-
1
-
-
84891013681
-
Viral bioterrorism and antiviral countermeasures
-
Torrence, P. F., Ed.; John Wiley & Sons: New York
-
Bray, M. Viral Bioterrorism and Antiviral Countermeasures. In Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats; Torrence, P. F., Ed.; John Wiley & Sons: New York, 2005; p 17.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 17
-
-
Bray, M.1
-
2
-
-
84890987149
-
Introduction: Pestilence, plague, bioterrorism
-
Torrence, P. F., Ed.; John Wiley & Sons: New York
-
Torrence, P. F. Introduction: Pestilence, Plague, Bioterrorism. In Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats: Torrence, P. F., Ed.; John Wiley & Sons: New York, 2005; p 3.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 3
-
-
Torrence, P.F.1
-
3
-
-
84891029068
-
Overview of antiviral drug discovery and development
-
Torrence, P. F., Ed.; John Wiley & Sons: New York
-
Tseng, C. K. Overview of Antiviral Drug Discovery and Development. In Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats; Torrence, P. F., Ed.; John Wiley & Sons: New York, 2005; p 31.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 31
-
-
Tseng, C.K.1
-
4
-
-
84891010611
-
Discovery and development of new antivirals for smallpox
-
Torrence, P. F., Ed.; John Wiley & Sons: New York
-
Kern, E. R. Discovery and Development of New Antivirals for Smallpox. In Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats; Torrence, P. F., Ed.; John Wiley & Sons: New York, 2005; p 331.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 331
-
-
Kern, E.R.1
-
5
-
-
84891005770
-
Antiviral drug targets and strategies for emerging viral disease and bioterrorism threats
-
Torrence, P. F., Ed.; John Wiley & Sons: New York
-
De Clercq, E. Antiviral Drug Targets and Strategies for Emerging Viral Disease and Bioterrorism Threats. In Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats; Torrence, P. F., Ed.; John Wiley & Sons: New York, 2005; p 83.
-
(2005)
Antiviral Drug Discovery for Emerging Diseases and Bioterrorism Threats
, pp. 83
-
-
De Clercq, E.1
-
6
-
-
0037161131
-
Orally available cidofovir derivative active against smallpox
-
Bradbury, J. Orally available cidofovir derivative active against smallpox. Lancet 2002, 359 (9311), 1041.
-
(2002)
Lancet
, vol.359
, Issue.9311
, pp. 1041
-
-
Bradbury, J.1
-
7
-
-
1242283917
-
Efficacy of oral active ether lipid analogs of cidofovir in a lethal mousepox model
-
Buller, R. M.; Owens, G.; Schriewer, J.; Melman, L.; Beadle, J. R.; Hostetler, K. Y. Efficacy of oral active ether lipid analogs of cidofovir in a lethal mousepox model. Virology 2004, 318 (2), 474.
-
(2004)
Virology
, vol.318
, Issue.2
, pp. 474
-
-
Buller, R.M.1
Owens, G.2
Schriewer, J.3
Melman, L.4
Beadle, J.R.5
Hostetler, K.Y.6
-
8
-
-
0042632872
-
Esterification of cidofovir with alkoxyalkanols increases oral bioavailability and diminishes drug accumulation in kidney
-
Ciesla, S. L.; Trahan, J.; Wan, W. B.; Beadle, J. R.; Aldern, K. A.; Painter, G. R.; Hostetler, K. Y. Esterification of cidofovir with alkoxyalkanols increases oral bioavailability and diminishes drug accumulation in kidney. Antiviral Res. 2003, 59 (3), 163.
-
(2003)
Antiviral Res.
, vol.59
, Issue.3
, pp. 163
-
-
Ciesla, S.L.1
Trahan, J.2
Wan, W.B.3
Beadle, J.R.4
Aldern, K.A.5
Painter, G.R.6
Hostetler, K.Y.7
-
9
-
-
0037333556
-
Increased antiviral activity of 1-O-hexadecyloxypropyl-[2-(14)C]- cidofovir in MRC-5 human lung fibroblasts is explained by unique cellular uptake and metabolism
-
Aldern, K. A.; Ciesla, S. L.; Winegarden, K. L.; Hosteller, K. Y. Increased antiviral activity of 1-O-hexadecyloxypropyl-[2-(14)C]-cidofovir in MRC-5 human lung fibroblasts is explained by unique cellular uptake and metabolism. Mol. Pharmacol. 2003, 63 (3), 678.
-
(2003)
Mol. Pharmacol.
, vol.63
, Issue.3
, pp. 678
-
-
Aldern, K.A.1
Ciesla, S.L.2
Winegarden, K.L.3
Hosteller, K.Y.4
-
10
-
-
2142715953
-
Inhibitory activity of alkoxyalkyl and alkyl esters of cidofovir and cyclic cidofovir against orthopoxvirus replication in vitro
-
Keith, K. A.; Wan, W. B.; Ciesla, S. L.; Beadle, J. R.; Hostetler, K. Y.; Kern, E. R. Inhibitory activity of alkoxyalkyl and alkyl esters of cidofovir and cyclic cidofovir against orthopoxvirus replication in vitro. Antimicrob. Agents Chemother. 2004, 48 (5), 1869.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, Issue.5
, pp. 1869
-
-
Keith, K.A.1
Wan, W.B.2
Ciesla, S.L.3
Beadle, J.R.4
Hostetler, K.Y.5
Kern, E.R.6
-
11
-
-
7644238046
-
New class of orthopoxvirus antiviral drugs that block viral maturation
-
Byrd, C. M.; Bolken, T. C.; Mjalli, A. M.; Arimilli, M. N.; Andrews, R. C.; Rothlein, R.; Andrea, T.; Rao, M.; Owens, K. L.; Hruby, D. E. New class of orthopoxvirus antiviral drugs that block viral maturation. J. Virol. 2004, 78 (22), 12147.
-
(2004)
J. Virol.
, vol.78
, Issue.22
, pp. 12147
-
-
Byrd, C.M.1
Bolken, T.C.2
Mjalli, A.M.3
Arimilli, M.N.4
Andrews, R.C.5
Rothlein, R.6
Andrea, T.7
Rao, M.8
Owens, K.L.9
Hruby, D.E.10
-
12
-
-
26444587116
-
An orally bioavailable antipoxvirus compound (ST-246) inhibits extracellular virus formation and protects mice from lethal orthopoxvirus challenge
-
Yang, G.; Pevear, D. C.; Davies, M. H.; Collett, M. S.; Bailey, T.; Rippen, S.; Barone, L.; Burns, C.; Rhodes, G.; Tohan, S.; Huggins, J. W.; Baker, R. O.; Buller, R. L.; Touchette, E.; Waller, K.; Schriewer, J.; Neyts, J.; DeClercq, E.; Jones, K.; Hruby, D.; Jordan, R. An orally bioavailable antipoxvirus compound (ST-246) inhibits extracellular virus formation and protects mice from lethal orthopoxvirus challenge. J. Virol. 2005, 79 (20), 13139.
-
(2005)
J. Virol.
, vol.79
, Issue.20
, pp. 13139
-
-
Yang, G.1
Pevear, D.C.2
Davies, M.H.3
Collett, M.S.4
Bailey, T.5
Rippen, S.6
Barone, L.7
Burns, C.8
Rhodes, G.9
Tohan, S.10
Huggins, J.W.11
Baker, R.O.12
Buller, R.L.13
Touchette, E.14
Waller, K.15
Schriewer, J.16
Neyts, J.17
Declercq, E.18
Jones, K.19
Hruby, D.20
Jordan, R.21
more..
-
13
-
-
14944382916
-
Antiviral chemotherapy facilitates control of poxvirus infections through inhibition of cellular signal transduction
-
Yang, H.; Kim, S. K.; Kim, M.; Reche, P. A.; Morehead, T. J.; Damon, I. K.; Welsh, R. M.; Reinherz, E. L. Antiviral chemotherapy facilitates control of poxvirus infections through inhibition of cellular signal transduction. J. Clin. Invest. 2005, 115 (2), 379.
-
(2005)
J. Clin. Invest.
, vol.115
, Issue.2
, pp. 379
-
-
Yang, H.1
Kim, S.K.2
Kim, M.3
Reche, P.A.4
Morehead, T.J.5
Damon, I.K.6
Welsh, R.M.7
Reinherz, E.L.8
-
14
-
-
14944376682
-
Host-based antipoxvirus therapeutic strategies: Turning the tables
-
Fauci, A. S.; Challberg, M. D. Host-based antipoxvirus therapeutic strategies: turning the tables. J. Clin. Invest. 2005, 115 (2), 231.
-
(2005)
J. Clin. Invest.
, vol.115
, Issue.2
, pp. 231
-
-
Fauci, A.S.1
Challberg, M.D.2
-
15
-
-
22544470270
-
Disabling poxvirus pathogenesis by inhibition of Abl-family tyrosine kinases
-
Reeves, P. M.; Bommarius, B.; Lebeis, S.; McNulty, S.; Christensen, J.; Swimm, A.; Chahroudi, A.; Chavan, R.; Feinberg, M. B.; Veach, D.; Bornmann, W.; Sherman, M.; Kalman, D. Disabling poxvirus pathogenesis by inhibition of Abl-family tyrosine kinases. Nat. Med. 2005, 11 (7), 731.
-
(2005)
Nat. Med.
, vol.11
, Issue.7
, pp. 731
-
-
Reeves, P.M.1
Bommarius, B.2
Lebeis, S.3
McNulty, S.4
Christensen, J.5
Swimm, A.6
Chahroudi, A.7
Chavan, R.8
Feinberg, M.B.9
Veach, D.10
Bornmann, W.11
Sherman, M.12
Kalman, D.13
-
16
-
-
33747095922
-
A Pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity
-
in press
-
Fan, X.; Zhang, X.; Zhou, L., Keith, K. A.; Kern, E. R.; Torrence, P. F. A Pyrimidine-pyrazolone nucleoside chimera with potent in vitro anti-orthopoxvirus activity. Bioorg. Med. Chem. Lett. , in press.
-
Bioorg. Med. Chem. Lett.
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Kern, E.R.5
Torrence, P.F.6
-
17
-
-
33744793223
-
5-(Dimethoxymethyl)-27prime;deoxyuridine: A novel gem diether nucleoside with anti-orthopoxvirus activity
-
in press
-
Fan, X.; Zhang, X.; Zhou, L.; Keith, K. A.; Kern, E. R.; Torrence, P. F. 5-(Dimethoxymethyl)-27prime;deoxyuridine: A novel gem diether nucleoside with anti-orthopoxvirus activity. J. Med. Chem., in press.
-
J. Med. Chem.
-
-
Fan, X.1
Zhang, X.2
Zhou, L.3
Keith, K.A.4
Kern, E.R.5
Torrence, P.F.6
-
18
-
-
4243159924
-
Privileged structures: Applications in drug discovery
-
DeSimone, R. W.; Currie, K. S.; Mitchell, S. A.; Darrow, J. W.; Pippin, D. A. Privileged structures: applications in drug discovery. Comb. Chem. High Throughput Screening 2004, 7 (5), 473.
-
(2004)
Comb. Chem. High Throughput Screening
, vol.7
, Issue.5
, pp. 473
-
-
Desimone, R.W.1
Currie, K.S.2
Mitchell, S.A.3
Darrow, J.W.4
Pippin, D.A.5
-
19
-
-
0036942484
-
Exploring privileged structures: The combinatorial synthesis of cyclic peptides
-
Horton, D. A.; Bourne, G. T.; Smythe, M. L. Exploring privileged structures: the combinatorial synthesis of cyclic peptides. Mol. Diversity 2002, 5 (4), 289.
-
(2002)
Mol. Diversity
, vol.5
, Issue.4
, pp. 289
-
-
Horton, D.A.1
Bourne, G.T.2
Smythe, M.L.3
-
20
-
-
4444256678
-
Antivirals and antiviral strategies
-
De Clercq, E. Antivirals and antiviral strategies. Nat. Rev. Microbiol. 2004, 2 (9), 704.
-
(2004)
Nat. Rev. Microbiol.
, vol.2
, Issue.9
, pp. 704
-
-
De Clercq, E.1
-
21
-
-
0042121318
-
Medicinal chemistry of target family-directed masterkeys
-
Muller, G. Medicinal chemistry of target family-directed masterkeys. Drug Discovery Today 2003, 8 (15), 681.
-
(2003)
Drug Discovery Today
, vol.8
, Issue.15
, pp. 681
-
-
Muller, G.1
-
22
-
-
0346251240
-
Use of multicomponent, domino, and other one-pot syntheses on solid phase: Powerful tools for the generation of libraries of diverse and complex compounds
-
Pulici, M.; Cervi, G.; Martina, K.; Quartieri, F. Use of multicomponent, domino, and other one-pot syntheses on solid phase: powerful tools for the generation of libraries of diverse and complex compounds. Comb. Chem. High Throughput Screening 2003, 6 (7), 693.
-
(2003)
Comb. Chem. High Throughput Screening
, vol.6
, Issue.7
, pp. 693
-
-
Pulici, M.1
Cervi, G.2
Martina, K.3
Quartieri, F.4
-
23
-
-
0347132224
-
Decoration of dihydropyrimidine and dihydropyridine scaffolds with sugars via Biginelli and Hantzsch multicomponent reactions: An efficient entry to a collection of artificial nucleosides
-
Dondoni, A.; Massi, A. Decoration of dihydropyrimidine and dihydropyridine scaffolds with sugars via Biginelli and Hantzsch multicomponent reactions: an efficient entry to a collection of artificial nucleosides. Mol. Diversity 2003, 6 (3-4), 261.
-
(2003)
Mol. Diversity
, vol.6
, Issue.3-4
, pp. 261
-
-
Dondoni, A.1
Massi, A.2
-
24
-
-
3543031001
-
A reexamination of Biginelli-like multicomponent condensation reaction: One-pot regioselective synthesis of spiro heterobicyclic rings
-
Shaabani, A.; Bazgir, A.; Bijanzadeh, H. R. A reexamination of Biginelli-like multicomponent condensation reaction: one-pot regioselective synthesis of spiro heterobicyclic rings. Mol. Diversity 2004, 8 (2), 141.
-
(2004)
Mol. Diversity
, vol.8
, Issue.2
, pp. 141
-
-
Shaabani, A.1
Bazgir, A.2
Bijanzadeh, H.R.3
-
25
-
-
3242695438
-
Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot Sila-Stetter/Paal-Knorr strategy
-
Bharadwaj, A. R.; Scheidt, K. A. Catalytic multicomponent synthesis of highly substituted pyrroles utilizing a one-pot Sila-Stetter/Paal-Knorr strategy. Org. Lett. 2004, 6 (14), 2465.
-
(2004)
Org. Lett.
, vol.6
, Issue.14
, pp. 2465
-
-
Bharadwaj, A.R.1
Scheidt, K.A.2
-
26
-
-
0027967842
-
Nucleosides and nucleotides. 131. Synthesis and properties of oligonucleotides containing 5-formyl-2′-deoxyuridine
-
Ono, A.; Okamoto, T.; Inada, M.; Nara, H.; Matsuda, A. Nucleosides and nucleotides. 131. Synthesis and properties of oligonucleotides containing 5-formyl-2′-deoxyuridine. Chem. Pharm. Bull. (Tokyo) 1994, 42 (11), 2231.
-
(1994)
Chem. Pharm. Bull. (Tokyo)
, vol.42
, Issue.11
, pp. 2231
-
-
Ono, A.1
Okamoto, T.2
Inada, M.3
Nara, H.4
Matsuda, A.5
-
27
-
-
0019122046
-
Oxime and dithiolane derivatives of 5-formyl-2′-deoxyuridine and their 5′-phosphates: Antiviral effects and thymidylate synthetase inhibition
-
Park, J. S.; Chang, C. T.; Schmidt, C. L.; Golander, Y.; De Clercq, E.; Descamps, J.; Merles, M. P. Oxime and dithiolane derivatives of 5-formyl-2′-deoxyuridine and their 5′-phosphates: antiviral effects and thymidylate synthetase inhibition. J. Med. Chem. 1980, 23 (6), 661.
-
(1980)
J. Med. Chem.
, vol.23
, Issue.6
, pp. 661
-
-
Park, J.S.1
Chang, C.T.2
Schmidt, C.L.3
Golander, Y.4
De Clercq, E.5
Descamps, J.6
Merles, M.P.7
-
28
-
-
0017185621
-
Synthesis of 5-substituted 2′-deoxyuridines
-
Kampf, A.; Pillar, C. J.; Woodford, W. J.; Merles, M. P. Synthesis of 5-substituted 2′-deoxyuridines. J. Med. Chem. 1976, 19 (7), 909.
-
(1976)
J. Med. Chem.
, vol.19
, Issue.7
, pp. 909
-
-
Kampf, A.1
Pillar, C.J.2
Woodford, W.J.3
Merles, M.P.4
-
29
-
-
0022567362
-
Antiviral activity of flavones and flavans
-
Selway, J. W. Antiviral activity of flavones and flavans. Prog. Clin. Biol Res. 1986, 213, 521.
-
(1986)
Prog. Clin. Biol Res.
, vol.213
, pp. 521
-
-
Selway, J.W.1
-
30
-
-
0036654692
-
Antiviral properties of prodelphinidin B-2 3′-O-gallate from green tea leaf
-
Cheng, H. Y.; Lin, C. C.; Lin, T. C. Antiviral properties of prodelphinidin B-2 3′-O-gallate from green tea leaf. Antiviral Chem. Chemother. 2002, 13, (4), 223.
-
(2002)
Antiviral Chem. Chemother.
, vol.13
, Issue.4
, pp. 223
-
-
Cheng, H.Y.1
Lin, C.C.2
Lin, T.C.3
-
31
-
-
0019870602
-
4′,6-Dichloroflavan (BW683C), a new antirhinovirus compound
-
Bauer, D. J.; Selway, J. W.; Batchelor, J. F.; Tisdale, M.; Caldwell, I. C.; Young, D. A. 4′,6-Dichloroflavan (BW683C), a new antirhinovirus compound. Nature 1981, 292 (5821), 369.
-
(1981)
Nature
, vol.292
, Issue.5821
, pp. 369
-
-
Bauer, D.J.1
Selway, J.W.2
Batchelor, J.F.3
Tisdale, M.4
Caldwell, I.C.5
Young, D.A.6
-
32
-
-
19444362115
-
Antioxidant and antiviral activities of plastoquinones from the brown alga Sargassum micracanthum, and a new chromene derivative converted from the plastoquinones
-
Iwashima, M.; Mori, J.; Ting, X.; Matsunaga, T.; Hayashi, K.; Shinoda, D.; Saito, H.; Sankawa, U.; Hayashi, T. Antioxidant and antiviral activities of plastoquinones from the brown alga Sargassum micracanthum, and a new chromene derivative converted from the plastoquinones. Biol. Pharm. Bull. 2005, 28 (2), 374.
-
(2005)
Biol. Pharm. Bull.
, vol.28
, Issue.2
, pp. 374
-
-
Iwashima, M.1
Mori, J.2
Ting, X.3
Matsunaga, T.4
Hayashi, K.5
Shinoda, D.6
Saito, H.7
Sankawa, U.8
Hayashi, T.9
-
33
-
-
16044365071
-
A synthetic entry into fused pyran derivatives through carbon transfer reactions of 1,3-oxazinanes and oxazolidines with carbon nucleophiles
-
Singh, K.; Singh, J.; Singh, H. A synthetic entry into fused pyran derivatives through carbon transfer reactions of 1,3-oxazinanes and oxazolidines with carbon nucleophiles. Tetrahedron 1996, 52 (45), 14273.
-
(1996)
Tetrahedron
, vol.52
, Issue.45
, pp. 14273
-
-
Singh, K.1
Singh, J.2
Singh, H.3
-
34
-
-
0037282348
-
In vitro activity of potential anti-poxvirus agents
-
Kern, E. R. In vitro activity of potential anti-poxvirus agents. Antiviral Res. 2003, 57(1-2), 35.
-
(2003)
Antiviral Res.
, vol.57
, Issue.1-2
, pp. 35
-
-
Kern, E.R.1
-
35
-
-
20444457155
-
The 4′,4′-difluoro analog of 5′-noraristeromycin: A new structural prototype for possible antiviral drug development toward orthopoxvirus and cytomegalovirus
-
Roy, A.; Schneller, S. W.; Keith, K. A.; Hartline, C. B.; Kern, E. R. The 4′,4′-difluoro analog of 5′-noraristeromycin: A new structural prototype for possible antiviral drug development toward orthopoxvirus and cytomegalovirus. Bioorg. Med. Chem. 2005, 13, 4443.
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 4443
-
-
Roy, A.1
Schneller, S.W.2
Keith, K.A.3
Hartline, C.B.4
Kern, E.R.5
-
36
-
-
0038312076
-
Evaluation of nucleoside phosphonates and their analogs and prodrugs for inhibition of orthopoxvirus replication
-
Keith, K. A.; Hitchcock, M. J.; Lee, W. A.; Holy, A.; Kern, E. R. Evaluation of nucleoside phosphonates and their analogs and prodrugs for inhibition of orthopoxvirus replication. Antimicrob. Agents Chemother. 2003, 47 (7), 2193.
-
(2003)
Antimicrob. Agents Chemother.
, vol.47
, Issue.7
, pp. 2193
-
-
Keith, K.A.1
Hitchcock, M.J.2
Lee, W.A.3
Holy, A.4
Kern, E.R.5
-
37
-
-
17444427138
-
Combinatorial optimization of isatin-β-thiosemicarbazones as antipoxvirus agents
-
Pirrung, M. C.; Pansare, S. V.; Sarma, K. D.; Keith, K. A.; Kern, E. R. Combinatorial optimization of isatin-β-thiosemicarbazones as antipoxvirus agents. J. Med. Chem. 2005, 48 (8), 3045.
-
(2005)
J. Med. Chem.
, vol.48
, Issue.8
, pp. 3045
-
-
Pirrung, M.C.1
Pansare, S.V.2
Sarma, K.D.3
Keith, K.A.4
Kern, E.R.5
-
38
-
-
0027978137
-
The SPI-1 gene of rabbitpox virus determines host range and is required for hemorrhagic pock formation
-
Ali, A. N.; Turner, P. C.; Brooks, M. A.; Moyer, R. W. The SPI-1 gene of rabbitpox virus determines host range and is required for hemorrhagic pock formation. Virology 1994, 202 (1), 305.
-
(1994)
Virology
, vol.202
, Issue.1
, pp. 305
-
-
Ali, A.N.1
Turner, P.C.2
Brooks, M.A.3
Moyer, R.W.4
-
39
-
-
0036803250
-
Cidofovir in the therapy and short-term prophylaxis of poxvirus infections
-
De Clercq, E. Cidofovir in the therapy and short-term prophylaxis of poxvirus infections. Trends Pharmacol. Sci. 2002, 23 (10), 456.
-
(2002)
Trends Pharmacol. Sci.
, vol.23
, Issue.10
, pp. 456
-
-
De Clercq, E.1
-
40
-
-
0035997915
-
Cidofovir in the treatment of poxvirus infections
-
De Clercq, E. Cidofovir in the treatment of poxvirus infections. Antiviral Res. 2002, 55 (1), 1.
-
(2002)
Antiviral Res.
, vol.55
, Issue.1
, pp. 1
-
-
De Clercq, E.1
-
41
-
-
0035074340
-
Vaccinia virus inhibitors as a paradigm for the chemotherapy of poxvirus infections
-
De Clercq, E. Vaccinia virus inhibitors as a paradigm for the chemotherapy of poxvirus infections. Clin. Microbiol. Rev. 2001, 14 (2), 382.
-
(2001)
Clin. Microbiol. Rev.
, vol.14
, Issue.2
, pp. 382
-
-
De Clercq, E.1
-
42
-
-
0019513848
-
Cell-free synthesis of enzymatically active vaccinia virus thymidine kinase
-
Hruby, D. E.; Ball, L. A. Cell-free synthesis of enzymatically active vaccinia virus thymidine kinase. Virology 1981, 113 (2), 594.
-
(1981)
Virology
, vol.113
, Issue.2
, pp. 594
-
-
Hruby, D.E.1
Ball, L.A.2
-
43
-
-
0025130909
-
Identification of the ATP-binding domain of vaccinia virus thymidine kinase
-
Black, M. E.; Hruby, D. E. Identification of the ATP-binding domain of vaccinia virus thymidine kinase. J Biol Chem 1990, 265 (29), 17584.
-
(1990)
J Biol Chem
, vol.265
, Issue.29
, pp. 17584
-
-
Black, M.E.1
Hruby, D.E.2
-
44
-
-
0025353109
-
Quaternary structure of vaccinia virus thymidine kinase
-
Black, M. E.; Hruby, D. E. Quaternary structure of vaccinia virus thymidine kinase. Biochem. Biophys. Res. Commun. 1990, 169 (3), 1080.
-
(1990)
Biochem. Biophys. Res. Commun.
, vol.169
, Issue.3
, pp. 1080
-
-
Black, M.E.1
Hruby, D.E.2
-
45
-
-
0026730771
-
Site-directed mutagenesis of a conserved domain in vaccinia virus thymidine kinase. Evidence for a potential role in magnesium binding
-
Black, M. E.; Hruby, D. E. Site-directed mutagenesis of a conserved domain in vaccinia virus thymidine kinase. Evidence for a potential role in magnesium binding. J. Biol. Chem. 1992, 267 (10), 6801.
-
(1992)
J. Biol. Chem.
, vol.267
, Issue.10
, pp. 6801
-
-
Black, M.E.1
Hruby, D.E.2
-
46
-
-
0026655908
-
A single amino acid substitution abolishes feedback inhibition of vaccinia virus thymidine kinase
-
Black, M. E.; Hruby, D. E. A single amino acid substitution abolishes feedback inhibition of vaccinia virus thymidine kinase. J. Biol. Chem. 1992, 267(14), 9743.
-
(1992)
J. Biol. Chem.
, vol.267
, Issue.14
, pp. 9743
-
-
Black, M.E.1
Hruby, D.E.2
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