Seasonal induction of GABAergic excitation in the central mammalian clock

由 Farajnia, Sahar, van Westering, Tirsa L. E., Meijer, Johanna H., Michel, Stephan
出版 2014

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

由 van Westering, Tirsa L. E., Betts, Corinne A., Wood, Matthew J. A.
發表在 Molecules (2015)

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

由 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
發表在 Hum Mol Genet (2018)

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

由 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.
發表在 J Cachexia Sarcopenia Muscle (2019)

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

由 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.
發表在 Mol Cell Proteomics (2020)

Cmah-dystrophin deficient mdx mice display an accelerated cardiac phenotype that is improved following peptide-PMO exon skipping treatment

由 Betts, Corinne A, McClorey, Graham, Healicon, Richard, Hammond, Suzan M, Manzano, Raquel, Muses, Sofia, Ball, Vicky, Godfrey, Caroline, Merritt, Thomas M, van Westering, Tirsa, O’Donovan, Liz, Wells, Kim E, Gait, Michael J, Wells, Dominic J, Tyler, Damian, Wood, Matthew J
發表在 Hum Mol Genet (2019)

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

由 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
發表在 EBioMedicine (2018)