BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

363 related articles for article (PubMed ID: 21696697)

  • 1. A novel EDA gene mutation in a Spanish family with X-linked hypohidrotic ectodermal dysplasia.
    Cañueto J; Zafra-Cobo MI; Ciria S; Unamuno P; González-Sarmiento R
    Actas Dermosifiliogr; 2011 Nov; 102(9):722-5. PubMed ID: 21696697
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel mutation of the bovine EDA gene associated with anhidrotic ectodermal dysplasia in Holstein cattle.
    Ogino A; Kohama N; Ishikawa S; Tomita K; Nonaka S; Shimizu K; Tanabe Y; Okawa H; Morita M
    Hereditas; 2011 Feb; 148(1):46-9. PubMed ID: 21410470
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus.
    Piccione M; Serra G; Sanfilippo C; Andreucci E; Sani I; Corsello G
    Minerva Pediatr; 2012 Feb; 64(1):59-64. PubMed ID: 22350046
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel 4-bp insertion mutation in EDA1 gene in a Pakistani family with X-linked hypohidrotic ectodermal dysplasia.
    Tariq M; Wasif N; Ayub M; Ahmad W
    Eur J Dermatol; 2007; 17(3):209-12. PubMed ID: 17478381
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.
    Zhang J; Han D; Song S; Wang Y; Zhao H; Pan S; Bai B; Feng H
    Eur J Med Genet; 2011; 54(4):e377-82. PubMed ID: 21457804
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of X-linked hypohidrotic ectodermal dysplasia in a Taiwanese family.
    Chao SC; Chung CH; Yang CC; Yang MH; Lee JY
    J Formos Med Assoc; 2003 Jun; 102(6):412-7. PubMed ID: 12923595
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
    Schneider H; Hammersen J; Preisler-Adams S; Huttner K; Rascher W; Bohring A
    J Med Genet; 2011 Jun; 48(6):426-32. PubMed ID: 21357618
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia.
    Kobielak K; Kobielak A; Roszkiewicz J; Wierzba J; Limon J; Trzeciak WH
    Am J Med Genet; 2001 May; 100(3):191-7. PubMed ID: 11343303
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Missense mutation of the EDA gene in a Jordanian family with X-linked hypohidrotic ectodermal dysplasia: phenotypic appearance and speech problems.
    Khabour OF; Mesmar FS; Al-Tamimi F; Al-Batayneh OB; Owais AI
    Genet Mol Res; 2010 May; 9(2):941-8. PubMed ID: 20486090
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.
    Hashiguchi T; Yotsumoto S; Kanzaki T
    Exp Dermatol; 2003 Aug; 12(4):518-22. PubMed ID: 12930312
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A frameshift mutation of the ED1 gene in sibling cases with X-linked hypohidrotic ectodermal dysplasia.
    Nishibu A; Hashiguchi T; Yotsumoto S; Takahashi M; Nakamura K; Kanzaki T; Kaneko F
    Dermatology; 2003; 207(2):178-81. PubMed ID: 12920369
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Detection of ED1 gene mutations in six pedigrees with hypohidrotic ectodermal dysplasia].
    Wu QH; Shi HR; Liu BC; Zhao ZH; Jiang M; Lu N; Kong XD
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):447-51. PubMed ID: 22875504
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.
    Yang Y; Luo L; Xu J; Zhu P; Xue W; Wang J; Li W; Wang M; Cheng K; Liu S; Tang Z; Ring BZ; Su L
    J Dent Res; 2013 Jun; 92(6):500-6. PubMed ID: 23625373
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.