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Jae-Hyun Park

Researcher at University of Chicago

Publications -  94
Citations -  4053

Jae-Hyun Park is an academic researcher from University of Chicago. The author has contributed to research in topics: Cancer & T cell. The author has an hindex of 34, co-authored 93 publications receiving 3459 citations. Previous affiliations of Jae-Hyun Park include University of Tokyo & Seoul National University.

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Imaging Tumor-Stroma Interactions during Chemotherapy Reveals Contributions of the Microenvironment to Resistance

TL;DR: Live imaging of chemotherapy-treated mouse mammary carcinomas allowed us to follow drug distribution, cell death, and tumor-stroma interactions, and associations between vascular leakage and response to doxorubicin, showing that the microenvironment contributes critically to drug response via regulation of vascular permeability and innate immune cell infiltration.
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Identification of Genes with Differential Expression in Acquired Drug-Resistant Gastric Cancer Cells Using High-Density Oligonucleotide Microarrays

TL;DR: Midkine (MDK), a heparin-binding growth factor, was overexpressed in all drug-resistant cell lines, strongly suggesting that MDK might contribute to multidrug resistance in gastric cancer cells.
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PDZ-Binding Kinase/T-LAK Cell-Originated Protein Kinase, a Putative Cancer/Testis Antigen with an Oncogenic Activity in Breast Cancer

TL;DR: It is suggested that PBK/TOPK is the cancer/testis antigen and its kinase function is likely to be related to its oncogenic activity, and it is suggested to be a promising molecular target for breast cancer therapy.
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Involvement of maternal embryonic leucine zipper kinase (MELK) in mammary carcinogenesis through interaction with Bcl-G, a pro-apoptotic member of the Bcl-2 family.

TL;DR: The findings suggest that the kinase activity of MELK is likely to affect mammary carcinogenesis through inhibition of the pro-apoptotic function of Bcl-GL.
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Myasthenic crisis and polymyositis induced by one dose of nivolumab

TL;DR: T cell receptor repertoire analysis using next‐generation sequencing technologies and identified infiltration of clonally expanded T cell populations in the skeletal muscle after nivolumab treatment, implying a very strong T cell immune response against muscular cells.