Preston M. McCourt

Xanthine oxidase is hyper‐active in Duchenne muscular dystrophy

J. Ervasti, A. Lindsay, D. Lowe, 2018, Free radical biology & medicine.

Tetrahydrobiopterin synthesis and metabolism is impaired in dystrophin‐deficient mdx mice and humans

J. Ervasti, A. Lindsay, D. Lowe, 2021, Acta physiologica.

Independent variability of microtubule perturbations associated with dystrophinopathy.

J. Ervasti, G. Gundersen, Christopher M. Chamberlain, 2016, Human molecular genetics.

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

M. Kyba, J. Ervasti, A. Lindsay, 2018, Human molecular genetics.

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

J. Ervasti, W. M. Southern, James S. Hodges, 2019, The FEBS journal.

Distinct mechanical properties in homologous spectrin-like repeats of utrophin

J. Ervasti, Sayan Ghosal, M. Salapaka, 2019, Scientific Reports.

Impaired muscle relaxation and mitochondrial fission associated with genetic ablation of cytoplasmic actin isoforms

J. Ervasti, David D. Thomas, E. Spangenburg, 2018, The FEBS journal.