Author

C. Tei

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

Signature Assays, Organisms & Methods

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Assay:CRISPR screen· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:DNA methylation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:variant calling· 1 Approach:wet-lab / biochemical assay· 1

Frequent Co-Authors

A. Mabuchi· 2 shared A. Toyoda· 2 shared D. Kitagawa· 2 shared M. Fukuyama· 2 shared S. Hata· 2 shared T. Chinen· 2 shared K. K. Ito· 1 shared M. Genova· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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2 shared papersCell Biology

A. Mabuchi

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Author profile →

2 papers

Recent·Most cited

Comprehensive analysis of end-modified long dsDNA donors in CRISPR-mediated endogenous tagging

R. Takagi, S. Hata, C. Tei, A. Mabuchi, R. Anzai, M. Fukuyama, S. Yamamoto, T. Chinen, A. Toyoda, D. Kitagawa

This study analyzes end-modified long dsDNA donors in CRISPR-mediated endogenous tagging, showing that 5 biotinylation reduces imprecise insertions and enhances HDR efficiency.

bioRxiv · Jun 28, 2024 · PreprintCell Biology

ssDNA is not superior to dsDNA as long HDR donors for CRISPR-mediated endogenous gene tagging in human diploid cells

A. Mabuchi, S. Hata, M. Genova, C. Tei, K. K. Ito, M. Hirota, T. Komori, M. Fukuyama, T. Chinen, A. Toyoda, D. Kitagawa

This study compares ssDNA and dsDNA as HDR donors for CRISPR-mediated gene tagging in human diploid cells, finding dsDNA more efficient for precise insertion.

bioRxiv · Jun 1, 2022 · PreprintCell Biology