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P2X7 purinoceptor alterations in dystrophic mdx mouse muscles: relationship to pathology and potential target for treatment
Duchenne muscular dystrophy (DMD) is a lethal inherited muscle disorder. Pathological characteristics of DMD skeletal muscles include, among others, abnormal Ca(2+) homeostasis and cell signalling. Here, in the mdx mouse model of DMD, we demonstrate significant P2X7 receptor abnormalities in isolate...
Autores principales: | Young, Christopher N J, Brutkowski, Wojciech, Lien, Chun-Fu, Arkle, Stephen, Lochmüller, Hanns, Zabłocki, Krzysztof, Górecki, Dariusz C |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4365874/ https://www.ncbi.nlm.nih.gov/pubmed/21794079 http://dx.doi.org/10.1111/j.1582-4934.2011.01397.x |
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