Author

Y. Fijita

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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Biochemistry· 1 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1 Research Focus:development & morphogenesis· 1 Research Focus:host-pathogen & immune response· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

A. Wiberg· 1 shared D. Bi· 1 shared D. Furniss· 1 shared H. K. Senapati· 1 shared K. B. Paiva· 1 shared K. Dzobo· 1 shared K. Inoue· 1 shared M. Inada· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperBiochemistry

A. Wiberg

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Mechanical imbalance between normal and transformed cells drives epithelial homeostasis through cell competition

P. Gupta, S. Kayal, N. Tanimura, S. P. Pothapragada, H. K. Senapati, P. Devendran, Y. Fijita, D. Bi, T. Das

This study identifies a mechanical imbalance between normal and transformed cells in epithelial tissue, showing that transformed cells are more compressible due to weakened adhesions, driving cell competition and homeostasis.

bioRxiv · Sep 27, 2023 · PreprintBiophysics

A Ca2+ wave generates a force during cell extrusion in zebrafish

S. Yamada, Y. Bessho, Y. Fijita, Y. Hosokawa, T. Matsui

This study shows that a Ca2+ wave in zebrafish generates force during cell extrusion by inducing polarized movements via IP3 receptor and trpc1.

bioRxiv · Jul 14, 2021 · PreprintCell Biology

An SNP variant MT1-MMP with a defect in its collagenolytic activity confers the fibrotic phenotype of Dupuytren's Disease

Y. Itoh, M. Ng, A. Wiberg, K. Inoue, N. Hirata, K. B. Paiva, N. Ito, K. Dzobo, N. Sato, V. Gifford, Y. Fijita, M. Inada, D. Furniss

This study identifies an SNP variant in MMP14 that reduces collagenolytic activity, contributing to the fibrotic phenotype of Dupuytren's Disease.

bioRxiv · Jun 9, 2020Biochemistry