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Jin Ho Oh

Researcher at Samsung

Publications -  17
Citations -  458

Jin Ho Oh is an academic researcher from Samsung. The author has contributed to research in topics: Circulating tumor cell & Filter (video). The author has an hindex of 10, co-authored 17 publications receiving 417 citations. Previous affiliations of Jin Ho Oh include Cedars-Sinai Medical Center.

Papers
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Journal ArticleDOI

Highly efficient assay of circulating tumor cells by selective sedimentation with a density gradient medium and microfiltration from whole blood.

TL;DR: It is observed that greater than 99% of leukocytes in whole blood were effectively removed at an optimal centrifugal force, due to differences in their sedimentation rates, yielding a much purer sample compared to other filter-based methods.
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Efficient Isolation and Accurate In Situ Analysis of Circulating Tumor Cells Using Detachable Beads and a High‐Pore‐Density Filter

TL;DR: A novel approach for isolation and subsequent in situ protein-expression analysis of CTCs is demonstrated using detachable beads termed RIA (reversible bead attachment for cell isolation and analysis), demonstrating the incompatibility of in situ quantitative analysis with bead-based capture methods.
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Fully Automated Circulating Tumor Cell Isolation Platform with Large-Volume Capacity Based on Lab-on-a-Disc

TL;DR: A novel centrifugal microfluidic platform that can isolate the rare cells from a large volume of whole blood and performs epidermal growth factor receptor (EGFR) mutation analysis with HCC827 lung cancer cells and the isolated cells were successfully detected for the mutation by PCR clamping and direct sequencing.
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Simultaneous capture and in situ analysis of circulating tumor cells using multiple hybrid nanoparticles.

TL;DR: Using hybrid nanoparticles (HNPs), it is possible to count, analyze in situ protein expression, and culture CTCs, all from the same set of cells, enabling a wide range of molecular- and cellular-based studies using C TCs.
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A microchip filter device incorporating slit arrays and 3-D flow for detection of circulating tumor cells using CAV1-EpCAM conjugated microbeads.

TL;DR: A microchip filter device incorporating slit arrays and 3-dimensional flow that can separate heterogeneous population of cells with marker for CTCs is reported, enabling the enhanced capture yield from metastatic breast cancer patients and obtained cells that expressed various EMT markers.