Notch signaling reveals developmental plasticity of Pax4+ pancreatic endocrine progenitors and shunts them to a duct fate

Mechanisms of Development

Volumn 124, Issue 2, 2007, Pages 97-107

  Greenwood, Amy L ^a   Li, Sui ^a   Jones, Kevin ^a   Melton, Douglas A ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

Cell fate specification; Cre recombinase; Duct; Endocrine; Lineage; Notch; Pancreas development; Pax4

Indexed keywords

NOTCH RECEPTOR; TRANSCRIPTION FACTOR PAX4;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL FATE; CELL LINEAGE; CELL MATURATION; CELL SPECIFICITY; CELL TYPE; CONTROLLED STUDY; EMBRYO; ENDOCRINE CELL; MOUSE; NONHUMAN; PANCREAS DUCT; PANCREAS ISLET ALPHA CELL; PANCREAS ISLET BETA CELL; PANCREAS ISLET CELL; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN FUNCTION; STEM CELL;

MUS;

EID: 33846338921     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mod.2006.11.002     Document Type: Article

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