TY  - JOUR
AU  - Trigueros-Motos, Laia
AU  - Gonzalez, Jose M
AU  - Rivera-Torres, Jose
AU  - Andres, Vicente
PY  - 2011
DO  - 10.2741/226
UR  - http://hdl.handle.net/20.500.12105/7659
AB  - Hutchinson-Gilford Progeria Syndrome (HGPS), a rare human disease characterized by premature aging, is mainly caused by the abnormal accumulation of progerin, a mutant form of the mammalian nuclear envelope component lamin A. HGPS patients exhibit...
LA  - eng
KW  - Aging
KW  - Alternative Splicing
KW  - Animals
KW  - Cardiovascular Diseases
KW  - Cholesterol
KW  - Diphosphonates
KW  - Genetic Therapy
KW  - Humans
KW  - Lamin Type A
KW  - Membrane Proteins
KW  - Metalloendopeptidases
KW  - Mice
KW  - Mice, Knockout
KW  - Nuclear Proteins
KW  - Oligonucleotides
KW  - Oxidative Stress
KW  - Progeria
KW  - Protein Precursors
KW  - Terpenes
TI  - Hutchinson-Gilford progeria syndrome, cardiovascular disease and oxidative stress
TY  - journal article
ER  -