T. Yamazaki

The paper determines the dimeric structure of VanX using NMR and identifies a monomeric form for inhibitor screening.

The paper identifies how NEAT1 domains specify shell protein composition in paraspeckles, enabling their independence from nuclear speckles through phase separation.

The paper investigates the bioluminescence mechanism of Gaussia Luciferase using azacoelenterazine, revealing the role of salt and monovalent anions and structural changes in catalysis.

This study identifies YwfG as a cell-surface protein in Lactococcus lactis that binds α-1,2-linked mannose, revealing its role in interactions with yeast cells.

The paper develops a theoretical model explaining how nascent pre-rRNAs suppress fibrillar center growth in nucleoli through lateral pressure, supported by experimental validation.

The paper models paraspeckles as triblock copolymer micelles and predicts structural changes based on arcRNA block length, validated by experiments.

This paper determines the solution structure of Gaussia Luciferase using NMR and identifies a potential coelenterazine binding cavity involved in bioluminescence.

This study develops a Western blot method with deglycosylation to detect Epo and ESAs in urine and plasma, showing the kidney as the main site of Epo production under hypoxia.