Spatial transcriptomics reveal markers of histopathological changes in Duchenne muscular dystrophy mouse models by L.G.M. Heezen, T. Abdelaal, M. van Putten, A. Aartsma-Rus, A. Mahfouz, P. Spitali

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Deacetylation Inhibition Reverses PABPN1-Dependent Muscle Wasting by Cyriel S. Olie, Muhammad Riaz, Rebecca Konietzny, Philip D. Charles, Adan Pinto-Fernandez, Szymon M. Kiełbasa, A. Aartsma-Rus, Jelle J. Goeman, Benedikt M. Kessler, Vered Raz

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Natural disease history of mouse models for limb girdle muscular dystrophy types 2D and 2F. by S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, J W Boertje-van der Meulen, L van Vliet, M Overzier, J J Plomp, A Aartsma-Rus, M van Putten

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Natural disease history of the dy2J mouse model of laminin α2 (merosin)-deficient congenital muscular dystrophy. by S Pasteuning-Vuhman, K Putker, C L Tanganyika-de Winter, J W Boertje-van der Meulen, L van Vliet, M Overzier, J J Plomp, A Aartsma-Rus, M van Putten

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