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Journal Abstract Search

189 related items for PubMed ID: 28965043

  • 1. A novel PAX9 mutation causing oligodontia.
    Daw EM, Saliba C, Grech G, Camilleri S.
    Arch Oral Biol; 2017 Dec; 84():100-105. PubMed ID: 28965043
    [Abstract] [Full Text] [Related]

  • 2. A novel initiation codon mutation of PAX9 in a family with oligodontia.
    Liang J, Qin C, Yue H, He H, Bian Z.
    Arch Oral Biol; 2016 Jan; 61():144-8. PubMed ID: 26571067
    [Abstract] [Full Text] [Related]

  • 3. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.
    Wang J, Jian F, Chen J, Wang H, Lin Y, Yang Z, Pan X, Lai W.
    Arch Oral Biol; 2011 Oct; 56(10):1027-34. PubMed ID: 21530942
    [Abstract] [Full Text] [Related]

  • 4. A novel missense mutation in the paired domain of human PAX9 causes oligodontia.
    Zhao J, Hu Q, Chen Y, Luo S, Bao L, Xu Y.
    Am J Med Genet A; 2007 Nov 01; 143A(21):2592-7. PubMed ID: 17910065
    [Abstract] [Full Text] [Related]

  • 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 01; 59(8):377-85. PubMed ID: 27365112
    [Abstract] [Full Text] [Related]

  • 6. Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.
    Gerits A, Nieminen P, De Muynck S, Carels C.
    Orthod Craniofac Res; 2006 Aug 01; 9(3):129-36. PubMed ID: 16918677
    [Abstract] [Full Text] [Related]

  • 7. Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.
    Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y.
    Arch Oral Biol; 2008 Aug 01; 53(8):773-9. PubMed ID: 18374898
    [Abstract] [Full Text] [Related]

  • 8. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
    Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H.
    Eur J Oral Sci; 2007 Aug 01; 115(4):330-3. PubMed ID: 17697174
    [Abstract] [Full Text] [Related]

  • 9. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene.
    Šerý O, Bonczek O, Hloušková A, Černochová P, Vaněk J, Míšek I, Krejčí P, Izakovičová Hollá L.
    Eur J Oral Sci; 2015 Apr 01; 123(2):65-71. PubMed ID: 25683653
    [Abstract] [Full Text] [Related]

  • 10. Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
    Qin H, Xu HZ, Xuan K.
    Arch Oral Biol; 2013 Sep 01; 58(9):1180-6. PubMed ID: 23731659
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. 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 30; 126(1):24-32. PubMed ID: 29114927
    [Abstract] [Full Text] [Related]

  • 13. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
    Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S.
    Genet Mol Res; 2013 Oct 10; 12(4):4446-58. PubMed ID: 24222224
    [Abstract] [Full Text] [Related]

  • 14. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
    Wong SW, Han D, Zhang H, Liu Y, Zhang X, Miao MZ, Wang Y, Zhao N, Zeng L, Bai B, Wang YX, Liu H, Frazier-Bowers SA, Feng H.
    J Dent Res; 2018 Feb 10; 97(2):155-162. PubMed ID: 28910570
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 155A(7):1616-22. PubMed ID: 21626677
    [Abstract] [Full Text] [Related]

  • 16. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?
    Bock NC, Lenz S, Ruiz-Heiland G, Ruf S.
    J Orofac Orthop; 2017 Mar 10; 78(2):112-120. PubMed ID: 28204848
    [Abstract] [Full Text] [Related]

  • 17. Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.
    Goldenberg M, Das P, Messersmith M, Stockton DW, Patel PI, D'Souza RN.
    J Dent Res; 2000 Jul 10; 79(7):1469-75. PubMed ID: 11005730
    [Abstract] [Full Text] [Related]

  • 18. Novel mutation of the initiation codon of PAX9 causes oligodontia.
    Klein ML, Nieminen P, Lammi L, Niebuhr E, Kreiborg S.
    J Dent Res; 2005 Jan 10; 84(1):43-7. PubMed ID: 15615874
    [Abstract] [Full Text] [Related]

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