Neurobiology of Disease, 2014 Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disease caused by lack of dystrophin, a sub-sarcolemmal protein, which leads to dramatic muscle deterioration.
Sara Vianello +8 more
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Ets-2 Repressor Factor Silences Extrasynaptic Utrophin by N-Box–mediated Repression in Skeletal Muscle [PDF]
, 2007 Kelly J. Perkins +9 more
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Structural and biochemical characterization of actin binding by dystrophin and utrophin [PDF]
, 2008 M. Muthu, Amanda Smith
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Prevention of Dystrophic Pathology in Severely Affected Dystrophin/Utrophin-deficient Mice by Morpholino-oligomer-mediated Exon-skipping [PDF]
, 2009 Aurélie Goyenvalle +6 more
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Myotendinous Junction Defects and Reduced Force Transmission in Mice that Lack α7 Integrin and Utrophin [PDF]
, 2009 Jennifer V. Welser +7 more
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Molecular pathways involved in the control of contractile and metabolic properties of skeletal muscle fibers as potential therapeutic targets for Duchenne muscular dystrophy. [PDF]
Front PhysiolBonato A, Raparelli G, Caruso M.
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Correction to: The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophy. [PDF]
Hum Mol Genet, 2023 europepmc +1 more source
Phenotypic features of genetically modified DMD-XKOXWT pigs. [PDF]
Regen Ther, 2023 Okamoto K +14 more
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Pharmacological activation of PPAR / stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice [PDF]
, 2009 Pedro Miura +6 more
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