Ronald Cohn
Affiliations: | Human Genetics | Johns Hopkins University, Baltimore, MD |
Area:
Genetics, Molecular Biology, Cell BiologyGoogle:
"Ronald Cohn"Children
Sign in to add traineeTyesha N. Burks | grad student | 2012 | Johns Hopkins |
Jessica L. Simmers | grad student | 2013 | Johns Hopkins |
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Publications
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Rok M, Ying Wong TW, Maino E, et al. (2023) Prevention of early-onset cardiomyopathy in exon 52-54 deletion mice by CRISPR-Cas9-mediated exon skipping. Molecular Therapy. Methods & Clinical Development. 30: 246-258 |
Fatehi S, Marks RM, Rok MJ, et al. (2023) Advances in CRISPR/Cas9 Genome Editing for the Treatment of Muscular Dystrophies. Human Gene Therapy |
Wong TWY, Ahmed A, Yang G, et al. (2020) A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy. Disease Models & Mechanisms. 13 |
Kemaladewi DU, Cohn RD. (2019) Development of therapeutic genome engineering in laminin-α2-deficient congenital muscular dystrophy. Emerging Topics in Life Sciences. 3: 11-18 |
Kemaladewi DU, Bassi PS, Erwood S, et al. (2019) A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene. Nature |
Kemaladewi DU, Benjamin JS, Hyatt E, et al. (2019) Increased polyamines as protective disease modifiers in congenital muscular dystrophy. Human Molecular Genetics. 27: 1905-1912 |
Kemaladewi DU, Cohn RD. (2019) Development of therapeutic genome engineering in laminin-α2-deficient congenital muscular dystrophy Emerging Topics in Life Sciences. 3: 11-18 |
Wong TWY, Cohn RD. (2017) Therapeutic Applications of CRISPR/Cas for Duchenne Muscular Dystrophy. Current Gene Therapy |
Kemaladewi DU, Maino E, Hyatt E, et al. (2017) Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism. Nature Medicine |
Zou Y, Donkervoort S, Salo AM, et al. (2017) P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye. Human Molecular Genetics |