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Journal Abstract Search

201 related items for PubMed ID: 37985977

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  • 4. ENAM Mutations Can Cause Hypomaturation Amelogenesis Imperfecta.
    Wang YL, Lin HC, Liang T, Lin JC, Simmer JP, Hu JC, Wang SK.
    J Dent Res; 2024 Jun; 103(6):662-671. PubMed ID: 38716742
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  • 7. AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta.
    Wang SK, Zhang H, Lin HC, Wang YL, Lin SC, Seymen F, Koruyucu M, Simmer JP, Hu JC.
    Int J Mol Sci; 2024 Jun 01; 25(11):. PubMed ID: 38892321
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  • 9. Novel ENAM and LAMB3 mutations in Chinese families with hypoplastic amelogenesis imperfecta.
    Wang X, Zhao Y, Yang Y, Qin M.
    PLoS One; 2015 Jun 01; 10(3):e0116514. PubMed ID: 25769099
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  • 10. 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 01; 52(3):209-17. PubMed ID: 17125728
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  • 11. A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta.
    Barron MJ, Brookes SJ, Kirkham J, Shore RC, Hunt C, Mironov A, Kingswell NJ, Maycock J, Shuttleworth CA, Dixon MJ.
    Hum Mol Genet; 2010 Apr 01; 19(7):1230-47. PubMed ID: 20067920
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  • 13. Alteration of Exon Definition Causes Amelogenesis Imperfecta.
    Kim YJ, Kang J, Seymen F, Koruyucu M, Zhang H, Kasimoglu Y, Bayram M, Tuna-Ince EB, Bayrak S, Tuloglu N, Hu JC, Simmer JP, Kim JW.
    J Dent Res; 2020 Apr 01; 99(4):410-418. PubMed ID: 31999931
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  • 15. Amelogenesis imperfecta in two families with defined AMELX deletions in ARHGAP6.
    Hu JC, Chan HC, Simmer SG, Seymen F, Richardson AS, Hu Y, Milkovich RN, Estrella NM, Yildirim M, Bayram M, Chen CF, Simmer JP.
    PLoS One; 2012 Apr 01; 7(12):e52052. PubMed ID: 23251683
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  • 16. Target gene analyses of 39 amelogenesis imperfecta kindreds.
    Chan HC, Estrella NM, Milkovich RN, Kim JW, Simmer JP, Hu JC.
    Eur J Oral Sci; 2011 Dec 01; 119 Suppl 1(Suppl 1):311-23. PubMed ID: 22243262
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  • 17. Translational Attenuation by an Intron Retention in the 5' UTR of ENAM Causes Amelogenesis Imperfecta.
    Kim YJ, Lee Y, Zhang H, Wright JT, Simmer JP, Hu JC, Kim JW.
    Biomedicines; 2021 Apr 22; 9(5):. PubMed ID: 33922212
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  • 18. Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
    Hart PS, Aldred MJ, Crawford PJ, Wright NJ, Hart TC, Wright JT.
    Arch Oral Biol; 2002 Apr 22; 47(4):261-5. PubMed ID: 11922869
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  • 19. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta.
    Santos MC, Hart PS, Ramaswami M, Kanno CM, Hart TC, Line SR.
    Head Face Med; 2007 Jan 31; 3():8. PubMed ID: 17266769
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