| 1 | EDAR, EDARADD
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| Functional studies for a dominant mutation in the EDAR gene responsible for hypohidrotic ectodermal dysplasia.
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| Okita T, Asano N, Yasuno S, Shimomura Y.
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| J Dermatol. Aug;46(8):710-715. doi: 10.1111/1346-8138.14983. Epub 2019 Jun 27 2019
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| 2 | ED12, ED3, EDA, EDAR, EDARADD, HEDAD, OODD, WNT10A
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| Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases.
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| 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.
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| Hum Mutat 32(1):70-2. 2011
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| 3 | EDAR, EDARADD
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| A Missense Mutation in the Death Domain of EDAR Abolishes the Interaction with EDARADD and Underlies Hypohidrotic Ectodermal Dysplasia.
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| Masui Y, Farooq M, Sato N, Fujimoto A, Fujikawa H, Ito M, Shimomura Y.
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| Dermatology ermatology. 2011 Aug 29. [Epub ahead of print]
2011
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| 4 | EDARADD, HEDAD
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| Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
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| Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N.
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| Am J Med Genet A 155A(7):1616-22. doi: 10.1002/ajmg.a.34045. Epub 2011 May 27.
2011
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| 5 | EDARADD, HEDAD
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| A Mongolian patient with hypohidrotic ectodermal dysplasia with a novel P121S variant in EDARADD.
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| Suda N, Bazar A, Bold O, Jigjid B, Garidkhuu A, Ganburged G, Moriyama K.
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| Orthod Craniofac Res 13(2):114-7.
2010
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| 6 | EDARADD, HEDAD
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| Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia cases.
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| Chassaing N, Cluzeau C, Bal E, Guigue P, Vincent MC, Viot G, Ginisty D, Munnich A, Smahi A, Calvas P.
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| Br J Dermatol 162(5):1044-8. Epub 2010 Mar 5.
2010
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| 7 | ED1, ED3, EDA, EDAR, EDARADD
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| Molecular aspects of hypohidrotic ectodermal dysplasia.
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| Mikkola ML.
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| Am J Med Genet A 149A(9):2031-6. Review.PMID: 19681132 2009
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| 8 | EDARADD,HEDAD
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| Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.
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| Bal E, Baala L, Cluzeau C, El Kerch F, Ouldim K, Hadj-Rabia S, Bodemer C, Munnich A, Courtois G, Sefiani A, Smahi A.
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| Hum Mutat 28(7):703-9. 2007
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| 9 | EDAR, EDARADD, MAP3K7, TAB2, TRAF6
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| TAB2, TRAF6 and TAK1 are involved in NF-kappaB activation induced by the TNF-receptor, Edar and its adaptator Edaradd.
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| Morlon A, Munnich A, Smahi A.
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| Hum Mol Genet 14(23):3751-7. Epub 2005 Oct 26. 2005
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| 10 | ED1, EDAR, EDARADD
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| The ectodysplasin pathway in feather tract development.
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| Houghton L, Lindon C, Morgan BA.
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| Development 132(5):863-72. Epub 2005 Jan 26.
2005
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| 11 | EDARADD
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| Identification of a novel death domain-containing adaptor molecule forectodysplasin-A receptor that is mutated in crinkled mice.
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| Yan M, Zhang Z, Brady JR, Schilbach S, Fairbrother WJ, Dixit VM.
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| Curr Biol 12(5):409-13. 2002
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| 12 | EDAR, EDARADD, EDA2R
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| The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes.
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| Smahi A, Courtois G, Rabia SH, Doffinger R, Bodemer C, Munnich A, Casanova JL, Israel A.
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| Hum Mol Genet 11(20):2371-5. 2002
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| 13 | EDARADD
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| Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice.
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| Yan M, Zhang Z, Brady JR, Schilbach S, Fairbrother WJ, Dixit VM.
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| Curr Biol 12(5):409-13.
2002
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| 14 | EDAR, EDARADD, HEDAD
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| Gene defect in ectodermal dysplasia implicates a death domain adapter in development.
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| Headon DJ, Emmal SA, Ferguson BM, Tucker AS, Justice MJ, Sharpe PT, Zonana J, Overbeek PA.
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| Nature 414(6866):913-6. 2001
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