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Journal Abstract Search

365 related items for PubMed ID: 15723871

  • 1. ENAM mutations in autosomal-dominant amelogenesis imperfecta.
    Kim JW, Seymen F, Lin BP, Kiziltan B, Gencay K, Simmer JP, Hu JC.
    J Dent Res; 2005 Mar; 84(3):278-82. PubMed ID: 15723871
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  • 2. Phenotype and enamel ultrastructure characteristics in patients with ENAM gene mutations g.13185-13186insAG and 8344delG.
    Pavlic A, Petelin M, Battelino T.
    Arch Oral Biol; 2007 Mar; 52(3):209-17. PubMed ID: 17125728
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  • 3. Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
    Gutierrez SJ, Chaves M, Torres DM, Briceño I.
    Arch Oral Biol; 2007 May; 52(5):503-6. PubMed ID: 17316551
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  • 4. Phenotype of ENAM mutations is dosage-dependent.
    Ozdemir D, Hart PS, Firatli E, Aren G, Ryu OH, Hart TC.
    J Dent Res; 2005 Nov; 84(11):1036-41. PubMed ID: 16246937
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  • 5. Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.
    Hart PS, Michalec MD, Seow WK, Hart TC, Wright JT.
    Arch Oral Biol; 2003 Aug; 48(8):589-96. PubMed ID: 12828988
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  • 6. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI).
    Masuya H, Shimizu K, Sezutsu H, Sakuraba Y, Nagano J, Shimizu A, Fujimoto N, Kawai A, Miura I, Kaneda H, Kobayashi K, Ishijima J, Maeda T, Gondo Y, Noda T, Wakana S, Shiroishi T.
    Hum Mol Genet; 2005 Mar 01; 14(5):575-83. PubMed ID: 15649948
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  • 7. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M, Bazrafshani MR, Poulton K, Jaber S, Naeem E, Blinkhorn AS.
    J Investig Clin Dent; 2011 Feb 01; 2(1):16-22. PubMed ID: 25427323
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  • 12. Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation at the exon-intron boundary.
    Kida M, Ariga T, Shirakawa T, Oguchi H, Sakiyama Y.
    J Dent Res; 2002 Nov 01; 81(11):738-42. PubMed ID: 12407086
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  • 13. A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2).
    Mårdh CK, Bäckman B, Holmgren G, Hu JC, Simmer JP, Forsman-Semb K.
    Hum Mol Genet; 2002 May 01; 11(9):1069-74. PubMed ID: 11978766
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  • 14. Enamelin and autosomal-dominant amelogenesis imperfecta.
    Hu JC, Yamakoshi Y.
    Crit Rev Oral Biol Med; 2003 May 01; 14(6):387-98. PubMed ID: 14656895
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  • 15. Altered enamelin phosphorylation site causes amelogenesis imperfecta.
    Chan HC, Mai L, Oikonomopoulou A, Chan HL, Richardson AS, Wang SK, Simmer JP, Hu JC.
    J Dent Res; 2010 Jul 01; 89(7):695-9. PubMed ID: 20439930
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  • 16. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta.
    Wang X, Zhao Y, Yang Y, Qin M.
    PLoS One; 2015 Jul 01; 10(3):e0116514. PubMed ID: 25769099
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