Inhibition of protein kinase c signaling maintains rat embryonic stem cell pluripotency

Journal of Biological Chemistry

Volumn 288, Issue 34, 2013, Pages 24351-24362

  Rajendran, Ganeshkumar ^a   Dutta, Debasree ^a,c   Hong, James ^b   Paul, Arindam ^a   Saha, Biswarup ^a   Mahato, Biraj ^a   Ray, Soma ^a   Home, Pratik ^a   Ganguly, Avishek ^a   Weiss, Mark L ^b   Paul, Soumen ^a  

^a UNIVERSITY OF KANSAS SCHOOL OF MEDICINE   (United States)

^b KANSAS STATE UNIVERSITY   (United States)

^c RAJIV GANDHI CENTRE FOR BIOTECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

DEVELOPMENTAL POTENTIAL; EFFICIENT STRATEGY; EMBRYONIC FIBROBLASTS; EMBRYONIC STEM CELLS; EPIGENETIC MODIFICATION; INDUCED PLURIPOTENT STEM CELLS; PLURIPOTENT STEM CELLS; SIGNALING MECHANISMS;

CELL CULTURE; ENZYMES; GENE EXPRESSION; PROTEINS; RATS; RNA; STEM CELLS;

SIGNALING;

2 [1 (3 DIMETHYLAMINOPROPYL) 5 METHOXY 1H INDOL 3 YL] 3 (1H INDOL 3 YL)MALEIMIDE; CHIR 99021; EMFILERMIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; MICRORNA 21; MICRORNA 29; N (2,3 DIHYDROXYPROPOXY) 3,4 DIFLUORO 2 (2 FLUORO 4 IODOANILINO)BENZAMIDE; PROTEIN KINASE C; PROTEIN KINASE C INHIBITOR; PROTEIN KINASE C ZETA; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLASTOCYST; CELL CULTURE; CELL DIFFERENTIATION; CELL ISOLATION; CELL RENEWAL; CELL VIABILITY; CHIMERA; CONCENTRATION RESPONSE; CONTROLLED STUDY; DNA MODIFICATION; DRUG TARGETING; EMBRYO; EMBRYONIC STEM CELL; ENZYME ACTIVITY; ENZYME INHIBITION; EPIGENETICS; FEMALE; FIBROBLAST; GENE EXPRESSION; GERM LINE; MALE; MOUSE; NONHUMAN; NUCLEAR REPROGRAMMING; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; PROTEIN TARGETING; RAT; REPORTER GENE; SIGNAL TRANSDUCTION; TRANSCRIPTION REGULATION;

CHROMATIN MODIFICATION; EMBRYONIC STEM CELL; NF-ΚB; PKC; RAT;

ANIMALS; EMBRYONIC STEM CELLS; INDOLES; MALEIMIDES; MICRORNAS; NF-KAPPA B; PLURIPOTENT STEM CELLS; PROTEIN KINASE C-EPSILON; PROTEIN KINASE INHIBITORS; RATS; SIGNAL TRANSDUCTION;

EID: 84883141564     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.455725     Document Type: Article

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