| Literature DB >> 22158542 |
Hana Lango Allen1, Sarah E Flanagan1, Charles Shaw-Smith1, Elisa De Franco1, Ildem Akerman2,3,4, Richard Caswell1, Jorge Ferrer2,3,4, Andrew T Hattersley1, Sian Ellard1.
Abstract
Understanding the regulation of pancreatic development is key for efforts to develop new regenerative therapeutic approaches for diabetes. Rare mutations in PDX1 and PTF1A can cause pancreatic agenesis, however, most instances of this disorder are of unknown origin. We report de novo heterozygous inactivating mutations in GATA6 in 15/27 (56%) individuals with pancreatic agenesis. These findings define the most common cause of human pancreatic agenesis and establish a key role for the transcription factor GATA6 in human pancreatic development.Entities:
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Year: 2011 PMID: 22158542 PMCID: PMC4062962 DOI: 10.1038/ng.1035
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330