Ji-Yeon Kim on Muck Rack

Ji-Yeon Kim

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As seen in: Nature, Wiley Online Library, Cardiology in the Young, IEEE, MDPI, JAMA Oncology, Royal Society of Chemistry, Cell Reports Medicine, ONCOLOGY journal, Archives of Pathology and
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Articles

Whole-genome landscapes of 1,364 breast cancers - Nature

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By Jonghan Yu, Brian Oh, Ji-Yeon Kim, Young Lee, Kabsoo Shin, Jun Mo Kang, Yuna Lee Verified, Won-Chul Lee, Jeongmin Lee, Young Seok Ju, Soo Yeon Bae
| Nature Verified
Abstract Breast cancer remains a major global health challenge1. Here, to comprehensively characterize its genomic landscape and the clinical significance of genomic characteristics, we analysed whole-genome sequences from 1,364 clinically annotated breast cancers, with transcriptome data available for most cases. Our study expands the repertoire of oncogenic alterations and identifies novel driver genes, recurrent gene fusions, structural variants and copy number alterations.
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Single-cell transcriptomics of the myeloid milieu reveals an angiogenic niche in triple-negative breast cancer - Experimental & Molecular Medicine

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By Ji-Yeon Kim, Paul Robson, Charles Lee, Minkyu Shim
| Nature Verified
Abstract Intratumoral myeloid cells are highly heterogeneous in terms of development and function and are pivotal for forming and regulating the tumor microenvironment. However, the myeloid milieu in triple-negative breast cancer (TNBC) remains poorly understood. Here, to elucidate this myeloid milieu, we integrated in-house and public single-cell RNA sequencing data. We detected diverse neutrophil and mononuclear-phagocyte subtypes and delineated their developmental trajectories and functions.
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Keratin degradation reflects a starvation survival strategy in Fervidobacterium islandicum AW-1

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By Byoung-Chan Kim, Dong-Woo Lee, Ji-Yeon Kim, Jae-Yoon Sung
| biorxiv.org
Abstract Keratin is a highly cross-linked, disulfide-rich protein that resists proteolysis, which poses a major challenge for microbial degradation. Here, we show that Fervidobacterium islandicum AW-1 initiates a starvation-induced keratinolytic program involving membrane-associated proteases and redox-mediated sulfitolysis.
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