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Journal Abstract Search

129 related items for PubMed ID: 9189622

  • 41. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.
    Lagerström-Fermér M, Nilsson M, Bäckman B, Salido E, Shapiro L, Pettersson U, Landegren U.
    Genomics; 1995 Mar 01; 26(1):159-62. PubMed ID: 7782077
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  • 43. Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.
    Smith CE, Murillo G, Brookes SJ, Poulter JA, Silva S, Kirkham J, Inglehearn CF, Mighell AJ.
    Hum Mol Genet; 2016 Aug 15; 25(16):3578-3587. PubMed ID: 27412008
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  • 47. Detection of a novel mutation in X-linked amelogenesis imperfecta.
    Kindelan SA, Brook AH, Gangemi L, Lench N, Wong FS, Fearne J, Jackson Z, Foster G, Stringer BM.
    J Dent Res; 2000 Dec 15; 79(12):1978-82. PubMed ID: 11201048
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  • 48. Protein-to-protein interactions: criteria defining the assembly of the enamel organic matrix.
    Paine ML, Krebsbach PH, Chen LS, Paine CT, Yamada Y, Deutsch D, Snead ML.
    J Dent Res; 1998 Mar 15; 77(3):496-502. PubMed ID: 9496923
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  • 55. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation.
    Shore RC, Bäckman B, Elcock C, Brook AH, Brookes SJ, Kirkham J.
    Cells Tissues Organs; 2010 Mar 15; 191(4):301-6. PubMed ID: 19923784
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  • 58. The use of animal models to explore amelogenin variants in amelogenesis imperfecta.
    Gibson CW, Kulkarni AB, Wright JT.
    Cells Tissues Organs; 2005 Mar 15; 181(3-4):196-201. PubMed ID: 16612085
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  • 59. Stim1 Regulates Enamel Mineralization and Ameloblast Modulation.
    Furukawa Y, Haruyama N, Nikaido M, Nakanishi M, Ryu N, Oh-Hora M, Kuremoto K, Yoshizaki K, Takano Y, Takahashi I.
    J Dent Res; 2017 Nov 15; 96(12):1422-1429. PubMed ID: 28732182
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  • 60. [Phenotype analysis and the molecular mechanism of enamel hypoplasia].
    Lv P, Gao XJ.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Feb 18; 41(1):121-3. PubMed ID: 19221580
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