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Molecules (Basel, Switzerland)
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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.
F1000Research
|
July 20, 2017
Current progress and future perspectives in the development of anti-polo-like kinase 1 therapeutic agents
Jung-Eun Park, David Hymel, Terrence R Burke, et al.
Frontiers in Immunology
|
September 10, 2019
Conventional and Chemically Programmed Asymmetric Bispecific Antibodies Targeting Folate Receptor 1
Junpeng Qi, David Hymel, Christopher G Nelson, et al.
RSC Chemical Biology
|
September 21, 2022
Development of ultra-high affinity bivalent ligands targeting the polo-like kinase 1
Kohei Tsuji, David Hymel, Buyong Ma, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 4, 2018
Histidine N(τ)-cyclized macrocycles as a new genre of polo-like kinase 1 polo-box domain-binding inhibitors
David Hymel, Robert A Grant, Kohei Tsuji, et al.
Chemical Communications (Cambridge, England)
|
August 20, 2015
Fluorescent mimics of cholesterol that rapidly bind surfaces of living mammalian cells
David Hymel, Sutang Cai, Qi Sun, et al.
Angewandte Chemie (International Ed. in English)
|
April 25, 2020
Chemically Programmable and Switchable CAR-T Therapy
Junpeng Qi, Kohei Tsuji, David Hymel, et al.
ACS Omega
|
August 29, 2019
Antibody-Drug Conjugate that Exhibits Synergistic Cytotoxicity with an Endosome-Disruptive Peptide
Kelsey E Knewtson, Chamani Perera, David Hymel, et al.
Diabetes Care
|
February 21, 2009
Lower total adipocyte number but no evidence for small adipocyte depletion in patients with type 2 diabetes
Magdalena Pasarica, Hui Xie, David Hymel, 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 macrocycles
David Hymel, Kohei Tsuji, Robert A Grant, et al.
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Search research articles
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Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
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.
F1000Research
|
July 20, 2017
Current progress and future perspectives in the development of anti-polo-like kinase 1 therapeutic agents
Jung-Eun Park, David Hymel, Terrence R Burke, et al.
Frontiers in Immunology
|
September 10, 2019
Conventional and Chemically Programmed Asymmetric Bispecific Antibodies Targeting Folate Receptor 1
Junpeng Qi, David Hymel, Christopher G Nelson, et al.
RSC Chemical Biology
|
September 21, 2022
Development of ultra-high affinity bivalent ligands targeting the polo-like kinase 1
Kohei Tsuji, David Hymel, Buyong Ma, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 4, 2018
Histidine N(τ)-cyclized macrocycles as a new genre of polo-like kinase 1 polo-box domain-binding inhibitors
David Hymel, Robert A Grant, Kohei Tsuji, et al.
Chemical Communications (Cambridge, England)
|
August 20, 2015
Fluorescent mimics of cholesterol that rapidly bind surfaces of living mammalian cells
David Hymel, Sutang Cai, Qi Sun, et al.
Angewandte Chemie (International Ed. in English)
|
April 25, 2020
Chemically Programmable and Switchable CAR-T Therapy
Junpeng Qi, Kohei Tsuji, David Hymel, et al.
ACS Omega
|
August 29, 2019
Antibody-Drug Conjugate that Exhibits Synergistic Cytotoxicity with an Endosome-Disruptive Peptide
Kelsey E Knewtson, Chamani Perera, David Hymel, et al.
Diabetes Care
|
February 21, 2009
Lower total adipocyte number but no evidence for small adipocyte depletion in patients with type 2 diabetes
Magdalena Pasarica, Hui Xie, David Hymel, 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 macrocycles
David Hymel, Kohei Tsuji, Robert A Grant, et al.
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of 3