Author

H. Wanibuchi

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cancer Biology· 1 Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

M. Gi· 2 shared A. Vachiraarunwong· 1 shared D. Inaoka· 1 shared D. Oikawa· 1 shared D. Tsuruta· 1 shared F. Okada· 1 shared F. Tokunaga· 1 shared G. Qiu· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersPharmacology & Toxicology

M. Gi

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A Novel Support Vector Machine-Based One-Day, Single-Dose Prediction Model of Genotoxic Hepatocarcinogenicity in Rats

M. Gi, S. Suzuki, M. Kanki, M. Yokohira, T. Tsukamoto, M. Fujioka, A. Vachiraarunwong, G. Qiu, R. Guo, H. Wanibuchi

This paper develops a support vector machine-based model to predict genotoxic hepatocarcinogens in rats using gene expression data from a single dose and day of exposure.

bioRxiv · Feb 19, 2024Pharmacology & Toxicology

OTUD1 deubiquitylase regulates NF-κB- and KEAP1-mediated inflammatory responses and reactive oxygen species-associated cell death pathways

D. Oikawa, M. Gi, H. Kosako, K. Shimizu, H. Takahashi, M. Shiota, S. Hosomi, K. Komakura, H. Wanibuchi, D. Tsuruta, T. Sawasaki, F. Tokunaga

This study identifies OTUD1 as a deubiquitylase that suppresses NF-κB and KEAP1-mediated inflammatory and oxidative stress responses, while promoting antiviral pathways and ROS-associated cell death.

bioRxiv · Dec 26, 2021 · PreprintCell Biology

PITX1 protein interacts with ZCCHC10 to regulate hTERT mRNA transcription

T. Ohira, H. Kojima, Y. Kuroda, D. Inaoka, M. Osaki, H. Wanibuchi, F. Okada, M. Oshimura, H. Kugoh

The paper identifies a ZCCHC10-PITX1 complex that suppresses hTERT transcription, contributing to telomerase regulation in melanoma.

bioRxiv · May 16, 2019Cancer Biology