Author

J. Imai

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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Immunology· 1 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:host-pathogen & immune response· 2 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

A. Nusrat· 1 shared A. Rosevelt· 1 shared C. Alteri· 1 shared C. K. Muraleedharan· 1 shared C. McCarthy· 1 shared E. Koike· 1 shared H. Nagao-Kitamoto· 1 shared J. L. Golob· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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

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1 shared paperMicrobiology

A. Nusrat

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Mucolytic bacteria license pathobionts to acquire host-derived nutrients during dietary nutrient restriction

K. Sugihara, S. Kitamoto, P. Saraithong, H. Nagao-Kitamoto, C. McCarthy, M. Hoostal, A. Rosevelt, C. K. Muraleedharan, M. G. Gillilland, J. Imai, M. Omi, S. Bishu, J. Y. Kao, C. Alteri, N. Barnich, , N. Kamada

The paper shows that mucolytic bacteria enable pathobionts to acquire host-derived nutrients during dietary restriction, allowing them to thrive in the gut.

bioRxiv · Jan 17, 2022Microbiology

A novel effect of the antigenic peptides position for presentation upon MHC class I

J. Imai, M. Otani, E. Koike, Y. Yokoyama, M. Maruya, S. Koyasu, T. Sakai

The paper identifies that N-terminal antigenic peptides are more efficiently presented by MHC-I than C-terminal peptides, linked to rapid degradation of newly synthesized proteins.

bioRxiv · May 29, 2019 · PreprintImmunology