Transient Activation of Autophagy via Sox2-Mediated Suppression of mTOR Is an Important Early Step in Reprogramming to Pluripotency

Cell Stem Cell

Volumn 13, Issue 5, 2013, Pages 617-625

  Wang, Shuo ^a   Xia, Pengyan ^a   Ye, Buqing ^a   Huang, Guanling ^a   Liu, Jing ^a   Fan, Zusen ^a  

^a INSTITUTE OF BIOPHYSICS   (China)

Author keywords

[No Author keywords available]

Indexed keywords

HISTONE DEACETYLASE; MAMMALIAN TARGET OF RAPAMYCIN; TRANSCRIPTION FACTOR SOX2; ATG5 PROTEIN, MOUSE; MICROTUBULE ASSOCIATED PROTEIN; SOX2 PROTEIN, MOUSE; TARGET OF RAPAMYCIN KINASE; TRANSCRIPTION FACTOR SOX;

ANIMAL CELL; ARTICLE; AUTOPHAGY; CONTROLLED STUDY; DOWN REGULATION; EMBRYO; EMBRYO DEVELOPMENT; GENE EXPRESSION; GENE REPRESSION; INDUCED PLURIPOTENT STEM CELL; MOUSE; NONHUMAN; NUCLEAR REPROGRAMMING; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN BINDING; SOMATIC CELL; ANIMAL; BIOLOGICAL MODEL; CHEMISTRY; CYTOLOGY; GENETICS; METABOLISM; PHYSIOLOGY; PLURIPOTENT STEM CELL;

ANIMALS; AUTOPHAGY; INDUCED PLURIPOTENT STEM CELLS; MICE; MICROTUBULE-ASSOCIATED PROTEINS; MODELS, BIOLOGICAL; NUCLEAR REPROGRAMMING; PROMOTER REGIONS, GENETIC; SOXB1 TRANSCRIPTION FACTORS; TOR SERINE-THREONINE KINASES;

EID: 84901349234     PISSN: 19345909     EISSN: 18759777     Source Type: Journal    
DOI: 10.1016/j.stem.2013.10.005     Document Type: Article

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