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...
Main Authors: | G Lattanzi, NM Maraldi, C Vigouroux, G Novelli, M Caron, M Auclair, C Le Dour, MR D’Apice, D Camozzi, C Capanni, E Schena, M Magnani, V Fiori, S Dominici |
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Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2009-03-01
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Series: | European Journal of Histochemistry |
Online Access: | http://ejh.pagepress.org/index.php/ejh/article/view/1232 |
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