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 *

398 related articles for article (PubMed ID: 23603338)

  • 1. Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
    Nikopensius T; Annilo T; Jagomägi T; Gilissen C; Kals M; Krjutškov K; Mägi R; Eelmets M; Gerst-Talas U; Remm M; Saag M; Hoischen A; Metspalu A
    J Dent Res; 2013 Jun; 92(6):507-11. PubMed ID: 23603338
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Oligodontia and curly hair occur with ectodysplasin-a mutations.
    Lee KE; Ko J; Shin TJ; Hyun HK; Lee SH; Kim JW
    J Dent Res; 2014 Apr; 93(4):371-5. PubMed ID: 24487376
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.
    Han D; Gong Y; Wu H; Zhang X; Yan M; Wang X; Qu H; Feng H; Song S
    Eur J Med Genet; 2008; 51(6):536-46. PubMed ID: 18657636
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel missense mutation in the EDA gene in a family affected by oligodontia.
    Ruiz-Heiland G; Jabir S; Wende W; Blecher S; Bock N; Ruf S
    J Orofac Orthop; 2016 Jan; 77(1):31-8. PubMed ID: 26753551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A; Zadurska M; Rakowska A; Lianeri M; Jagodziński PP
    Eur J Oral Sci; 2013 Oct; 121(5):403-11. PubMed ID: 24028587
    [TBL] [Abstract][Full Text] [Related]  

  • 9. De novo EDA mutations: Variable expression in two Egyptian families.
    Gaczkowska A; Abdalla EM; Dowidar KM; Elhady GM; Jagodzinski PP; Mostowska A
    Arch Oral Biol; 2016 Aug; 68():21-8. PubMed ID: 27054699
    [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. [EDA mutation screening and phenotype analysis in patients with tooth agenesis].
    He HY; Liu Y; Han D; Liu HC; Bai BJ; Feng HL
    Beijing Da Xue Xue Bao Yi Xue Ban; 2016 Aug; 48(4):686-691. PubMed ID: 29263514
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis.
    Zeng B; Zhao Q; Li S; Lu H; Lu J; Ma L; Zhao W; Yu D
    Genes (Basel); 2017 Oct; 8(10):. PubMed ID: 28981473
    [No Abstract]   [Full Text] [Related]  

  • 13. Novel EDA mutation in X-linked hypohidrotic ectodermal dysplasia and genotype-phenotype correlation.
    Zeng B; Lu H; Xiao X; Zhou L; Lu J; Zhu L; Yu D; Zhao W
    Oral Dis; 2015 Nov; 21(8):994-1000. PubMed ID: 26411740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
    Zhang H; Kong X; Ren J; Yuan S; Liu C; Hou Y; Liu Y; Meng L; Zhang G; Du Q; Shen W
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1684. PubMed ID: 33943035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Non-syndromic tooth agenesis in two Chinese families associated with novel missense mutations in the TNF domain of EDA (ectodysplasin A).
    Li S; Li J; Cheng J; Zhou B; Tong X; Dong X; Wang Z; Hu Q; Chen M; Hua ZC
    PLoS One; 2008 Jun; 3(6):e2396. PubMed ID: 18545687
    [TBL] [Abstract][Full Text] [Related]  

  • 16. EDA gene mutations underlie non-syndromic oligodontia.
    Song S; Han D; Qu H; Gong Y; Wu H; Zhang X; Zhong N; Feng H
    J Dent Res; 2009 Feb; 88(2):126-31. PubMed ID: 19278982
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K; Lian M; Zou D; Huang W; Zhou W; Shen Y; Wang F; Wu Y
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Novel PAX9 mutations cause non-syndromic tooth agenesis.
    Mitsui SN; Yasue A; Masuda K; Watanabe K; Horiuchi S; Imoto I; Tanaka E
    J Dent Res; 2014 Mar; 93(3):245-9. PubMed ID: 24436340
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.