Author

T. Ishibashi

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

Biology Disciplines

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Biochemistry· 2 Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:ATAC-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:chromatin & epigenetic regulation· 1 Assay:scRNA-seq· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Iida· 1 shared A. Matsushima· 1 shared A. Sato· 1 shared D. Ding· 1 shared E. Hondo· 1 shared E. Yoshihara· 1 shared H. Shimoda· 1 shared K. Tagawa· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperPharmacology & Toxicology

A. Iida

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Epithelial cell chirality emerges through the dynamic concentric pattern of actomyosin cytoskeleton

T. Yamamoto, T. Ishibashi, Y. Mimori-Kiyosue, S. Hiver, N. Tokushige, M. Tarama, M. Takeichi, T. Shibata

This study investigates how molecular chirality leads to cellular chirality in epithelial cells, revealing that concentric actomyosin filaments drive intracellular rotation.

bioRxiv · Aug 16, 2023Cell Biology

FDA-approved drug screening identified micafungin as an antiviral agent against bat-borne emerging zoonotic Pteropine orthoreovirus

T. Katta, A. Sato, N. Kadofusa, T. Ishibashi, H. Shimoda, A. Iida, E. Hondo

The paper screens FDA-approved drugs to identify micafungin as an antiviral agent against Pteropine orthoreovirus.

bioRxiv · Sep 21, 2022 · PreprintPharmacology & Toxicology

Testis-specific H2BFWT disrupts nucleosome integrity through reductions of DNA-histone interactions

D. Ding, M. Y. H. Pang, M. Deng, T. T. Nguyen, X. Sun, Z. Xu, Y. Zhang, Y. Zhai, Y. Yan, T. Ishibashi

This study identifies H2BFWT's role in spermatogenesis by showing its impact on nucleosome stability and gene expression through structural and functional analyses.

bioRxiv · Jul 20, 2022 · PreprintBiochemistry

Bisphenol A derivatives act as novel coactivator binding inhibitors for estrogen receptor β

M. Iwamoto, T. Masuya, M. Hosose, K. Tagawa, T. Ishibashi, E. Yoshihara, M. Downes, R. M. Evans, A. Matsushima

This study identifies bisphenol A derivatives as novel coactivator binding inhibitors for estrogen receptor β, showing dual agonist/antagonist activities and a new ligand interaction site.

bioRxiv · May 10, 2021Biochemistry