Dangerous Entrapment for NRF2.
Cell
; 165(6): 1312-1313, 2016 Jun 02.
Article
em En
| MEDLINE
| ID: mdl-27259142
Progerin, a mutated lamin A, causes the severe premature-aging syndrome Hutchinson-Gilford progeria (HGPS). Kubben et al. present a driving mechanism for HGPS involving trapping of NRF2 at the nuclear periphery by progerin. This local restriction results in impaired NRF2 signaling and chronic oxidative stress.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Progéria
/
Lamina Tipo A
Limite:
Humans
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article