Author

J. Y. 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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Biochemistry· 1 Cancer Biology· 1 Immunology· 1 Microbiology· 1 Plant Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Organism:human· 4 Assay:bulk RNA-seq· 2 Research Focus:host-pathogen & immune response· 2 Approach:biophysical modeling· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1

Frequent Co-Authors

H. J. Kim· 2 shared H. S. Lee· 2 shared A. K. Shukla· 1 shared A. Talebi· 1 shared B. Y. Park· 1 shared C. Goncalves· 1 shared D. Jung· 1 shared F. Cai· 1 shared

Activity by Year

2019-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersImmunology

H. J. Kim

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

Disrupting peroxisomes alters lipid metabolism in melanoma and uncovers a novel therapeutic vulnerability in combination with MAPK-targeted therapies

F. Huang, F. Cai, M. S. Dahabieh, K. Gunawardena, A. Talebi, J. Dehairs, F. El-Turk, J. Y. Park, C. Goncalves, N. Gagnon, J. Su, P. Gaub, J.-S. Joyal, J. J. Mitchell, J. V. Swinnen, , S. V. del Rincon

This paper identifies a metabolic vulnerability in melanoma cells by disrupting peroxisomes and shows that combining this with MAPK-targeted therapies enhances anti-tumor effects.

bioRxiv · Oct 25, 2022 · PreprintCancer Biology

Plant-derived insulator-like sequences for control of transgene expression

J. Y. Park, L. Kovar, P. R. LaFayette, J. Wallace, W. A. Parrott

This study identifies plant-derived insulator-like sequences that reduce ectopic transgene expression but also decrease promoter effectiveness, suggesting they function as silencers with potential utility in plant transformation.

bioRxiv · Nov 4, 2021 · PreprintPlant Biology

E prostanoid receptor 4 expressing macrophages promote the regeneration of the intestinal epithelial barrier upon inflammation

Y. R. Na, D. Jung, M. Stakenborg, G. J. Gu, M. R. Jeong, H. R. Jang, S. Y. Suh, H. J. Kim, Y. H. Kwon, T. S. Sung, S. B. Ryoo, K. J. Park, J. P. Im, J. Y. Park, Y. S. Lee, , S. H. Seok

The paper identifies EP4-expressing intestinal macrophages that promote mucosal healing by secreting CXCL1 during inflammation resolution.

bioRxiv · May 4, 2020Immunology

Naringenin as an antibacterial reagent controlling of biofilm formation and fatty acid metabolism in MRSA

H.-S. Song, S. K. Bhatia, R. Gurav, T.-R. Choi, H. J. Kim, Y.-L. Park, Y.-H. Han, J. Y. Park, S. m. Lee, S. L. Park, H. S. Lee, W. Kim, Y.-G. Kim, Y.-H. Yang

This study identifies naringenin as an antibacterial agent that reduces biofilm formation and fatty acid secretion in MRSA and shows synergy with oxacillin.

bioRxiv · Mar 8, 2020 · PreprintMicrobiology

Crystal structure of β-arrestin 2 in complex with an atypical chemokine receptor phosphopeptide reveals an alternative active conformation

K. Min, H.-J. Yoon, J. Y. Park, M. Baidya, H. Dwivedi, J. Maharana, K. Y. Chung, A. K. Shukla, H. H. Lee

The paper presents a crystal structure of β-arrestin 2 bound to a phosphopeptide from ACKR3, revealing an alternative active conformation distinct from β-arrestin 1.

bioRxiv · Sep 29, 2019 · PreprintBiochemistry