E De Clercq|P F Torrence|B Witkop - JoVE Visualize

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Journal of Virology|October 1, 1972

Recovery of cell-bound interferonW E Stewart, E De Clercq, P De Somer

Journal of Virology|November 1, 1972

Cellular alteration by interferon: a virus-free system for assaying interferonW E Stewart, E De Clercq, P De Somer

Journal of Medicinal Chemistry|February 1, 1990

Synthesis, antiretrovirus effects, and phosphorylation kinetics of 3'-isocyano-3'-deoxythymidine and 3'-isocyano-2',3'-dideoxyuridineJ Hiebl, E Zbiral, J Balzarini, et al.

Oncology Research|January 1, 1997

The sulfonic acid polymers PAMPS [poly(2-acrylamido-2-methyl-1-propanesulfonic acid)] and related analogues are highly potent inhibitors of angiogenesisS Liekens, J Neyts, B Degrève, et al.

Antiviral Research|March 1, 1983

Efficacy of (E)-5-(2-bromovinyl)-2'-deoxyuridine in the treatment of experimental herpes simplex virus encephalitis in miceN H Park, D Pavan-Langston, E de Clercq

Methods and Findings in Experimental and Clinical Pharmacology|January 1, 1985

Incorporation of 5-substituted pyrimidine nucleoside analogues into DNA of a thymidylate synthetase-deficient murine FM3A carcinoma cell lineJ Balzarini, E De Clercq, D Ayusawa, et al.

Carcinogenesis|August 1, 1985

Potent anti-viral 5-(2-bromovinyl) uracil nucleosides are inactive at inducing gene mutations in Salmonella typhimurium and V79 Chinese hamster cells and unscheduled DNA synthesis in primary rat hepatocytesH Marquardt, J Westendorf, E De Clercq, et al.

Microbiology and Immunology|January 1, 1988

Inhibitory activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine on the salmonid herpesviruses, Oncorhynchus masou virus (OMV) and Herpesvirus salmonisT Kimura, T Nishizawa, M Yoshimizu, et al.

Journal of Virology|January 22, 2000

CXC-chemokine receptor 4 is not a coreceptor for human herpesvirus 7 entry into CD4(+) T cellsY Zhang, S Hatse, E De Clercq, et al.

Bioorganic & Medicinal Chemistry Letters|July 13, 2000

Thiosugars. Part 5: synthesis and biological activity of 1-(4-thio-L-arabinofuranosyl)-5-halopyrimidine nucleosidesJ Wirsching, J Voss, J Balzarini, et al.

Pageof 125

Showing results (311-320 of 1,246) with videos related to

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Pageof 125

Journal of Virology|October 1, 1972

Recovery of cell-bound interferonW E Stewart, E De Clercq, P De Somer

Journal of Virology|November 1, 1972

Cellular alteration by interferon: a virus-free system for assaying interferonW E Stewart, E De Clercq, P De Somer

Journal of Medicinal Chemistry|February 1, 1990

Synthesis, antiretrovirus effects, and phosphorylation kinetics of 3'-isocyano-3'-deoxythymidine and 3'-isocyano-2',3'-dideoxyuridineJ Hiebl, E Zbiral, J Balzarini, et al.

Oncology Research|January 1, 1997

The sulfonic acid polymers PAMPS [poly(2-acrylamido-2-methyl-1-propanesulfonic acid)] and related analogues are highly potent inhibitors of angiogenesisS Liekens, J Neyts, B Degrève, et al.

Antiviral Research|March 1, 1983

Efficacy of (E)-5-(2-bromovinyl)-2'-deoxyuridine in the treatment of experimental herpes simplex virus encephalitis in miceN H Park, D Pavan-Langston, E de Clercq

Methods and Findings in Experimental and Clinical Pharmacology|January 1, 1985

Incorporation of 5-substituted pyrimidine nucleoside analogues into DNA of a thymidylate synthetase-deficient murine FM3A carcinoma cell lineJ Balzarini, E De Clercq, D Ayusawa, et al.

Carcinogenesis|August 1, 1985

Potent anti-viral 5-(2-bromovinyl) uracil nucleosides are inactive at inducing gene mutations in Salmonella typhimurium and V79 Chinese hamster cells and unscheduled DNA synthesis in primary rat hepatocytesH Marquardt, J Westendorf, E De Clercq, et al.

Microbiology and Immunology|January 1, 1988

Inhibitory activity of (E)-5-(2-bromovinyl)-2'-deoxyuridine on the salmonid herpesviruses, Oncorhynchus masou virus (OMV) and Herpesvirus salmonisT Kimura, T Nishizawa, M Yoshimizu, et al.

Journal of Virology|January 22, 2000

CXC-chemokine receptor 4 is not a coreceptor for human herpesvirus 7 entry into CD4(+) T cellsY Zhang, S Hatse, E De Clercq, et al.

Bioorganic & Medicinal Chemistry Letters|July 13, 2000

Thiosugars. Part 5: synthesis and biological activity of 1-(4-thio-L-arabinofuranosyl)-5-halopyrimidine nucleosidesJ Wirsching, J Voss, J Balzarini, et al.

Pageof 125