Combinatorial modulation of signaling pathways reveals cell-type-specific requirements for highly efficient and synchronous iPSC reprogramming

Stem Cell Reports

Volumn 3, Issue 4, 2014, Pages 574-584

  Vidal, Simon E ^a   Amlani, Bhishma ^a   Chen, Taotao ^a   Tsirigos, Aristotelis ^a   Stadtfeld, Matthias ^a  

^a NEW YORK UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE; TRANSFORMING GROWTH FACTOR BETA; WNT PROTEIN; ASCORBIC ACID;

ANIMAL CELL; ARTICLE; CELL DIFFERENTIATION; CELL POPULATION; CELL TYPE; CHROMATIN ASSEMBLY AND DISASSEMBLY; CONTROLLED STUDY; EMBRYONIC STEM CELL; ENZYME ACTIVITY; FIBROBLAST; HEMATOPOIETIC STEM CELL; INTRACELLULAR SIGNALING; LIVER DEVELOPMENT; MOUSE; NONHUMAN; NUCLEAR REPROGRAMMING; NUCLEOTIDE SEQUENCE; PLURIPOTENT STEM CELL; PROTEIN EXPRESSION; SOMATIC CELL; WNT SIGNALING PATHWAY; ANIMAL; CELL CULTURE; CYTOLOGY; DRUG EFFECTS; INDUCED PLURIPOTENT STEM CELL; METABOLISM; SIGNAL TRANSDUCTION;

ANIMALS; ASCORBIC ACID; CELLS, CULTURED; CELLULAR REPROGRAMMING; EMBRYONIC STEM CELLS; FIBROBLASTS; INDUCED PLURIPOTENT STEM CELLS; MAP KINASE SIGNALING SYSTEM; MICE; TRANSFORMING GROWTH FACTOR BETA; WNT SIGNALING PATHWAY;

EID: 84908031698     PISSN: 22136711     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.stemcr.2014.08.003     Document Type: Article

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