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Research and Practice in Technology Enhanced Learning
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January 8, 2019
Practice supporting system with related problem set generator based on targeted educational effects
Yasuhiro Noguchi, Satoru Kogure, Tatsuhiro Konishi, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 5, 2017
Histone H3 peptides incorporating modified lysine residues as lysine-specific demethylase 1 inhibitors
Taeko Kakizawa, Yosuke Ota, Yukihiro Itoh, et al.
Molecules (Basel, Switzerland)
|
May 9, 2018
Design, Synthesis, and In Vitro Evaluation of Novel Histone H3 Peptide-Based LSD1 Inactivators Incorporating α,α-Disubstituted Amino Acids with γ-Turn-Inducing Structures
Yosuke Ota, Taeko Kakizawa, Yukihiro Itoh, et al.
Current Opinion in Chemical Biology
|
March 3, 2022
Recent progress on small molecules targeting epigenetic complexes
Yukihiro Itoh, Yuri Takada, Yasunobu Yamashita, et al.
Computational and Structural Biotechnology Journal
|
April 24, 2014
Synthesis, LSD1 Inhibitory Activity, and LSD1 Binding Model of Optically Pure Lysine-PCPA Conjugates
Yukihiro Itoh, Daisuke Ogasawara, Yosuke Ota, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 2, 2015
Histone H3 peptide based LSD1-selective inhibitors
Taeko Kakizawa, Yosuke Ota, Yukihiro Itoh, et al.
The Journal of Chemical Physics
|
April 2, 2018
Computational analysis for selectivity of histone deacetylase inhibitor by replica-exchange umbrella sampling molecular dynamics simulations
Shuichiro Tsukamoto, Yoshitake Sakae, Yukihiro Itoh, et al.
Bioorganic & Medicinal Chemistry
|
October 22, 2011
Design, synthesis and biological evaluation of nuclear receptor-degradation inducers
Yukihiro Itoh, Risa Kitaguchi, Minoru Ishikawa, et al.
Molecular Biosystems
|
September 12, 2014
Recent advances in the structure-based rational design of TNKSIs
Peng Zhan, Yu'ning Song, Yukihiro Itoh, et al.
Bioorganic & Medicinal Chemistry
|
January 3, 2024
Structural optimization of a lysine demethylase 5 inhibitor for improvement of its cellular activity
Mitsuhiro Terao, Yasunobu Yamashita, Yuri Takada, et al.
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Search research articles
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Showing results (11-20 of 79) with videos related to
Sort By:
Page
of 8
Research and Practice in Technology Enhanced Learning
|
January 8, 2019
Practice supporting system with related problem set generator based on targeted educational effects
Yasuhiro Noguchi, Satoru Kogure, Tatsuhiro Konishi, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 5, 2017
Histone H3 peptides incorporating modified lysine residues as lysine-specific demethylase 1 inhibitors
Taeko Kakizawa, Yosuke Ota, Yukihiro Itoh, et al.
Molecules (Basel, Switzerland)
|
May 9, 2018
Design, Synthesis, and In Vitro Evaluation of Novel Histone H3 Peptide-Based LSD1 Inactivators Incorporating α,α-Disubstituted Amino Acids with γ-Turn-Inducing Structures
Yosuke Ota, Taeko Kakizawa, Yukihiro Itoh, et al.
Current Opinion in Chemical Biology
|
March 3, 2022
Recent progress on small molecules targeting epigenetic complexes
Yukihiro Itoh, Yuri Takada, Yasunobu Yamashita, et al.
Computational and Structural Biotechnology Journal
|
April 24, 2014
Synthesis, LSD1 Inhibitory Activity, and LSD1 Binding Model of Optically Pure Lysine-PCPA Conjugates
Yukihiro Itoh, Daisuke Ogasawara, Yosuke Ota, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 2, 2015
Histone H3 peptide based LSD1-selective inhibitors
Taeko Kakizawa, Yosuke Ota, Yukihiro Itoh, et al.
The Journal of Chemical Physics
|
April 2, 2018
Computational analysis for selectivity of histone deacetylase inhibitor by replica-exchange umbrella sampling molecular dynamics simulations
Shuichiro Tsukamoto, Yoshitake Sakae, Yukihiro Itoh, et al.
Bioorganic & Medicinal Chemistry
|
October 22, 2011
Design, synthesis and biological evaluation of nuclear receptor-degradation inducers
Yukihiro Itoh, Risa Kitaguchi, Minoru Ishikawa, et al.
Molecular Biosystems
|
September 12, 2014
Recent advances in the structure-based rational design of TNKSIs
Peng Zhan, Yu'ning Song, Yukihiro Itoh, et al.
Bioorganic & Medicinal Chemistry
|
January 3, 2024
Structural optimization of a lysine demethylase 5 inhibitor for improvement of its cellular activity
Mitsuhiro Terao, Yasunobu Yamashita, Yuri Takada, et al.
Page
of 8