Activation of Akt signaling is sufficient to maintain pluripotency in mouse and primate embryonic stem cells

Oncogene

Volumn 25, Issue 19, 2006, Pages 2697-2707

  Watanabe, S ^a   Umehara, H ^a   Murayama, K ^b   Okabe, M ^c   Kimura, T ^b   Nakano, T ^a,b  

^a OSAKA UNIVERSITY   (Japan)

^b OSAKA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c OSAKA UNIVERSITY   (Japan)

Author keywords

Akt; ES cells; Pluripotency; Stem cell system

Indexed keywords

4 HYDROXYTAMOXIFEN; HYBRID PROTEIN; LEUKEMIA INHIBITORY FACTOR; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL RENEWAL; CELL TYPE; CONTROLLED STUDY; EMBRYO; EMBRYONIC STEM CELL; ENZYME ACTIVATION; ENZYME ACTIVITY; GENE DELETION; GERM CELL; MONKEY; MOUSE; MYRISTYLATION; NEURAL STEM CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PLURIPOTENT STEM CELL; PRIMATE; PRIORITY JOURNAL; SIGNAL TRANSDUCTION;

ANIMALS; BETA CATENIN; CELL CULTURE TECHNIQUES; CELL DIFFERENTIATION; CELL PROLIFERATION; EMBRYO; ENZYME ACTIVATION; ESTROGEN ANTAGONISTS; INTERLEUKIN-6; LEUKEMIA INHIBITORY FACTOR; MACACA FASCICULARIS; MICE; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; MYRISTIC ACID; PHENOTYPE; PLURIPOTENT STEM CELLS; PROTO-ONCOGENE PROTEINS C-AKT; RECOMBINANT FUSION PROTEINS; SIGNAL TRANSDUCTION; STAT3 TRANSCRIPTION FACTOR; TAMOXIFEN;

ANIMALIA; MACACA FASCICULARIS; PRIMATES;

EID: 33646549601     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/sj.onc.1209307     Document Type: Article

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