Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations

The nuclear face of the nuclear membrane is enriched with the intermediate filament protein lamin A. Mutations in LMNA, the gene encoding lamin A, lead to a diverse set of inherited conditions including myopathies that affect both the heart and skeletal muscle. To gain insight about lamin A protein...

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Foilsithe in:Hum Mol Genet
Main Authors: Depreux, Frederic F., Puckelwartz, Megan J., Augustynowicz, Aleksandra, Wolfgeher, Don, Labno, Christine M., Pierre-Louis, Dynora, Cicka, Danielle, Kron, Stephen J., Holaska, James, McNally, Elizabeth M.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Oxford University Press 2015
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Articles
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4492393/
https://ncbi.nlm.nih.gov/pubmed/25948554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv160
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