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A novel dystrophin/utrophin-associated protein is an enzymatically inactive member of the phosphoglucomutase superfamilyMechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubesDown-regulation of a novel actin-binding molecule, skeletrophin, in malignant melanomaRecent advances in innovative therapeutic approaches for Duchenne muscular dystrophy: from discovery to clinical trialsMetabogenic and Nutriceutical Approaches to Address Energy Dysregulation and Skeletal Muscle Wasting in Duchenne Muscular DystrophyCaveolae regulation of mechanosensitive channel function in myotubesAtomic Force Microscopy Protocol for Measurement of Membrane Plasticity and Extracellular Interactions in Single Neurons in EpilepsyBiomechanics of the sarcolemma and costameres in single skeletal muscle fibers from normal and dystrophin-null miceImmunolocalisation of neuronal nitric oxide synthase at the neuromuscular junction of MDX mice: a confocal microscopy studyChanges in mechanosensitive channel gating following mechanical stimulation in skeletal muscle myotubes from the mdx mouseDysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brainPregnancy-induced amelioration of muscular dystrophy phenotype in mdx mice via muscle membrane stabilization effect of glucocorticoidIdentification and characterisation of transcript and protein of a new short N-terminal utrophin isoformStrains at the myotendinous junction predicted by a micromechanical model.Embryonic cardiomyocytes beat best on a matrix with heart-like elasticity: scar-like rigidity inhibits beatingCardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations.Recombinant MG53 protein modulates therapeutic cell membrane repair in treatment of muscular dystrophyAtomic force microscopy probing in the measurement of cell mechanics.Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophyGene-mediated restoration of normal myofiber elasticity in dystrophic muscles.Mechanical and electrophysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: col6a1-/- and mdxDystrophin and utrophin: genetic analyses of their role in skeletal muscle.Sarcoglycans in muscular dystrophy.Expression levels of sarcolemmal membrane repair proteins following prolonged exercise training in miceRegulation and functional significance of utrophin expression at the mammalian neuromuscular synapse.Myocardial atrophy in children with mitochondrial disease and Duchenne muscular dystrophy.Mechanisms of muscle weakness in muscular dystrophyMechanical perturbation elicits a phenotypic difference between Dictyostelium wild-type cells and cytoskeletal mutants.Local measurements of viscoelastic parameters of adherent cell surfaces by magnetic bead microrheometry.Skeletal muscle satellite cells: mediators of muscle growth during development and implications for developmental disorders.Physiological characterization of muscle strength with variable levels of dystrophin restoration in mdx mice following local antisense therapy.Elastic energy storage and radial forces in the myofilament lattice depend on sarcomere length.Muscle degeneration without mechanical injury in sarcoglycan deficiencyAquapuncture Using Stem Cell Therapy to Treat Mdx Mice.Correlating In Vitro Splice Switching Activity With Systemic In Vivo Delivery Using Novel ZEN-modified Oligonucleotides.Increased resting intracellular calcium modulates NF-κB-dependent inducible nitric-oxide synthase gene expression in dystrophic mdx skeletal myotubesTopographical significance of membrane skeletal component protein 4.1 B in mammalian organs.A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells.Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.Myotubes differentiate optimally on substrates with tissue-like stiffness: pathological implications for soft or stiff microenvironments
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh
1995年學術文章
@zh-hant
name
Mechanical function of dystrophin in muscle cells
@ast
Mechanical function of dystrophin in muscle cells
@en
type
label
Mechanical function of dystrophin in muscle cells
@ast
Mechanical function of dystrophin in muscle cells
@en
prefLabel
Mechanical function of dystrophin in muscle cells
@ast
Mechanical function of dystrophin in muscle cells
@en
P2093
P2860
P356
P1476
Mechanical function of dystrophin in muscle cells
@en
P2093
P2860
P304
P356
10.1083/JCB.128.3.355
P407
P577
1995-02-01T00:00:00Z