Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9373709 | Journal of Pediatric Surgery | 2005 | 4 Pages |
Abstract
Fibroblast growth factor-10 serves as a regulator in normal duodenal growth and development. Its deletion leads to duodenal atresia and challenges traditionally accepted theories of pathogenesis. This novel, genetically mediated duodenal malformation reflects an animal model that will allow further evaluation of the pathogenesis of this surgically correctable disease. By studying the mechanism of Fgf10 function in foregut development, the authors hope to better understand these anomalies and to explore possible therapeutic alternatives.
Keywords
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Perinatology, Pediatrics and Child Health
Authors
Robert C. Kanard, Timothy J. Fairbanks, Stijn P. De Langhe, Fred G. Sala, Pierre M. Del Moral, Chrissy A. Lopez, David Warburton, Kathryn D. Anderson, Saverio Bellusci, R. Cartland Burns,