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Journal Abstract Search

342 related items for PubMed ID: 12784514

  • 1. [Ectodermal dysplasia syndrome].
    Mortier K, Wackens G.
    Ned Tijdschr Tandheelkd; 2003 May; 110(5):190-2. PubMed ID: 12784514
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  • 2. 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. PubMed ID: 12629675
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  • 3. Novel mutations in the EDAR gene in two Pakistani consanguineous families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Naeem M, Muhammad D, Ahmad W.
    Br J Dermatol; 2005 Jul; 153(1):46-50. PubMed ID: 16029325
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  • 4. [Anhidrotic ectodermal dysplasia. Apropos of a case report of quadruplets].
    Delaire J, Schmidt J, Lumineau JP, Pressard J, Billet J.
    Rev Stomatol Chir Maxillofac; 1984 Jul; 85(1):34-7. PubMed ID: 6584956
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  • 5. [Syndromes 17. Hypohidrotic ectodermal dysplasia].
    Baart JA, van Hagen JM.
    Ned Tijdschr Tandheelkd; 2000 Jan; 107(1):12-4. PubMed ID: 12621820
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  • 6. [A patient with anhidrotic ectodermal dysplasia].
    Wolff AA, Hermans JB.
    Ned Tijdschr Geneeskd; 1981 Dec 05; 125(49):2015-8. PubMed ID: 7322221
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  • 12. Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
    Azeem Z, Naqvi SK, Ansar M, Wali A, Naveed AK, Ali G, Hassan MJ, Tariq M, Basit S, Ahmad W.
    Arch Dermatol Res; 2009 Sep 05; 301(8):625-9. PubMed ID: 19551394
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  • 13. The Ectodysplasin and NFkappaB signalling pathways in odontogenesis.
    Courtney JM, Blackburn J, Sharpe PT.
    Arch Oral Biol; 2005 Feb 05; 50(2):159-63. PubMed ID: 15721144
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  • 14. 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; 2011 Jan 05; 32(1):70-2. PubMed ID: 20979233
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  • 15. [Anhydrotic ectodermal dysplasia].
    Worret WI, Burgdorf WH, Kusch SL.
    Hautarzt; 1982 May 05; 33(5):289-90. PubMed ID: 7096095
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  • 16. 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 05; 22(4):366-9. PubMed ID: 10431241
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