A truncated lamin A in the Lmna(−/−) mouse line: Implications for the understanding of laminopathies

During recent years a number of severe clinical syndromes, collectively termed laminopathies, turned out to be caused by various, distinct mutations in the human LMNA gene. Arising from this, remarkable progress has been made to unravel the molecular pathophysiology underlying these disorders. A gre...

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Hlavní autoři: Jahn, Daniel, Schramm, Sabine, Schnölzer, Martina, Heilmann, Clemens J., de Koster, Chris G., Schütz, Wolfgang, Benavente, Ricardo, Alsheimer, Manfred
Médium: Artigo
Jazyk:Inglês
Vydáno: Landes Bioscience 2012
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Research Paper
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3474667/
https://ncbi.nlm.nih.gov/pubmed/22895093
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/nucl.21676
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