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A mutation in desmin makes skeletal muscle less vulnerable to acute muscle damage after eccentric loading in rats
Desminopathy is the most common intermediate filament disease in humans. The most frequent mutation causing desminopathy in patients is a R350P DES missense mutation. We have developed a rat model with an analogous mutation in R349P Des. To investigate the role of R349P Des in mechanical loading, we...
Autores principales: | Langer, Henning T., Mossakowski, Agata A., Avey, Alec M., Wohlgemuth, Ross P., Smith, Lucas R., Zbinden‐Foncea, Herman, Baar, Keith |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292853/ https://www.ncbi.nlm.nih.gov/pubmed/34411340 http://dx.doi.org/10.1096/fj.202100711RR |
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