TY  - JOUR
AU  - Rivera-Torres, Jose
AU  - Acin-Perez, Rebeca
AU  - Cabezas-Sánchez, Pablo
AU  - Osorio, Fernando G
AU  - Gonzalez-Gomez, Cristina
AU  - Megias Vazquez, Diego
AU  - Cámara, Carmen
AU  - López-Otín, Carlos
AU  - Enriquez, Jose Antonio
AU  - Luque-García, José L
AU  - Andres, Vicente
PY  - 2013
DO  - 10.1016/j.jprot.2013.08.008
SN  - 1874-3919
UR  - http://hdl.handle.net/20.500.12105/7755
AB  - UNLABELLED: Hutchinson-Gilford progeria syndrome (HGPS) is a rare segmental premature aging disorder that recapitulates some biological and physical aspects of physiological aging. The disease is caused by a sporadic dominant mutation in the LMNA gene...
LA  - eng
PB  - Elsevier
KW  - ATP synthase, H+ transporting, mitochondrial F0 complex, subunit B1
KW  - ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit
KW  - ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1
KW  - ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide
KW  - ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide
KW  - ATP5A1
KW  - ATP5B
KW  - ATP5C1
KW  - ATP5F1
KW  - ATP5O
KW  - Accelerated aging
KW  - COX
KW  - CS
KW  - ENO2
KW  - FTI
KW  - FpSDH
KW  - HGPS
KW  - Hutchinson–Gilford progeria syndrome
KW  - Lamin A
KW  - MAF
KW  - Mitochondrial dysfunction
KW  - Molecular biology of aging
KW  - OXPHOS
KW  - PKM
KW  - Progerin
KW  - SILAC
KW  - Zmpste24
KW  - citrate synthase
KW  - cytochrome c oxidase
KW  - eIF2
KW  - eIF4
KW  - Enolase 2
KW  - Eukaryotic translation initiation factor 2
KW  - Eukaryotic translation initiation factor 4
KW  - Farnesyltransferase inhibitor
KW  - Flavoprotein subunit of succinate dehydrogenase
KW  - mTOR
KW  - Mammalian target of rapamycin
KW  - Mouse adult fibroblast
KW  - Oxidative phosphorylation
KW  - p70S6K
KW  - Pyruvate kinase, muscle
KW  - Ribosomal protein S6 kinase, 70kDa, polypeptide 1
KW  - Stable isotope labeling with amino acids in cell culture
KW  - Zinc metalloproteinase STE24 homolog
TI  - Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture
TY  - journal article
ER  -