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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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Vydáno v:Hum Mol Genet
Hlavní autoři: 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.
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2015
Témata:
On-line přístup: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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