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Terrence R Burke

Showing results (81-90 of 169) with videos related to

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Viruses|December 28, 2021
INSTIs and NNRTIs Potently Inhibit HIV-1 Polypurine Tract Mutants in a Single Round Infection AssaySteven J Smith, Andrea Ferris, Xuezhi Zhao, et al.
Journal of Medicinal Chemistry|March 30, 2011
Utilization of nitrophenylphosphates and oxime-based ligation for the development of nanomolar affinity inhibitors of the Yersinia pestis outer protein H (YopH) phosphataseMedhanit Bahta, George T Lountos, Beverly Dyas, et al.
Organic & Biomolecular Chemistry|August 4, 2021
Design and synthesis of a new orthogonally protected glutamic acid analog and its use in the preparation of high affinity polo-like kinase 1 polo-box domain - binding peptide macrocyclesDavid Hymel, Kohei Tsuji, Robert A Grant, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Effect of HIV integrase inhibitors on the RAG1/2 recombinaseMeni Melek, Jessica M Jones, Mary H O'Dea, et al.
Journal of Medicinal Chemistry|August 5, 2005
Design and synthesis of 4-(alpha-hydroxymalonyl)phenylalanine as a new phosphotyrosyl mimetic and its use in growth factor receptor bound 2 src-homology 2 (Grb2 SH2) domain-binding peptidesSang-Uk Kang, Karen M Worthy, Lakshman K Bindu, et al.
ACS Infectious Diseases|February 12, 2024
<i>N</i>-Substituted Bicyclic Carbamoyl Pyridones: Integrase Strand Transfer Inhibitors that Potently Inhibit Drug-Resistant HIV-1 Integrase MutantsPankaj S Mahajan, Steven J Smith, Min Li, et al.
Journal of Medicinal Chemistry|February 6, 2004
Synthesis of a 5-methylindolyl-containing macrocycle that displays ultrapotent Grb2 SH2 domain-binding affinityZhen-Dan Shi, Kyeong Lee, Chang-Qing Wei, et al.
Chembiochem : a European Journal of Chemical Biology|July 26, 2008
SAR by oxime-containing peptide libraries: application to Tsg101 ligand optimizationFa Liu, Andrew G Stephen, Abdul A Waheed, et al.
Molecular Pharmacology|July 30, 2009
An allosteric mechanism for inhibiting HIV-1 integrase with a small moleculeJacques J Kessl, Jocelyn O Eidahl, Nikolozi Shkriabai, et al.
The Journal of Biological Chemistry|November 1, 2005
Integration requires a specific interaction of the donor DNA terminal 5'-cytosine with glutamine 148 of the HIV-1 integrase flexible loopAllison A Johnson, Webster Santos, Godwin C G Pais, et al.
Pageof 17

Showing results (81-90 of 169) with videos related to

Sort By:
Pageof 17
Viruses|December 28, 2021
INSTIs and NNRTIs Potently Inhibit HIV-1 Polypurine Tract Mutants in a Single Round Infection AssaySteven J Smith, Andrea Ferris, Xuezhi Zhao, et al.
Journal of Medicinal Chemistry|March 30, 2011
Utilization of nitrophenylphosphates and oxime-based ligation for the development of nanomolar affinity inhibitors of the Yersinia pestis outer protein H (YopH) phosphataseMedhanit Bahta, George T Lountos, Beverly Dyas, et al.
Organic & Biomolecular Chemistry|August 4, 2021
Design and synthesis of a new orthogonally protected glutamic acid analog and its use in the preparation of high affinity polo-like kinase 1 polo-box domain - binding peptide macrocyclesDavid Hymel, Kohei Tsuji, Robert A Grant, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 5, 2002
Effect of HIV integrase inhibitors on the RAG1/2 recombinaseMeni Melek, Jessica M Jones, Mary H O'Dea, et al.
Journal of Medicinal Chemistry|August 5, 2005
Design and synthesis of 4-(alpha-hydroxymalonyl)phenylalanine as a new phosphotyrosyl mimetic and its use in growth factor receptor bound 2 src-homology 2 (Grb2 SH2) domain-binding peptidesSang-Uk Kang, Karen M Worthy, Lakshman K Bindu, et al.
ACS Infectious Diseases|February 12, 2024
<i>N</i>-Substituted Bicyclic Carbamoyl Pyridones: Integrase Strand Transfer Inhibitors that Potently Inhibit Drug-Resistant HIV-1 Integrase MutantsPankaj S Mahajan, Steven J Smith, Min Li, et al.
Journal of Medicinal Chemistry|February 6, 2004
Synthesis of a 5-methylindolyl-containing macrocycle that displays ultrapotent Grb2 SH2 domain-binding affinityZhen-Dan Shi, Kyeong Lee, Chang-Qing Wei, et al.
Chembiochem : a European Journal of Chemical Biology|July 26, 2008
SAR by oxime-containing peptide libraries: application to Tsg101 ligand optimizationFa Liu, Andrew G Stephen, Abdul A Waheed, et al.
Molecular Pharmacology|July 30, 2009
An allosteric mechanism for inhibiting HIV-1 integrase with a small moleculeJacques J Kessl, Jocelyn O Eidahl, Nikolozi Shkriabai, et al.
The Journal of Biological Chemistry|November 1, 2005
Integration requires a specific interaction of the donor DNA terminal 5'-cytosine with glutamine 148 of the HIV-1 integrase flexible loopAllison A Johnson, Webster Santos, Godwin C G Pais, et al.
Pageof 17