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Receptor and post-receptor abnormalities contribute to insulin resistance in myotonic dystrophy type 1 and type 2 skeletal muscle

Myotonic dystrophy type 1 (DM1) and type 2 (DM2) are autosomal dominant multisystemic disorders caused by expansion of microsatellite repeats. In both forms, the mutant transcripts accumulate in nuclear foci altering the function of alternative splicing regulators which are necessary for the physiol...

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Bibliografiske detaljer
Udgivet i:PLoS One
Main Authors: Renna, Laura Valentina, Bosè, Francesca, Iachettini, Sara, Fossati, Barbara, Saraceno, Lorenzo, Milani, Valentina, Colombo, Roberto, Meola, Giovanni, Cardani, Rosanna
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2017
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5600405/
https://ncbi.nlm.nih.gov/pubmed/28915272
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0184987
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