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References

These sources were used to develop the Genetics Home Reference gene summary on the EDA gene.

Courtney JM, Blackburn J, Sharpe PT. The Ectodysplasin and NFkappaB signalling pathways in odontogenesis. Arch Oral Biol. 2005 Feb;50(2):159-63. Review. PubMed citation
Drögemüller C, Distl O, Leeb T. X-linked anhidrotic ectodermal dysplasia (ED1) in men, mice, and cattle. Genet Sel Evol. 2003;35 Suppl 1:S137-45. Review. PubMed citation
Entrez Gene
Gaide O. New developments in the history of hypohidrotic ectodermal dysplasia. Dermatology. 2003;207(2):123-4. PubMed citation
Gene Review: Hypohidrotic Ectodermal Dysplasia
Hashiguchi T, Yotsumoto S, Kanzaki T. Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia. Exp Dermatol. 2003 Aug;12(4):518-22. PubMed citation
Mikkola ML, Thesleff I. Ectodysplasin signaling in development. Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):211-24. Review. PubMed citation
Smahi A, Courtois G, Rabia SH, Döffinger R, Bodemer C, Munnich A, Casanova JL, Israël A. The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes. Hum Mol Genet. 2002 Oct 1;11(20):2371-5. Review. PubMed citation
Vincent MC, Biancalana V, Ginisty D, Mandel JL, Calvas P. Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia. Eur J Hum Genet. 2001 May;9(5):355-63. PubMed citation
Wiśniewski SA, Kobielak A, Trzeciak WH, Kobielak K. Recent advances in understanding of the molecular basis of anhidrotic ectodermal dysplasia: discovery of a ligand, ectodysplasin A and its two receptors. J Appl Genet. 2002;43(1):97-107. Review. PubMed citation


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