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Journal Abstract Search

261 related items for PubMed ID: 12097313

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

  • 2. 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; 111(5):365-70. PubMed ID: 12974677
    [Abstract] [Full Text] [Related]

  • 3. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
    Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
    Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
    [Abstract] [Full Text] [Related]

  • 4. A novel MSX1 intronic mutation associated with autosomal dominant non-syndromic oligodontia in a large Chinese family pedigree.
    Xue J, Gao Q, Huang Y, Zhang X, Yang P, Cram DS, Liang D, Wu L.
    Clin Chim Acta; 2016 Oct 01; 461():135-40. PubMed ID: 27485761
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.
    Vieira AR, Meira R, Modesto A, Murray JC.
    J Dent Res; 2004 Sep 01; 83(9):723-7. PubMed ID: 15329380
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 79(7):1469-75. PubMed ID: 11005730
    [Abstract] [Full Text] [Related]

  • 8. The role of MSX1 in tooth agenesis in Iranians.
    Seifi M, Kazemi B, Golkar P.
    Int J Paediatr Dent; 2007 Jul 01; 17(4):254-8. PubMed ID: 17559452
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. 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]

  • 11.
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  • 12. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Aug 01; 10(3):105-13. PubMed ID: 17651126
    [Abstract] [Full Text] [Related]

  • 13. Craniofacial disorders caused by mutations in homeobox genes MSX1 and MSX2.
    Cohen MM.
    J Craniofac Genet Dev Biol; 2000 Aug 01; 20(1):19-25. PubMed ID: 10879654
    [Abstract] [Full Text] [Related]

  • 14. An aberrant splice acceptor site due to a novel intronic nucleotide substitution in MSX1 gene is the cause of congenital tooth agenesis in a Japanese family.
    Tatematsu T, Kimura M, Nakashima M, Machida J, Yamaguchi S, Shibata A, Goto H, Nakayama A, Higashi Y, Miyachi H, Shimozato K, Matsumoto N, Tokita Y.
    PLoS One; 2015 Aug 01; 10(6):e0128227. PubMed ID: 26030286
    [Abstract] [Full Text] [Related]

  • 15. [Research advances in tooth agenesis].
    Feng HL, Zhang XX, Wu H.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2007 Feb 18; 39(1):13-7. PubMed ID: 17304318
    [Abstract] [Full Text] [Related]

  • 16. MSX1 and orofacial clefting with and without tooth agenesis.
    Modesto A, Moreno LM, Krahn K, King S, Lidral AC.
    J Dent Res; 2006 Jun 18; 85(6):542-6. PubMed ID: 16723652
    [Abstract] [Full Text] [Related]

  • 17. Gene defect in hypodontia: exclusion of MSX1 and MSX2 as candidate genes.
    Nieminen P, Arte S, Pirinen S, Peltonen L, Thesleff I.
    Hum Genet; 1995 Sep 18; 96(3):305-8. PubMed ID: 7649547
    [Abstract] [Full Text] [Related]

  • 18. Msx1 mutations: how do they cause tooth agenesis?
    Wang Y, Kong H, Mues G, D'Souza R.
    J Dent Res; 2011 Mar 18; 90(3):311-6. PubMed ID: 21297014
    [Abstract] [Full Text] [Related]

  • 19. 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 18; 97(2):155-162. PubMed ID: 28910570
    [Abstract] [Full Text] [Related]

  • 20. Two novel mutations in MSX1 causing oligodontia.
    Yang L, Liang J, Yue H, Bian Z.
    PLoS One; 2020 Feb 18; 15(1):e0227287. PubMed ID: 31914153
    [Abstract] [Full Text] [Related]

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