Author

S. Ohata

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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Microbiology· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:drug response / drug discovery· 2 Organism:fungi (other)· 2 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

M. Ishii· 3 shared T. Yamada· 3 shared H. Uga· 1 shared M. Monod· 1 shared T. Katada· 1 shared Y. Matsumoto· 1 shared

Activity by Year

2023-2024 · peak 2/yr

Co-Author Collaboration Network

6 top collaborators · 12 mutual co-author links

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3 shared papersMicrobiology

M. Ishii

Mutual co-authors in cluster

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3 papers

Recent·Most cited

An efficient gene targeting system using Δku80 and functional analysis of Cyp51A in Trichophyton rubrum.

M. Ishii, T. Yamada, S. Ohata

This paper develops an efficient gene targeting system in Trichophyton rubrum using a Δku80 strain and shows that Cyp51A contributes to azole drug tolerance by responding to efinaconazole.

bioRxiv · Apr 18, 2024Microbiology

Targeting dermatophyte Cdc42 and Rac GTPase signaling to hinder hyphal elongation and virulence

M. Ishii, Y. Matsumoto, T. Yamada, H. Uga, T. Katada, S. Ohata

This study identifies Cdc42 and Rac GTPase inhibition as a strategy to block hyphal elongation and virulence in Trichophyton rubrum, with EHop-016 showing promise as an antifungal lead.

bioRxiv · Mar 4, 2024Microbiology

The Ptk2-Pma1 pathway enhances tolerance to terbinafine in Trichophyton rubrum

M. Ishii, T. Yamada, M. Monod, S. Ohata

This study identifies the TrPtk2-TrPma1 pathway in Trichophyton rubrum as critical for terbinafine tolerance and suggests it as a target for antifungal therapy.

bioRxiv · Dec 7, 2023Microbiology