Ota, Y.; Kakizawa, T.; Itoh, Y.; Suzuki, T.
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. Molecules 2018, 23, 1099.
https://doi.org/10.3390/molecules23051099
AMA Style
Ota Y, Kakizawa T, Itoh Y, Suzuki T.
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. Molecules. 2018; 23(5):1099.
https://doi.org/10.3390/molecules23051099
Chicago/Turabian Style
Ota, Yosuke, Taeko Kakizawa, Yukihiro Itoh, and Takayoshi Suzuki.
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" Molecules 23, no. 5: 1099.
https://doi.org/10.3390/molecules23051099
APA Style
Ota, Y., Kakizawa, T., Itoh, Y., & Suzuki, T.
(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. Molecules, 23(5), 1099.
https://doi.org/10.3390/molecules23051099