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Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
Lamin A is a component of the nuclear lamina mutated in a group of human inherited disorders known as laminopathies. Among laminopathies, progeroid syndromes and lipodystrophies feature accumulation of prelamin A, the precursor protein which, in normal cells, undergoes a multi-step processing to yie...
Autores principales: | Dominici, S., Fiori, V., Magnani, M., Schena, E., Capanni, C., Camozzi, D., D’Apice, M.R., Le Dour, C., Auclair, M., Caron, M., Novelli, G., Vigouroux, C., Maraldi, N.M., Lattanzi, G. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3167279/ https://www.ncbi.nlm.nih.gov/pubmed/30256865 http://dx.doi.org/10.4081/ejh.2009.e6 |
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