Benjamin Edwards
Affiliations: | Physiology, Anatomy and Genetics | University of Oxford, Oxford, United Kingdom |
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| Meijboom KE, Sutton ER, McCallion E, et al. (2022) Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice. Skeletal Muscle. 12: 18 |
| Lovering RM, Iyer SR, Edwards B, et al. (2020) Alterations of neuromuscular junctions in Duchenne muscular dystrophy. Neuroscience Letters. 135304 |
| Babbs A, Berg A, Chatzopoulou M, et al. (2020) Synthesis of SMT022357 enantiomers and evaluation in a Duchenne muscular dystrophy mouse model. Tetrahedron. 76: 130819 |
| Babbs A, Berg A, Chatzopoulou M, et al. (2020) 2-Arylbenzo[d]oxazole phosphinate esters as second-generation modulators of utrophin for the treatment of Duchenne Muscular Dystrophy. Journal of Medicinal Chemistry |
| Guiraud S, Edwards B, Babbs A, et al. (2019) The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophy. Human Molecular Genetics |
| Guiraud S, Edwards B, Squire SE, et al. (2018) Embryonic myosin is a regeneration marker to monitor utrophin based therapies for DMD. Human Molecular Genetics |
| Guiraud S, Edwards B, Squire SE, et al. (2017) Identification of serum protein biomarkers for utrophin based DMD therapy. Scientific Reports. 7: 43697 |
| Guiraud S, Squire SE, Edwards B, et al. (2015) Second-generation compound for the modulation of utrophin in the therapy of DMD. Human Molecular Genetics. 24: 4212-24 |
| Liu KX, Edwards B, Lee S, et al. (2015) Neuron-specific antioxidant OXR1 extends survival of a mouse model of amyotrophic lateral sclerosis. Brain : a Journal of Neurology. 138: 1167-81 |
| Paton L, Bitoun E, Kenyon J, et al. (2014) A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathology. The Journal of Biological Chemistry. 289: 26709-21 |