The senescence-related mitochondrial/oxidative stress pathway is repressed in human induced pluripotent stem cells

Stem Cells

Volumn 28, Issue 4, 2010, Pages 721-733

  Prigione, Alessandro ^a   Fauler, Beatrix ^a   Lurz, Rudi ^a   Lehrach, Hans ^a   Adjaye, James ^a  

^a MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

Author keywords

Aging; Differentiation; Embryonic stem cells; Gene expression; Induced pluripotency; iPS; Reprogramming

Indexed keywords

ADENOSINE TRIPHOSPHATE; LACTIC ACID; MITOCHONDRIAL DNA;

AEROBIC METABOLISM; ARTICLE; CELL AGING; CELL ASSAY; CELL DIFFERENTIATION; CELL LEVEL; CELL MATURATION; CELL STRUCTURE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DNA DETERMINATION; EMBRYO; EMBRYONIC STEM CELL; GLYCOLYSIS; HUMAN; HUMAN CELL; MITOCHONDRION; NEWBORN; OXIDATIVE STRESS; PLURIPOTENT STEM CELL; PROTEIN EXPRESSION; SENESCENCE;

ANAEROBIOSIS; CELL AGING; CELLS, CULTURED; DNA, MITOCHONDRIAL; GENE DOSAGE; GENE EXPRESSION PROFILING; GLYCOLYSIS; HUMANS; INDUCED PLURIPOTENT STEM CELLS; KARYOTYPING; MICROSCOPY, ELECTRON, TRANSMISSION; MITOCHONDRIA; OXIDATIVE STRESS; TRANSCRIPTION, GENETIC;

IPS;

EID: 77951002352     PISSN: 10665099     EISSN: None     Source Type: Journal    
DOI: 10.1002/stem.404     Document Type: Article

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