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Journal Abstract Search

222 related items for PubMed ID: 25203534

  • 1. Whole genome sequencing reveals novel non-synonymous mutation in ectodysplasin A (EDA) associated with non-syndromic X-linked dominant congenital tooth agenesis.
    Sarkar T, Bansal R, Das P.
    PLoS One; 2014; 9(9):e106811. PubMed ID: 25203534
    [Abstract] [Full Text] [Related]

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

  • 3. Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.
    He H, Han D, Feng H, Qu H, Song S, Bai B, Zhang Z.
    PLoS One; 2013; 8(11):e80393. PubMed ID: 24312213
    [Abstract] [Full Text] [Related]

  • 4. Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis.
    Mues G, Tardivel A, Willen L, Kapadia H, Seaman R, Frazier-Bowers S, Schneider P, D'Souza RN.
    Eur J Hum Genet; 2010 Jan; 18(1):19-25. PubMed ID: 19623212
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Deleterious Variants in WNT10A, EDAR, and EDA Causing Isolated and Syndromic Tooth Agenesis: A Structural Perspective from Molecular Dynamics Simulations.
    Parveen A, Khan SA, Mirza MU, Bashir H, Arshad F, Iqbal M, Ahmad W, Wahab A, Fiaz A, Naz S, Ashraf F, Mobeen T, Aziz S, Ahmed SS, Muhammad N, Hassib NF, Mostafa MI, Gaboon NE, Gul R, Khan S, Froeyen M, Shoaib M, Wasif N.
    Int J Mol Sci; 2019 Oct 24; 20(21):. PubMed ID: 31652981
    [Abstract] [Full Text] [Related]

  • 7. 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 24; 93(4):371-5. PubMed ID: 24487376
    [Abstract] [Full Text] [Related]

  • 8. 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 24; 68():21-8. PubMed ID: 27054699
    [Abstract] [Full Text] [Related]

  • 9. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
    Shahid M, Balto HA, Al-Hammad N, Joshi S, Khalil HS, Somily AM, Sinjilawi NA, Al-Ghamdi S, Faiyaz-Ul-Haque M, Dhillon VS.
    Eur J Med Genet; 2016 Aug 24; 59(8):377-85. PubMed ID: 27365112
    [Abstract] [Full Text] [Related]

  • 10. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct 24; 121(5):403-11. PubMed ID: 24028587
    [Abstract] [Full Text] [Related]

  • 11. EDA Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis.
    Su L, Lin B, Yu M, Liu Y, Sun S, Feng H, Liu H, Han D.
    Int J Mol Sci; 2024 Sep 27; 25(19):. PubMed ID: 39408781
    [Abstract] [Full Text] [Related]

  • 12. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.
    Wang SK, Chan HC, Makovey I, Simmer JP, Hu JC.
    PLoS One; 2012 Sep 27; 7(12):e51533. PubMed ID: 23227268
    [Abstract] [Full Text] [Related]

  • 13. Missense mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis.
    Andreoni F, Sgattoni C, Bencardino D, Simonetti O, Forabosco A, Magnani M.
    Mol Genet Genomic Med; 2021 Jan 27; 9(1):e1555. PubMed ID: 33205897
    [Abstract] [Full Text] [Related]

  • 14. 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 27; 92(6):500-6. PubMed ID: 23625373
    [Abstract] [Full Text] [Related]

  • 15. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
    Salvi A, Giacopuzzi E, Bardellini E, Amadori F, Ferrari L, De Petro G, Borsani G, Majorana A.
    Int J Mol Med; 2016 Nov 27; 38(5):1338-1348. PubMed ID: 27665865
    [Abstract] [Full Text] [Related]

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  • 18. 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 27; 49(12):1399-402. PubMed ID: 21091672
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  • 20. 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 05; 8(10):. PubMed ID: 28981473
    [Abstract] [Full Text] [Related]

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