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Publication : Neuronal defects in genotyped dominant megacolon (Dom) mouse embryos, a model for Hirschsprung disease.

First Author  Puliti A Year  1996
Journal  Neuroreport Volume  7
Issue  2 Pages  489-92
PubMed ID  8730812 Mgi Jnum  J:32994
Mgi Id  MGI:80482 Doi  10.1097/00001756-199601310-00027
Citation  Puliti A, et al. (1996) Neuronal defects in genotyped dominant megacolon (Dom) mouse embryos, a model for Hirschsprung disease. Neuroreport 7(2):489-92
abstractText  Dominant megacolon (Dom) is one of four mutations in the mouse which can produce a phenotype similar to Hirschsprung disease in man. Here, we report that it is possible to take advantage of two microsatellite markers to genotype Dom embryos and to study enteric neuronal development in Dom embryos using whole-mount immunohistochemistry. Dom embryos present a variable defect in the ileo-caecal region, as do embryos of other murine models of Hirschsprung disease.
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