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In-Joong Kim

Researcher at Kansas State University

Publications -  25
Citations -  568

In-Joong Kim is an academic researcher from Kansas State University. The author has contributed to research in topics: Virus & Herpes simplex virus. The author has an hindex of 10, co-authored 23 publications receiving 479 citations. Previous affiliations of In-Joong Kim include South Korean Ministry for Food, Agriculture, Forestry and Fisheries & Princeton University.

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Multiplex real-time RT-PCR for the simultaneous detection and quantification of transmissible gastroenteritis virus and porcine epidemic diarrhea virus.

TL;DR: This assay provides an effective etiological diagnostic tool for detecting and quantifying viral loads and may also prove useful for detecting infections, ultimately leading to better disease control on farms.
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DNA-Protein Vaccination Strategy Does Not Protect from Challenge with African Swine Fever Virus Armenia 2007 Strain

TL;DR: While the vaccinated pigs developed antigen-specific antibodies, immunized pig sera at the time of challenge lacked the capacity to neutralize virus, and instead was observed to enhance ASFV infection in vitro, points to a putative immune enhancement mechanism involved in ASFF pathogenesis that warrants further investigation.
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Molecular epidemiology of rabies virus isolates from South Korea.

TL;DR: The results of these studies supported the conclusion of previous studies (Kuzmin et al.) that the raccoon dogs take part in the circulation of rabies virus within their natural territories in the Far East.
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Genetic characterization of porcine epidemic diarrhea virus in Korea from 1998 to 2013

TL;DR: Although Korean PEDVs have been evolving slowly, their diverse antigenicity and genetics imply that multilateral efforts to prevent future PED outbreaks are required, suggesting that the evolution of Korean strains has been slow.
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Herpes Simplex Virus 1 Glycoprotein M and the Membrane-Associated Protein UL11 Are Required for Virus-Induced Cell Fusion and Efficient Virus Entry

TL;DR: Results indicate that gM and UL11 are required for efficient membrane fusion events during virus entry and virus spread.