Y. Sekiguchi

Identification of protein kinase CK2 inhibitors using solvent dipole ordering virtual screening.

K. Kitaura, G. Tsujimoto, T. Kinoshita, 2015, European journal of medicinal chemistry.

Synthesis of (−)-(5R,6S)-6-acetoxyhexadecanolide based on l-proline-catalyzed asymmetric aldol reactions

H. Kotsuki, Y. Sekiguchi, Y. Ichikawa, 2006 .

Ligand binding to human prostaglandin E receptor EP4 at the lipid-bilayer interface

T. Hirokawa, S. Narumiya, S. Iwata, 2018, Nature Chemical Biology.

A detailed thermodynamic profile of cyclopentyl and isopropyl derivatives binding to CK2 kinase

K. Kitaura, G. Tsujimoto, H. Fukada, 2011, Molecular and Cellular Biochemistry.

Strained surface layers of quartz plates produced by lapping and polishing and their influence on quartz resonator performance

H. Funakubo, Y. Sekiguchi, 1980 .

Structure of human protein kinase CK2 alpha 2 with a potent indazole-derivative inhibitor.

K. Kitaura, G. Tsujimoto, T. Kinoshita, 2009, Acta crystallographica. Section F, Structural biology and crystallization communications.

High-Pressure-Promoted Asymmetric Aldol Reactions of Ketones with Aldehydes Catalyzed by l-Proline

H. Kotsuki, Y. Sekiguchi, A. Sasaoka, 2003 .

A new class of chiral pyrrolidine-pyridine conjugate base catalysts for use in asymmetric Michael addition reactions.

T. Ishii, H. Kotsuki, Y. Sekiguchi, 2004, Journal of the American Chemical Society.

Structural and functional studies of the Apical Sodium Dependent Bile Acid Transporter

Y. Sekiguchi, 2014 .

Structural insight into human CK2alpha in complex with the potent inhibitor ellagic acid.

K. Kitaura, G. Tsujimoto, T. Kinoshita, 2009, Bioorganic & medicinal chemistry letters.

Crystal structure of human CK2α at 1.06 Å resolution

T. Kinoshita, I. Nakanishi, Shinya Nakamura, 2013, Journal of synchrotron radiation.