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Embryonic myosin is a regeneration marker to monitor utrophin-based therapies for DMD.

Journal article

Guiraud S. et al, (2019), Hum Mol Genet, 28, 307 - 319

Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice.

Journal article

Kennedy TL. et al, (2018), Mol Ther Methods Clin Dev, 11, 92 - 105

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle.

Journal article

Kennedy TL. et al, (2017), Skelet Muscle, 7

Identification of serum protein biomarkers for utrophin based DMD therapy.

Journal article

Guiraud S. et al, (2017), Sci Rep, 7

Second-generation compound for the modulation of utrophin in the therapy of DMD.

Journal article

Guiraud S. et al, (2015), Hum Mol Genet, 24, 4212 - 4224

New orally available compounds which modulate utrophin expression for the therapy of Duchenne muscular dystrophy (DMD)

Conference paper

Fairclough RJ. et al, (2014), NEUROMUSCULAR DISORDERS, 24, 821 - 821

Identification of new chemical compounds with upregulate utrophin for the therapy of Duchenne muscular dystrophy

Conference paper

Fairclough RJ. et al, (2012), NEUROMUSCULAR DISORDERS, 22, S3 - S3

Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin.

Journal article

Nowak KJ. et al, (2009), J Cell Biol, 185, 903 - 915

Non-toxic ubiquitous over-expression of utrophin in the mdx mouse.

Journal article

Fisher R. et al, (2001), Neuromuscul Disord, 11, 713 - 721

Analysis of mutations in Survival of Motor Neuron (SMN1) gene through model systems.

Journal article

Owen N. et al, (2001), AMERICAN JOURNAL OF HUMAN GENETICS, 69, 368 - 368

Non-toxic ubiquitous overexpression of utrophin in the mdx mouse.

Journal article

Fisher R. et al, (2000), AMERICAN JOURNAL OF HUMAN GENETICS, 67, 428 - 428

Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.

Journal article

Rafael JA. et al, (2000), Hum Mol Genet, 9, 1357 - 1367