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Scientific Reports|June 8, 2021
A cell-free assay implicates a role of sphingomyelin and cholesterol in STING phosphorylationKanoko Takahashi, Takahiro Niki, Emari Ogawa, et al.Proceedings of the National Academy of Sciences of the United States of America|August 10, 2006
Glycoproteomic probes for fluorescent imaging of fucosylated glycans in vivoMasaaki Sawa, Tsui-Ling Hsu, Takeshi 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.Bioorganic & Medicinal Chemistry Letters|November 9, 2019
An isoform-selective inhibitor of tropomyosin receptor kinase A behaves as molecular glueNoritaka Furuya, Takaki Momose, Kenji Katsuno, et al.European Journal of Medicinal Chemistry|March 11, 2017
Discovery of novel furanone derivatives as potent Cdc7 kinase inhibitorsTakayuki Irie, Tokiko Asami, Ayako Sawa, et al.Journal of Medicinal Chemistry|February 8, 2002
New strategy for antedrug application: development of metalloproteinase inhibitors as antipsoriatic drugsMasaaki Sawa, Takako Tsukamoto, Takao Kiyoi, et al.Bioorganic & Medicinal Chemistry Letters|February 3, 2005
Tryptamine-based human beta3-adrenergic receptor agonists. Part 3: improved oral bioavailability via modification of the sulfonamide moietyMasaaki Sawa, Kazuhiro Mizuno, Hiroshi Harada, et al.Bioorganic & Medicinal Chemistry|January 18, 2005
Discovery of 1,7-cyclized indoles as a new class of potent and highly selective human beta3-adrenergic receptor agonists with high cell permeabilityKazuhiro Mizuno, Masaaki Sawa, Hiroshi Harada, et al.Scientific Reports|December 11, 2019
Cdc7 kinase stimulates Aurora B kinase in M-phaseSayuri Ito, Hidemasa Goto, Kinue Kuniyasu, et al.Nature Communications|August 27, 2016
TNIK inhibition abrogates colorectal cancer stemnessMari Masuda, Yuko Uno, Naomi Ohbayashi, et al.Pageof 7