Found: 17
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Transplanted hematopoietic stem cells demonstrate impaired sarcoglycan expression after engraftment into cardiac and skeletal muscle.
- Published in:
- Journal of Clinical Investigation, 2004, v. 114, n. 11, p. 1577, doi. 10.1172/JCI200423071
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- Publication type:
- Article
Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury.
- Published in:
- PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1007070
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- Publication type:
- Article
Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0136679
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- Publication type:
- Article
Translational Control of FOG-2 Expression in Cardiomyocytes by MicroRNA-130a.
- Published in:
- PLoS ONE, 2009, v. 4, n. 7, p. 1, doi. 10.1371/journal.pone.0006161
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- Publication type:
- Article
Abcc9 is required for the transition to oxidative metabolism in the newborn heart.
- Published in:
- FASEB Journal, 2014, v. 28, n. 7, p. 2804, doi. 10.1096/fj.13-244459
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- Publication type:
- Article
Myoferlin is required for insulin-like growth factor response and muscle growth.
- Published in:
- FASEB Journal, 2010, v. 24, n. 4, p. 1284, doi. 10.1096/fj.09-136309
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- Publication type:
- Article
Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Targeting latent TGFβ release in muscular dystrophy.
- Published in:
- Science Translational Medicine, 2014, v. 6, n. 259, p. 1, doi. 10.1126/scitranslmed.3010018
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- Publication type:
- Article
Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6722, doi. 10.1093/hmg/ddu390
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- Publication type:
- Article
Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu390
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- Publication type:
- Article
SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 5, p. 894, doi. 10.1093/hmg/ddq528
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- Publication type:
- Article
Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 4, p. 779, doi. 10.1093/hmg/ddq522
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- Publication type:
- Article
Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 4, p. 607, doi. 10.1093/hmg/ddn386
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- Publication type:
- Article
Reduced life span with heart and muscle dysfunction in Drosophila sarcoglycan mutants.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 23, p. 2933, doi. 10.1093/hmg/ddm254
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- Publication type:
- Article
Nuclear sequestration of δ-sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 4, p. 355, doi. 10.1093/hmg/ddl453
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- Publication type:
- Article
Overexpression of Latent TGFβ Binding Protein 4 in Muscle Ameliorates Muscular Dystrophy through Myostatin and TGFβ.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006019
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- Publication type:
- Article