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Erratum to: dysregulation of matricellular proteins is an early signature of pathology in laminindeficient muscular dystrophy
Skeletal Musclevolume 4, Article number: 17 (2014)
The original article was published in Skeletal Muscle 2014 4:14
After publication of this work , we noted that while we were initially going to include muscle function tests in this study, as our manuscript evolved and we decided to include earlier time points for characterization, we decided to remove it because pups younger than 2 weeks cannot be measured. While we removed this from the results, we missed retracting them from the methods section of the abstract. Therefore, the methods section of the abstract should instead read:
We sought out to examine the dysregulation of various pathways throughout early development (postnatal weeks 1–4) in the DyW mouse, the most commonly used mouse model of laminin-deficient muscular dystrophy. Gene (qRT-PCR) and protein levels (western blot, ELISA) as well as histology (H&E, picrosirius red staining) and immunohistochemistry (fibronectin, TUNEL assay) were used to assess dysregulation of matricellular proteins.
Mehuron T, Kumar A, Duarte L, Yamauchi J, Accorsi A, Girgenrath M: Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy. Skeletal Muscle 2014, 4: 14. 10.1186/2044-5040-4-14
The online version of the original article can be found at 10.1186/2044-5040-4-14