Differential histological features and myogenic protein levels in distinct muscles of d-sarcoglycan null muscular dystrophy mouse model
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,General Medicine,Physiology,Histology
Link
https://link.springer.com/content/pdf/10.1007/s10735-023-10136-7.pdf
Reference38 articles.
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2. Alonso-Perez J, Gonzalez-Quereda L, Bello L et al (2020) New genotype-phenotype correlations in a large european cohort of patients with sarcoglycanopathy. Brain 143:2696–2708. https://doi.org/10.1093/brain/awaa228
3. Barateau A, Vadrot N, Agbulut O, Vicart P, Batonnet-Pichon S, Buendia B (2017) Distinct fiber type signature in mouse muscles expressing a mutant lamin a responsible for congenital muscular dystrophy in a patient. Cells. https://doi.org/10.3390/cells6020010
4. Bassel-Duby R, Olson EN (2006) Signaling pathways in skeletal muscle remodeling. Annu Rev Biochem 75:19–37. https://doi.org/10.1146/annurev.biochem.75.103004.142622
5. Bloemberg D, Quadrilatero J (2012) Rapid determination of myosin heavy chain expression in rat, mouse, and human skeletal muscle using multicolor immunofluorescence analysis. PLoS ONE 7:e35273. https://doi.org/10.1371/journal.pone.0035273
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