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Gene Therapy of mdx Mice With Large Truncated Dystrophins Generated by Recombination Using rAAV6.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 1, p. 36, doi. 10.1038/mt.2010.205
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- Article
Microutrophin Delivery Through rAAV6 Increases Lifespan and Improves Muscle Function in Dystrophic Dystrophin/Utrophin-deficient Mice.
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- Molecular Therapy, 2008, v. 16, n. 9, p. 1539, doi. 10.1038/mt.2008.149
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- Article
Recombinant adeno-associated viral ( rAAV) vectors mediate efficient gene transduction in cultured neonatal and adult microglia.
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- Journal of Neurochemistry, 2016, v. 136, p. 49, doi. 10.1111/jnc.13081
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- Article
Muscle Structure Influences Utrophin Expression in <i>mdx</i> Mice.
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- PLoS Genetics, 2014, v. 10, n. 6, p. 1, doi. 10.1371/journal.pgen.1004431
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- Article
Validation of ultrasonography for non-invasive assessment of diaphragm function in muscular dystrophy.
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- Journal of Physiology, 2016, v. 594, n. 24, p. 7215, doi. 10.1113/JP272707
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- Article
rAAV6-Microdystrophin Rescues Aberrant Golgi Complex Organization in mdx Skeletal Muscles.
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- Traffic, 2007, v. 8, n. 10, p. 1424, doi. 10.1111/j.1600-0854.2007.00622.x
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- Article
Progress and prospects of gene therapy clinical trials for the muscular dystrophies.
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- Human Molecular Genetics, 2016, v. 25, n. R1, p. R9, doi. 10.1093/hmg/ddv420
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- Publication type:
- Article
Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting.
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- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6697, doi. 10.1093/hmg/ddu388
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- Publication type:
- Article
Phosphorylation within the cysteine-rich region of dystrophin enhances its association with β-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting.
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- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu388
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- Publication type:
- Article
Corrigendum: Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
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- Nature Communications, 2017, v. 8, n. 6, p. 16007, doi. 10.1038/ncomms16007
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- Publication type:
- Article
Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
- Published in:
- Nature Communications, 2017, v. 8, n. 2, p. 14454, doi. 10.1038/ncomms14454
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- Publication type:
- Article
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle.
- Published in:
- Skeletal Muscle, 2023, v. 13, n. 1, p. 1, doi. 10.1186/s13395-023-00325-z
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- Publication type:
- Article
Biomarkers for Duchenne muscular dystrophy progression: impact of age in the mdx tongue spared muscle.
- Published in:
- Skeletal Muscle, 2023, v. 13, n. 1, p. 1, doi. 10.1186/s13395-023-00325-z
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- Publication type:
- Article
Microutrophin expression in dystrophic mice displays myofiber type differences in therapeutic effects.
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- PLoS Genetics, 2020, v. 16, n. 11, p. 1, doi. 10.1371/journal.pgen.1009179
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- Article
Predicting Mammalian SINE Subfamily Activity from A-tail Length.
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- Molecular Biology & Evolution, 2004, v. 21, n. 11, p. 2140, doi. 10.1093/molbev/msh225
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- Article
Barnes Woodhall, M.D., 1905-1985.
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- Journal of Neurosurgery, 1985, v. 63, n. 4, p. 483
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- Article
Effect of Common Carotid Ligation on Size of Internal Carotid Aneurysms and Distal Intracarotid and Retinal Artery Pressures.
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- Journal of Neurosurgery, 1966, v. 25, n. 5, p. 503, doi. 10.3171/jns.1966.25.5.0503
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- Article
Cytological Changes in Cerebrospinal Fluid Associated with Resect ions of Intracranial Neoplasms.
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- Journal of Neurosurgery, 1966, v. 25, n. 1, p. 23, doi. 10.3171/jns.1966.25.1.0024
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- Article
Preclinical Studies for Gene Therapy of Duchenne Muscular Dystrophy.
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- Journal of Child Neurology, 2010, v. 25, n. 9, p. 1149, doi. 10.1177/0883073810371006
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- Article
Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16–17.
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- Human Molecular Genetics, 2018, v. 27, n. 17, p. 2978, doi. 10.1093/hmg/ddy197
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- Article