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Chemistry (Weinheim an Der Bergstrasse, Germany)|July 14, 2018
Orthogonal γPNA Dimerization Domains Empower DNA Binders with Cooperativity and Versatility Mimicking that of Transcription Factor PairsZutao Yu, Wei-Che Hsieh, Sefan Asamitsu, et al.Journal of Molecular Biology|July 19, 2011
Functional characterization of human cyclin T1 N-terminal region for human immunodeficiency virus-1 Tat transcriptional activationKaori Asamitsu, Yurina Hibi, Kenichi Imai, et al.Bioorganic & Medicinal Chemistry Letters|December 30, 2024
Design and synthesis of novel triazine derivatives as antimalarial agentsYuko Asamitsu, Aki Ishiyama, Yui Iwamae, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 10, 2005
Growth inhibition of multiple myeloma cells by a novel IkappaB kinase inhibitorTakaomi Sanda, Shinsuke Iida, Hiroka Ogura, et al.Oncogene|February 20, 2020
Cancer-derived UTX TPR mutations G137V and D336G impair interaction with MLL3/4 complexes and affect UTX subcellular localizationHiroyuki Kato, Kaori Asamitsu, Wendi Sun, et al.AIDS Research and Human Retroviruses|March 31, 1998
Inhibition of human immunodeficiency virus type 1 replication by a bioavailable serine/threonine kinase inhibitor, fasudil hydrochlorideT Sato, K Asamitsu, J P Yang, et al.Biochemical and Biophysical Research Communications|February 10, 2020
Identification and immunohistochemical characterization of G-quadruplexes in mouse brainSefan Asamitsu, Yoshiki Imai, Yasushi Yabuki, et al.Bioorganic & Medicinal Chemistry|June 16, 2016
Sequence-specific DNA binding by long hairpin pyrrole-imidazole polyamides containing an 8-amino-3,6-dioxaoctanoic acid unitYoshito Sawatani, Gengo Kashiwazaki, Anandhakumar Chandran, et al.Plos One|July 23, 2013
Identification of highly selective and potent histone deacetylase 3 inhibitors using click chemistry-based combinatorial fragment assemblyTakayoshi Suzuki, Yuki Kasuya, Yukihiro Itoh, et al.Journal of Medicinal Chemistry|September 15, 2018
Design and Synthesis of Novel Amino-triazine Analogues as Selective Bruton's Tyrosine Kinase Inhibitors for Treatment of Rheumatoid ArthritisWataru Kawahata, Tokiko Asami, Takao Kiyoi, et al.Pageof 9