John T. Olthoff

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

Persistent upregulation of the β-tubulin tubb6, linked to muscle regeneration, is a source of microtubule disorganization in dystrophic muscle

Davide Randazzo, Umara Khalique, Joseph J. Belanto et al. · Human Molecular Genetics · 2018 · 49 citations · Full text

Muscle Function, Cytoskeleton, Cellular Physiology +17

Loss of peroxiredoxin-2 exacerbates eccentric contraction-induced force loss in dystrophin-deficient muscle

John T. Olthoff, Angus Lindsay, Reem Abo‐Zahrah et al. · Nature Communications · 2018 · 44 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

Use of fully modified 2′‐O‐methyl antisense oligos for loss‐of‐function studies in vertebrate embryos

Patricia N. Schneider, John T. Olthoff, Abby J. Matthews et al. · genesis · 2010 · 16 citations · Full text

Antisense Oligos, Zebrafish Chordin, Molecular Biology +22