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PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 26104267

  • 1.
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  • 2. Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.
    Zhao N, Han D, Liu H, Li Y, Wong SW, Cao Z, Xu J, Zhang X, Cai T, Wang Y, Feng H.
    Sci Rep; 2016 Dec 07; 6():38680. PubMed ID: 27924851
    [Abstract] [Full Text] [Related]

  • 3. Craniofacial variations in the tricho-dento-osseous syndrome.
    Nguyen T, Phillips C, Frazier-Bower S, Wright T.
    Clin Genet; 2013 Apr 07; 83(4):375-9. PubMed ID: 22671030
    [Abstract] [Full Text] [Related]

  • 4. DLX3 promotes bone marrow mesenchymal stem cell proliferation through H19/miR-675 axis.
    Zhao N, Zeng L, Liu Y, Han D, Liu H, Xu J, Jiang Y, Li C, Cai T, Feng H, Wang Y.
    Clin Sci (Lond); 2017 Nov 15; 131(22):2721-2735. PubMed ID: 28963438
    [Abstract] [Full Text] [Related]

  • 5. DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.
    Nieminen P, Lukinmaa PL, Alapulli H, Methuen M, Suojärvi T, Kivirikko S, Peltola J, Asikainen M, Alaluusua S.
    Cells Tissues Organs; 2011 Nov 15; 194(1):49-59. PubMed ID: 21252474
    [Abstract] [Full Text] [Related]

  • 6. Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.
    Liu H, Wang Y, Liu H, Yu M, Zheng J, Feng H, Liu Y, Han D.
    Arch Oral Biol; 2022 Sep 15; 141():105479. PubMed ID: 35714441
    [Abstract] [Full Text] [Related]

  • 7. Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis.
    Zhang Z, Tian H, Lv P, Wang W, Jia Z, Wang S, Zhou C, Gao X.
    PLoS One; 2015 Sep 15; 10(3):e0121288. PubMed ID: 25815730
    [Abstract] [Full Text] [Related]

  • 8. Tricho-dento-osseous syndrome. Features of the hair and teeth.
    Wright JT, Roberts MW, Wilson AR, Kudhail R.
    Oral Surg Oral Med Oral Pathol; 1994 May 15; 77(5):487-93. PubMed ID: 8028872
    [Abstract] [Full Text] [Related]

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  • 10. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome.
    Haldeman RJ, Cooper LF, Hart TC, Phillips C, Boyd C, Lester GE, Wright JT.
    Bone; 2004 Oct 15; 35(4):988-97. PubMed ID: 15454107
    [Abstract] [Full Text] [Related]

  • 11. DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells.
    Zeng L, Zhao N, Han D, Liu H, Liu Y, Wang Y, Feng H.
    Arch Oral Biol; 2017 May 15; 77():12-17. PubMed ID: 28135572
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  • 13. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome.
    Price JA, Bowden DW, Wright JT, Pettenati MJ, Hart TC.
    Hum Mol Genet; 1998 Mar 15; 7(3):563-9. PubMed ID: 9467018
    [Abstract] [Full Text] [Related]

  • 14. miR-675 promotes odontogenic differentiation of human dental pulp cells by epigenetic regulation of DLX3.
    Zeng L, Zhao N, Li F, Han D, Liu Y, Liu H, Sun S, Wang Y, Feng H.
    Exp Cell Res; 2018 Jun 01; 367(1):104-111. PubMed ID: 29604248
    [Abstract] [Full Text] [Related]

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  • 16. Tricho-dento-osseous syndrome and amelogenesis imperfecta with taurodontism are genetically distinct conditions.
    Price JA, Wright JT, Walker SJ, Crawford PJ, Aldred MJ, Hart TC.
    Clin Genet; 1999 Jul 01; 56(1):35-40. PubMed ID: 10466415
    [Abstract] [Full Text] [Related]

  • 17. DLX3 mutation in a new family and its phenotypic variations.
    Lee SK, Lee ZH, Lee SJ, Ahn BD, Kim YJ, Lee SH, Kim JW.
    J Dent Res; 2008 Apr 01; 87(4):354-7. PubMed ID: 18362318
    [Abstract] [Full Text] [Related]

  • 18. A dominant mutation etiologic for human tricho-dento-osseous syndrome impairs the ability of DLX3 to downregulate ΔNp63α.
    Di Costanzo A, Festa L, Roscigno G, Vivo M, Pollice A, Morasso M, La Mantia G, Calabrò V.
    J Cell Physiol; 2011 Aug 01; 226(8):2189-97. PubMed ID: 21520071
    [Abstract] [Full Text] [Related]

  • 19. A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.
    Quan J, Liu Y, Ji L, Zhao Y, Zheng S.
    Arch Oral Biol; 2024 Jan 01; 157():105849. PubMed ID: 38006713
    [Abstract] [Full Text] [Related]

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