Author

Satoshi Suzuki

Kyoto UniversityORCID 0009-0003-7478-5808Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Assay:CRISPR screen· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1

Frequent Co-Authors

Chikako OkuboiD· 2 shared Kazutoshi TakahashiiD· 2 shared Mari Hamao· 2 shared Michiko NakamuraiD· 2 shared Knut WoltjeniD· 1 shared Lu NiiD· 1 shared Qi FangiD· 1 shared Takuya MurakamiiD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

8 top collaborators · 24 mutual co-author links

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2 shared papersCell Biology

Chikako OkuboORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintMay 20, 2026

EIF3H Sustains Translational Programs Essential for Proliferation in Human Primed Pluripotency

Satoshi Suzuki, Chikako Okubo, Michiko Nakamura…·Kazutoshi Takahashi

This study identifies EIF3H as essential for human primed pluripotency by regulating translation of metallothionein genes, impacting proliferation and differentiation.

DOI 10.64898/2026.05.18.725809

humanbulk RNA-seq

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Cell BiologybioRxivPreprintMay 14, 2026

Comparative benchmarking of CRISPRi and CasRx in standardized pluripotent stem cell platforms reveals context-dependent knockdown performance

Lu Ni, Takuya Murakami, Satoshi Suzuki…·Kazutoshi Takahashi

This study compares CRISPRi and CasRx for gene knockdown in human pluripotent stem cells, finding CRISPRi provides faster and stronger repression but slower recovery, while CasRx offers reversible knockdown with isoform resolution but lower efficiency.

DOI 10.64898/2026.05.13.724469

humanCRISPR screen

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