Author

Y. M. Park

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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Cancer Biology· 2 Plant Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Approach:statistical model· 2 Organism:Arabidopsis· 1 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1

Frequent Co-Authors

J. Kim· 2 shared C. J. Lee· 1 shared C. Lambing· 1 shared D. Byun· 1 shared D. C. Nageswaran· 1 shared D. H. Kim· 1 shared D. Kim· 1 shared E.-J. Kim· 1 shared

Activity by Year

2019-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersPlant Biology

J. Kim

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

HEAT SHOCK FACTOR BINDING PROTEIN limits meiotic crossovers by repressing HEI10 transcription

J. Kim, J. Park, H. Kim, N. Son, C. Lambing, E.-J. Kim, J. Kim, D. Byun, Y. Lee, Y. M. Park, D. C. Nageswaran, P. Kuo, T. V. T. Dang, I. Hwang, I. R. Henderson, K. Choi

This study identifies HSBP as a repressor of HEI10 transcription and meiotic crossovers in Arabidopsis by binding to HSFs and maintaining DNA methylation at the HEI10 promoter.

bioRxiv · Oct 17, 2021Plant Biology

Visualizing cancer-originated acetate uptake through MCT1 in reactive astrocytes demarcates tumor border and extends survival in glioblastoma patients

H. Y. Ko, J.-I. Chung, D. Kim, Y. M. Park, H. H. Jo, S. Lee, S. Y. Kim, J. Kim, J.-H. Chun, K.-S. Han, M. Lee, Y. Ju, S. J. Park, K. D. Park, M.-H. Nam, , M. Yun

This study uses AcePET to visualize tumor boundaries and reactive astrocytes in GBM, showing that targeting MCT1 improves survival by enabling complete resection of cancer stem cells.

bioRxiv · Apr 13, 2021 · PreprintCancer Biology

Single-cell transcriptome analysis reveals TOX as a promoting factor for T-cell exhaustion and a predictor for anti-PD1 responses in human cancer

K. Kim, S. Park, S. Y. Park, G. Kim, S. M. Park, J.-W. Cho, D. H. Kim, Y. M. Park, Y. W. Koh, H. R. Kim, S.-J. Ha, I. Lee

The paper identifies TOX as a factor promoting T-cell exhaustion and predicts its role in anti-PD1 therapy outcomes using single-cell transcriptome data from cancer patients.

bioRxiv · Dec 3, 2019 · PreprintCancer Biology