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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

599 related items for PubMed ID: 27665865

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  • 2. 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; 59(8):377-85. PubMed ID: 27365112
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  • 3. Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.
    Haddaji Mastouri M, De Coster P, Zaghabani A, Jammali F, Raouahi N, Ben Salem A, Saad A, Coucke P, H'mida Ben Brahim D.
    Eur J Oral Sci; 2018 Feb; 126(1):24-32. PubMed ID: 29114927
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  • 4. Mutations in WNT10A are present in more than half of isolated hypodontia cases.
    van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK.
    J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971
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  • 6. Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.
    Mostowska A, Biedziak B, Zadurska M, Dunin-Wilczynska I, Lianeri M, Jagodzinski PP.
    Clin Genet; 2013 Nov; 84(5):429-40. PubMed ID: 23167694
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  • 7. 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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  • 8. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr 27; 25(3):646-651. PubMed ID: 29969831
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  • 9. 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 Apr 27; 8(8):e73705. PubMed ID: 23991204
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  • 10. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth.
    Kirac D, Eraydin F, Avcilar T, Ulucan K, Özdemir F, Guney AI, Kaspar EÇ, Keshi E, Isbir T.
    Cell Mol Biol (Noisy-le-grand); 2016 Nov 30; 62(13):78-84. PubMed ID: 28040065
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  • 13. Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
    Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N.
    Am J Med Genet A; 2011 Jul 30; 155A(7):1616-22. PubMed ID: 21626677
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  • 14. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct 30; 121(5):403-11. PubMed ID: 24028587
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  • 19. WNT10B mutations associated with isolated dental anomalies.
    Kantaputra PN, Hutsadaloi A, Kaewgahya M, Intachai W, German R, Koparal M, Leethanakul C, Tolun A, Ketudat Cairns JR.
    Clin Genet; 2018 May 30; 93(5):992-999. PubMed ID: 29364501
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