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Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.
- Published in:
- Nature, 2006, v. 444, n. 7119, p. 574, doi. 10.1038/nature05282
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- Publication type:
- Article
Inflammation Converts Human Mesoangioblasts Into Targets of Alloreactive Immune Responses: Implications for Allogeneic Cell Therapy of DMD.
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- Molecular Therapy, 2014, v. 22, n. 7, p. 1342, doi. 10.1038/mt.2014.62
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- Publication type:
- Article
Extracellular HMGB1, a signal of tissue damage, induces mesoangioblast migration and proliferation.
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- Journal of Cell Biology, 2004, v. 164, n. 3, p. 441, doi. 10.1083/jcb.200304135
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- Publication type:
- Article
PW1/Peg3 expression regulates key properties that determine mesoangioblast stem cell competence.
- Published in:
- Nature Communications, 2015, v. 6, n. 3, p. 6364, doi. 10.1038/ncomms7364
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- Publication type:
- Article
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor.
- Published in:
- 1997
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- Publication type:
- Correction notice
Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor.
- Published in:
- EMBO Journal, 1997, v. 16, n. 10, p. 2892, doi. 10.1093/emboj/16.10.2892
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- Publication type:
- Article
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy.
- Published in:
- EMBO Molecular Medicine, 2024, v. 16, n. 4, p. 927, doi. 10.1038/s44321-024-00031-3
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- Publication type:
- Article
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next‐generation human artificial chromosomes for Duchenne muscular dystrophy.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 2, p. 254, doi. 10.15252/emmm.201607284
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- Publication type:
- Article
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.
- Published in:
- EMBO Molecular Medicine, 2016, v. 8, n. 12, p. 1470, doi. 10.15252/emmm.201607129
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- Publication type:
- Article
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.
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- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1513, doi. 10.15252/emmm.201505636
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- Publication type:
- Article
Spectrum of mutations in fucosidosis.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 1, p. 60, doi. 10.1038/sj.ejhg.5200272
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- Publication type:
- Article
Skeletal Muscle Differentiation of Embryonic Mesoangioblasts Requires Pax3 Activity.
- Published in:
- Stem Cells, 2009, v. 27, n. 1, p. 157, doi. 10.1634/stemcells.2008-0503
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- Publication type:
- Article
The increase of pericyte population in human neuromuscular disorders supports their role in muscle regeneration in vivo.
- Published in:
- Journal of Pathology, 2012, v. 228, n. 4, p. 544, doi. 10.1002/path.4083
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- Publication type:
- Article
Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.
- Published in:
- Nature, 2014, v. 507, n. 7491, p. 262, doi. 10.1038/nature13143
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- Publication type:
- Article
Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.
- Published in:
- 2013
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- Publication type:
- Erratum
Mesoangioblasts at 20: From the embryonic aorta to the patient bed.
- Published in:
- Frontiers in Genetics, 2023, v. 13, p. 1, doi. 10.3389/fgene.2022.1056114
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- Publication type:
- Article
Pericytes of human skeletal muscle are myogenic precursors distinct from satellite cells.
- Published in:
- Nature Cell Biology, 2007, v. 9, n. 3, p. 255, doi. 10.1038/ncb1542
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- Publication type:
- Article
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A.
- Published in:
- Skeletal Muscle, 2015, v. 5, n. 1, p. 1, doi. 10.1186/s13395-015-0055-5
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- Publication type:
- Article
Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy.
- Published in:
- Science Translational Medicine, 2012, v. 4, n. 140, p. 1, doi. 10.1126/scitranslmed.3003541
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- Publication type:
- Article
Stem Cell-Mediated Transfer of a Human Artificial Chromosome Ameliorates Muscular Dystrophy.
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- Science Translational Medicine, 2011, v. 3, n. 96, p. 1, doi. 10.1126/scitranslmed.3002342
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- Publication type:
- Article
Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease.
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- Cellular & Molecular Life Sciences, 2021, v. 78, n. 1, p. 351, doi. 10.1007/s00018-020-03510-1
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- Publication type:
- Article
Human circulating AC133 + stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
- Published in:
- Journal of Clinical Investigation, 2004, v. 114, n. 2, p. 182, doi. 10.1172/JCI200420325
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- Publication type:
- Article
Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
- Published in:
- 2004
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- Publication type:
- journal article
Two New Nonsense mutations (Q80X; Q389X) in patients with severe hunter syndrome ( mucopolysaccharidosis type II).
- Published in:
- Human Mutation, 1996, v. 7, n. 2, p. 184, doi. 10.1002/humu.1380070204
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- Publication type:
- Article