Shinji Takechi

Professor

Sojo University

Japan

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Professor Shinji Takechi is a faculty member at Sojo University in Japan. His research areas focus on enzymology, particularly the role of UDP-glucuronosyltransferases and their interactions with other cellular mechanisms. Recent publications include studies on oxidative stress, inflammatory responses, and the impact of specific compounds on cellular functions. He is actively contributing to the understanding of drug metabolism and the molecular mechanisms underlying cytotoxicity.

Articles (11)

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2025

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2025

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2024

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2024

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2023

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2022

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2022

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2021

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2021

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2020

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2020

Collaborators (1)

Peter Mackenzie

Flinders University

AUSTRALIA

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Shinji Takechi

Research Interests

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Articles (11)

Disulfide bond-mediated stabilization of the oligomers of UDP-glucuronosyltransferase 2B7

SDS-stable homo-oligomers of UDP-Glucuronosyltransferase 2B7: Involvement of disulfide bond formation via a specific cystein residue

Saponin Esculeoside A and Aglycon Esculeogenin A from Ripe Tomatoes Inhibit Dendritic Cell Function by Attenuation of Toll-like Receptor 4 Signaling

Dihydropyrazine induces endoplasmic reticulum stress and inhibits autophagy in HepG2 human hepatoma cells

Oxidative stress and cellular toxicity induced by dihydropyrazine: a comparative study with other Maillard reaction products

Use of a Baculovirus-Mammalian Cell Expression-System for Expression of Drug-Metabolizing Enzymes: Optimization of Infection With a Focus on Cytochrome P450 3A4

Dihydropyrazine suppresses TLR4-dependent inflammatory responses by blocking MAPK signaling in human hepatoma HepG2 cells

Functional Interaction between Cytochrome P450 and UDP-Glucuronosyltransferase on the Endoplasmic Reticulum Membrane: One of Post-translational Factors Which Possibly Contributes to Their Inter-Individual Differences

Molecular mechanism of dihydropyrazine-induced cytotoxicity: the possibility of an independent pathway from the receptor for advanced glycation end products

The carboxyl-terminal di-lysine motif is essential for catalytic activity of UDP-glucuronosyltransferase 1A9

The effect of dihydropyrazines on lipopolysaccharide-stimulated human hepatoma HepG2 cells via regulating the TLR4-MyD88-mediated NF-κB signaling pathway

Collaborators (1)

Peter Mackenzie

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