphonomethoxy)propyl]-adenine, CMX157, as a potential treatment for human immunodeficiency virus type 1 and hepatitis B virus infections. Antimicrob. Agents Chemother. 51, 3505-3509 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 3505-3509
-
-
Painter, G.R.1
Almond, M.R.2
Trost, L.C.3
-
6
-
-
0347928672
-
Inhibition of hepatitis B virus replication by drug-induced depletion of nucleocapsids
-
Deres K, Schröder CH, Paessens A et al.: Inhibition of hepatitis B virus replication by drug-induced depletion of nucleocapsids. Science 299, 893-896 (2003).
-
(2003)
Science
, vol.299
, pp. 893-896
-
-
Deres, K.1
Schröder, C.H.2
Paessens, A.3
-
7
-
-
0344131411
-
Development of resistance and perspectives for future therapies against hepatitis B infections: Lessons to be learned from HIV
-
Deres K, Rübsamen-Waigmann H: Development of resistance and perspectives for future therapies against hepatitis B infections: lessons to be learned from HIV. Infection 27, S45-S51 (1999).
-
(1999)
Infection
, vol.27
-
-
Deres, K.1
Rübsamen-Waigmann, H.2
-
8
-
-
33751517736
-
Antiviral agents active against influenza A viruses
-
De Clercq E: Antiviral agents active against influenza A viruses. Nat. Rev. Drug Discov. 5, 1015-1025 (2006).
-
(2006)
Nat. Rev. Drug Discov
, vol.5
, pp. 1015-1025
-
-
De Clercq, E.1
-
9
-
-
36749056771
-
The war against influenza: Discovery and development of sialidase inhibitors
-
von Itzstein M: The war against influenza: discovery and development of sialidase inhibitors. Nat. Rev. Drug Discov. 6, 967-974 (2007).
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 967-974
-
-
von Itzstein, M.1
-
11
-
-
27844455955
-
Acyclic nucleoside phosphonates: A key class of antiviral drugs
-
De Clercq E, Holy A: Acyclic nucleoside phosphonates: a key class of antiviral drugs. Nat. Rev. Drug Discov. 4, 928-940 (2005).
-
(2005)
Nat. Rev. Drug Discov
, vol.4
, pp. 928-940
-
-
De Clercq, E.1
Holy, A.2
-
12
-
-
38649102173
-
Cidofovir and (S)-9-[3-hydroxy-(2-phosphonomethoxy)propyl]adenine are highly effective inhibitors of vaccinia virus DNA polymerase when incorporated into the template strand
-
Magee WC, Aldern KA, Hostetler KY, Evans DH: Cidofovir and (S)-9-[3-hydroxy-(2-phosphonomethoxy)propyl]adenine are highly effective inhibitors of vaccinia virus DNA polymerase when incorporated into the template strand. Antimicrob. Agents Chemother. 52, 586-597 (2008).
-
(2008)
Antimicrob. Agents Chemother
, vol.52
, pp. 586-597
-
-
Magee, W.C.1
Aldern, K.A.2
Hostetler, K.Y.3
Evans, D.H.4
-
13
-
-
26444587116
-
An orally bioavailable antipoxvirus compound (ST-246) inhibits extracellular virus formation and protects mice from lethal orthopoxvirus challenge
-
Yang G, Pevear DC, Davies MH et al.: An orally bioavailable antipoxvirus compound (ST-246) inhibits extracellular virus formation and protects mice from lethal orthopoxvirus challenge. J. Virol. 79, 13139-13149 (2005).
-
(2005)
J. Virol
, vol.79
, pp. 13139-13149
-
-
Yang, G.1
Pevear, D.C.2
Davies, M.H.3
-
14
-
-
33846623695
-
Efficacy of delayed treatment with ST-246 given orally against systemic orthopoxvirus infections in mice
-
Quenelle DC, Buller RML, Parker S et al.: Efficacy of delayed treatment with ST-246 given orally against systemic orthopoxvirus infections in mice. Antimicrob. Agents Chemother. 51, 689-695 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 689-695
-
-
Quenelle, D.C.1
Buller, R.M.L.2
Parker, S.3
-
15
-
-
34249742507
-
Efficacy of the antipoxvirus compound ST-246 for treatment of severe orthopoxvirus infection
-
Sbrana E, Jordan R, Hruby DE et al.: Efficacy of the antipoxvirus compound ST-246 for treatment of severe orthopoxvirus infection. Am. J. Trop. Med. Hyg. 76, 768-773 (2007).
-
(2007)
Am. J. Trop. Med. Hyg
, vol.76
, pp. 768-773
-
-
Sbrana, E.1
Jordan, R.2
Hruby, D.E.3
-
16
-
-
14944382916
-
Antiviral chemotherapy facilitates control of poxvirus infections through inhibition of cellular signal transduction
-
Yang H, Kim SK, Kim M et al.: Antiviral chemotherapy facilitates control of poxvirus infections through inhibition of cellular signal transduction. J. Clin. Invest. 115, 379-387 (2005).
-
(2005)
J. Clin. Invest
, vol.115
, pp. 379-387
-
-
Yang, H.1
Kim, S.K.2
Kim, M.3
-
17
-
-
22544470270
-
Disabling poxvirus pathogenesis by inhibition of Abi-family tyrosine kinases
-
Reeves PM, Bommarius B, Lebeis S et al.: Disabling poxvirus pathogenesis by inhibition of Abi-family tyrosine kinases. Nat. Med. 11, 731-739 (2005).
-
(2005)
Nat. Med
, vol.11
, pp. 731-739
-
-
Reeves, P.M.1
Bommarius, B.2
Lebeis, S.3
-
18
-
-
36749040780
-
Activities of several classes of acyclic nucleoside phosphonates against camelpox virus replication in different cell culture models
-
Duraffour S, Snoeck R, Kremerová M et al.: Activities of several classes of acyclic nucleoside phosphonates against camelpox virus replication in different cell culture models. Antimicrob. Agents Chemother. 51, 4410-4419 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 4410-4419
-
-
Duraffour, S.1
Snoeck, R.2
Kremerová, M.3
-
19
-
-
35848929516
-
Effect of oral treatment with hexadecyloxypropyl-[(S)-9-(3-hydroxy-2- phosphonylmethoxypropyl)adenine] [(S)-HPMPA] or octadecyloxyethyl-(S)-HPMPA on cowpox or vaccinia virus infections in mice
-
Quenelle DC, Collins DJ, Herrod BP et al.: Effect of oral treatment with hexadecyloxypropyl-[(S)-9-(3-hydroxy-2- phosphonylmethoxypropyl)adenine] [(S)-HPMPA] or octadecyloxyethyl-(S)-HPMPA on cowpox or vaccinia virus infections in mice. Antimicrob. Agents Chemother., 3940-3947 (2007).
-
(2007)
Antimicrob. Agents Chemother
, pp. 3940-3947
-
-
Quenelle, D.C.1
Collins, D.J.2
Herrod, B.P.3
-
20
-
-
33847083535
-
-
Hostetler KY, Beadle JR, Trahan J et al.: Oral 1-O-octadecyl-2-[i O-benzyl-sn-glycero-3-cidofovir targets the lung and is effective against a lethal respiratory challenge with ectromelia virus in mice. Antiviral Res. 73, 212-218 (2007).
-
Hostetler KY, Beadle JR, Trahan J et al.: Oral 1-O-octadecyl-2-[i O-benzyl-sn-glycero-3-cidofovir targets the lung and is effective against a lethal respiratory challenge with ectromelia virus in mice. Antiviral Res. 73, 212-218 (2007).
-
-
-
-
21
-
-
35848968505
-
Synergistic efficacy of the combination of ST-246 with CMX001 against orthopoxviruses
-
Quenelle DC, Prichard MN, Keith KA et al.: Synergistic efficacy of the combination of ST-246 with CMX001 against orthopoxviruses. Antimicrob. Agents Chemother. 51, 4118-4124 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 4118-4124
-
-
Quenelle, D.C.1
Prichard, M.N.2
Keith, K.A.3
-
22
-
-
35948949782
-
RSV604, a novel inhibitor of respiratory syncytial virus replication
-
Chapman J, Abbott E, Alber DG et al.: RSV604, a novel inhibitor of respiratory syncytial virus replication. Antimicrob. Agents Chemother. 51, 3346-3353 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 3346-3353
-
-
Chapman, J.1
Abbott, E.2
Alber, D.G.3
-
23
-
-
0036107516
-
Herpes simplex virus helicase-primase inhibitors are active in animal models of human disease
-
Crute JJ, Grygon CA, Hargrave KD et al.: Herpes simplex virus helicase-primase inhibitors are active in animal models of human disease. Nat. Med. 8, 386-391 (2002).
-
(2002)
Nat. Med
, vol.8
, pp. 386-391
-
-
Crute, J.J.1
Grygon, C.A.2
Hargrave, K.D.3
-
24
-
-
0036111626
-
New helicase-primase inhibitors as drug candidates for the treatment of herpes simplex disease
-
Kleymann G, Fischer R, Betz UA et al.: New helicase-primase inhibitors as drug candidates for the treatment of herpes simplex disease. Nat. Med. 8, 392-398 (2002).
-
(2002)
Nat. Med
, vol.8
, pp. 392-398
-
-
Kleymann, G.1
Fischer, R.2
Betz, U.A.3
-
25
-
-
0036093580
-
Potent in vivo antiviral activity of the herpes simplex virus primase-helicase inhibitor BAY 57-1293
-
Betz UA, Fischer R, Kleymann G, Hendrix M, Rübsamen-Waigmann H: Potent in vivo antiviral activity of the herpes simplex virus primase-helicase inhibitor BAY 57-1293. Antimicrob. Agents Chemother. 46, 1766-1772 (2002).
-
(2002)
Antimicrob. Agents Chemother
, vol.46
, pp. 1766-1772
-
-
Betz, U.A.1
Fischer, R.2
Kleymann, G.3
Hendrix, M.4
Rübsamen-Waigmann, H.5
-
26
-
-
33947286682
-
Superior efficacy of helicase-primase inhibitor BAY 57-1293 for herpes infection and latency in the guinea pig model of human genital herpes disease
-
Baumeister J, Fischer R, Eckenberg P, Henninger K, Ruebsamen-Waigmann H, Kleymann G: Superior efficacy of helicase-primase inhibitor BAY 57-1293 for herpes infection and latency in the guinea pig model of human genital herpes disease. Antiviral Chem. Chemother. 18, 35-48 (2007).
-
(2007)
Antiviral Chem. Chemother
, vol.18
, pp. 35-48
-
-
Baumeister, J.1
Fischer, R.2
Eckenberg, P.3
Henninger, K.4
Ruebsamen-Waigmann, H.5
Kleymann, G.6
-
27
-
-
33947241644
-
The helicase primase inhibitor, BAY 57-1293 shows potent therapeutic antiviral activity superior to famciclovir in BALB/c mice infected with herpes simplex virus type 1
-
Biswas S, Jennens L, Field HJ: The helicase primase inhibitor, BAY 57-1293 shows potent therapeutic antiviral activity superior to famciclovir in BALB/c mice infected with herpes simplex virus type 1. Antiviral Res. 75, 30-35 (2007).
-
(2007)
Antiviral Res
, vol.75
, pp. 30-35
-
-
Biswas, S.1
Jennens, L.2
Field, H.J.3
-
28
-
-
8644267364
-
Isolation and characterization of herpes simplex virus type 1 resistant to aminothiazolylphenyl-based inhibitors of the viral helicase-primase
-
Liuzzi M, Kibler P, Bousquet C et al.: Isolation and characterization of herpes simplex virus type 1 resistant to aminothiazolylphenyl-based inhibitors of the viral helicase-primase. Antiviral Res. 64, 161-170 (2004).
-
(2004)
Antiviral Res
, vol.64
, pp. 161-170
-
-
Liuzzi, M.1
Kibler, P.2
Bousquet, C.3
-
29
-
-
34547837615
-
Detection of HSV-1 variants highly resistant to the helicase-primase inhibitor BAY 57-1293 at high frequency in 2 of 10 recent clinical isolates of HSV-1
-
Biswas S, Smith C, Field HJ: Detection of HSV-1 variants highly resistant to the helicase-primase inhibitor BAY 57-1293 at high frequency in 2 of 10 recent clinical isolates of HSV-1. J. Antimicrob. Chemother. 60, 274-279 (2007).
-
(2007)
J. Antimicrob. Chemother
, vol.60
, pp. 274-279
-
-
Biswas, S.1
Smith, C.2
Field, H.J.3
-
30
-
-
33947220269
-
High frequency of spontaneous helicase-primase inhibitor (BAY 57-1293) drug-resistant variants in certain laboratory isolates of HSV-1
-
Biswas S, Swift M, Field HJ: High frequency of spontaneous helicase-primase inhibitor (BAY 57-1293) drug-resistant variants in certain laboratory isolates of HSV-1. Antiviral Chem. Chemother. 18, 13-23 (2007).
-
(2007)
Antiviral Chem. Chemother
, vol.18
, pp. 13-23
-
-
Biswas, S.1
Swift, M.2
Field, H.J.3
-
31
-
-
0037404522
-
Highly potent and selective inhibition of varicella-zoster virus replication by bicyclic furo [2,3-d]pyrimidine nucleoside analogues
-
De Clercq E: Highly potent and selective inhibition of varicella-zoster virus replication by bicyclic furo [2,3-d]pyrimidine nucleoside analogues. Med. Res. Rev. 23, 253-274 (2003).
-
(2003)
Med. Res. Rev
, vol.23
, pp. 253-274
-
-
De Clercq, E.1
-
32
-
-
36448956849
-
Preclinical development of bicyclic nucleoside analogues as potent and selective inhibitros of varicella zoster virus
-
McGuigan C, Pathirana RN, Migliore M et al.: Preclinical development of bicyclic nucleoside analogues as potent and selective inhibitros of varicella zoster virus. J. Antimicrob. Chemother. 60. 1316-1330 (2007).
-
(2007)
J. Antimicrob. Chemother
, vol.60
, pp. 1316-1330
-
-
McGuigan, C.1
Pathirana, R.N.2
Migliore, M.3
-
33
-
-
14744269097
-
Susceptibilities of several clinical varicella-zoster virus (VZV) isolates and drug-resistant VZV strains to bicyclic furano pyrimidine nucleosides
-
Andrei G, Sienaert R, McGuigan C, De Clercq E, Balzarini J, Snoeck R: Susceptibilities of several clinical varicella-zoster virus (VZV) isolates and drug-resistant VZV strains to bicyclic furano pyrimidine nucleosides. Antimicrob. Agents Chemother. 49, 1081-1086 (2005).
-
(2005)
Antimicrob. Agents Chemother
, vol.49
, pp. 1081-1086
-
-
Andrei, G.1
Sienaert, R.2
McGuigan, C.3
De Clercq, E.4
Balzarini, J.5
Snoeck, R.6
-
34
-
-
33747141729
-
Antiviral drugs for cytomegalovirus diseases
-
Biron KK: Antiviral drugs for cytomegalovirus diseases. Antiviral Res. 71, 154-163 (2006).
-
(2006)
Antiviral Res
, vol.71
, pp. 154-163
-
-
Biron, K.K.1
-
35
-
-
37349039721
-
Accelerated evolution of maribavir resistance in a cytomegalovirus exonuclease domain II mutant
-
Chou S, Marousek GI: Accelerated evolution of maribavir resistance in a cytomegalovirus exonuclease domain II mutant. J. Virol. 82, 246-253 (2008).
-
(2008)
J. Virol
, vol.82
, pp. 246-253
-
-
Chou, S.1
Marousek, G.I.2
-
36
-
-
0035050725
-
Inhibition of murine cytomegalovirus and human cytomegalovirus by a novel non-nucleoside compound in vivo
-
Weber O, Bender W, Eckenberg P et al.: Inhibition of murine cytomegalovirus and human cytomegalovirus by a novel non-nucleoside compound in vivo. Antiviral Res. 49, 179-189 (2001).
-
(2001)
Antiviral Res
, vol.49
, pp. 179-189
-
-
Weber, O.1
Bender, W.2
Eckenberg, P.3
-
37
-
-
0035656411
-
Novel non-nucleoside inhibitors of cytomegalovirus (BAY 38-4766): In vitro and in vivo antiviral activity and mechanism of action
-
Reefschläger J, Bender W, Hallenberger S et al.: Novel non-nucleoside inhibitors of cytomegalovirus (BAY 38-4766): in vitro and in vivo antiviral activity and mechanism of action. J. Antimicrob. Chemother. 48, 757-767 (2001).
-
(2001)
J. Antimicrob. Chemother
, vol.48
, pp. 757-767
-
-
Reefschläger, J.1
Bender, W.2
Hallenberger, S.3
-
38
-
-
0034855634
-
A novel nonnucleoside inhibitor specifically targets cytomegalovirus DNA maturation via the UL89 and UL56 gene products
-
Buerger J, Reefschläger J, Bender W et al.: A novel nonnucleoside inhibitor specifically targets cytomegalovirus DNA maturation via the UL89 and UL56 gene products. J. Virol. 75, 9077-9086 (2001).
-
(2001)
J. Virol
, vol.75
, pp. 9077-9086
-
-
Buerger, J.1
Reefschläger, J.2
Bender, W.3
-
39
-
-
34548031594
-
In search of effective anti-HHV-6 agents
-
De Clercq E, Naesens L: In search of effective anti-HHV-6 agents. J. Clin. Virol. 47, S82-S86 (2006).
-
(2006)
J. Clin. Virol
, vol.47
-
-
De Clercq, E.1
Naesens, L.2
-
40
-
-
34247225861
-
Antiviral activity of diverse classes of broad-acting agents and natural compounds in HHV-6-infected lymphoblasts
-
Naesens L, Bonnafous P, Agut H, De Clercq E: Antiviral activity of diverse classes of broad-acting agents and natural compounds in HHV-6-infected lymphoblasts. J. Clin. Virol. 37(Suppl. 1), S69-S75 (2006).
-
(2006)
J. Clin. Virol
, vol.37
, Issue.SUPPL. 1
-
-
Naesens, L.1
Bonnafous, P.2
Agut, H.3
De Clercq, E.4
-
41
-
-
34249089649
-
Origins of major human infectious diseases
-
Wolfe ND, Dunavan CP, Diamond J: Origins of major human infectious diseases. Nature 447, 279-283 (2007).
-
(2007)
Nature
, vol.447
, pp. 279-283
-
-
Wolfe, N.D.1
Dunavan, C.P.2
Diamond, J.3
-
42
-
-
35948957769
-
In vitro and in vivo activities of T-705 against arenavirus and bunyavirus infections
-
Gowen BB, Wong MH, Jung KH et al.: In vitro and in vivo activities of T-705 against arenavirus and bunyavirus infections. Antimicrob. Agents Chemother. 51, 3168-3176 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 3168-3176
-
-
Gowen, B.B.1
Wong, M.H.2
Jung, K.H.3
-
43
-
-
0035997942
-
3-deazaneplanocin A induces massively increased interferon-α production in Ebola virus-infected mice
-
Bray M, Raymond JL, Geisbert T, Baker RO: 3-deazaneplanocin A induces massively increased interferon-α production in Ebola virus-infected mice. Antiviral Res. 55, 151-159 (2002).
-
(2002)
Antiviral Res
, vol.55
, pp. 151-159
-
-
Bray, M.1
Raymond, J.L.2
Geisbert, T.3
Baker, R.O.4
-
44
-
-
34250179837
-
Activty of T-1106 in a hamster model of yellow fever virus infection
-
Julander JG, Furuta Y, Shafer K, Sidwell RW: Activty of T-1106 in a hamster model of yellow fever virus infection. Antimicrob. Agents Chemother. 51, 1962-1966 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 1962-1966
-
-
Julander, J.G.1
Furuta, Y.2
Shafer, K.3
Sidwell, R.W.4
-
46
-
-
42049112379
-
Potential use of antiviral agents in polio eradication
-
De Palma AM. Pürstinger G, Wimmer E et al.: Potential use of antiviral agents in polio eradication. Emerg. Infect. Dis. 14, 545-551 (2008).
-
(2008)
Emerg. Infect. Dis
, vol.14
, pp. 545-551
-
-
De Palma, A.M.1
Pürstinger, G.2
Wimmer, E.3
-
47
-
-
4444256678
-
Antivirals and antiviral strategies
-
De Clercq E: Antivirals and antiviral strategies. Nat. Rev. Microbiol. 2, 704-720 (2004).
-
(2004)
Nat. Rev. Microbiol
, vol.2
, pp. 704-720
-
-
De Clercq, E.1
-
48
-
-
33645102511
-
The anti-yellow fever virus activity of ribavirin is independent of error-prone replication
-
Leyssen P, De Clercq E, Neyts J: The anti-yellow fever virus activity of ribavirin is independent of error-prone replication. Mol. Pharmacol. 69, 1461-1467 (2006).
-
(2006)
Mol. Pharmacol
, vol.69
, pp. 1461-1467
-
-
Leyssen, P.1
De Clercq, E.2
Neyts, J.3
-
49
-
-
33845992567
-
Activity of ribavirin against Hantaan virus correlates with production of ribavirin-5′ -triphosphate, not with inhibition of IMP dehydrogenase
-
Sun Y, Chung D-H, Chu Y-K, Jonsson CB, Parker WB: Activity of ribavirin against Hantaan virus correlates with production of ribavirin-5′ -triphosphate, not with inhibition of IMP dehydrogenase. Antimicrob. Agents Chemother. 51, 84-88 (2007).
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 84-88
-
-
Sun, Y.1
Chung, D.-H.2
Chu, Y.-K.3
Jonsson, C.B.4
Parker, W.B.5
-
50
-
-
36749001029
-
The way forward in HCV treatment - finding the right path
-
Manns MP, Foster GR, Rockstroh JK, Zeuzem S, Zoulim F, Houghton M: The way forward in HCV treatment - finding the right path. Nat. Rev. Drug Discov. 6, 991-1000 (2007).
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 991-1000
-
-
Manns, M.P.1
Foster, G.R.2
Rockstroh, J.K.3
Zeuzem, S.4
Zoulim, F.5
Houghton, M.6
-
51
-
-
36749069393
-
Interferons at age 50: Past, current and future impact on biomedicine
-
Borden EC, Sen GC, Uze G et al.: Interferons at age 50: past, current and future impact on biomedicine. Nat. Rev. Drug Discov. 6, 975-990 (2007).
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 975-990
-
-
Borden, E.C.1
Sen, G.C.2
Uze, G.3
|