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Trends in Molecular Medicine|May 15, 2024
Pig models for translational Duchenne muscular dystrophy researchMichael Stirm, Nikolai Klymiuk, Hiroshi Nagashima, et al.
Pituitary|July 3, 2024
Decreased β-cell volume and insulin secretion but preserved glucose tolerance in a growth hormone insensitive pig modelLaeticia Laane, Simone Renner, Elisabeth Kemter, et al.
STAR Protocols|February 13, 2026
Protocol for in vivo analysis of muscle function in porcine models for muscular dystrophiesHristiyan Hristov, Michaela Blasi, Igor Neves Barbosa, et al.
Cells|June 25, 2025
Multi-Modal Analysis of Satellite Cells Reveals Early Impairments at Pre-Contractile Stages of Myogenesis in Duchenne Muscular DystrophySophie Franzmeier, Shounak Chakraborty, Armina Mortazavi, et al.
Regenerative Therapy|September 29, 2023
Phenotypic features of genetically modified DMD-XKOXWT pigsKazutoshi Okamoto, Hitomi Matsunari, Kazuaki Nakano, et al.
Journal of Cachexia, Sarcopenia and Muscle|October 1, 2025
Reduced Muscle Force in Dystrophic DMDΔ52 Pigs Is Incompletely Restored by Systemic Transcript Reframing (DMDΔ51-52)Michaela Blasi, Hristiyan Hristov, Jan B Stöckl, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 10, 2023
Systemic deletion of DMD exon 51 rescues clinically severe Duchenne muscular dystrophy in a pig model lacking DMD exon 52Michael Stirm, Bachuki Shashikadze, Andreas Blutke, et al.
Advanced Healthcare Materials|February 18, 2025
Mimicking the Dystrophic Cardiac Extracellular Environment through DystroGelMaila Chirivì, Fabio Maiullari, Marika Milan, et al.
Neuromuscular Disorders : NMD|June 6, 2022
Pig models for Duchenne muscular dystrophy - from disease mechanisms to validation of new diagnostic and therapeutic conceptsMichael Stirm, Lina Marie Fonteyne, Bachuki Shashikadze, et al.
Disease Models & Mechanisms|November 19, 2021
A scalable, clinically severe pig model for Duchenne muscular dystrophyMichael Stirm, Lina Marie Fonteyne, Bachuki Shashikadze, et al.
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