Article
Evaluation of quantitative muscle MRI and an intelligent phenotyping housing system as advanced phenotyping methods in a mouse model of calpain 3-deficient muscular dystrophy.
Animal models and experimental medicine - 1 Jul 2026
Südkamp Nicolina, Rohm Marlena, Russo Gabriele, Helluy Xavier, Kocabas Abdulhadi, Froeling Martijn, Kleefeld Felix, Manahan-Vaughan Denise, Ruck Tobias, Jacobsen Frank, Vorgerd Matthias, Forsting Johannes, Schlaffke Lara
Abstract excerpt
Calpainopathy is a rare genetic myopathy without causal treatment available. Recent advances have produced promising treatment strategies, including genetic treatment and immunomodulation, that are currently being tested pre-clinically in murine models. Traditional behavioral assays frequently fail to detect early motor deficits in corresponding mouse models. Thus, this study investigated whether more...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
