Preston M. McCourt

Independent variability of microtubule perturbations associated with dystrophinopathy

Joseph J. Belanto, John T. Olthoff, Tara L. Mader et al. · Human Molecular Genetics · 2016 · 55 citations · Full text

Pathology, Cytoskeleton, Cellular Physiology +21

Centromere defects, chromosome instability, and cGAS-STING activation in systemic sclerosis

Souren Paul, Mark H. Kaplan, Dinesh Khanna et al. · Nature Communications · 2022 · 36 citations · Full text

Xanthine oxidase is hyper-active in Duchenne muscular dystrophy

Angus Lindsay, Preston M. McCourt, Peter Karachunski et al. · Free Radical Biology and Medicine · 2018 · 30 citations

Biochemistry, Skeletal Muscle, Physiology +6

Variable cytoplasmic actin expression impacts the sensitivity of different dystrophin‐deficient <i>mdx</i> skeletal muscles to eccentric contraction

Angus Lindsay, William M. Southern, Preston M. McCourt et al. · FEBS Journal · 2019 · 23 citations · Full text

Mouse models of two missense mutations in actin-binding domain 1 of dystrophin associated with Duchenne or Becker muscular dystrophy

Jackie L. McCourt, Dana M Talsness, Angus Lindsay et al. · Human Molecular Genetics · 2017 · 18 citations · Full text

Missense Mutations, Proteasome Inhibitors, Protein Function +11