Found: 20
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Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes.
- Published in:
- Nature Biotechnology, 2011, v. 29, n. 4, p. 341, doi. 10.1038/nbt.1807
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- Article
Corrigendum: Identification of novel, therapy-responsive protein biomarkers in a mouse model of Duchenne muscular dystrophy by aptamer-based serum proteomics.
- Published in:
- Scientific Reports, 2016, p. 37047, doi. 10.1038/srep37047
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- Publication type:
- Article
Identification of novel, therapy-responsive protein biomarkers in a mouse model of Duchenne muscular dystrophy by aptamer-based serum proteomics.
- Published in:
- Scientific Reports, 2015, p. 17014, doi. 10.1038/srep17014
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- Publication type:
- Article
Dystrophin involvement in peripheral circadian SRF signalling.
- Published in:
- Life Science Alliance, 2021, v. 4, n. 10, p. 1, doi. 10.26508/lsa.202101014
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- Publication type:
- Article
fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 4, p. 699, doi. 10.1093/hmg/ddy377
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- Article
Cmah -dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatment.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 3, p. 396, doi. 10.1093/hmg/ddy346
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- Article
Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 20, p. 3582, doi. 10.1093/hmg/ddy249
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- Article
Selective release of muscle-specific, extracellular microRNAs during myogenic differentiation.
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- Human Molecular Genetics, 2016, v. 25, n. 18, p. 3960, doi. 10.1093/hmg/ddw237
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- Article
How much dystrophin is enough: the physiological consequences of different levels of dystrophin in the mdx mouse.
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- Human Molecular Genetics, 2015, v. 24, n. 15, p. 4225, doi. 10.1093/hmg/ddv155
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- Article
In vitro evaluation of novel antisense oligonucleotides is predictive of in vivo exon skipping activity for Duchenne muscular dystrophy.
- Published in:
- Journal of Gene Medicine, 2010, v. 12, n. 4, p. 354, doi. 10.1002/jgm.1446
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- Article
Pip5 Transduction Peptides Direct High Efficiency Oligonucleotide-mediated Dystrophin Exon Skipping in Heart and Phenotypic Correction in mdx Mice.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 7, p. 1295, doi. 10.1038/mt.2011.79
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- Publication type:
- Article
Functional Rescue of Dystrophin-deficient mdx Mice by a Chimeric Peptide-PMO.
- Published in:
- Molecular Therapy, 2010, v. 18, n. 10, p. 1822, doi. 10.1038/mt.2010.151
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- Publication type:
- Article
Optimization of Peptide Nucleic Acid Antisense Oligonucleotides for Local and Systemic Dystrophin Splice Correction in the mdx Mouse.
- Published in:
- Molecular Therapy, 2010, v. 18, n. 4, p. 819, doi. 10.1038/mt.2009.310
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- Article
Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy.
- Published in:
- Scientific Reports, 2015, p. 11632, doi. 10.1038/srep11632
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- Article
Prevention of exercised induced cardiomyopathy following Pip-PMO treatment in dystrophic mdx mice.
- Published in:
- Scientific Reports, 2015, p. 8986, doi. 10.1038/srep08986
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- Article
Current Understanding of Molecular Pathology and Treatment of Cardiomyopathy in Duchenne Muscular Dystrophy.
- Published in:
- Molecules, 2015, v. 20, n. 5, p. 8823, doi. 10.3390/molecules20058823
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- Article
Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology.
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- Journal of Cachexia, Sarcopenia & Muscle, 2020, v. 11, n. 2, p. 578, doi. 10.1002/jcsm.12506
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- Article
Diaphragm rescue alone prevents heart dysfunction in dystrophic mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 413, doi. 10.1093/hmg/ddq477
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- Publication type:
- Article
A fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 22, p. 4405, doi. 10.1093/hmg/ddp395
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- Publication type:
- Article
Peptide-conjugated phosphodiamidate oligomer-mediated exon skipping has benefits for cardiac function in mdx and Cmah-/-mdx mouse models of Duchenne muscular dystrophy.
- Published in:
- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0198897
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- Article