Current Understanding of Molecular Pathology and Treatment of Cardiomyopathy in Duchenne Muscular Dystrophy

por van Westering, Tirsa L. E., Betts, Corinne A., Wood, Matthew J. A.
Publicado 2015

Light modulation ameliorates expression of circadian genes and disease progression in spinal muscular atrophy mice

por Walter, Lisa M, Koch, Christiane E, Betts, Corinne A, Ahlskog, Nina, Meijboom, Katharina E, van Westering, Tirsa L E, Hazell, Gareth, Bhomra, Amarjit, Claus, Peter, Oster, Henrik, Wood, Matthew J A, Bowerman, Melissa
Publicado 2018

Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology

por van Westering, Tirsa L.E., Lomonosova, Yulia, Coenen‐Stass, Anna M.L., Betts, Corinne A., Bhomra, Amarjit, Hulsker, Margriet, Clark, Lucy E., McClorey, Graham, Aartsma‐Rus, Annemieke, van Putten, Maaike, Wood, Matthew J.A., Roberts, Thomas C.
Publicado 2019

Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy

por van Westering, Tirsa L. E., Johansson, Henrik J., Hanson, Britt, Coenen-Stass, Anna M. L., Lomonosova, Yulia, Tanihata, Jun, Motohashi, Norio, Yokota, Toshifumi, Takeda, Shin'ichi, Lehtiö, Janne, Wood, Matthew J. A., EL Andaloussi, Samir, Aoki, Yoshitsugu, Roberts, Thomas C.
Publicado 2020

Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice

por Walter, Lisa M., Deguise, Marc-Olivier, Meijboom, Katharina E., Betts, Corinne A., Ahlskog, Nina, van Westering, Tirsa L.E., Hazell, Gareth, McFall, Emily, Kordala, Anna, Hammond, Suzan M., Abendroth, Frank, Murray, Lyndsay M., Shorrock, Hannah K., Prosdocimo, Domenick A., Haldar, Saptarsi M., Jain, Mukesh K., Gillingwater, Thomas H., Claus, Peter, Kothary, Rashmi, Wood, Matthew J.A., Bowerman, Melissa
Publicado 2018