Author

Y. Shindo

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 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Organism:Drosophila· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

A. A. Amodeo· 1 shared A. Arakawa· 1 shared A. Nakagawa· 1 shared A. Tada· 1 shared C. Ono· 1 shared D. M. Standley· 1 shared E. E. Nakayama· 1 shared H. Arase· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperCell Biology

A. A. Amodeo

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2 papers

Recent·Most cited

An infectivity-enhancing site on the SARS-CoV-2 spike protein is targeted by COVID-19 patient antibodies

Y. Liu, W. T. Soh, A. Tada, A. Arakawa, S. Matsuoka, E. E. Nakayama, S. Li, C. Ono, S. Torii, K. Kishida, H. Jin, W. Nakai, N. Arase, A. Nakagawa, Y. Shindo, , H. Arase

This study identifies an NTD site on SARS-CoV-2 spike protein that enhances infectivity when targeted by antibodies, and finds these antibodies are present in hospitalized patients and some uninfected donors.

bioRxiv · Dec 18, 2020Microbiology

Excess histone H3 is a Chk1 inhibitor that controls embryonic cell cycle progression

Y. Shindo, A. A. Amodeo

This study shows that excess histone H3 inhibits Chk1 to promote cell cycle progression in Drosophila embryos, revealing a mechanism for MBT regulation.

bioRxiv · Jun 9, 2020 · PreprintCell Biology