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Environmental Pollution (Barking, Essex : 1987)|December 3, 2015
Different cesium-137 transfers to forest and stream ecosystemsMasaru Sakai, Takashi Gomi, Junjiro N Negishi, et al.
Acta Crystallographica. Section D, Biological Crystallography|June 5, 2003
Preparation and crystallization of human flap endonuclease FEN-1 in complex with proliferating-cell nuclear antigen, PCNAShigeru Sakurai, Ken Kitano, Kengo Okada, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|March 3, 2007
Preparation and preliminary X-ray diffraction analysis of crystals of bacterial flagellar sigma factor sigma 28 in complex with the sigma 28-binding region of its antisigma factor, FlgMKengo Okada, Hisako Ichihara, Hiroyuki Takahashi, et al.
Cell|November 18, 2006
Crystal structure of the DsbB-DsbA complex reveals a mechanism of disulfide bond generationKenji Inaba, Satoshi Murakami, Mamoru Suzuki, et al.
Biochemical and Biophysical Research Communications|May 15, 2017
Discovery of a novel prolyl-tRNA synthetase inhibitor and elucidation of its binding mode to the ATP site in complex with l-prolineRyutaro Adachi, Kengo Okada, Robert Skene, et al.
Bioorganic & Medicinal Chemistry|September 14, 2010
N-phenyl-N'-[4-(5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)phenyl]ureas as novel inhibitors of VEGFR and FGFR kinasesYuya Oguro, Naoki Miyamoto, Terufumi Takagi, et al.
The EMBO Journal|December 24, 2004
Structural basis for recruitment of human flap endonuclease 1 to PCNAShigeru Sakurai, Ken Kitano, Hiroto Yamaguchi, et al.
Molecular Pharmaceutics|October 28, 2025
Insights into In Vivo Performance of Amorphous Solid Dispersions: Evaluation Using a Surrogate Marker for Drug Release Profiles and Pharmacokinetic AnalysisShoko Takeyama, Kengo Okada, Takato Masada, et al.
Bioorganic & Medicinal Chemistry|September 14, 2010
Design, synthesis, and evaluation of 5-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine derivatives: novel VEGFR2 kinase inhibitors binding to inactive kinase conformationYuya Oguro, Naoki Miyamoto, Kengo Okada, et al.
Nature|July 22, 2014
High-resolution structure of the human GPR40 receptor bound to allosteric agonist TAK-875Ankita Srivastava, Jason Yano, Yoshihiko Hirozane, et al.
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