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Kyoungmi Kim on Muck Rack

Kyoungmi Kim

As seen in: Nature, PLOS, MDPI, JAMA Dermatology, BioRxiv
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Articles

In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON - Nature Communications

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By Sanghun J. Kim, Seongho Hong, Sol Kim, Soo-Ji Park, Lark Kyun Kim, Seonghyun Lee, Kyoung Yul Seo, Je Kyung Seong, Kyoungmi Kim, Jin-Soo Kim
| Nature Verified
Abstract Leber hereditary optic neuropathy (LHON), a maternally inherited mitochondrial disorder, results from point mutations in mitochondrial DNA (mtDNA), primarily affecting the MT-ND4 gene. To date, no animal model harboring authentic LHON mutations has been available, limiting therapeutic development.
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Comprehensive phenotypic assessment of nonsense mutations in mitochondrial ND5 in mice - Experimental & Molecular Medicine

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By Sanghun J. Kim, Kyoung-Jin Oh, Ki-Hoan Nam, Kyoungmi Kim, Je Kyung Seong
| Nature Verified
Abstract Mitochondrial dysfunction induced by mitochondrial DNA (mtDNA) mutations has been implicated in various human diseases. A comprehensive analysis of mitochondrial genetic disorders requires suitable animal models for human disease studies. While gene knockout via premature stop codons is a powerful method for investigating the unique functions of target genes, achieving knockout of mtDNA has been rare. Here, we report the genotypes and phenotypes of heteroplasmic MT-ND5 gene-knockout mice.
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Navigating the CRISPR/Cas Landscape for Enhanced Diagnosis and Treatment of Wilson’s Disease

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By Woong Choi, Seongkwang Cha, Kyoungmi Kim
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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