Jung Min Lim, Hyongbum Henry Kim. Yonsei Med J 2022
Times Cited: 3
Times Cited: 3
Times Cited
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Minchul Kim, Vedran Franke, Bettina Brandt, Elijah D Lowenstein, Verena Schöwel, Simone Spuler, Altuna Akalin, Carmen Birchmeier. Nat Commun 2020
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Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome.
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Genomic analysis of a large set of currently-and historically-important human adenovirus pathogens.
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In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.
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Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.
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CRISPR/Cas9 gene editing for curing sickle cell disease.
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In Vivo AAV-CRISPR/Cas9-Mediated Gene Editing Ameliorates Atherosclerosis in Familial Hypercholesterolemia.
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Search-and-replace genome editing without double-strand breaks or donor DNA.
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Cas9-specific immune responses compromise local and systemic AAV CRISPR therapy in multiple dystrophic canine models.
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Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo.
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