Author

D. Saigusa

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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Cell Biology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:genetic perturbation / CRISPR· 1 Organism:mouse· 1

Frequent Co-Authors

H. Kato· 1 shared H. Nishizawa· 1 shared H. Shimokawa· 1 shared K. Igarashi· 1 shared K. Suzuki· 1 shared M. Matsumoto· 1 shared M. Sato· 1 shared T. Shindo· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperCell Biology

H. Kato

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1 paper

Recent·Most cited

Ferroptosis is programmed by the coordinated regulation of glutathione and iron metabolism by BACH1

H. Nishizawa, M. Matsumoto, T. Shindo, D. Saigusa, H. Kato, K. Suzuki, M. Sato, Y. Ishii, H. Shimokawa, K. Igarashi

This study identifies BACH1 as a regulator of ferroptosis by modulating glutathione and iron metabolism, showing its role in myocardial infarction resistance.

bioRxiv · May 21, 2019Cell Biology