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Page 1
Cardiac Involvement in Dystrophin-Deficient Females: Current Understanding and Implications for the Treatment of Dystrophinopathies.
Genes (Basel). 2020 Jul 8;11(7):765. doi: 10.3390/genes11070765.
Genes (Basel). 2020.
PMID: 32650403
Free PMC article.
Review.
In Vivo Evaluation of Exon 51 Skipping in hDMD/Dmd-null Mice.
Sheri N, Yokota T.
Sheri N, et al.
Methods Mol Biol. 2023;2640:327-336. doi: 10.1007/978-1-0716-3036-5_23.
Methods Mol Biol. 2023.
PMID: 36995605
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Novel heterozygous PRPH2 variant identified in a patient with spinocerebellar ataxia type 14 and macular dystrophy.
Chen TS, Sheri N, Ehmann DS, Benson MD.
Chen TS, et al. Among authors: sheri n.
Ophthalmic Genet. 2024 Feb 29:1-4. doi: 10.1080/13816810.2024.2321883. Online ahead of print.
Ophthalmic Genet. 2024.
PMID: 38419591
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eSkip-Finder: a machine learning-based web application and database to identify the optimal sequences of antisense oligonucleotides for exon skipping.
Chiba S, Lim KRQ, Sheri N, Anwar S, Erkut E, Shah MNA, Aslesh T, Woo S, Sheikh O, Maruyama R, Takano H, Kunitake K, Duddy W, Okuno Y, Aoki Y, Yokota T.
Chiba S, et al. Among authors: sheri n.
Nucleic Acids Res. 2021 Jul 2;49(W1):W193-W198. doi: 10.1093/nar/gkab442.
Nucleic Acids Res. 2021.
PMID: 34104972
Free PMC article.
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