Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

Background: Skeletal muscle disorders associated with mutations of lamin A/C gene include autosomal Emery–Dreifuss muscular dystrophy and limb girdle muscular dystrophy 1B. The pathogenic mechanism underlying these diseases is unknown. Recent data suggest an impairment of signalling mechanisms as a...

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Hlavní autoři: Cenni, V, Sabatelli, P, Mattioli, E, Marmiroli, S, Capanni, C, Ognibene, A, Squarzoni, S, Maraldi, N, Bonne, G, Columbaro, M, Merlini, L, Lattanzi, G
Médium: Artigo
Jazyk:Inglês
Vydáno: BMJ Group 2005
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1736020/
https://ncbi.nlm.nih.gov/pubmed/15744034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.026112
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