V. Schöwel

Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells

A. Akalin, C. Birchmeier, V. Franke, 2020, Nature Communications.

Full-length Dysferlin Transfer by the Hyperactive Sleeping Beauty Transposase Restores Dysferlin-deficient Muscle

Z. Izsvák, Andreas Marg, S. Spuler, 2016, Molecular therapy. Nucleic acids.

4-Phenylbutyrate restores localization and membrane repair to human dysferlin mutations

L. Guarente, M. Viswanathan, S. Spuler, 2021, iScience.

Exon Skipping in a Dysf-Missense Mutant Mouse Model

Andreas Marg, A. Goyenvalle, L. García, 2018, Molecular therapy. Nucleic acids.

Potent cytochrome P450 2C19 genotype–related interaction between voriconazole and the cytochrome P450 3A4 inhibitor ritonavir

Gerd Mikus, Walter E Haefeli, W. Haefeli, 2006, Clinical pharmacology and therapeutics.

Loss of Ptpn11 (Shp2) drives satellite cells into quiescence

C. Birchmeier, M. Nazaré, Charles Keller, 2017, eLife.

Ahnak1 abnormally localizes in muscular dystrophies and contributes to muscle vesicle release

I. Morano, B. Purfürst, S. Spuler, 2011, Journal of Muscle Research and Cell Motility.

Exon skipping in a Dysf-missense mutant mouse model 1

A. Goyenvalle, C. Beley, S. Spuler, 2018 .