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ProteomicsProteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and enhanced cysteine metabolic pathways
Equine myofibrillar myopathy (MFM) causes exertional muscle pain and is characterized by myofibrillar disarray and ectopic protein aggregates of unknown origin. To investigate the pathophysiology of MFM, we compared the skeletal muscle proteome and 3 h post-exercise transcriptome of gluteal muscle i...
ORGANISM(S): Equus caballus (Horse) 
2019-11-12 | PXD009362 | Pride
Myopathy Horse Antioxidant Proteome 
ProteomicsEquine gluteal muscle LC-MSMS: Warmblood
Myofibrillar myopathy (MFM) in horses is a late onset disease that affects performance and athleticism. It is characterized by myofibrillar disarray and protein aggregation with no known cause. The objective of this study was to elucidate the molecular drivers of MFM in Warmblood (WB) horses by prot...
ORGANISM(S): Equus caballus (Horse) 
2021-09-09 | PXD019187 | Pride
Horse Lc-msms Gluteal muscle 
UnknownClinical and histopathological features of myofibrillar myopathy in Warmblood horses.
Not available
S-EPMC5640499 | biostudies-literature
UnknownMitochondrial dysfunction in myofibrillar myopathy.
Not available
S-EPMC5066370 | biostudies-literature
ProteomicsComparison of the skeletal muscle proteomes in wt and hBAG3P209L overexpressing mice
Myofibrillar myopathy-6 (MFM6) is rare, autosomal dominant neuromuscular disease that is characterised by devastating childhood muscular dystrophy, restrictive cardiomyopathy, and respiratory insufficiency. MFM-6 is caused by single base mutation in the gene encoding the co-chaperone BAG3 (Bcl-2 ass...
ORGANISM(S): Mus musculus (Mouse) 
2025-12-11 | PXD047942 | Pride
Myofibrillar myopathy-6  mouse model  proteome  skeletal muscle Bag3p209l Bag3 
UnknownFLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.
Not available
S-EPMC8237399 | biostudies-literature
UnknownA mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.
Not available
S-EPMC1224531 | biostudies-literature
UnknownCommercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis.
Not available
S-EPMC7937766 | biostudies-literature
UnknownTitin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure.
Not available
S-EPMC6558248 | biostudies-literature
UnknownProteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways.
Not available
S-EPMC6337024 | biostudies-literature
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