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Post-natal myogenic and adipogenic developmental: Defects and metabolic impairment upon loss of A-type lamins

A-type lamins are a major component of the nuclear lamina. Mutations in the LMNA gene, which encodes the A-type lamins A and C, cause a set of phenotypically diverse diseases collectively called laminopathies. While adult LMNA null mice show various symptoms typically associated with laminopathies,...

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Detalhes bibliográficos
Main Authors: Kubben, Nard, Voncken, Jan Willem, Konings, Gonda, van Weeghel, Michel, van den Hoogenhof, Maarten MG, Gijbels, Marion, van Erk, Arie, Schoonderwoerd, Kees, van den Bosch, Bianca, Dahlmans, Vivian, Calis, Chantal, Houten, Sander M, Misteli, Tom, Pinto, Yigal M
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3149880/
https://ncbi.nlm.nih.gov/pubmed/21818413
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/nucl.2.3.15731
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