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PUBMED FOR HANDHELDS

Journal Abstract Search


276 related items for PubMed ID: 15329380

  • 1. 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]

  • 2. Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis.
    Vieira AR, Modesto A, Meira R, Barbosa AR, Lidral AC, Murray JC.
    Am J Med Genet A; 2007 Mar 15; 143A(6):538-45. PubMed ID: 17318851
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 111(3):272-6. PubMed ID: 12786960
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 59(8):377-85. PubMed ID: 27365112
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region.
    Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ.
    Cleft Palate Craniofac J; 2003 May 30; 40(3):274-9. PubMed ID: 12733956
    [Abstract] [Full Text] [Related]

  • 7. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.
    Seo YJ, Park JW, Kim YH, Baek SH.
    Angle Orthod; 2013 Nov 30; 83(6):1036-42. PubMed ID: 23718693
    [Abstract] [Full Text] [Related]

  • 8. 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 30; 111(5):365-70. PubMed ID: 12974677
    [Abstract] [Full Text] [Related]

  • 9. 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 Oct 30; 39(2):111-2. PubMed ID: 11374781
    [Abstract] [Full Text] [Related]

  • 10. Transforming growth factor-alfa gene (TGFA), human tooth agenesis, and evidence of segmental uniparental isodisomy.
    Callahan N, Modesto A, Deeley K, Meira R, Vieira AR.
    Eur J Oral Sci; 2009 Feb 30; 117(1):20-6. PubMed ID: 19196314
    [Abstract] [Full Text] [Related]

  • 11. Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis.
    Vieira AR.
    J Dent Res; 2003 Mar 30; 82(3):162-5. PubMed ID: 12598542
    [Abstract] [Full Text] [Related]

  • 12. 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 30; 97(2):155-162. PubMed ID: 28910570
    [Abstract] [Full Text] [Related]

  • 13. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
    Paixão-Côrtes VR, Braga T, Salzano FM, Mundstock K, Mundstock CA, Bortolini MC.
    Arch Oral Biol; 2011 Apr 30; 56(4):337-44. PubMed ID: 21111400
    [Abstract] [Full Text] [Related]

  • 14. 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 30; 84(1):43-7. PubMed ID: 15615874
    [Abstract] [Full Text] [Related]

  • 15. The role of MSX1 in human tooth agenesis.
    Lidral AC, Reising BC.
    J Dent Res; 2002 Apr 30; 81(4):274-8. PubMed ID: 12097313
    [Abstract] [Full Text] [Related]

  • 16. 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 30; 79(7):1469-75. PubMed ID: 11005730
    [Abstract] [Full Text] [Related]

  • 17. Identification of genetic risk factors for maxillary lateral incisor agenesis.
    Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I.
    J Dent Res; 2014 May 30; 93(5):452-8. PubMed ID: 24554542
    [Abstract] [Full Text] [Related]

  • 18. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis.
    Pinho T, Silva-Fernandes A, Bousbaa H, Maciel P.
    Eur J Orthod; 2010 Oct 30; 32(5):582-8. PubMed ID: 20660504
    [Abstract] [Full Text] [Related]

  • 19. A novel mutation in human PAX9 causes molar oligodontia.
    Frazier-Bowers SA, Guo DC, Cavender A, Xue L, Evans B, King T, Milewicz D, D'Souza RN.
    J Dent Res; 2002 Feb 30; 81(2):129-33. PubMed ID: 11827258
    [Abstract] [Full Text] [Related]

  • 20. In a Vietnamese population, MSX1 variants contribute to cleft lip and palate.
    Suzuki Y, Jezewski PA, Machida J, Watanabe Y, Shi M, Cooper ME, Viet le T, Nguyen TD, Hai H, Natsume N, Shimozato K, Marazita ML, Murray JC.
    Genet Med; 2004 Feb 30; 6(3):117-25. PubMed ID: 15354328
    [Abstract] [Full Text] [Related]


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