Author

Jiyeon Ohk

Yonsei University

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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Bioengineering· 1 Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

Hosung JungiD· 3 shared Heon Yung GeeiD· 2 shared Jae Won RohiD· 2 shared Ji Won HongiD· 2 shared Ala WooiD· 1 shared Annie LiniD· 1 shared Chul Hoon KimiD· 1 shared Hae-Sol Shin· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersBioengineering

Hosung JungORCID

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Author profile →

3 papers

Recent·Most cited

MechanoMR microparticle (M3) sensors reveal dynamic stress loading as a driver of epithelial-mesenchymal transition

Minji An, Ri Yu, Annie Lin, Jinho Jang, Jiyeon Ohk, Young‐Joo Kim, Hosung Jung, Minsuk Kwak, Young‐wook Jun, Jinwoo Cheon

The paper introduces M3 sensors to measure tissue stress dynamics and shows that abrupt stress increases drive epithelial-mesenchymal transition in cancer.

bioRxiv · Dec 13, 2025 · PreprintBioengineering

TMEM145 is a key component in stereociliary link structures of outer hair cells

Jae Won Roh, Kyung Seok Oh, Jiahn Lee, Yujin Choi, Soomin Kim, Ji Won Hong, Yelim Kim, Hogun Lew, Seung Hyun Jang, Hae-Sol Shin, Jiyeon Ohk, Hosung Jung, Kyoung Yul Seo, Jinwoong Bok, Chul Hoon Kim, Heon Yung Gee

This study identifies TMEM145 as a critical transmembrane protein in OHC stereociliary structures, showing its necessity for structural integrity and auditory function.

bioRxiv · Feb 10, 2025 · PreprintNeuroscience

The founder missense mutation of WFDC2 leads to severe respiratory distress accompanied by bronchiectasis and rhinosinusitis

Jae Won Roh, Jiyoung Oh, Se Jin Kim, Ji Won Hong, Jiyeon Ohk, Hyo Sup Shim, Hyung‐Ju Cho, Ala Woo, Song Yee Kim, Young Ae Kang, Hosung Jung, Kyung Won Kim, Moo Suk Park, Heon Yung Gee

This study identifies a novel WFDC2 mutation causing severe respiratory disease with features similar to cystic fibrosis and primary ciliary dyskinesia in Korean patients.

medRxiv · Nov 16, 2024 · PreprintGenetic & Genomic Medicine