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Bioorganic & Medicinal Chemistry
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March 14, 2017
Enhancing polo-like kinase 1 selectivity of polo-box domain-binding peptides
Xue Zhi Zhao, David Hymel, Terrence R Burke
Expert Opinion on Therapeutic Targets
|
July 16, 2008
Grb2 signaling in cell motility and cancer
Alessio Giubellino, Terrence R Burke, Donald P Bottaro
Bioorganic & Medicinal Chemistry Letters
|
September 15, 2016
Application of oxime-diversification to optimize ligand interactions within a cryptic pocket of the polo-like kinase 1 polo-box domain
Xue Zhi Zhao, David Hymel, Terrence R Burke
Bioorganic & Medicinal Chemistry Letters
|
February 26, 2004
Design and synthesis of photoactivatable aryl diketo acid-containing HIV-1 integrase inhibitors as potential affinity probes
Xuechun Zhang, Christophe Marchand, Yves Pommier, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 7, 2002
Design and synthesis of a beta-amino phosphotyrosyl mimetic suitably protected for peptide synthesis
Kyeong Lee, Manchao Zhang, Dajun Yang, et al.
The EMBO Journal
|
February 17, 2006
Retroviral DNA integration: reaction pathway and critical intermediates
Min Li, Michiyo Mizuuchi, Terrence R Burke, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 17, 2008
Application of a trifunctional reactive linker for the construction of antibody-drug hybrid conjugates
Joshua D Thomas, Thomas Hofer, Christoph Rader, et al.
The Journal of Biological Chemistry
|
July 5, 2012
Chemically programmed bispecific antibodies that recruit and activate T cells
Huiting Cui, Joshua D Thomas, Terrence R Burke, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 23, 2008
An engineered selenocysteine defines a unique class of antibody derivatives
Thomas Hofer, Joshua D Thomas, Terrence R Burke, et al.
Molecules (Basel, Switzerland)
|
April 25, 2019
Development of Highly Selective 1,2,3-Triazole-containing Peptidic Polo-like Kinase 1 Polo-box Domain-binding Inhibitors
Xue Zhi Zhao, Kohei Tsuji, David Hymel, et al.
Page
of 17
Search research articles
Search
Showing results (21-30 of 169) with videos related to
Sort By:
Page
of 17
Bioorganic & Medicinal Chemistry
|
March 14, 2017
Enhancing polo-like kinase 1 selectivity of polo-box domain-binding peptides
Xue Zhi Zhao, David Hymel, Terrence R Burke
Expert Opinion on Therapeutic Targets
|
July 16, 2008
Grb2 signaling in cell motility and cancer
Alessio Giubellino, Terrence R Burke, Donald P Bottaro
Bioorganic & Medicinal Chemistry Letters
|
September 15, 2016
Application of oxime-diversification to optimize ligand interactions within a cryptic pocket of the polo-like kinase 1 polo-box domain
Xue Zhi Zhao, David Hymel, Terrence R Burke
Bioorganic & Medicinal Chemistry Letters
|
February 26, 2004
Design and synthesis of photoactivatable aryl diketo acid-containing HIV-1 integrase inhibitors as potential affinity probes
Xuechun Zhang, Christophe Marchand, Yves Pommier, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 7, 2002
Design and synthesis of a beta-amino phosphotyrosyl mimetic suitably protected for peptide synthesis
Kyeong Lee, Manchao Zhang, Dajun Yang, et al.
The EMBO Journal
|
February 17, 2006
Retroviral DNA integration: reaction pathway and critical intermediates
Min Li, Michiyo Mizuuchi, Terrence R Burke, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 17, 2008
Application of a trifunctional reactive linker for the construction of antibody-drug hybrid conjugates
Joshua D Thomas, Thomas Hofer, Christoph Rader, et al.
The Journal of Biological Chemistry
|
July 5, 2012
Chemically programmed bispecific antibodies that recruit and activate T cells
Huiting Cui, Joshua D Thomas, Terrence R Burke, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 23, 2008
An engineered selenocysteine defines a unique class of antibody derivatives
Thomas Hofer, Joshua D Thomas, Terrence R Burke, et al.
Molecules (Basel, Switzerland)
|
April 25, 2019
Development of Highly Selective 1,2,3-Triazole-containing Peptidic Polo-like Kinase 1 Polo-box Domain-binding Inhibitors
Xue Zhi Zhao, Kohei Tsuji, David Hymel, et al.
Page
of 17