Identification of mitochondrial dysfunction in Hutchinson-Gilford progeria syndrome through use of stable isotope labeling with amino acids in cell culture.
J Proteomics
; 91: 466-77, 2013 Oct 08.
Article
em En
| MEDLINE
| ID: mdl-23969228
Palavras-chave
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit B1; ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit; ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1; ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide; ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide; ATP5A1; ATP5B; ATP5C1; ATP5F1; ATP5O; Accelerated aging; COX; CS; ENO2; FTI; FpSDH; HGPS; HutchinsonGilford progeria syndrome; Lamin A; MAF; Mitochondrial dysfunction; Molecular biology of aging; OXPHOS; PKM; Progerin; SILAC; Zmpste24; citrate synthase; cytochrome c oxidase; eIF2; eIF4; enolase 2; eukaryotic translation initiation factor 2; eukaryotic translation initiation factor 4; farnesyltransferase inhibitor; flavoprotein subunit of succinate dehydrogenase; mTOR; mammalian target of rapamycin; mouse adult fibroblast; oxidative phosphorylation; p70S6K; pyruvate kinase, muscle; ribosomal protein S6 kinase, 70kDa, polypeptide 1; stable isotope labeling with amino acids in cell culture; zinc metalloproteinase STE24 homolog
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Progéria
/
Regulação da Expressão Gênica
/
Aminoácidos
/
Mitocôndrias
Tipo de estudo:
Diagnostic_studies
/
Prognostic_studies
Limite:
Adolescent
/
Animals
/
Child
/
Female
/
Humans
/
Male
Idioma:
En
Revista:
J Proteomics
Assunto da revista:
BIOQUIMICA
Ano de publicação:
2013
Tipo de documento:
Article
País de publicação:
Holanda