These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

367 related articles for article (PubMed ID: 19171226)

  • 1. [Anhidrotic ectodermal dysplasia. Report of a rare mutation in EDA1].
    Tomb R; Soutou B; Zalloua P
    Ann Dermatol Venereol; 2009 Jan; 136(1):28-31. PubMed ID: 19171226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Novel missense mutation in the EDA1 gene identified in a family with hypohidrotic ectodermal dysplasia.
    Pozo-Molina G; Reyes-Reali J; Mendoza-Ramos MI; Villalobos-Molina R; Garrido-Guerrero E; Méndez-Cruz AR
    Int J Dermatol; 2015 Jul; 54(7):790-4. PubMed ID: 25626993
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A case of anhidrotic ectodermal dysplasia diagnosed during investigation of asthmatic attack].
    Hara J; Nishi K; Herai Y; Mizuguchi M; Myou S; Fujimura M
    Nihon Kokyuki Gakkai Zasshi; 2004 Sep; 42(9):848-53. PubMed ID: 15500155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patients.
    Conte C; Gambardella S; Bulli C; Rinaldi F; Di Marino D; Falconi M; Bramanti P; Desideri A; Novelli G
    Genet Test; 2008 Sep; 12(3):437-42. PubMed ID: 18666859
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation A1270G of the EDA1 gene causing Tyr343Cys substitution in ectodysplasin-A in a family with anhidrotic ectodermal dysplasia.
    Kobielak A; Kobielak K; Biedziak B; Trzeciak WH
    Acta Biochim Pol; 2003; 50(1):255-8. PubMed ID: 12673367
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 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. The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia.
    Pääkkönen K; Cambiaghi S; Novelli G; Ouzts LV; Penttinen M; Kere J; Srivastava AK
    Hum Mutat; 2001 Apr; 17(4):349. PubMed ID: 11295832
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ-Siemens-Touraine syndrome.
    Kinyó A; Vályi P; Farkas K; Nagy N; Gergely B; Tripolszki K; Török D; Bata-Csörgő Z; Kemény L; Széll M
    Arch Dermatol Res; 2014 Jan; 306(1):97-100. PubMed ID: 23989902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia.
    Ayub M; ur-Rehman F; Yasinzai M; Ahmad W
    Int J Dermatol; 2010 Dec; 49(12):1399-402. PubMed ID: 21091672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mutation in the ED1, Ala349Thr in a patient with X-linked hypohidrotic ectodermal dysplasia].
    Salas-Alanis JC; Cepeda-Valdés R; González-Santos A; Amaya-Guerra M; Kurban M; Christiano AM
    Rev Med Chil; 2011 Dec; 139(12):1601-4. PubMed ID: 22446708
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A single point mutation within the ED1 gene disrupts correct splicing at two different splice sites and leads to anhidrotic ectodermal dysplasia in cattle.
    Drögemüller C; Peters M; Pohlenz J; Distl O; Leeb T
    J Mol Med (Berl); 2002 May; 80(5):319-23. PubMed ID: 12021844
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Prenatal Genetic Testing for X-Linked Hypohidrotic Ectodermal Dysplasia.
    Yapijakis C; Gintoni I; Chrousos G
    Adv Exp Med Biol; 2021; 1339():337-340. PubMed ID: 35023123
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.
    Zhang H; Quan C; Sun LD; Lv HL; Gao M; Zhou FS; Xiao FL; Fang QY; Shen YJ; Zhou L; Yang S; Zhang XJ
    Clin Exp Dermatol; 2009 Jan; 34(1):74-6. PubMed ID: 18702659
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 19.