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Jeong Moon

Researcher at Korea Research Institute of Bioscience and Biotechnology

Publications -  25
Citations -  612

Jeong Moon is an academic researcher from Korea Research Institute of Bioscience and Biotechnology. The author has contributed to research in topics: Medicine & Coating. The author has an hindex of 10, co-authored 21 publications receiving 253 citations. Previous affiliations of Jeong Moon include KAIST.

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Nanogap-Rich Au Nanowire SERS Sensor for Ultrasensitive Telomerase Activity Detection: Application to Gastric and Breast Cancer Tissues Diagnosis

TL;DR: A nanogap‐rich Au nanowire (NW) surface‐enhanced Raman scattering (SERS) sensor is reported for detection of telomerase activity in various cancer cells and tissues and can diagnose gastric and breast cancer tissues accurately.
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Clustered Regularly Interspaced Short Palindromic Repeats-Mediated Surface-Enhanced Raman Scattering Assay for Multidrug-Resistant Bacteria

TL;DR: A clustered regularly interspaced short palindromic repeats-mediated surface-enhanced Raman scattering (SERS) assay for multidrug-resistant (MDR) bacteria is reported, which may prove effective for the accurate diagnosis of MDR bacterial pathogens, thus preventing severe infection by ensuring appropriate antibiotic treatment.
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Au@ZIF-8 SERS paper for food spoilage detection.

TL;DR: A metal-organic framework (MOF)-coated surface-enhanced Raman scattering (SERS) paper platform for the detection of putrescine and cadaverine is developed in this article.
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Colorimetric Detection of SARS-CoV-2 and Drug-Resistant pH1N1 Using CRISPR/dCas9.

TL;DR: A colorimetric viral detection method based on the clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 endonuclease dead (dCas9) system that successfully identified SARS-CoV-2, pH1N1, and pH1n1/H275Y viruses by the naked eye is reported.
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Simple and rapid detection of bacteria using a nuclease-responsive DNA probe

TL;DR: The probe consisting of a fluorescent dye and a quencher at the 5' and 3' termini was designed to be cleaved by nucleases such as endonucleases, exon nucleases, and DNases, which are released from bacteria using an optimized lysis buffer.