Sp1 and Sp3 physically interact and co-operate with GABP for the activation of the utrophin promoter [PDF]
Federico Galvagni+2 more
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iNOS Expression In Dystrophinopathies Can Be Reduced By Somatic Gene Transfer of Dystrophin or Utrophin [PDF]
Jean‐Pierre Louboutin+4 more
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Biglycan : a multivalent proteoglycan providing structure and signals [PDF]
Research over the past few years has provided fascinating results indicating that biglycan, besides being a ubiquitous structural component of the extracellular matrix (ECM), may act as a signaling molecule.
Năstase, Mădălina-Viviana+2 more
core
Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system [PDF]
Sarah Squire+7 more
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Comparative Analysis of the Human Dystrophin and Utrophin Gene Structures [PDF]
Uberto Pozzoli+5 more
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Social stress is lethal in the mdx model of Duchenne muscular dystrophy
Background: Duchenne muscular dystrophy (DMD) is caused by the loss of dystrophin. Severe and ultimately lethal, DMD progresses relatively slowly in that patients become wheelchair bound only around age twelve with a survival expectancy reaching the ...
Maria Razzoli+10 more
doaj
Utrophin Binds Laterally along Actin Filaments and Can Couple Costameric Actin with Sarcolemma When Overexpressed in Dystrophin-deficient Muscle [PDF]
Inna N. Rybakova+4 more
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Compensation for dystrophin-deficiency: ADAM12 overexpression in skeletal muscle results in increased 7 integrin, utrophin and associated glycoproteins [PDF]
Behzad Moghadaszadeh
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262. Chronic Inflammation-Induced Extrasynaptic Utrophin Upregulation in Muscle Fibers of Immune Competent mdx Mice Is Related to Reduced Calpain Activity of Muscle [PDF]
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