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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

173 related items for PubMed ID: 11037750

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  • 5. Cloning, characterization and immunolocalization of human ameloblastin.
    MacDougall M, Simmons D, Gu TT, Forsman-Semb K, Mårdh CK, Mesbah M, Forest N, Krebsbach PH, Yamada Y, Berdal A.
    Eur J Oral Sci; 2000 Aug; 108(4):303-10. PubMed ID: 10946765
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  • 6. 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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  • 8. Cloning and characterization of the mouse and human enamelin genes.
    Hu JC, Zhang CH, Yang Y, Kärrman-Mårdh C, Forsman-Semb K, Simmer JP.
    J Dent Res; 2001 Mar 01; 80(3):898-902. PubMed ID: 11379892
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  • 9. Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta.
    Rajpar MH, Harley K, Laing C, Davies RM, Dixon MJ.
    Hum Mol Genet; 2001 Aug 01; 10(16):1673-7. PubMed ID: 11487571
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  • 10. A mutation in the enamelin gene in a mouse model.
    Seedorf H, Klaften M, Eke F, Fuchs H, Seedorf U, Hrabe de Angelis M.
    J Dent Res; 2007 Aug 01; 86(8):764-8. PubMed ID: 17652207
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  • 11. Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta.
    Hart PS, Wright JT, Savage M, Kang G, Bensen JT, Gorry MC, Hart TC.
    Eur J Oral Sci; 2003 Aug 01; 111(4):326-31. PubMed ID: 12887398
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  • 13. Amelogenesis imperfecta in a new animal model--a mutation in chromosome 5 (human 4q21).
    Seedorf H, Springer IN, Grundner-Culemann E, Albers HK, Reis A, Fuchs H, Hrabe de Angelis M, Açil Y.
    J Dent Res; 2004 Aug 01; 83(8):608-12. PubMed ID: 15271968
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  • 19. The enamelin (tuftelin) gene.
    Deutsch D, Palmon A, Dafni L, Catalano-Sherman J, Young MF, Fisher LW.
    Int J Dev Biol; 1995 Feb 01; 39(1):135-43. PubMed ID: 7626400
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  • 20. Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q.
    Kärrman C, Bäckman B, Holmgren G, Forsman K.
    Arch Oral Biol; 1996 Feb 01; 41(8-9):893-900. PubMed ID: 9022927
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