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Journal Abstract Search

411 related items for PubMed ID: 27054699

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. EDA, EDAR, EDARADD and WNT10A allelic variants in patients with ectodermal derivative impairment in the Spanish population.
    Martínez-Romero MC, Ballesta-Martínez MJ, López-González V, Sánchez-Soler MJ, Serrano-Antón AT, Barreda-Sánchez M, Rodriguez-Peña L, Martínez-Menchon MT, Frías-Iniesta J, Sánchez-Pedreño P, Carbonell-Meseguer P, Glover-López G, Guillén-Navarro E, GIEDE (Spanish multidisciplinary research group for ectodermal dysplasia).
    Orphanet J Rare Dis; 2019 Dec 03; 14(1):281. PubMed ID: 31796081
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  • 3. 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]

  • 4. 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 24; 21(8):994-1000. PubMed ID: 26411740
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  • 5. 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]

  • 6. Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations.
    Ahmed HA, El-Kamah GY, Rabie E, Mostafa MI, Abouzaid MR, Hassib NF, Mehrez MI, Abdel-Kader MA, Mohsen YH, Zada SK, Amr KS, Sayed ISM.
    Genes (Basel); 2021 Sep 08; 12(9):. PubMed ID: 34573371
    [Abstract] [Full Text] [Related]

  • 7. 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 08; 78(3):257-66. PubMed ID: 20236127
    [Abstract] [Full Text] [Related]

  • 8. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr 08; 25(3):646-651. PubMed ID: 29969831
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  • 13. 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 08; 92(6):500-6. PubMed ID: 23625373
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  • 14. 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 08; 32(1):70-2. PubMed ID: 20979233
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  • 15. 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 08; 301(8):625-9. PubMed ID: 19551394
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  • 16. 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
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  • 17. 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
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  • 19. 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
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  • 20. Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
    Arte S, Parmanen S, Pirinen S, Alaluusua S, Nieminen P.
    PLoS One; 2013 Oct 05; 8(8):e73705. PubMed ID: 23991204
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