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Young Hwan Chang

Researcher at Oregon Health & Science University

Publications -  157
Citations -  3010

Young Hwan Chang is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Computer science & Cancer. The author has an hindex of 20, co-authored 140 publications receiving 2034 citations. Previous affiliations of Young Hwan Chang include Korea Institute of Science and Technology & University of California, Berkeley.

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Toward Minimal Residual Disease-Directed Therapy in Melanoma.

TL;DR: Single-cell RNA sequencing to malignant cells isolated from BRAF mutant patient-derived xenograft melanoma cohorts exposed to concurrent RAF/MEK-inhibition identifies NCSCs as key drivers of resistance and highlights how gene regulatory network architecture reprogramming may be therapeutically exploited to limit cellular heterogeneity.
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Quantitative Multiplex Immunohistochemistry Reveals Myeloid-Inflamed Tumor-Immune Complexity Associated with Poor Prognosis

TL;DR: A multiplexed immunohistochemical platform with computational image processing workflows, including image cytometry, enabling simultaneous evaluation of 12 biomarkers in one formalin-fixed paraffin-embedded tissue section is described, revealing differential immune profiles based on lymphoid and myeloid cell densities, correlating with human papilloma virus status and prognosis.
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The Human Tumor Atlas Network: Charting Tumor Transitions Across Space and Time at Single-Cell Resolution

Orit Rozenblatt-Rosen, +373 more
- 16 Apr 2020 - 
TL;DR: The Human Tumor Atlas Network (HTAN), part of the NCI Cancer Moonshot Initiative, will establish a clinical, experimental, computational, and organizational framework to generate informative and accessible three-dimensional atlases of cancer transitions for a diverse set of tumor types.
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Modeling Tumor Phenotypes In Vitro with Three-Dimensional Bioprinting.

TL;DR: It is demonstrated that multi-cell-type bioprinted tissues can recapitulate aspects of in vivo neoplastic tissues and provide a manipulable system for the interrogation of multiple tumorigenic endpoints in the context of distinct tumor microenvironments.
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IFNγ-activated dermal lymphatic vessels inhibit cytotoxic T cells in melanoma and inflamed skin.

TL;DR: IFN&ggr;R is identified as an immunological switch in lymphatic vessels that balances protective immunity and immunopathology leading to adaptive immune resistance in melanoma.