BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

321 related articles for article (PubMed ID: 16435307)

  • 1. 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. PubMed ID: 16435307
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia.
    van der Hout AH; Oudesluijs GG; Venema A; Verheij JB; Mol BG; Rump P; Brunner HG; Vos YJ; van Essen AJ
    Eur J Hum Genet; 2008 Jun; 16(6):673-9. PubMed ID: 18231121
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 20222921
    [TBL] [Abstract][Full Text] [Related]  

  • 5. EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families.
    Lind LK; Stecksén-Blicks C; Lejon K; Schmitt-Egenolf M
    BMC Med Genet; 2006 Nov; 7():80. PubMed ID: 17125505
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 10431241
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 32(1):70-2. PubMed ID: 20979233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India.
    Bashyam MD; Chaudhary AK; Reddy EC; Reddy V; Acharya V; Nagarajaram HA; Devi AR; Bashyam L; Dalal AB; Gupta N; Kabra M; Agarwal M; Phadke SR; Tainwala R; Kumar R; Hariharan SV
    Br J Dermatol; 2012 Apr; 166(4):819-29. PubMed ID: 22032522
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 15373768
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 301(8):625-9. PubMed ID: 19551394
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 17354266
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A compound heterozygous mutation in the EDAR gene in a Spanish family with autosomal recessive hypohidrotic ectodermal dysplasia.
    Moya-Quiles MR; Ballesta-Martínez MJ; López-González V; Glover G; Guillén-Navarro E
    Arch Dermatol Res; 2010 May; 302(4):307-10. PubMed ID: 20033817
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic analysis of consanguineous Pakistani families with autosomal recessive hypohidrotic ectodermal dysplasia.
    Bibi N; Ahmad S; Ahmad W; Naeem M
    Australas J Dermatol; 2011 Feb; 52(1):37-42. PubMed ID: 21332691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 21876339
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings.
    Clauss F; Chassaing N; Smahi A; Vincent MC; Calvas P; Molla M; Lesot H; Alembik Y; Hadj-Rabia S; Bodemer C; Manière MC; Schmittbuhl M
    Clin Genet; 2010 Sep; 78(3):257-66. PubMed ID: 20236127
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Two novel mutations in the gene EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia.
    Naqvi SK; Wasif N; Javaid H; Ahmad W
    Orthod Craniofac Res; 2011 Aug; 14(3):156-9. PubMed ID: 21771270
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel 7-bp deletion mutation in a Taiwanese family with X-linked hypohidrotic ectodermal dysplasia.
    Lin TK; Huang CY; Lin MH; Chao SC
    Clin Exp Dermatol; 2004 Sep; 29(5):536-8. PubMed ID: 15347342
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypohidrotic ectodermal dysplasia.
    Lu PD; Schaffer JV
    Dermatol Online J; 2008 Oct; 14(10):22. PubMed ID: 19061621
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia.
    Vincent MC; Biancalana V; Ginisty D; Mandel JL; Calvas P
    Eur J Hum Genet; 2001 May; 9(5):355-63. PubMed ID: 11378824
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.