BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 15663448)

  • 1. A point mutation of the ED1 gene in a Japanese family with X-linked hypohidrotic ectodermal dysplasia.
    Sekiguchi H; Wang XJ; Minaguchi K; Yakushiji M
    Int J Paediatr Dent; 2005 Jan; 15(1):73-7. PubMed ID: 15663448
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.
    Gunadi ; Miura K; Ohta M; Sugano A; Lee MJ; Sato Y; Matsunaga A; Hayashi K; Horikawa T; Miki K; Wataya-Kaneda M; Katayama I; Nishigori C; Matsuo M; Takaoka Y; Nishio H
    Pediatr Res; 2009 Apr; 65(4):453-7. PubMed ID: 19127222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia.
    Zhang XJ; Chen JJ; Song YX; Yang S; Xiong XY; Zhang AP; He PP; Gao M; Li YB; Lin D; Huang W
    Arch Dermatol Res; 2003 Apr; 295(1):38-42. PubMed ID: 12682853
    [No Abstract]   [Full Text] [Related]  

  • 5. X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation.
    Savasta S; Carlone G; Castagnoli R; Chiappe F; Bassanese F; Piras R; Salpietro V; Brazzelli V; Verrotti A; Marseglia GL
    Cytogenet Genome Res; 2017; 152(3):111-116. PubMed ID: 28877528
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia.
    Zhao J; Hua R; Zhao X; Meng Y; Ao Y; Liu Q; Shang D; Sun M; Lo WH; Zhang X
    Br J Dermatol; 2008 Mar; 158(3):614-7. PubMed ID: 18076698
    [No Abstract]   [Full Text] [Related]  

  • 8. A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia.
    Hertz JM; Nørgaard Hansen K; Juncker I; Kjeldsen M; Gregersen N
    Clin Genet; 1998 Mar; 53(3):205-9. PubMed ID: 9630076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families.
    Visinoni AF; de Souza RL; Freire-Maia N; Gollop TR; Chautard-Freire-Maia EA
    Am J Med Genet A; 2003 Sep; 122A(1):51-5. PubMed ID: 12949972
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation in the ED1 gene, Ala349Thr, in a Korean patient with X-linked hypohidrotic ectodermal dysplasia developing de novo.
    Na GY; Kim DW; Lee SJ; Chung SL; Park DJ; Kim JC; Kim MK
    Pediatr Dermatol; 2004; 21(5):568-72. PubMed ID: 15461765
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia.
    Tao R; Jin B; Guo SZ; Qing W; Feng GY; Brooks DG; Liu L; Xu J; Li T; Yan Y; He L
    J Hum Genet; 2006; 51(5):498-502. PubMed ID: 16583127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetical diagnosis in a family with X-linked hypohidrotic ectodermal dysplasia].
    Zhang H; Quan C; Gao M; Xiao FL; Lu WS; Shen YJ; Zhou FS; Yang S; Zhang XJ
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2007 Apr; 29(2):201-4. PubMed ID: 17536268
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A novel 22-bp deletion mutation in a Chinese family with X-linked hypohidrotic ectodermal dysplasia.
    Li M; Xu TY; Yang LJ; Zhu XH
    Arch Dermatol Res; 2008 Aug; 300(7):389-91. PubMed ID: 18427821
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds.
    Fan H; Ye X; Shi L; Yin W; Hua B; Song G; Shi B; Bian Z
    Eur J Oral Sci; 2008 Oct; 116(5):412-7. PubMed ID: 18821982
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein.
    Kere J; Srivastava AK; Montonen O; Zonana J; Thomas N; Ferguson B; Munoz F; Morgan D; Clarke A; Baybayan P; Chen EY; Ezer S; Saarialho-Kere U; de la Chapelle A; Schlessinger D
    Nat Genet; 1996 Aug; 13(4):409-16. PubMed ID: 8696334
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypohidrotic ectodermal dysplasia--a case report.
    Gopinath VK; Manoj KM; Mahesh K
    J Indian Soc Pedod Prev Dent; 1999 Sep; 17(3):90-2. PubMed ID: 10863497
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.