Author

H. Fujisaki

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Biophysics· 1 Cell Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

S. Hattori· 2 shared T. Hayashi· 2 shared A. Kidera· 1 shared D. O. Wang· 1 shared E. Zu· 1 shared K. Mizuno· 1 shared K. Moritsugu· 1 shared K. Sekiguchi· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

Click any collaborator node to inspect or filter shared papers

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

Curved chords = mutual co-authorship

2 shared papersPhysiology

S. Hattori

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Bi-phasic effect of gelatin in myogenesis and skeletal muscle regeneration

X. l. Liu, E. Zu, X. Y. Chang, Z. Q. Wang, X. R. Li, Q. Yu, K.-i. Kamei, T. Hayashi, K. Mizuno, S. Hattori, H. Fujisaki, T. Ikejima, D. O. Wang

This study identifies a bi-phasic effect of gelatin on skeletal muscle regeneration through ROS-mediated signaling, showing low-dose gelatin promotes regeneration while high-dose inhibits it.

bioRxiv · May 26, 2021Physiology

Adhesion to type I collagen fibrous gels induces E- to N- cadherin switching without other EMT-related phenotypes in lung carcinoma cell A549

H. Fujisaki, S. Futaki, M. Yamada, K. Sekiguchi, T. Hayashi, S. Hattori

This study shows that A549 lung cancer cells cultured on type I collagen gels switch from E-cadherin to N-cadherin without other epithelial-mesenchymal transition features.

bioRxiv · Oct 2, 2020 · PreprintCell Biology

Energetics and Conformational Pathways of Functional Rotation in the Multidrug Transporter AcrB

Y. Matsunaga, T. Yamane, T. Terada, K. Moritsugu, H. Fujisaki, S. Murakami, M. Ikeguchi, A. Kidera

This study calculates the minimum free energy pathway of functional rotation in AcrB, linking it to proton translocation and drug transport at the atomic level.

bioRxiv · Aug 8, 2017Biophysics