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Downstream utrophin enhancer is required for expression of utrophin in skeletal muscle.
- Published in:
- Journal of Gene Medicine, 2008, v. 10, n. 6, p. 702, doi. 10.1002/jgm.1190
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- Publication type:
- Article
The utrophin promoter A drives high expression of the transgenic LacZ gene in liver, testis, colon, submandibular gland, and small intestine.
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- Journal of Gene Medicine, 2005, v. 7, n. 2, p. 237, doi. 10.1002/jgm.651
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- Publication type:
- Article
Establishment of bipotent progenitor cell clone from rat skeletal muscle.
- Published in:
- Animal Science Journal, 2011, v. 82, n. 6, p. 764, doi. 10.1111/j.1740-0929.2011.00907.x
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- Publication type:
- Article
Perlecan Facilitates Neuronal Nitric Oxide Synthase Delocalization in Denervation-Induced Muscle Atrophy.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 11, p. 2524, doi. 10.3390/cells9112524
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- Publication type:
- Article
Reprogramming efficiency and quality of induced Pluripotent Stem Cells (iPSCs) generated from muscle-derived fibroblasts of mdx mice at different ages.
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- PLoS Currents, 2011, p. 525, doi. 10.1371/currents.RRN1274
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- Publication type:
- Article
Generation of transplantable, functional satellite-like cells from mouse embryonic stem cells.
- Published in:
- FASEB Journal, 2009, v. 23, n. 6, p. 1907, doi. 10.1096/fj.08-123661
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- Publication type:
- Article
Coordinate control of axon defasciculation and myelination by laminin-2 and -8.
- Published in:
- Journal of Cell Biology, 2005, v. 168, n. 4, p. 655, doi. 10.1083/jcb.200411158
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- Publication type:
- Article
α-Syntrophin-deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration.
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- Journal of Cell Biology, 2002, v. 158, n. 6, p. 1097, doi. 10.1083/jcb.200204076
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- Publication type:
- Article
Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3003, doi. 10.1093/hmg/ddt157
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- Publication type:
- Article
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 4, p. 621, doi. 10.1093/hmg/ddn387
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- Publication type:
- Article
Laminin α1 chain reduces muscular dystrophy in laminin α2 chain deficient mice.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 16, p. 1775, doi. 10.1093/hmg/ddh190
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- Publication type:
- Article
Erratum: G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy.
- Published in:
- Nature Communications, 2015, v. 6, n. 6, p. 7295, doi. 10.1038/ncomms8295
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- Publication type:
- Article
G-CSF supports long-term muscle regeneration in mouse models of muscular dystrophy.
- Published in:
- Nature Communications, 2015, v. 6, n. 4, p. 6745, doi. 10.1038/ncomms7745
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- Publication type:
- Article
Induction of Pluripotent Stem Cells from a Manifesting Carrier of Duchenne Muscular Dystrophy and Characterization of Their X-Inactivation Status.
- Published in:
- Stem Cells International, 2017, p. 1, doi. 10.1155/2017/7906843
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- Publication type:
- Article
Periostin Is Required for the Maintenance of Muscle Fibers during Muscle Regeneration.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3627, doi. 10.3390/ijms22073627
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- Publication type:
- Article
Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains.
- Published in:
- Glycobiology, 2014, v. 24, n. 3, p. 314, doi. 10.1093/glycob/cwt116
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- Publication type:
- Article
Autologous Transplantation of SM/C-2.6<sup>+</sup> Satellite Cells Transduced with Micro-dystrophin CS1 cDNA by Lentiviral Vector into mdx Mice.
- Published in:
- Molecular Therapy, 2007, v. 15, n. 12, p. 2178, doi. 10.1038/sj.mt.6300295
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- Publication type:
- Article
36. Transplantation of SM/C-2.6+ Satellite Cells Transduced with Micro-Dystrophin CS1 cDNA by Lentiviral Vector into mdx Mice.
- Published in:
- Molecular Therapy, 2006, v. 13, p. S15, doi. 10.1016/j.ymthe.2006.08.049
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- Publication type:
- Article
253. An AAV Vector-Mediated Gene Transfer into Canine Skeletal Muscle
- Published in:
- 2005
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- Publication type:
- Abstract
AAV vector-mediated microdystrophin expression in a relatively small percentage of mdx myofibers improved the mdx phenotype
- Published in:
- Molecular Therapy, 2004, v. 10, n. 5, p. 821, doi. 10.1016/j.ymthe.2004.07.025
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- Publication type:
- Article
Skeletal Muscle Cells Generated from Pluripotent Stem Cells.
- Published in:
- 2017
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- Publication type:
- Editorial
Calcitonin receptor and Odz4 are differently expressed in Pax7-positive cells during skeletal muscle regeneration.
- Published in:
- Journal of Molecular Histology, 2012, v. 43, n. 5, p. 581, doi. 10.1007/s10735-012-9421-3
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- Publication type:
- Article
Molecular Signature of Quiescent Satellite Cells in Adult Skeletal Muscle.
- Published in:
- Stem Cells, 2007, v. 25, n. 10, p. 2448, doi. 10.1634/stemcells.2007-0019
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- Publication type:
- Article
Laminin regulates postnatal oligodendrocyte production by promoting oligodendrocyte progenitor survival in the subventricular zone.
- Published in:
- Glia, 2012, v. 60, n. 10, p. 1451, doi. 10.1002/glia.22365
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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
NO production results in suspension-induced muscle atrophy through dislocation of neuronal NOS.
- Published in:
- 2007
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- Publication type:
- journal article
Schwann cell myelination occurred without basal lamina formation in laminin α2 chain-null mutant ( dy<sup>3K</sup>/ dy<sup>3K</sup>) mice.
- Published in:
- Glia, 2001, v. 35, n. 2, p. 101, doi. 10.1002/glia.1075
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- Publication type:
- Article
Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy.
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- PLoS Genetics, 2020, v. 16, n. 5, p. 1, doi. 10.1371/journal.pgen.1008826
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- Publication type:
- Article
Prostaglandin EP2 receptor downstream of Notch signaling inhibits differentiation of human skeletal muscle progenitors in differentiation conditions.
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- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-0904-6
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- Publication type:
- Article
Antioxidants restore store‐operated Ca<sup>2+</sup> entry in patient‐iPSC‐derived myotubes with tubular aggregate myopathy‐associated Ile484ArgfsX21 STIM1 mutation via upregulation of binding immunoglobulin protein.
- Published in:
- FASEB Bioadvances, 2023, v. 5, n. 11, p. 453, doi. 10.1096/fba.2023-00069
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- Publication type:
- Article
Activation of calcium signaling through Trpv1 by nNOS and peroxynitrite as a key trigger of skeletal muscle hypertrophy.
- Published in:
- Nature Medicine, 2013, v. 19, n. 1, p. 101, doi. 10.1038/nm.3019
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- Publication type:
- Article
Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 11, p. 1006, doi. 10.1093/hmg/ddab100
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- Publication type:
- Article
α1-Syntrophin-deficient mice exhibit impaired muscle force recovery after osmotic shock.
- Published in:
- Muscle & Nerve, 2014, v. 49, n. 5, p. 728, doi. 10.1002/mus.23990
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- Publication type:
- Article
iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin.
- Published in:
- 2020
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- Publication type:
- journal article
Mesenchymal stem cells derived from human induced pluripotent stem cells improve the engraftment of myogenic cells by secreting urokinase-type plasminogen activator receptor (uPAR).
- Published in:
- Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-021-02594-1
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- Publication type:
- Article
Association of neuronal nitric oxide synthase (nNOS) with α1-syntrophin at the sarcolemma.
- Published in:
- Microscopy Research & Technique, 2001, v. 55, n. 3, p. 164, doi. 10.1002/jemt.1167
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- Publication type:
- Article
Merosin and congenital muscular dystrophy.
- Published in:
- Microscopy Research & Technique, 2000, v. 48, n. 3/4, p. 181, doi. 10.1002/(SICI)1097-0029(20000201/15)48:3/4<181::AID-JEMT6>3.0.CO;2-Q
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- Publication type:
- Article