Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
Farnesylated prelamin A is a processing intermediate produced in the lamin A maturation pathway. Accumulation of a truncated farnesylated prelamin A form, called progerin, is a hallmark of the severe premature ageing syndrome, Hutchinson-Gilford progeria. Progerin elicits toxic effects in cells, lea...
Main Authors: | Cenni, V., Capanni, C., Columbaro, M., Ortolani, M., D'Apice, M.R., Novelli, G., Fini, M., Marmiroli, S., Scarano, E., Maraldi, N.M., Squarzoni, S., Prencipe, S., Lattanzi, G. |
---|---|
Format: | Online |
Language: | English |
Published: |
PAGEPress Publications
2011
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3284238/ |
Similar Items
-
Erratum - Autophagic Degradation of Farnesylated Prelamin a as a Therapeutic Approach to Lamin-Linked Progeria
by: Cenni, V., et al.
Published: (2013) -
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria
by: Dominici, S., et al.
Published: (2009) -
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment
by: Camozzi, Daria, et al.
Published: (2012) -
Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics
by: Cenni, Vittoria, et al.
Published: (2014) -
All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype
by: Pellegrini, Camilla, et al.
Published: (2015)