Author

Tae Min Kim

Seoul National UniversityPrimary ORCID profile (0000-0003-0015-2701 · 1 paper)Unclaimed ORCID profile · follow to get notified of new preprints

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

Same name, identified by ORCID

Tae Min KimiD1 paper · Rural Development Administration

Biology Disciplines

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Genomics· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Assay:flow cytometry· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Bhumsuk Keam· 1 shared Dae Seog Heo· 1 shared Dong-Wan Kim· 1 shared Jaeku KangiD· 1 shared Jong Woo ParkiD· 1 shared Joonghoon ParkiD· 1 shared Juhyun Jin· 1 shared Su Cheong YeomiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperImmunology

Bhumsuk Keam

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2 papers

Recent·Most cited

8-OxoG in GC-rich Sp1 binding sites enhances gene transcription during adipose tissue development in juvenile mice

Jong Woo Park, Young In Han, Tae Min Kim, Tae Min Kim, Su Cheong Yeom, Jaeku Kang, Joonghoon Park

Scientific Reports · Oct 30, 2019Peer-reviewedGenomics

The CD56bright CD62L+ NKG2A+ immature cell subset is dominantly expanded in human cytokine-induced memory-like NK cells

Juhyun Jin, Yong-Oon Ahn, Tae Min Kim, Bhumsuk Keam, Dong-Wan Kim, Dae Seog Heo

This study identifies CD56bright CD62L+ NKG2A+ immature NK cells as the dominant subset in cytokine-induced memory-like NK cells and shows their distinct functional properties.

bioRxiv · Sep 9, 2018 · PreprintImmunology