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Journal Abstract Search

218 related items for PubMed ID: 12786960

  • 1. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia.
    Mostowska A, Kobielak A, Biedziak B, Trzeciak WH.
    Eur J Oral Sci; 2003 Jun; 111(3):272-6. PubMed ID: 12786960
    [Abstract] [Full Text] [Related]

  • 2. 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; 79(7):1469-75. PubMed ID: 11005730
    [Abstract] [Full Text] [Related]

  • 3. 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; 84(1):43-7. PubMed ID: 15615874
    [Abstract] [Full Text] [Related]

  • 4. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.
    Vieira AR, Meira R, Modesto A, Murray JC.
    J Dent Res; 2004 Sep; 83(9):723-7. PubMed ID: 15329380
    [Abstract] [Full Text] [Related]

  • 5. 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; 97(2):155-162. PubMed ID: 28910570
    [Abstract] [Full Text] [Related]

  • 6. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.
    Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S.
    Eur J Hum Genet; 2001 Oct; 9(10):743-6. PubMed ID: 11781684
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition.
    Mostowska A, Kobielak A, Trzeciak WH.
    Eur J Oral Sci; 2003 Oct 01; 111(5):365-70. PubMed ID: 12974677
    [Abstract] [Full Text] [Related]

  • 10. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
    Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR.
    Hum Genet; 2004 Feb 01; 114(3):242-9. PubMed ID: 14689302
    [Abstract] [Full Text] [Related]

  • 11. The novel polymorphic variants within the paired box of the PAX9 gene are associated with selective tooth agenesis.
    Kobielak A, Kobielak K, Wiśniewski AS, Mostowska A, Biedziak B, Trzeciak WH.
    Folia Histochem Cytobiol; 2001 Feb 01; 39(2):111-2. PubMed ID: 11374781
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 93(3):245-9. PubMed ID: 24436340
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 38(5):1338-1348. PubMed ID: 27665865
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 61():144-8. PubMed ID: 26571067
    [Abstract] [Full Text] [Related]

  • 15. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.
    Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P.
    Eur J Hum Genet; 2003 Nov 01; 11(11):866-71. PubMed ID: 14571272
    [Abstract] [Full Text] [Related]

  • 16. Novel MSX1 frameshift causes autosomal-dominant oligodontia.
    Kim JW, Simmer JP, Lin BP, Hu JC.
    J Dent Res; 2006 Mar 01; 85(3):267-71. PubMed ID: 16498076
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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]

  • 19. Non-syndromic oligodontia with a novel mutation of PAX9.
    Suda N, Ogawa T, Kojima T, Saito C, Moriyama K.
    J Dent Res; 2011 Mar 01; 90(3):382-6. PubMed ID: 21098475
    [Abstract] [Full Text] [Related]

  • 20. 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]

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