Author

K. Teranishi

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 Biophysics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:flow cytometry· 2 Research Focus:batch correction / integration· 1 Approach:biophysical modeling· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

S. Ota· 2 shared Y. Yanagihashi· 2 shared A. Applebaum· 1 shared A. K. Okada· 1 shared A. Siemer· 1 shared A. Tsubouchi· 1 shared E. Mochizuki· 1 shared F. Meier· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersCell Biology

S. Ota

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Label-free ghost cytometry for manufacturing of cell therapy products

K. Teranishi, K. Wagatsuma, K. Toda, H. Nomaru, Y. Yanagihashi, H. Ochiai, S. Akai, E. Mochizuki, Y. Onda, K. Nakagawa, K. Sugimoto, S. Takahashi, H. Yamaguchi, S. Ota

This paper introduces label-free ghost cytometry (LF-GC) for cell therapy manufacturing, showing it can quantify cell count, viability, and identify cell subsets and impurities without staining.

bioRxiv · Jul 9, 2023Cell Biology

Pooled CRISPR screening of high-content cellular phenotypes by ghost cytometry

A. Tsubouchi, Y. An, Y. Kawamura, Y. Yanagihashi, Y. Murata, K. Teranishi, S. Ishiguro, H. Aburatani, N. Yachie, S. Ota

The paper introduces a ghost cytometry-based method for fast pooled CRISPR screening of high-content cellular phenotypes, including fluorescence and label-free modes, enabling genome-wide analysis of gene effects on cellular processes.

bioRxiv · Jan 26, 2023 · PreprintCell Biology

Huntingtin fibrils with different toxicity, structure, and seeding potential can be reversibly interconverted

J. M. Isas, N. K. Pandey, K. Teranishi, A. K. Okada, A. Applebaum, F. Meier, R. Langen, A. Siemer

This study shows that HTTex1 fibrils with different toxicity and structure can be reversibly interconverted through changes in C-terminal domain dynamics.

bioRxiv · Jul 16, 2019 · PreprintBiophysics