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Journal Abstract Search

148 related items for PubMed ID: 15454107

  • 1. 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; 35(4):988-97. PubMed ID: 15454107
    [Abstract] [Full Text] [Related]

  • 2. Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity.
    Islam M, Lurie AG, Reichenberger E.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Dec; 100(6):736-42. PubMed ID: 16301156
    [Abstract] [Full Text] [Related]

  • 3. A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.
    Price JA, Wright JT, Kula K, Bowden DW, Hart TC.
    J Med Genet; 1998 Oct; 35(10):825-8. PubMed ID: 9783705
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  • 4. 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; 7(3):563-9. PubMed ID: 9467018
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  • 5. Tricho-dento-osseous syndrome: heterogeneity or clinical variability.
    Shapiro SD, Quattromani FL, Jorgenson RJ, Young RS.
    Am J Med Genet; 1983 Oct; 16(2):225-36. PubMed ID: 6650567
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  • 6. Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.
    Li Y, Han D, Zhang H, Liu H, Wong S, Zhao N, Qiu L, Feng H.
    Eur J Oral Sci; 2015 Aug; 123(4):228-34. PubMed ID: 26104267
    [Abstract] [Full Text] [Related]

  • 7. 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; 226(8):2189-97. PubMed ID: 21520071
    [Abstract] [Full Text] [Related]

  • 8. Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.
    Mayer DE, Baal C, Litschauer-Poursadrollah M, Hemmer W, Jarisch R.
    J Dtsch Dermatol Ges; 2010 Feb; 8(2):102-4. PubMed ID: 20151948
    [Abstract] [Full Text] [Related]

  • 9. 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 Feb; 194(1):49-59. PubMed ID: 21252474
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  • 12. DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.
    Wright JT, Hong SP, Simmons D, Daly B, Uebelhart D, Luder HU.
    Am J Med Genet A; 2008 Feb 01; 146A(3):343-9. PubMed ID: 18203197
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  • 13. Expression pattern of Dlx3 during cell differentiation in mineralized tissues.
    Ghoul-Mazgar S, Hotton D, Lézot F, Blin-Wakkach C, Asselin A, Sautier JM, Berdal A.
    Bone; 2005 Dec 01; 37(6):799-809. PubMed ID: 16172034
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  • 15. 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
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  • 17. 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
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  • 18. Molecular consequences of a frameshifted DLX3 mutant leading to Tricho-Dento-Osseous syndrome.
    Duverger O, Lee D, Hassan MQ, Chen SX, Jaisser F, Lian JB, Morasso MI.
    J Biol Chem; 2008 Jul 18; 283(29):20198-208. PubMed ID: 18492670
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  • 19. Analysis of the tricho-dento-osseous syndrome genotype and phenotype.
    Wright JT, Kula K, Hall K, Simmons JH, Hart TC.
    Am J Med Genet; 1997 Oct 17; 72(2):197-204. PubMed ID: 9382143
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