TY  - JOUR
AU  - Hamczyk, Magda R.
AU  - Villa-Bellosta, Ricardo
AU  - Quesada, Víctor
AU  - Gonzalo, Pilar
AU  - Vidak, Sandra
AU  - Nevado, Rosa M
AU  - Andres-Manzano, Maria J.
AU  - Misteli, Tom
AU  - López-Otín, Carlos
AU  - Andres, Vicente
PY  - 2019
DO  - 10.15252/emmm.201809736
SN  - 1757-4676
UR  - http://hdl.handle.net/20.500.12105/7510
AB  - Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder caused by progerin, a mutant lamin A variant. HGPS patients display accelerated aging and die prematurely, typically from atherosclerosis complications. Recently, we demonstrated...
LA  - eng
PB  - EMBO Press
KW  - Aging
KW  - Endoplasmic reticulum stress
KW  - Progeria
KW  - Unfolded protein response
KW  - Vascular smooth muscle cell
TI  - Progerin accelerates atherosclerosis by inducing endoplasmic reticulum stress in vascular smooth muscle cells
TY  - journal article
ER  -