Author

R. S. Kasai

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· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 2 Assay:imaging· 2 Approach:microscopy & imaging analysis· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1

Frequent Co-Authors

A. Kusumi· 3 shared T. A. Tsunoyama· 2 shared T. K. Fujiwara· 2 shared B. Tang· 1 shared C. Hoffmann· 1 shared C. Tan· 1 shared D. Milovanovic· 1 shared D. Sasaki· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersCell Biology

A. Kusumi

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A nano-liquid hub integrating growth and immune-evasion signaling to promote cell survival

T. A. Tsunoyama, C. Hoffmann, D. Sasaki, C. Tan, B. Tang, K. M. Hirosawa, Y. L. Nemoto, R. S. Kasai, T. Fujiwara, K. G. Suzuki, Y. Sugita, H. Ishikawa, D. Milovanovic, A. Kusumi

The paper identifies GEM, a nano-liquid hub that integrates growth and immune-evasion signaling to enhance cell survival in mice.

bioRxiv · Dec 30, 2021 · PreprintCell Biology

High-speed single-molecule imaging reveals signal transduction by induced transbilayer raft phases

I. Koyama-Honda, T. K. Fujiwara, R. S. Kasai, K. G. N. Suzuki, E. Kajikawa, H. Tsuboi, T. A. Tsunoyama, A. Kusumi

High-speed single-molecule imaging shows outer-leaflet rafts induce transbilayer raft phases that recruit inner-leaflet signaling molecules via lipid interactions.

bioRxiv · Jun 20, 2020Cell Biology

Metastable GPCR dimers trigger the basal signal by recruiting G-proteins

R. S. Kasai, T. K. Fujiwara, A. Kusumi

This study shows that metastable GPCR homo-dimers recruit G-proteins to induce basal signals, and inverse agonists block this recruitment specifically in dimers.

bioRxiv · Feb 10, 2020 · PreprintBiochemistry