Robuta

https://pubmed.ncbi.nlm.nih.gov/8559162/ Tenascin-C expression in dystrophin-related muscular dystrophy The mdx mouse has a mutated dystrophin gene and is used as a model for the study of Duchenne muscular dystrophy (DMD). We investigated whether regenerating mdx... cexpressiondystrophinrelateddystrophy https://hsrc.himmelfarb.gwu.edu/gwhpubs/3042/ "Vamorolone improves Becker muscular dystrophy and increases dystrophin" by Nikki M. McCormack, Nhu... There is no approved therapy for Becker muscular dystrophy (BMD), a genetic muscle disease caused by in-frame dystrophin deletions. We previously developed the... becker muscular dystrophy https://experts.umn.edu/en/publications/isometric-resistance-training-increases-strength-and-alters-histo/ Isometric resistance training increases strength and alters histopathology of dystrophin-deficient... resistance trainingisometricincreasesstrength https://publications-cnrc.canada.ca/eng/view/object/?id=65b4e079-1772-4b31-8c53-b594918b9a1e Regeneration and myogenic cell proliferation correlate with taurine levels in dystrophin- and... Regeneration and myogenic cell proliferation correlate with taurine levels in dystrophin- and MyoD-deficient muscles cell proliferationregeneration https://pubmed.ncbi.nlm.nih.gov/7633443/ A novel dystrophin isoform is required for normal retinal electrophysiology Dystrophin is present in the outer plexiform layer of the retina and is required for normal retinal function as measured by electroretinography. We describe... a noveldystrophinisoformrequirednormal https://theses.gla.ac.uk/71488/ Analysis of dystrophin point mutations - Enlighten Theses analysisdystrophinpointmutationsenlighten https://pmc.ncbi.nlm.nih.gov/articles/PMC7971009/ Low dystrophin variability between muscles and stable expression over time in Becker muscular... Becker muscular dystrophy (BMD) is the milder allelic variant of Duchenne muscular dystrophy, with higher dystrophin levels. To anticipate on results of... https://experts.umn.edu/en/publications/a-multiple-site-side-binding-model-for-the-interaction-of-dystrop/ A multiple site, side binding model for the interaction of dystrophin with F-actin -... https://research-repository.uwa.edu.au/en/publications/multiple-exon-skipping-strategies-to-by-pass-dystrophin-mutations/ Multiple exon skipping strategies to by-pass dystrophin mutations - the UWA Profiles and Research... https://eprints.ncl.ac.uk/64360 Immunogold confirmation that utrophin is localized to the normal position of dystrophin in... https://experts.umn.edu/en/publications/disease-causing-missense-mutations-in-actin-binding-domain-1-of-d/ Disease-causing missense mutations in actin binding domain 1 of dystrophin induce thermodynamic... https://nrc-publications.canada.ca/eng/view/object/?id=15c380c0-31db-4b18-aaca-57b2f802d8b6 Sustained Improvement of Muscle Function One Year After Full-Length Dystrophin Gene Transfer into... Sustained Improvement of Muscle Function One Year After Full-Length Dystrophin Gene Transfer into mdx Mice by a Gutted Helper-Dependent Adenoviral Vector https://conservancy.umn.edu/items/a8ee64e9-7bd9-4af9-b0f4-d9256dd8d92a Biophysical and functional consequences of sequence changes on dystrophin and utrophin Mutations in the DMD gene result in Duchenne (DMD) and Becker (BMD) muscular dystrophies. The DMD gene encodes the protein, dystrophin that is predominantly... biophysicalfunctionalconsequenceschangesdystrophin https://pubmed.ncbi.nlm.nih.gov/9288751/ Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy The absence of dystrophin at the muscle membrane leads to Duchenne muscular dystrophy (DMD), a severe muscle-wasting disease that is inevitably fatal in early... as adystrophindeficientmice https://podcasts.ox.ac.uk/keywords/dystrophin dystrophin | University of Oxford Podcasts university of oxforddystrophinpodcasts https://iris.cnr.it/handle/20.500.14243/23735 Lack of dystrophin functionally affects alpha3beta2/beta4-nicotinic acethylcholine receptors in... lack ofdystrophinaffects https://eprints.ncl.ac.uk/232714 Investigating the effect of dystrophin deficiency on brain function in mouse models of Duchenne... https://publications-cnrc.canada.ca/eng/view/object/?id=ad12ae05-37b9-4687-83e6-551159785160 Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy... Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice https://nrc-publications.canada.ca/eng/view/object/?id=3342c507-b549-4037-ab00-4ae7a9d7178e Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene... Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding... https://conservancy.umn.edu/items/3e42c59a-dbed-4081-9f28-705bc3347fee Interdomain Force Dispersion within Spectrin Repeats of Dystrophin and its Influence on Secondary... Dystrophin is a large protein complex that connects the cytoskeleton to the extracellular matrix and functions to stabilize muscle cells when force is applied....