Genetic background affects properties of satellite cells and mdx phenotypes. - Wikidata - wikimedia - TriplyDB

Genetic background affects properties of satellite cells and mdx phenotypes.

Genetic background affects properties of satellite cells and mdx phenotypes.

http://www.wikidata.org/entity/Q33816419

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Marginal level dystrophin expression improves clinical outcome in a strain of dystrophin/utrophin double knockout mice Adult stem cell and mesenchymal progenitor theories of aging.Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy Hanging on for the ride: adhesion to the extracellular matrix mediates cellular responses in skeletal muscle morphogenesis and disease Biochemical and Functional Comparisons of mdx and Sgcg(-/-) Muscular Dystrophy Mouse Models.Contribution of human muscle-derived cells to skeletal muscle regeneration in dystrophic host mice.Generation of muscular dystrophy model rats with a CRISPR/Cas system.The effect of calorie restriction on mouse skeletal muscle is sex, strain and time-dependent.Are human and mouse satellite cells really the same?Duchenne muscular dystrophy gene therapy: Lost in translation?The FVB Background Does Not Dramatically Alter the Dystrophic Phenotype of Mdx Mice A Wnt-TGFβ2 axis induces a fibrogenic program in muscle stem cells from dystrophic mice.mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype: Transcriptome Comparative Analysis Searching for the Protective Factors Quantitative evaluation of the beneficial effects in the mdx mouse of epigallocatechin gallate, an antioxidant polyphenol from green tea.Serotonin and Histamine Therapy Increases Tetanic Forces of Myoblasts, Reduces Muscle Injury, and Improves Grip Strength Performance of Dmd(mdx) Mice.Effect of genetic background on the dystrophic phenotype in mdx mice.A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle.Plasma Membrane Repair in Health and Disease Voluntary stand-up physical activity enhances endurance exercise capacity in rats Satellite Cells in Muscular Dystrophy - Lost in Polarity.Modifying muscular dystrophy through transforming growth factor-β.Isolation, characterization, and molecular regulation of muscle stem cells.Impaired regenerative capacity and lower revertant fibre expansion in dystrophin-deficient mdx muscles on DBA/2 background.Roles of nonmyogenic mesenchymal progenitors in pathogenesis and regeneration of skeletal muscle.Current Translational Research and Murine Models For Duchenne Muscular Dystrophy.Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair.What do mouse models of muscular dystrophy tell us about the DAPC and its components?Fat deposition and accumulation in the damaged and inflamed skeletal muscle: cellular and molecular players.Drug Discovery of Therapies for Duchenne Muscular Dystrophy.Magnetic Resonance Monitoring of Disease Progression in mdx Mice on Different Genetic Backgrounds.Understanding the process of fibrosis in Duchenne muscular dystrophy.Vestigial-like 2 contributes to normal muscle fiber type distribution in mice.A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy.Fibrogenic Cell Plasticity Blunts Tissue Regeneration and Aggravates Muscular Dystrophy.Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscle.The Rag2⁻Il2rb⁻Dmd⁻ mouse: a novel dystrophic and immunodeficient model to assess innovating therapeutic strategies for muscular dystrophies.Traumatic muscle fibrosis: From pathway to prevention.Tracking progress: an update on animal models for Duchenne muscular dystrophy.Skeletal Muscle Metabolism in Duchenne and Becker Muscular Dystrophy-Implications for Therapies.

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Genetic background affects properties of satellite cells and mdx phenotypes.

http://www.wikidata.org/entity/Q33816419

description

2010 nî lūn-bûn

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2010 թուականի Մարտին հրատարակուած գիտական յօդուած

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2010 թվականի մարտին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

@zh-hk

2010年論文

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2010年論文

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2010年论文

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name

Genetic background affects properties of satellite cells and mdx phenotypes.

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Genetic background affects properties of satellite cells and mdx phenotypes.

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type

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Genetic background affects properties of satellite cells and mdx phenotypes.

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Genetic background affects properties of satellite cells and mdx phenotypes.

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prefLabel

Genetic background affects properties of satellite cells and mdx phenotypes.

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Genetic background affects properties of satellite cells and mdx phenotypes.

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AJPATH.2010.090887

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The American Journal of Pathology

P1476

Genetic background affects properties of satellite cells and mdx phenotypes.

@en

P2093

Daisuke Morikawa

http://www.w3.org/2001/XMLSchema#string

Hiroshi Yamamoto

http://www.w3.org/2001/XMLSchema#string

Kazutake Tsujikawa

http://www.w3.org/2001/XMLSchema#string

Masahiko Yamaguchi

http://www.w3.org/2001/XMLSchema#string

Noriaki Sumie

http://www.w3.org/2001/XMLSchema#string

Shin'ichi Takeda

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So-ichiro Fukada

http://www.w3.org/2001/XMLSchema#string

Takahito Ito

http://www.w3.org/2001/XMLSchema#string

Tokuyuki Yoshida

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Yukiko Yamamoto

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P2860

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

Cellular and molecular regulation of muscle regeneration

X chromosome-linked muscular dystrophy (mdx) in the mouse

Pax7 is required for the specification of myogenic satellite cells

Satellite cell of skeletal muscle fibers

Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis

Asymmetric self-renewal and commitment of satellite stem cells in muscle.

Genetic regulation of primitive hematopoietic stem cell senescence.

Purification and cell-surface marker characterization of quiescent satellite cells from murine skeletal muscle by a novel monoclonal antibody.

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2414-2424

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10.2353/AJPATH.2010.090887

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5

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176

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20304955

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