Citations for
1ED12, ED3, EDA, EDAR, EDARADD, HEDAD, OODD, WNT10A
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
Cluzeau C, Hadj-Rabia S, Jambou M, Mansour S, Guigue P, Masmoudi S, Bal E, Chassaing N, Vincent MC, Viot G, Clauss F, Manière MC, Toupenay S, Le Merrer M, Lyonnet S, Cormier-Daire V, Amiel J, Faivre L, de Prost Y, Munnich A, Bonnefont JP, Bodemer C, Smahi A.
Hum Mutat 32(1):70-2. 2011
2EDAR, EDARADD
A Missense Mutation in the Death Domain of EDAR Abolishes the Interaction with EDARADD and Underlies Hypohidrotic Ectodermal Dysplasia.
Masui Y, Farooq M, Sato N, Fujimoto A, Fujikawa H, Ito M, Shimomura Y.
Dermatology ermatology. 2011 Aug 29. [Epub ahead of print] 2011
3EDARADD, HEDAD
Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N.
Am J Med Genet A 155A(7):1616-22. doi: 10.1002/ajmg.a.34045. Epub 2011 May 27. 2011
4EDARADD, HEDAD
A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD.
Suda N, Bazar A, Bold O, Jigjid B, Garidkhuu A, Ganburged G, Moriyama K.
Orthod Craniofac Res 13(2):114-7. 2010
5EDARADD, HEDAD
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases.
Chassaing N, Cluzeau C, Bal E, Guigue P, Vincent MC, Viot G, Ginisty D, Munnich A, Smahi A, Calvas P.
Br J Dermatol 162(5):1044-8. Epub 2010 Mar 5. 2010
6ED1, ED3, EDA, EDAR, EDARADD
Molecular aspects of hypohidrotic ectodermal dysplasia.
Mikkola ML.
Am J Med Genet A 149A(9):2031-6. Review.PMID: 19681132 2009
7EDARADD,HEDAD
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.
Bal E, Baala L, Cluzeau C, El Kerch F, Ouldim K, Hadj-Rabia S, Bodemer C, Munnich A, Courtois G, Sefiani A, Smahi A.
Hum Mutat 28(7):703-9. 2007
8EDAR, EDARADD, MAP3K7, TAB2, TRAF6
TAB2, TRAF6 and TAK1 are involved in NF-kappaB activation induced by the TNF-receptor, Edar and its adaptator Edaradd.
Morlon A, Munnich A, Smahi A.
Hum Mol Genet 14(23):3751-7. Epub 2005 Oct 26. 2005
9ED1, EDAR, EDARADD
The ectodysplasin pathway in feather tract development.
Houghton L, Lindon C, Morgan BA.
Development 132(5):863-72. Epub 2005 Jan 26. 2005
10EDARADD
Identification of a novel death domain-containing adaptor molecule forectodysplasin-A receptor that is mutated in crinkled mice.
Yan M, Zhang Z, Brady JR, Schilbach S, Fairbrother WJ, Dixit VM.
Curr Biol 12(5):409-13. 2002
11EDAR, EDARADD, EDA2R
The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes.
Smahi A, Courtois G, Rabia SH, Doffinger R, Bodemer C, Munnich A, Casanova JL, Israel A.
Hum Mol Genet 11(20):2371-5. 2002
12EDARADD
Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice.
Yan M, Zhang Z, Brady JR, Schilbach S, Fairbrother WJ, Dixit VM.
Curr Biol 12(5):409-13. 2002
13EDAR, EDARADD, HEDAD
Gene defect in ectodermal dysplasia implicates a death domain adapter in development.
Headon DJ, Emmal SA, Ferguson BM, Tucker AS, Justice MJ, Sharpe PT, Zonana J, Overbeek PA.
Nature 414(6866):913-6. 2001