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Results: 1 to 20 of 129

Similar articles for PubMed (Select 11780064)

1.

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. 2001 Dec 20-27;414(6866):913-6.

PMID:
11780064
2.

The Ectodysplasin and NFkappaB signalling pathways in odontogenesis.

Courtney JM, Blackburn J, Sharpe PT.

Arch Oral Biol. 2005 Feb;50(2):159-63. Review.

PMID:
15721144
3.

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. 2005 Dec 1;14(23):3751-7. Epub 2005 Oct 26.

4.
5.

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. 2002 Mar 5;12(5):409-13.

6.

Ectodysplasin receptor-mediated signaling is essential for embryonic submandibular salivary gland development.

Jaskoll T, Zhou YM, Trump G, Melnick M.

Anat Rec A Discov Mol Cell Evol Biol. 2003 Apr;271(2):322-31.

7.

Signaling and subcellular localization of the TNF receptor Edar.

Koppinen P, Pispa J, Laurikkala J, Thesleff I, Mikkola ML.

Exp Cell Res. 2001 Oct 1;269(2):180-92.

PMID:
11570810
8.

Death receptor signaling giving life to ectodermal organs.

Thesleff I, Mikkola ML.

Sci STKE. 2002 May 7;2002(131):pe22. Review.

PMID:
11997580
9.

TRAF6-deficient mice display hypohidrotic ectodermal dysplasia.

Naito A, Yoshida H, Nishioka E, Satoh M, Azuma S, Yamamoto T, Nishikawa S, Inoue J.

Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8766-71. Epub 2002 Jun 11.

10.

A rare case of hypohidrotic ectodermal dysplasia caused by compound heterozygous mutations in the EDAR gene.

Shimomura Y, Sato N, Miyashita A, Hashimoto T, Ito M, Kuwano R.

J Invest Dermatol. 2004 Oct;123(4):649-55.

11.

Edar and Troy signalling pathways act redundantly to regulate initiation of hair follicle development.

Pispa J, Pummila M, Barker PA, Thesleff I, Mikkola ML.

Hum Mol Genet. 2008 Nov 1;17(21):3380-91. doi: 10.1093/hmg/ddn232. Epub 2008 Aug 9.

12.

Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis.

Tucker AS, Headon DJ, Schneider P, Ferguson BM, Overbeek P, Tschopp J, Sharpe PT.

Development. 2000 Nov;127(21):4691-700.

13.

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia.

Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J.

Nat Genet. 1999 Aug;22(4):366-9.

PMID:
10431241
14.

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. 2007 Jul;28(7):703-9.

PMID:
17354266
15.

Molecular aspects of hypohidrotic ectodermal dysplasia.

Mikkola ML.

Am J Med Genet A. 2009 Sep;149A(9):2031-6. doi: 10.1002/ajmg.a.32855. Review.

PMID:
19681132
16.

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. 2011;223(1):74-9. doi: 10.1159/000330557. Epub 2011 Aug 29.

PMID:
21876339
17.

A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene.

Kuramoto T, Yokoe M, Hashimoto R, Hiai H, Serikawa T.

BMC Genet. 2011 Oct 21;12:91. doi: 10.1186/1471-2156-12-91.

18.

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. 2010 May;162(5):1044-8. doi: 10.1111/j.1365-2133.2010.09670.x. Epub 2010 Mar 5.

PMID:
20222921
19.

The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A.

Kumar A, Eby MT, Sinha S, Jasmin A, Chaudhary PM.

J Biol Chem. 2001 Jan 26;276(4):2668-77. Epub 2000 Oct 16.

20.

Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia.

Chassaing N, Bourthoumieu S, Cossee M, Calvas P, Vincent MC.

Hum Mutat. 2006 Mar;27(3):255-9.

PMID:
16435307
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