Disruption of the palatal rugae pattern in Tabby (eda) mutant mice
Author:
Publisher
Wiley
Subject
General Dentistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0722.2007.00482.x/fullpdf
Reference43 articles.
1. The tabby syndrome in the mouse
2. Evidence from thiol histochemistry for homology between the Tabby-crinkled syndrome in mice and human ectodermal dysplasia.
3. Anhidrosis and Absence of Sweat Glands in Mice Hemizygous for the Tabby Gene; Supportive Evidence for the Hypothesis of Homology Between Tabby and Human Anhidrotic (Hypohidrotic) Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)
4. The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains
5. X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
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