Author

M. Fakruddin

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 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Research Focus:host-pathogen & immune response· 1 Assay:proteomics· 1

Frequent Co-Authors

H. Takizawa· 2 shared T. Morishima· 2 shared F. Butter· 1 shared F. Wei· 1 shared G. Nakato· 1 shared H. Baba· 1 shared J. Moon· 1 shared K. Tomizawa· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersCell Biology

H. Takizawa

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2 papers

Recent·Most cited

Mitochondrial translation regulates terminal erythroid differentiation by maintaining iron homeostasis

T. Morishima, M. Fakruddin, T. Masuda, Y. Wang, V. A. C. Schoonenberg, F. Butter, Y. Arima, T. Akaike, K. Tomizawa, F. Wei, T. Suda, H. Takizawa

This study shows that Mto1 dysfunction disrupts mitochondrial translation, leading to iron overload and defective erythroid differentiation.

bioRxiv · Mar 5, 2023Cell Biology

Hematopoietic stem and progenitor cells integrate Bacteroides-derived innate immune signals to promote gut tissue repair

Y. Hayashi, M. Sezaki, G. Nakato, S. Biswas, M. Fakruddin, T. Morishima, J. Moon, S. Ahn, P. Kim, Y. Miyamoto, H. Baba, S. Fukuda, H. Takizawa

This study shows that Bacteroides activates HSPCs in the BM during acute gut inflammation to promote tissue repair, but impairs HSC function in chronic inflammation and aging.

bioRxiv · Oct 5, 2021 · PreprintPathology