Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease-Reference-Cited by-同舟云学术

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Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease

Published:1998-04-28 Issue:9 Volume:95 Page:5161-5165
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Herbarth B.,Pingault V.,Bondurand N.,Kuhlbrodt K.,Hermans-Borgmeyer I.,Puliti A.,Lemort N.,Goossens M.,Wegner M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference29 articles.

1. Cellular and molecular biology of neural crest cell lineage determination

2. Association of Megacolon with Two Recessive Spotting Genes in the Mouse

3. Association of megacolon with a new dominant spotting gene (Dom) in the mouse

4. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

5. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice

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